Inhibition of the master growth regulator mTORC1 (mechanistic target of rapamycin complex 1) slows ageing across phyla, in part by reducing protein synthesis. Various stresses globally suppress protein synthesis through the integrated stress response (ISR), resulting in preferential translation of the transcription factor ATF-4. Here we show in C. elegans that inhibition of translation or mTORC1 increases ATF-4 expression, and that ATF-4 mediates longevity under these conditions independently of ISR signalling. ATF-4 promotes longevity by activating canonical anti-ageing mechanisms, but also by elevating expression of the transsulfuration enzyme CTH-2 to increase hydrogen sulfide (H2S) production. This H2S boost increases protein persulfidation, a protective modification of redox-reactive cysteines. The ATF-4/CTH-2/H2S pathway also mediates longevity and increased stress resistance from mTORC1 suppression. Increasing H2S levels, or enhancing mechanisms that H2S influences through persulfidation, may represent promising strategies for mobilising therapeutic benefits of the ISR, translation suppression, or mTORC1 inhibition.
Over the last three decades, genetic and phenotypic analyses of ageing have revealed that across eukaryotes, lifespan can be extended by inhibition of mechanisms that promote growth and proliferation1,2,3. Prominent among these is the serine/threonine kinase complex mTORC1, which coordinates the activity of multiple growth-related processes in response to growth factor and nutrient signals2,3,4. mTORC1 activity can be reduced by genetic perturbations, dietary restriction (DR), or pharmacological interventions such as rapamycin, an mTORC1 inhibitor that increases lifespan from yeast to mice2,3. However, while rapamycin represents a very exciting paradigm for anti-ageing pharmacology, mTORC1 suppression has wide-ranging effects on the organism2,3. Rapamycin is used clinically as an immunosuppressant, and mTORC1 broadly affects metabolism and supports the synthesis of proteins, nucleic acids, and lipids2,3,4. Elucidation of specific mechanisms through which mTORC1 influences longevity is critical not only for understanding the biology of ageing and longevity, but also for the development of molecularly targeted anti-ageing therapies that maintain health.
mTORC1 increases the rates at which numerous different mRNAs are translated, and a hallmark of mTORC1 inhibition is a reduction in overall protein synthesis2,3. Work in the model organisms C. elegans and Drosophila indicates that lifespan extension from mTORC1 inhibition is mediated in part through this global decrease in translation2,5,6. Furthermore, in C. elegans suppression of translation is sufficient to increase both lifespan and stress resistance7,8,9,10,11,12. A mechanistic understanding of how mRNA translation levels affect longevity should therefore provide mechanistic insights into how mTORC1 influences lifespan.
Suppression of new protein synthesis is also an important mechanism through which cells protect themselves from stressful conditions that include nutrient deprivation, and thermal-, oxidative-, and endoplasmic reticulum (ER) stress13,14. Those stresses induce the evolutionarily conserved ISR by activating kinases that phosphorylate and inhibit the translation initiation factor subunit eIF2α, thereby imposing a broad reduction in cap-dependent mRNA translation13,14. This suppression of translation leads in turn to preferential translation of the activating transcription factor ATF4, which mobilizes stress defense mechanisms to re-establish homeostasis13,14. Although the ISR has important protective functions, its effects on longevity and health are complex. In C. elegans, genetic or pharmacological interventions that impair the ISR extend lifespan by inducing preferential translation of selective mRNAs15. In older mice, pharmacological ISR inhibition enhances memory and cognition by allowing protein synthesis to be maintained14,16. On the other hand, in S. cerevisiae the ATF4 ortholog Gcn4 promotes longevity17,18, and in C. elegans hexosamine pathway activation enhances proteostasis through the ISR and ATF-419. It remains to be determined whether ATF4 is required and sufficient to promote metazoan longevity.
Here we have investigated whether and how ATF-4 affects lifespan in C. elegans. We find that ATF-4 but not upstream ISR signalling is required for longevity induced by conditions that inhibit protein synthesis, and that ATF-4 is a pro-longevity factor that extends lifespan when overexpressed on its own. ATF-4 increases lifespan not only by enhancing canonical anti-ageing mechanisms, but also by inducing transsulfuration enzyme-mediated H2S production and therefore levels of protein persulfidation. Importantly, the anti-ageing benefits of mTORC1 suppression depend upon this ATF-4-induced increase in H2S production, further supporting the idea that they derive from lower translation rates and suggesting that increases in ATF-4 and H2S levels may recapitulate these benefits.
ATF-4 responds to translation suppression to increase C. elegans lifespan
We investigated whether C. elegans atf-4 is regulated similarly to mammalian ATF4 at the level of mRNA translation. In mammals, 2–3 small upstream open reading frames (uORFs) within the ATF4 5′ untranslated region (UTR) occupy the translation machinery under normal conditions, inhibiting translation of the downstream ATF4 coding region14,20. By contrast, when translation initiation is impaired by eIF2α phosphorylation, the last uORF is bypassed and ATF4 is translated preferentially14,20. The C. elegans atf-4 ortholog (previously named atf-5) contains two 5′ UTR uORFs (Fig. 1a, Supplementary Fig. 1a, b), deletion of which increases translation of a transgenic reporter21, predicting that translation of the atf-4 mRNA may be increased under conditions of global translation suppression.
We tested this idea in C. elegans that express green fluorescent protein (GFP) driven by the atf-4 upstream region, including the two uORFs (Patf-4(uORF)::GFP, Fig. 1a). Patf-4(uORF)::GFP expression was extremely low under unstressed conditions, but increased when translation was suppressed by treatment with the translation elongation blocker cycloheximide, or RNA interference (RNAi)-mediated knockdown of the tRNA synthase rars-1 (Fig. 1b, Supplementary Fig. 1c–f). Compounds that induce ER stress and elicit the ISR, including tunicamycin (TM) or dithiothreitol (DTT), also strongly induced Patf-4(uORF)::GFP expression (Fig. 1b, Supplementary Fig. 1c, d). By contrast, TM treatment increased atf-4 mRNA levels by only 1.5-fold (Fig. 1c, Supplementary Fig. 1g). Treatment with alpha-amanitin, which blocks transcription, prevented TM from increasing the levels of the atf-4 mRNA but not Patf-4(uORF)::GFP fluorescence (Fig. 1c, d). Together, the data indicate that the Patf-4(uORF)::GFP reporter is regulated post-transcriptionally during ER stress. The endogenous atf-4 mRNA was expressed at steady levels during development and ageing (Supplementary Fig. 1h). By contrast, ribosome occupancy was decreased on its uORFs compared to the coding region as larval development progressed, with the lowest levels apparent during the L4 stage after the body plan has been formed and growth has slowed (Fig. 1e, f). This suggests that the endogenous atf-4 gene is regulated translationally through its uORF region under unstressed conditions, possibly in response to growth-related cues. We conclude that, like mammalian ATF4, C. elegans atf-4 is regulated translationally and preferentially translated upon conditions of reduced protein synthesis (Supplementary Fig. 1i).
Given that ATF-4 is upregulated by translation suppression during the ISR, we hypothesized that it might be important for lifespan extension by reduced protein synthesis. In C. elegans, RNAi-mediated knockdown of various translation initiation factors increases lifespan7,8,9,10,11,12. In the wild type (WT) background, neither a partial21 nor a complete (Fig. 2a, b, Supplementary Data 1) ablation of atf-4 activity decreased lifespan. By contrast, the lifespan increases that occurred in response to knockdown of ifg-1/eIF4G, ife-2/eIF4E, or eif-1A/eIF1AY, were abrogated in atf-4(tm4397) loss-of-function mutants (Fig. 2a, Supplementary Data 1). Similarly, a low dose of cycloheximide extended the lifespan of WT but not atf-4(tm4397) animals (Fig. 2b, Supplementary Data 1). Thus, atf-4 is required for longevity arising from a global reduction in protein synthesis.
The increase in ATF-4 translation that occurs during the canonical ISR is induced by translation suppression that is imposed through increased eIF2α phosphorylation22, but this might not be the case when translation is reduced by directly inhibiting translation initiation or elongation. Supporting this idea, the low dose of cycloheximide that was sufficient to extend lifespan (Fig. 2b) increased ATF-4 expression (Supplementary Fig. 1f), but not eIF2α phosphorylation (Fig. 2c, d). Similarly, depletion of the translation initiation factor ifg-1/eIF4G reduced protein synthesis and dramatically increased expression of Patf-4(uORF)::GFP, but knocking down either ifg-1 or eif-1A only modestly increased eIF2α phosphorylation (Fig. 2e–i). This suggests that treatments that inhibit translation can increase ATF-4 expression without triggering canonical induction of the ISR through eIF2α phosphorylation.
We next investigated whether translation inhibition might increase lifespan independently of this canonical ISR signalling, using a well-characterized eIF2α mutant (eif-2α(qd338)) in which the serine at which inhibitory phosphorylation occurs during the ISR (S49 in C. elegans; S51 in mammals) is mutated to phenylalanine, so that eIF2α phosphorylation and ISR induction are blocked23. A mutation that prevents phosphorylation of this serine partially suppresses lifespan extension from reduced insulin/IGF-1 signalling, suggesting that ISR signalling is important for longevity in this context24. Importantly, the eif-2α(qd338) mutation did not interfere with the atf-4-dependent increase in lifespan that was seen with ifg-1 knockdown (Fig. 2j). We conclude that canonical ISR signalling through eIF2α phosphorylation is not necessarily required for translation inhibition to induce preferential ATF-4 translation or increase lifespan through ATF-4.
ATF-4 mobilises canonical pro-longevity mechanisms
In C. elegans, a limited number of transcription factors have been identified that increase lifespan when overexpressed, including DAF-16/FOXO, HSF-1/HSF1, and SKN-1/NRF1,25. These evolutionarily conserved regulators are generally associated with enhancement of protective mechanisms such as stress resistance, protein folding or turnover, and immunity. To determine whether ATF-4 can actually promote longevity, as opposed to being required generally for health, we investigated whether an increase in ATF-4 levels might extend lifespan. Transgenic ATF-4-overexpressing animals (ATF-4OE) exhibited nuclear accumulation of ATF-4 in neuronal, hypodermal, and other somatic tissues under unstressed conditions (Patf-4::ATF-4(gDNA)::GFP; Supplementary Fig. 2a). TM treatment doubled ATF-4 protein levels (Supplementary Fig. 2b, Source data File), indicating that this ATF-4 transgene responds to environmental stimuli. Importantly, ATF-4 overexpression increased lifespan by 7–44% across >10 independent trials, which included two experiments without 5-Fluoro-2′deoxyuridine (FUdR) and analysis of two independent transgenic lines (Fig. 3a, Supplementary Data 1). ATF-4 overexpression also prolonged healthspan (Fig. 3b, Supplementary Fig. 2c, Supplementary Data 2). We conclude that the elevated activity of the ATF-4 transcriptional program is sufficient to extend lifespan and promote health.
To identify longevity-promoting mechanisms that are enhanced by ATF-4, we used RNA sequencing (RNA-seq) to compare gene expression profiles in atf-4 loss-of-function or ATF-4OE animals compared to WT under non-stressed conditions (Supplementary Fig. 3a, b, Supplementary Data 3). Only a modest number of genes were detectably up- or downregulated by atf-4 loss or overexpression, respectively (Fig. 3c, Supplementary Fig. 3c, d). Notably, ATF-4 overexpression upregulated several small heat shock protein (HSP) genes that are also controlled by HSF-1/HSF (heat shock factor) and DAF-16/FOXO (Fig. 3d), and are typically induced by longevity-assurance pathways1. Each of the ATF-4-upregulated chaperone genes sip-1/CRYAA, hsp-70/HSPA1L, hsp-16.2/HSPB1, and hsp-12.3/HSPB2 was required for lifespan extension from ATF-4 overexpression (Supplementary Fig. 3e; Supplementary Data 1). Translation of atf-4 was increased within minutes by a heat shock (Supplementary Fig. 3f), suggesting that ATF-4 functions in tandem with HSF-1/HSF1. Together, the data suggest that ATF-4 enhances proteostasis mechanisms that have been linked to longevity.
Other findings further linked ATF-4 to longevity-associated mechanisms. ATF-4 overexpression increased expression of the cytoprotective gene nit-1/Nitrilase (Fig. 3d), a canonical target of the xenobiotic response regulator SKN-1/NRF25, along with expression of collagen genes that are typically upregulated by SKN-1/NRF in response to lifespan extension interventions (Fig. 3c)26. The 3 kb predicted promoter regions of many ATF-4-upregulated genes included not only the binding consensus for mammalian ATF4 (-TGATG-)27,28, but also sites for DAF-16, HSF-1, and SKN-1 (Fig. 3d, Supplementary Data 4, 5). Furthermore, many genes that were upregulated by ATF-4 overexpression had been detected in chromatin immunoprecipitation (ChIP) analyses of these transcription factors (Supplementary Fig. 3g, Supplementary Data 5). Each of those transcription factors is critical for lifespan extension arising from suppression of translation10,11, and we determined that they are also needed for longevity conferred by ATF-4 overexpression (Fig. 3e, Supplementary Data 1). ATF-4 overexpression also robustly upregulated two adenine nucleotide translocase genes (ANT; ant-1.3 and ant-1.4, Fig. 3c). The ANT complex is important for transport of ATP from the mitochondrial space into the cytoplasm, as well as for mitophagy29. Both ant-1.3 and ant-1.4 were required for longevity by ATF-4 overexpression (Fig. 3f, Supplementary Data 1). Together, our findings suggest that while the transcriptional impact of ATF-4 may seem limited in breadth, it cooperates with other longevity factors to enhance the activity of multiple mechanisms that protect cellular functions, thereby driving lifespan extension.
ATF-4 increases lifespan through H2S production
To identify ATF-4-regulated genes that are conserved across species and might be particularly likely to have corresponding roles in humans, we queried our ATF-4OE vs WT RNA-seq results, and compared the top 200 significantly upregulated C. elegans genes against 152 mammalian genes that are thought to be regulated directly by ATF428. Seven orthologues of these genes were upregulated in ATF-4OE (Fig. 4a, Supplementary Data 4), four of which encoded components of the reverse transsulfuration (hereafter referred to as transsulfuration) pathway (cth-2/CTH), or associated mechanisms (glt-1/SLC1A2, C02D5.4/GSTO1, and F22F7.7/CHAC1) (Fig. 4b, Supplementary Data 4). The transsulfuration pathway provides a mechanism for utilising methionine to synthesize cysteine and glutathione when their levels are limiting30, but the CTH enzyme (cystathionine gamma-lyase, also known as CGL or CSE) also generates H2S as a direct product. Underscoring the potential importance of the H2S-generating enzyme CTH-2 for ATF-4 function, the levels of its mRNA and protein were each increased by ATF-4 overexpression (Fig. 4c–e, Source data File).
Regulation of amino acid biosynthesis genes is a conserved ATF4 function13, and reduced levels of methionine31 and higher levels of H2S32,33 have each been linked to longevity. We did not detect any differences in the relative abundance of amino acids between ATF-4OE and WT animals (Supplementary Data 6), suggesting that ATF-4 is unlikely to influence longevity by altering amino acid levels. By contrast, ATF-4 overexpression consistently increased H2S production capacity in a cth-2-dependent manner (Fig. 4f, Supplementary Fig. 4a–d). Using the fluorescent H2S probe MeRho-Az34, we also found that H2S levels are reduced by mutation of either atf-4 or cth-2 (Fig. 4g). Taken together, our data indicate that ATF-4 promotes H2S production by acting through CTH-2. The increases in longevity and stress resistance that are conferred by ATF-4 overexpression were abrogated by cth-2 mutation or knockdown (Fig. 4h, Supplementary Fig. 4e, Supplementary Data 1, 7). Similarly, ifg-1/eIF4G knockdown failed to extend lifespan in cth-2 mutant animals (Fig. 4i). We conclude that the increase in H2S production that derived from CTH-2 upregulation is a critical and beneficial aspect of ATF-4 function (Fig. 4j).
An important consequence of increased H2S levels is an increase in the proportion of protein cysteine thiols (-SH) that are converted to persulfides (-SSH)35,36. Redox modification at reactive cysteine residues is critical in growth signalling and other mechanisms36, and in C. elegans thousands of redox-regulated cysteine residues are present in proteins that are involved in translation regulation, lipid and carbohydrate metabolism, stress signalling, and other fundamental biological processes37. Under oxidising conditions, these thiols are readily converted to sulfenic acids (–SOH), which is a reversible and in many cases regulatory modification that can proceed to irreversible and potentially damaging oxidized forms (–SO2H, –SO3H) (Fig. 5a)36. H2S converts –SOH to –SSH in the process called persulfidation, preventing protein overoxidation and thereby preserving protein functions under stressed conditions (Fig. 5a)35,36. The levels of overall protein persulfidation (PSSH) can be visualised in individual animals by using chemical probes and confocal microscopy35. In C. elegans PSSH levels are decreased by mutation of the cth-2 paralog cth-1, suggesting that they depend upon a background level of H2S produced by the latter35. We found that PSSH levels are also reduced by mutation of either cth-2 or atf-4, and are modestly increased by ATF-4 overexpression (Fig. 5b, c). Taken together, our results show that ATF-4 acts through multiple mechanisms to promote stress resistance and longevity, and that a CTH-2-driven increase in H2S production and persulfidation is an essential aspect of this program.
A partial role for ATF-4 in some lifespan extension programs
Given that atf-4 is required for lifespan extension in response to reduced translation, we investigated whether atf-4 and its transcriptional target cth-2 might be generally required for C. elegans longevity. Although ATF4/ATF-4 has been implicated in responses to mitochondrial stress or protein synthesis imbalance27,38, atf-4 was dispensable for the increases in lifespan or oxidative stress resistance that follow from developmental impairment of mitochondrial function (Supplementary Fig. 5a–c, Supplementary Data 1, 8). The extent of lifespan extension by reduced insulin/IGF-1 signalling or germ cell proliferation was decreased by atf-4 mutation but did not depend upon cth-2, consistent with other transsulfuration components and H2S producers being implicated in the latter pathway (Supplementary Fig. 5d, e, Supplementary Data 1)39. The ATF-4-CTH-2 pathway of H2S production may therefore be fully essential specifically when lifespan extension is driven by suppression of protein synthesis.
We also investigated whether the ATF-4-CTH-2 pathway might be involved in longevity induced by DR, which extends lifespan in essentially all eukaryotes. An increase in H2S production capacity has been implicated in mediating some DR benefits in mammals33. In C. elegans, atf-4 was not required for lifespan to be extended by a liquid culture food-dilution DR protocol but was partially required for lifespan extension in the genetic DR-related model eat-2(ad1116) (Supplementary Fig. 5f, Supplementary Data 1). Consistent with these findings, transsulfuration pathway genes other than cth-2 are also partially required for eat-2 lifespan extension33,35, suggesting that in C. elegans other pathways than ATF-4-CTH-2 might also increase H2S production during DR. In mammals, restriction of sulfur-containing amino acids (methionine and cysteine) acts through ATF4 and CTH to boost endothelial H2S levels and angiogenesis40, and multiple longevity interventions increase CTH mRNA levels41, suggesting a possible role for the ATF4-CTH pathway in DR. Supporting this idea, our bioinformatic analysis revealed that CTH mRNA levels were increased in various mouse tissues in response to DR (32/36 profiles), rapamycin (4/6 profiles), or growth hormone insufficiency (8/8 profiles) (Supplementary Fig. 5g, Supplementary Data 11). Therefore, ATF4-induced H2S upregulation is likely to be evolutionarily conserved as a contributor to lifespan extension.
Longevity from mTORC1 suppression is driven by ATF-4 and H2S
Because mTORC1 inhibition increases lifespan in part by reducing protein synthesis2,5,6, we hypothesized that ATF-4 might be activated and required for lifespan extension when mTORC1 is inhibited. The heterodimeric RAG GTPases transduce amino acid signals to activate mTORC1 signalling, and are composed of RAGA-1 and RAGC-1 in C. elegans. mTORC1 is required for C. elegans larval development2, but lifespan can be increased by RNAi-mediated knockdown of either raga-1 or ragc-1 during adulthood, or by a partial loss-of-function mutation of raga-12,3. The former strategy allows mTORC1 activity to be reduced without any associated developmental effects. Adulthood RAG gene knockdown reduced protein synthesis (Fig. 2g, h), consistent with previous studies of mTORC12,3, but did not induce eIF2α phosphorylation (Fig. 2e, f). Under these conditions Patf-4(uORF)::GFP expression was increased robustly even when eIF2α phosphorylation was blocked genetically (Fig. 6a, b, Supplementary Data 9). We conclude that ATF-4 is preferentially translated when mTORC1 activity is reduced and translation rates are low, and that this occurs independently of the canonical ISR mechanism of increased eIF2α phosphorylation.
Importantly, the increases in lifespan extension, stress tolerance, and healthspan that resulted from loss of either raga-1 or ragc-1 function required atf-4 but not phosphorylation of eIF2α (Fig. 6c–f, Supplementary Figs. 2c, 5c, 6a, Supplementary Data 1–2, 7, 8, 10), consistent with our analyses of Patf-4(uORF)::GFP activation. In a single trial, the longevity induced by raga-1 knockdown was blunted by ATF-4 overexpression, suggesting that too much ATF-4 activity might be harmful (Supplementary Fig. 2c), but this has been observed for some other pro-longevity factors25. In summary, the data demonstrate that ATF-4 activation plays an essential role in the benefits of reducing mTORC1 activity.
Having determined that atf-4 is required for mTORC1 suppression to extend lifespan, we were surprised to find that atf-4 was dispensable for lifespan extension from rapamycin treatment, even though rapamycin increased ATF-4 translational reporter expression (Fig. 6g, Supplementary Fig. 6b, Supplementary Data 1, 9). Notably, mTOR is present in both the mTORC1 and mTORC2 complexes (Supplementary Fig. 6c)3. mTORC2 is not as well understood as mTORC1, but it functions in growth signalling and its activation involves binding to the ribosome, suggesting an association with translation regulation (Supplementary Fig. 6c)42. Rapamycin mechanistically inhibits mTORC1 activity, but continuous rapamycin treatment also reduces mTORC2 activity by blocking complex assembly43,44, leading us to investigate the possible involvement of atf-4 in mTORC2 effects. Knockdown of the essential mTORC2 subunit RICT-1 (Rictor) suppressed translation (Fig. 2g, h) and increased Patf-4(uORF)::GFP expression independently of eIF2α phosphorylation (Figs. 2e, f, 6b, Supplementary Data 9). The effects of mTORC2 on C. elegans lifespan are complex, but adulthood RNAi knockdown of rict-1 extends lifespan2,6. Lifespan extension by rict-1 knockdown required atf-4 (Fig. 6h, Supplementary Data 1). Interestingly, however, simultaneous inactivation of mTORC1 and mTORC2 by knocking down both raga-1 and rict-1 extended lifespan independently of atf-4 (Fig. 6i, Supplementary Data 1), as occurred with rapamycin treatment, suggesting that when the activity of both mTOR complexes is suppressed the requirement for atf-4 is relieved.
We investigated whether an ATF-4-mediated increase in H2S production is required for lifespan extension arising from inhibition of mTORC1 or mTORC2. Genetic inhibition of either mTORC1 or mTORC2 increased H2S production capability in an atf-4-dependent manner (Fig. 7a, b, Supplementary Fig. 6d, e). Furthermore, the ATF-4 target gene cth-2 was required for the increased lifespan of animals with reduced mTORC1 or mTORC2 activity (Fig. 7c, d, Supplementary Data 1, 7), suggesting that an ATF-4/CTH-2-mediated increase in H2S production is essential for the benefits of either mTORC1 or mTORC2 inhibition. Knockdown of cth-2 prevented mTORC1 inhibition from increasing stress resistance, further supporting this idea (Extended data Fig. 6f). Interestingly, simultaneous knockdown of raga-1 and rict-1 dramatically increased H2S production capability, and this was greatly reduced but not eliminated in the atf-4 loss-of-function mutant (Supplementary Fig. 6g). This result, together with the dispensable role for ATF-4 in longevity under these conditions, suggests that simultaneous inhibition of both mTOR complexes mobilizes mechanisms that increase lifespan independently of atf-4 and possibly H2S.
The observation that PSSH levels are reduced by lack of either ATF-4 or CTH-2 (Figs. 5b, c, 7e, f) suggests that the ATF-4/CTH-2 pathway might increase persulfidation in response to interventions that boost H2S production through this pathway, including mTORC1 inhibition. Accordingly, in raga-1 mutant adults PSSH levels were elevated in an atf-4-dependent manner (Fig. 7e, f). Taken together, our results show that reduced mTORC1 signalling leads to preferential translation of ATF-4, which acts through CTH-2 to promote stress resilience and healthy ageing by increasing H2S production, and possibly through the resulting increase in PSSH levels across the proteome (Fig. 7g).
We have identified ATF-4, the transcriptional effector of the ISR, as a pro-longevity factor that can extend C. elegans lifespan when overexpressed. Furthermore, conditions that reduce mRNA translation, including mTORC1 inhibition, increase ATF-4 expression without activating canonical ISR signalling that is downstream of eIF2α phosphorylation, and require ATF-4 for lifespan extension. Previous studies revealed that longevity arising from inhibition of translation depends upon preferential translation of protective genes45 and increased transcription of stress defence genes6,10. Our findings link these mechanisms by revealing that preferentially translated ATF-4 cooperates with DAF-16/FOXO, HSF-1/HSF, and SKN-1/NRF to drive protective gene transcription. Viewed alongside the well-documented pro-longevity activity of S. cerevisiae Gcn4 (ATF-4 ortholog)17,18 and evidence that ATF-4 levels and activity are increased in long-lived mouse models46,47, our results indicate that ATF-4 has an ancient and broadly conserved function in promoting longevity.
A striking aspect of our findings is that the longevity and health benefits of ATF-4 depend upon activation of its target transsulfuration pathway gene cth-2, and the resultant increase in H2S production. For many years an understanding of how H2S might promote health and longevity proved to be elusive48, but recent work has implicated increased PSSH and its salutary effects on the proteome35. This modification protects the proteome from the effects of oxidative stress by “rescuing” sulfenylated cysteine residues from the fate of further oxidation (Fig. 5a), declines during ageing, and is increased in other long-lived models35. Here we demonstrated that PSSH levels were increased or decreased by ATF-4 overexpression or cth-2 mutation, respectively, and that mTORC1 inhibition increased PSSH levels through ATF-4 (Figs. 5, 7). These results provide the first definition of a regulatory pathway through which a pro-longevity intervention increases H2S and PSSH levels (Fig. 7g). Although persulfides can be introduced during translation40, our results align with previous evidence that H2S levels may largely determine the extent of this protective cysteine modification35. It was particularly intriguing that the ATF-4/CTH-2 pathway, which boosts H2S formation and PSSH levels, was required for lifespan extension from mTORC1 suppression. This ATF-4/H2S-induced posttranslational shift in PSSH levels could influence many biological functions, including the activity of redox-regulated signalling pathways35,37, making it of interest to elucidate how these modifications mediate the downstream effects of mTORC1 signalling.
Our data add to the evidence that translation suppression is an essential effector of the longevity effects of mTORC1 inhibition5,6. We were surprised, however, to find that mTORC2 knockdown decreased protein synthesis levels and depended upon ATF-4 for lifespan extension (Figs. 2, 6). It will be very interesting to elucidate the mechanisms underlying the former observation. It was also surprising that either simultaneous mTORC1 and mTORC2 inhibition or rapamycin extended lifespan independently of ATF-4, suggesting that when both mTOR complexes are inhibited an independent mechanism compensates for lack of ATF-4. An understanding of how this occurs is likely to identify additional mechanisms that promote longevity.
Our evidence that reduced mTORC1 activity promotes longevity by increasing ATF-4 levels contrasts with mammalian evidence that pharmacological mTORC1 inhibition reduces ATF4 translation20,41. However, those findings were obtained in cultured cells in which mTORC1 activity was elevated genetically or by growth factor treatment, a very different scenario from adult C. elegans in vivo, in which growth has largely ceased and most tissues are post-mitotic. It seems logical that mTORC1 might increase ATF4 translation under the former conditions, given the importance of mTORC1 for translation of many genes and the need to maintain amino acid levels under conditions of high growth activity. On the other hand, it is consistent with our C. elegans results that analyses of mouse liver found that ATF4 protein levels and activity are increased in long-lived models that include rapamycin treatment and nutrient restriction46,47, and that mTORC1 hyperactivation (TSC1 deletion) decreases CTH expression and prevents DR from increasing CTH mRNA levels33. It will be interesting in the future to determine how mammalian mTORC1 influences ATF4 in vivo under different conditions, including analysis of tissues with varying rates of growth and levels of mTORC1 activity.
Although inhibition of mTORC1 has received widespread enthusiasm as an anti-ageing strategy, mTORC1 maintains fundamental processes that include protein synthesis, mRNA splicing, and metabolic pathways2,3,41,49,50, suggesting that not all effects of mTORC1 suppression are necessarily beneficial. Similarly, although conditions that suppress ISR signalling can promote longevity through effects on selective translation15, ISR signalling through eIF2α contributes to lifespan extension from reduced insulin/IGF-1 signalling24, and our results demonstrate that the downstream ISR effector ATF-4 is a potent pro-longevity factor. Furthermore, while pharmacological ISR inhibition preserves cognitive functions during ageing by maintaining protein synthesis14,16, our findings suggest that ISR suppression could reduce levels of H2S, which has been shown to prevent neurodegeneration51,52. In these and other settings, targeted mobilisation of beneficial mechanisms that are activated by ATF-4, including H2S production, might be of promising long-term value. Consistent with this notion, H2S confers many cardiovascular benefits in mammals, including a reduction in blood pressure52,53, and patients suffering from vascular diseases show reduced CTH and H2S levels54, prompting clinical trials of H2S-releasing agents for cardiovascular conditions (NCT02899364 and NCT02278276). It could be of considerable value to examine the potential benefits of ATF4 and H2S in various settings, including the prevention of ageing-related phenotypes and disease.
Caenorhabditis elegans strains were maintained on NGM plates and OP50 Escherichia coli bacteria. LD1499 [Patf-4(uORF)::GFP::unc-54(3’UTR)] was made by Chi Yun (1.8 kb promoter 5′ of atf-4 including both uORFs into pPD95.75)55. All strains used are listed in Supplementary Table 1. The C. elegans work described here was not covered by regulations concerning the ethical treatment of animals and did not require approval by a committee.
Generation of transgenic lines
To construct a translational fusion of ATF-4 with GFP, the plasmid pWM48 (Patf-4::ATF-4(gDNA)::GFP::unc-54(3’UTR)) was generated by introducing the 1.8 kb promoter region 5′ of atf-4 and the atf-4 genomic sequence into pAD1. This construct was used to generate two independent transgenic lines: wbmEx26 [pWM48 (Patf-4::ATF-4(gDNA)::GFP::unc-54(3’UTR), pRF4 (rol-6(su1006))] and wbmEx27 [pWM48 (Patf-4::ATF-4(gDNA)::GFP::unc-54(3’UTR), pRF4 (rol-6(su1006))]. UV irradiation was used for integration resulting in ldIs119 from wbmEx26 and ldIs120-1 from wbmEx27, which were outcrossed 8-10x against N2.
Genomic organisation and alignments
Alignment of C. elegans ATF-4 (T04C10.4, WBGene00000221, 208 amino acids, www.wormbase.org) with human ATF4 (350 amino acids, P18848; www.uniprot.org) or ATF5 (282 amino acids, Q9Y2D1; www.uniprot.org) sequences was performed by T-COFFEE (Version_11.00.d625267). The atf-4 genomic representation was made using Exon‐Intron Graphic Maker (http://wormweb.org/exonintron) from Nikhil Bhatla. DNA and mRNA sequences were from www.wormbase.org (WS258). For human ATF4 GenBank BC008090 mRNA sequence was used. The uORFs were predicted with ApE- A plasmid Editor v2.0.50b3. For amino acid alignments T-COFFEE (Version_11.00.d625267) was used.
Ribosome profiling analysis
Ribosome profiling sequencing data were downloaded from the NCBI Sequence Read Archive (S.R.A.) (http://www.ncbi.nlm.nih.gov/sra/) under accession number SRA055804. Data were analyzed as described54: Data analysis was performed with the help of Unix-based software tools. First, the quality of raw sequencing reads was determined by FastQC (Andrews, S. FastQC (Babraham Bioinformatics, 2010)). Reads were then filtered according to quality via FASTQ for a mean PHRED quality score above 30 (http://usegalaxy.org/u/dan/p/fastq). Filtered reads were mapped to the worm reference genome (Wormbase WS275) using B.W.A. (version 0.7.5), and S.A.M. files were converted into B.A.M. files by SAMtools (version 0.1.19). Read counts were then assigned to each gene or non-coding RNA. Library sizes were normalized using the EdgeR software package and the TMM normalization mode. Ribosome profiling was computed separately for each library as the average normalized read counts across all for normalized libraries. Thus, the mapped reads were determined and normalized based on library size for each transcript in each ribosome profiling library. The ATF-4 coverage data for each larval stage (L1, L2 and L4) and for the whole transcript (including 5’UTR, exons and 3’UTR) were calculated and exported by SAMtools. The stage-specific averaged coverage data for each gene were plotted using R (https://www.r-project.org).
Knockdown by RNA interference
RNAi clones were obtained from the Vidal and Ahringer RNAi libraries. RNAi bacteria cultures were grown overnight in LB with carbenicillin [100 μg/ml] and tetracycline [12.5 μg/ml], diluted to an OD600 of 1, and induced with 1 mM IPTG and spread onto NGM plates containing tetracycline [12.5 μg/ml] and ampicillin [50 μg/ml]. For empty RNAi vector (EV) plasmid pL4440 was used as control.
Manual lifespan assays
Adult lifespan was determined either with or without FUdR as described in Ewald and colleagues56. About 100 L4 C. elegans per strain were picked onto NGM plates containing OP50 bacteria. The next day, C. elegans (day-1-adults) were transferred onto either NGM plates containing 400 µM FUdR and OP50 bacteria or RNAi bacteria. For cycloheximide-treatment lifespan, day-1-adults were transferred on NGM OP50 plates either containing the solvent 0.25% dimethyl sulfoxide (DMSO) alone as a control or cycloheximide (Sigma #C7698) dissolved in 0.25% DMSO. The rapamycin lifespan and liquid DR lifespan assays were performed as described6,56. Animals were classified as dead if they failed to respond to prodding. Exploded, bagged, burrowed, or animals that left the agar were excluded from the statistics. The estimates of survival functions were calculated using the product-limit (Kaplan–Meier) method. The log-rank (Mantel–Cox) method was used to test the null hypothesis and calculate P values (JMP software v.9.0.2.).
Pharyngeal pumping was assessed as described previously26. Pharyngeal pumping was determined by counting grinder movements in 45 second intervals while the animals were feeding on the bacterial lawn.
Puromycin incorporation and detection assays were adapted from previous studies15,57. Approximately 500 L4 animals were resuspended in M9 and transferred to NGM plates containing 50 µM FUdR seeded with RNAi bacteria clones. After 3 days, worms were collected in M9 and then transferred to S-basal medium. Worms were incubated with 4 ml S-Basal that contained OP50 and 0.5 mg/ml puromycin for 1 h. Afterwards, worms were washed with S-basal for three times. Protein extraction and Western blots for puromycin detection were performed as described below.
Quantitative real-time polymerase chain reaction (qRT-PCR) assays
RNA was isolated with Trizol (TRI REAGENT Sigma), DNAse-treated, and cleaned over a column (RNA Clean & ConcentratorTM ZYMO Research). First-strand cDNA was synthesized in duplicate from each sample (Invitogen SuperScript III). SYBR green was used to perform qRT-PCR (ABI 7900). Primers are listed in Supplementary Table 2. For each primer set, a standard curve from genomic DNA accompanied the duplicate cDNA samples. mRNA levels relative to WT control were determined by normalizing to the number of C. elegans and the geometric mean of three reference genes (cdc-42, pmp-3, and Y45F10D.4). At least two independent biological replicates were examined for each sample. For statistical analysis, one-sample t-test, two-tailed, a hypothetical mean of 1 was used for comparison using Prism 6.0 software (GraphPad).
Three independent biological replicates were prepared by using sodium hypochlorite to harvest eggs and overnight L1 arrest in M9 buffer with 10 μg/ml cholesterol to synchronize C. elegans. For each sample, about 20000 C. elegans per strain were allowed to develop to the L4 stage under normal growth conditions on NGM OP50 plates at 20 °C (about 1000 C. elegans per one 10 cm NGM OP50 plate). WT, atf-4(tm4397), and ldIs119 were grown at the same time for each biological replicate. C. elegans were washed from the culturing NGM plates and washed additional 3 times with M9 buffer to wash away the OP50 bacteria. RNA was isolated with Trizol (TRI REAGENT Sigma), DNAse-treated, and cleaned over a column (RNA Clean & ConcentratorTM ZYMO Research). The RNA was sent to Dana-Farber Cancer Institute Center core for sequencing (http://mbcf.dfci.harvard.edu). The RNA Integrity Number (RIN) was then assessed by using the Bioanalyzer 2100 (Agilent Technologies), and only samples with a high RIN score were used to prepare cDNA libraries. All nine samples were multiplexed in a single lane. Single read 50 bp RNA-sequencing with poly(A) enrichment was performed using a HiSeq 2000 (Illumina). We aligned the FASTQ output files to the C. elegans WBcel235 reference genome using STAR 2.4.0j software (http://code.google.com/p/rna-star/) with an average >80% coverage mapping the reads to the genome. The differential gene expression analysis was performed using Bioconductor (http://bioconductor.org) as described in58. Rsubread 1.16.1 featureCounts was used to quantify the mapped reads in the aligned SAM output files. Transcripts with <1 count per million reads were discarded. Counts were scaled to Reads Per Kilobase of transcript per Million mapped reads (RPKM) and deposited as a final output file in (Supplementary Data 3). To analyze the differential expressed genes, we compared atf-4(tm4397), and ldIs119 to wild type using Degust (http://degust.erc.monash.edu) with the following settings: RPKM with minimum 5 counts using edgeR with a false discovery rate (FDR) of 0.1 and an absolute log fold change (FC) of 1 relative to WT. Results are displayed in MA-plots. Functional annotation clustering was performed with DAVID using high classification stringencies (https://david.ncifcrf.gov).
Comparison of RNA sequencing data with mammalian ATF4 target genes
The RNA-sequencing data described in the previous section was subjected to differential expression analysis using the limma package (Smyth, Gordon K. “Limma: linear models for microarray data.” Bioinformatics and computational biology solutions using R and Bioconductor. Springer, New York, NY, 2005. 397-420) available in the programming language R (Team, R. Core. “R: A language and environment for statistical computing.” (2013): 201). The 200 most-upregulated genes that were identified by comparison of ATF4 OE to WT and passed a Benjamini–Hochberg adjusted P-value threshold of 0.1 were analyzed further. Mammalian ATF4-specific gene targets were obtained from Quiros et al.27 and subjected to Ortholist2 to infer C. elegans orthologs based on a comparative genomic meta-analysis59. The intersection of the most-upregulated genes in our ATF4OE to WT expression analysis and the orthologs of the mammalian ATF4 targets is depicted as a heatmap showing all biological replicates (#1-3) (http://www.bioconductor.org/packages/devel/bioc/html/ComplexHeatmap.html). The atf-4 mutant samples are shown separately since the displayed genes were selected based on the comparison between ATF4OE and WT. The absolute expression levels are displayed in a blue (low) to white (medium) to red (high) colour gradient, with genes indicated as gene names or sequence names if the former is not available. Hierarchical clustering was applied to both genes (rows) and samples (columns). Additional information: GO term enrichment yielded a significant (P = 0.047, Benjamini–Hochberg corrected) enrichment of the membrane raft compartment (lec-2, lec-4, lec-5) while no significant enrichment for GO biological process, GO molecular function, KEGG- or REACTOME pathways were found.
Analysis of CTH expression levels in mice
Publicly-available expression datasets were analyzed to quantify the change of CTH expression levels in long-lived compared to normal-lived mice. A selected subset of comparisons displaying CTH upregulation in longevity is depicted in Fig. 6b, while the full table is provided in Supplementary Data 11. Microarray datasets and platform information were obtained from GEO (https://www.ncbi.nlm.nih.gov/geo/) followed by mapping probes to their corresponding genes and sequencing information was obtained from SRA (https://www.ncbi.nlm.nih.gov/sra) and processed using Trim Galore (https://www.bioinformatics.babraham.ac.uk/projects/trim_galore/) and Salmon60. Datasets were centered and scaled, and subsequently, the mean fold change, as well as its standard error, were computed for the CTH gene.
Manual thermotolerance assays
Day-1-adults were placed on NGM OP50 plates (maximum 20 C. elegans per plate) and placed in an incubator at 35 °C. Survival was scored every hour. Animals were classified as dead if they failed to respond to prodding. Exploded animals or animals that moved up on the side of the plate were censored from the analysis. The estimates of survival functions were calculated using the product-limit (Kaplan–Meier) method. The log-rank (Mantel–Cox) method was used to test the null hypothesis and calculate P values (JMP software v.9.0.2.).
Automated survival assays using the lifespan machine
Automated survival analysis was conducted using the lifespan machine described by Stroustrup and colleagues61. Approximately 500 L4 animals were resuspended in M9 and transferred to NGM plates containing 50 µM FUdR seeded with OP50 bacteria, RNAi bacteria supplemented with 100 μg/ml carbenicillin, heat-killed OP50 bacteria, or UV-inactivated E. coli strain NEC937 B (OP50 ΔuvrA; KanR) containing 100 μg/ml carbenicillin. For oxidative stress assays, tBOOH was added to 2 mM to the NGM immediately before pouring and seeding with heat-killed OP50 bacteria. Animals were kept at 20 °C until measurement. Heat and oxidative stress experiments were performed using regular petri dishes sealed with parafilm, while tight-fitting petri dishes (BD Falcon Petri Dishes, 50x9mm) were used for lifespan experiments. Tight-fitting plates were dried without lids in a laminar flow hood for 40 minutes before starting the experiment. Air-cooled Epson V800 scanners were utilized for all experiments operating at a scanning frequency of one scan per 10–30 min. Temperature probes (Thermoworks, Utah, U.S.) were used to monitor the temperature on the scanner flatbed and maintain 20 °C constantly. Animals which left the imaging area during the experiment were censored.
Population survival was determined using the statistical software R62 with the survival and survminer (https://rpkgs.datanovia.com/survminer/) packages. Lifespans were calculated from the L4 stage (=day 0). For stress survival assays the moment of exposure was utilized to define the time point zero of each experiment.
Manual oxidative stress assay (arsenite and tBOOH)
The manual oxidative stress assays were performed as described in detail in the bio-protocol63. L4 worms were manually picked onto fresh OP50 plates. The next day, 10–12 day-one old C. elegans were transferred into 24-well plates containing 1 mL M9 Buffer in quadruplicates for each strain and condition (three wells with sodium arsenite (Sigma-Aldrich) and one well M9 as control). For tBOOH stress assay, about 80 L4 C. elegans per condition were picked onto fresh RNAi plates. Three days later, 20 day-three-old C. elegans were picked onto NGM plates containing 15.4 mM tBOOH (Sigma-Aldrich). The survival was scored every hour until all animas died. Exploded animals were excluded from the statistics. The log-rank (Mantel–Cox) method was used to test the null hypothesis and calculate P values (JMP software v.9.0.2.).
Oxidative stress assay by quantifying movement
C. elegans were collected from NGM plates and washed four times by centrifugation, aspirating the supernatant and resuspending in fresh M9 buffer again. After the final wash, the supernatant was removed, and 10 µl of the C. elegans suspension pipetted into each well of a round-bottom 96-well microplate resulting in ~40–70 animals per well. To prevent desiccation, the wells were filled up immediately with either 30 µl M9, or 30 µl M9 containing 6.7 mM or 18.7 mM sodium arsenite yielding a final arsenite concentration of 0, 5, or 14 mM, respectively. Per C. elegans strain and conditions, we loaded two wells with M9 as control and six wells with either 5 or 14 mM arsenite as technical replicates. The plate was closed, sealed with Parafilm and briefly stirred and then loaded into the wMicrotracker device (NemaMetrix). Data acquisition was performed for 50 h, according to the manufacturer’s instructions. The acquired movement dataset was analyzed using the dplyr (https://dplyr.tidyverse.org/reference/dplyr-package.html, version 1.0.7) and ggplot2 (https://ggplot2.tidyverse.org, version 3.3.5) R packages.
H2S production capacity assay
The H2S production capacity assay was adapted from Hine and colleagues33. Synchronized C. elegans at the L1 stage were placed on RNAi or OP50 food, and harvested from NGM plates as young adults if not specified otherwise. Afterwards, worms were washed four times by centrifugation and resuspension with M9 to remove residual bacteria. Approximately 3000 animals were collected as a pellet and mixed with the same volume of 2× passive lysis buffer (Promega, E194A) on ice. Three freeze-thaw cycles were performed by freezing the samples in liquid nitrogen and thawing them again using a heat block set to 37 °C. Particles were removed by centrifuging at 12,000 × g for 10 min at 4 °C. The pellet was discarded, and the supernatant used further. The protein content of each sample was determined (BCA protein assay, Thermo scientific, 23225) and the sample sequentially diluted with distilled water to the required protein mass range, usually 25–200 µg protein. To produce the lead acetate paper, we submerged chromatography paper (Whatman paper 3M (GE Healthcare, 3030-917)) in a 20 mM lead acetate (Lead (II) acetate trihydrate (Sigma, 215902-25G)) solution for one minute and then let it dry overnight. The fuel mix was prepared freshly by mixing Pyridoxal 5′-phosphate hydrate (Sigma, P9255-5G) and L-Cysteine (Sigma, C7352-25G) in Phosphate Buffered Saline on ice at final concentrations of 2.5 mM and 25 mM, respectively. A 96-well plate was placed on ice, 80 µl of each sample were loaded into each well and mixed with 20 µl fuel mix and subsequently covered using the lead acetate paper. The assay plate was then incubated at 37 °C for 3 h under a weight of approximately 1 kg to keep the lead acetate paper firmly in place. For analysis, the exposed lead acetate paper was imaged using a photo scanner. H2S levels were quantified as the amount of lead sulfide captured on the paper, measured by the integrated density of each well area (Supplementary Data 12). Quantification of H2S production was performed by measuring the integrated density using ImageJ, compared to a well next to it that contained no protein for background.
We used two approaches to monitor H2S levels (see below). With this strategy we detected H2S and not other volatile sulfur compounds. For example, methanethiol is a thiol while H2S is not. Although methanethiol and H2S are each volatile, they have distinct reactivities. The lead acetate assay detects volatile H2S, which generates lead sulfide (which is black). Although this assay has its limitations52, it does not detect methanethiol and was used in the past to distinguish those two molecules in food sample analysis64,65,66. As for the MeRho-Az probe described in the next section, the mechanism of detection is based on a difference in chemical reactivity of H2S vs organic thiols, as tested by the authors who developed the probe34.
Detection of H2S levels by confocal microscopy
For the quantification of H2S levels, worms were synchronized and grown at 20 °C on regular NGM plates seeded with OP50-1 until they reached late L4 stage. At this point, 50 animals per strain were transferred to fresh plates containing fluorescent H2S probe to develop until the next day. Plates with H2S sensor were made by spreading 100 µl of 40 µM MeRho-Az solution (in DMSO; MeRho-Az was synthesized in-house following a previously described protocol34) on the plate surfaces and left to dry for at least 4 h. On the control plates, the same volume of DMSO was spread as a vehicle control. On the day 1 of adulthood, worms were collected by picking, transferred to a tube containing M9 buffer and centrifuged for 1 minute at 40 × g to remove bacteria. Fixation was done in 2% PFA for 20 min at 37 °C followed by incubation with 4% PFA (Sigma Aldrich, #P6148) for 20 min at RT with shaking. PFA was removed and worms were washed 3 times with PBS supplemented with 0.01% Triton and twice with PBS. PBS was removed and mounting media (Ibidi GmbH, Martinsried Germany, ref. 50001) was added directly to the tube. Worm suspension was transferred to the glass slide, covered with a cover slip and sealed with the nail polish. Samples were recorded on Leica TCS SP8 DLC Digital Light Sheet and Confocal microscope using ×10 air objective and VIS (488 nm) laser. Obtained images were first processed with Worm-align open source pipeline for straightening and then analyzed for fluorescence intensity using Cell Profiler software.
Persulfidation detection by confocal microscopy
Worms were synchronized by putting 15 gravid adults to lay eggs for 2 h. Once the animals reached day 1 of adulthood, they were washed off the plates with M9 buffer, collected into a 1.5 ml tube, and centrifuged for 1 min at 400 × g. After 3 washes, M9 was removed, and worms were snap frozen in liquid nitrogen. Samples were defrosted by putting the tubes shortly in the water bath, and 200 µl of 5 mM NBF-Cl (Sigma Aldrich, #163260) in PBS supplemented with 0.01% Triton was immediately added to tubes, followed by incubation at 37 °C for 1 h with shaking. Worms were washed for 1 minute with ice-cold methanol while mixing, followed by 3 washes with PBS-Triton to remove excess NBF-Cl. Methanol/acetone fixation was performed on ice by incubating the samples in the ice-cold methanol for 5 min and then with the ice-cold acetone for 5 min. Acetone was removed, and 3 washes with PBS-Triton were performed. Samples were then again incubated with 5 mM NBF-Cl for 30 min at 37 °C to ensure complete labelling. After the washes were performed in the same order as previously described, worms were incubated with 150 µl of 25 µM DAz-2:Cy-5 click mix (mix was made in-house following a previously described synthetic protocol35) for 1 h at 37 °C with shaking. For the negative control, worms were incubated with 25 μM DAz-2:Cy-5 click mix prepared without DAz-2. Samples were then washed 2 times for 5 minutes with ice-cold methanol and 3 times for 5 minutes with PBS-Triton to remove excess of the preclick product. DAPI staining was performed by incubating the samples with 300 nM DAPI solution in PBS-Triton for 5 min at RT with agitation. After several washes with PBS-Triton and PBS, worms were mounted on glass slide. Samples were recorded on Leica TCS SP8 DLC Digital Light Sheet and Confocal microscope using ×10 air objective and 405 nm laser for DAPI, 488 nm laser for NBF-adducts and 635 nm laser for PSSH. Images were first processed with the Worm-align open source pipeline for straightening and then analyzed for fluorescence intensity using Cell Profiler software.
Scoring of transgenic promoter-driven GFP
For Patf-4(uORF)::GFP, L4 stage transgenic animals were exposed to chemicals by top-coating with 500 μl of each reagent (alpha-amanitin (Sigma #A2263), cycloheximide (Sigma #C7698), tunicamycin (Sigma #T7765), sodium arsenite (Honeywell International #35000)) or control (DMSO or M9 buffer) onto 6 cm NGM OP50 plates for 30 min to 4 hours, except that rapamycin (LC laboratories) was added to the NGM agar as described6. Then GFP fluorescent levels were either (1) scored or (2) quantified. (1) GFP scoring: Transgenic animals were first inspected with a dissecting scope while on still on the plate. GFP intensity was scored in the following categories: 0 = none or very low GFP usually corresponding to untreated control, 1 = low, 2 = medium, and 3 = high GFP fluorescence visible. Animals were washed off chemical treated plates, washed again at least twice, placed on OP50 NGM plates and were picked from there and mounted onto slides and GFP fluorescence was scored using a Zeiss AxioSKOP2 or a Tritech Research BX-51-F microscope with optimized triple-band filter-sets to distinguish autofluorescence from GFP at 40x as described67. GFP was scored as the following: None: no GFP (excluding spermatheca), low: either only anterior or only posterior of the animal with weak GFP induction, Medium: both anterior and posterior of the animal with GFP but no GFP in the middle of the animal. High: GFP throughout the animal. P values were determined by Chi2 test. (2) Quantification of GFP fluorescent levels: Animals were washed off reagent-containing plates, washed an additional two times, then placed into 24-well plates containing 0.06% tetramisole dissolved in M9 buffer to immobilize animals. Fluorescent pictures were taken with the same exposure settings (1 s) at ×10 magnification using an Olympus Cellsens Standard Camera on an inverted microscope. GFP levels were assessed by drawing a line around the animal, measuring mean grey value and using the same area next to it for background using ImageJ. The arbitrary fluorescent value corresponds to mean grey value of the animals minus the background.
About 5000 C. elegans (L4 or day-1-adults indicated in figure legends) were sonicated in lysis buffer (RIPA buffer (ThermoFisher #89900), 20 mM sodium fluoride (Sigma #67414), 2 mM sodium orthovanadate (Sigma #450243), and protease inhibitor (Roche #04693116001)) and kept on ice for 15 min before being centrifuged for 10 min at 15,000 × g68. For equal loading, the protein concentration of the supernatant was determined with BioRad DC protein assay kit II (#5000116) and standard curve with Albumin (Pierce #23210). Samples were treated at 95 °C for 5 min, centrifuged for 1 min at 10,000 × g and 40 μg protein was loaded onto NuPAGE Bis-Tris 10% Protein Gels (ThermoFisher #NP0301BOX), and proteins were transferred to nitrocellulose membranes (Sigma #GE10600002). Western blot analysis was performed under standard conditions with antibodies against Tubulin (1:500, Sigma #T9026), GFP (1:1’000, Roche #11814460001), Cystathionase/CTH (1:2000, abcam #ab151769), Puromycin (1:10,000, Millipore #MABE343), and Phospho-eIF2α (Ser51) (1:1000, Cell Signaling #9721). HRP-conjugated goat anti-mouse (1:2000, Cell Signaling #7076) and goat anti-rabbit (1:2000, Cell Signaling #7074) secondary antibodies were used to detect the proteins by enhanced chemiluminescence (Bio-Rad #1705061). For loading control (i.e., Tubulin) either corresponding samples were run in parallel, membrane was cut if the size of Tubulin and protein of interest were not overlapping, membrane was incubated with loading control after detection of protein of interest on the same blot, or the blot was stripped (indicated in figure legends). For stripping, membranes were incubated for 5 min in acid buffer (0.2 M Glycine, 0.5 M NaCl, pH set to 2 with HCl) and afterwards for 10 min in basic buffer (0.5 M Tris, pH set to 11 with NaOH) and washed with TBS-T before blocking. Quantification of protein levels was determined by densitometry using ImageJ software and normalized to loading control (i.e., Tubulin). Uncropped blots are provided in the Source data File.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The RNA sequencing data in this publication have been deposited in NCBI’s Gene Expression Omnibus and are accessible through GEO Series accession number GSE173799. Figure legends refer to the raw and source data. Source data are provided with this paper.
Kenyon, C. J. The genetics of ageing. Nature 464, 504–512 (2010).
Blackwell, T. K., Sewell, A. K., Wu, Z. & Han, M. TOR Signaling in Caenorhabditis elegans development, metabolism, and aging. Genetics 213, 329–360 (2019).
Liu, G. Y. & Sabatini, D. M. mTOR at the nexus of nutrition, growth, ageing and disease. Nat. Rev. Mol. Cell Biol. 21, 183–203 (2020).
Ben-Sahra, I. & Manning, B. D. mTORC1 signaling and the metabolic control of cell growth. Curr. Opin. Cell Biol. 45, 72–82 (2017).
Bjedov, I. et al. Mechanisms of life span extension by rapamycin in the fruit fly Drosophila melanogaster. Cell Metab. 11, 35–46 (2010).
Robida-Stubbs, S. et al. TOR signaling and rapamycin influence longevity by regulating SKN-1/Nrf and DAF-16/FoxO. Cell Metab. 15, 713–724 (2012).
Pan, K. Z. et al. Inhibition of mRNA translation extends lifespan in Caenorhabditis elegans. Aging Cell 6, 111–119 (2007).
Curran, S. P. & Ruvkun, G. Lifespan regulation by evolutionarily conserved genes essential for viability. PLoS Genet. 3, e56 (2007).
Syntichaki, P., Troulinaki, K. & Tavernarakis, N. eIF4E function in somatic cells modulates ageing in Caenorhabditis elegans. Nature 445, 922–926 (2007).
Wang, J. et al. RNAi screening implicates a SKN-1-dependent transcriptional response in stress resistance and longevity deriving from translation inhibition. PLoS Genet. 6, https://doi.org/10.1371/journal.pgen.1001048 (2010).
Howard, A. C., Rollins, J., Snow, S., Castor, S. & Rogers, A. N. Reducing translation through eIF4G/IFG-1 improves survival under ER stress that depends on heat shock factor HSF-1 in Caenorhabditis elegans. Aging Cell 15, 1027–1038 (2016).
Hansen, M. et al. Lifespan extension by conditions that inhibit translation in Caenorhabditis elegans. Aging Cell 6, 95–110 (2007).
Harding, H. P. et al. An integrated stress response regulates amino acid metabolism and resistance to oxidative stress. Mol. Cell 11, 619–633 (2003).
Costa-Mattioli, M. & Walter, P. The integrated stress response: from mechanism to disease. Science 368, https://doi.org/10.1126/science.aat5314 (2020).
Derisbourg, M. J., Wester, L. E., Baddi, R. & Denzel, M. S. Mutagenesis screen uncovers lifespan extension through integrated stress response inhibition without reduced mRNA translation. Nat. Commun. 12, 1678 (2021).
Sidrauski, C. et al. Pharmacological brake-release of mRNA translation enhances cognitive memory. Elife 2, e00498 (2013).
Mittal, N. et al. The Gcn4 transcription factor reduces protein synthesis capacity and extends yeast lifespan. Nat. Commun. 8, 457 (2017).
Hu, Z. et al. Ssd1 and Gcn2 suppress global translation efficiency in replicatively aged yeast while their activation extends lifespan. Elife 7, https://doi.org/10.7554/eLife.35551 (2018).
Horn, M. et al. Hexosamine pathway activation improves protein homeostasis through the integrated stress response. iScience 23, 100887 (2020).
Park, Y., Reyna-Neyra, A., Philippe, L. & Thoreen, C. C. mTORC1 Balances cellular amino acid supply with demand for protein synthesis through post-transcriptional control of ATF4. Cell Rep. 19, 1083–1090 (2017).
Rousakis, A. et al. The general control nonderepressible-2 kinase mediates stress response and longevity induced by target of rapamycin inactivation in Caenorhabditis elegans. Aging Cell 12, 742–751 (2013).
Pakos-Zebrucka, K. et al. The integrated stress response. EMBO Rep. 17, 1374–1395 (2016).
Kulalert, W., Sadeeshkumar, H., Zhang, Y. K., Schroeder, F. C. & Kim, D. H. Molecular determinants of the regulation of development and metabolism by neuronal eIF2alpha phosphorylation in Caenorhabditis elegans. Genetics 206, 251–263 (2017).
Li, W. J. et al. Insulin signaling regulates longevity through protein phosphorylation in Caenorhabditis elegans. Nat. Commun. 12, 4568 (2021).
Blackwell, T. K., Steinbaugh, M. J., Hourihan, J. M., Ewald, C. Y. & Isik, M. SKN-1/Nrf, stress responses, and aging in Caenorhabditis elegans. Free Radic. Biol. Med. 88, 290–301 (2015).
Ewald, C. Y., Landis, J. N., Porter Abate, J., Murphy, C. T. & Blackwell, T. K. Dauer-independent insulin/IGF-1-signalling implicates collagen remodelling in longevity. Nature 519, 97–101 (2015).
Quiros, P. M. et al. Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals. J. Cell Biol. 216, 2027–2045 (2017).
Han, J. et al. ER-stress-induced transcriptional regulation increases protein synthesis leading to cell death. Nat. Cell Biol. 15, 481–490 (2013).
Hoshino, A. et al. The ADP/ATP translocase drives mitophagy independent of nucleotide exchange. Nature 575, 375–379 (2019).
Zhu, J. et al. Transsulfuration activity can support cell growth upon extracellular cysteine limitation. Cell Metab. 30, 865–876 (2019). e865.
Miller, R. A. et al. Methionine-deficient diet extends mouse lifespan, slows immune and lens aging, alters glucose, T4, IGF-I and insulin levels, and increases hepatocyte MIF levels and stress resistance. Aging Cell 4, 119–125 (2005).
Miller, D. L. & Roth, M. B. Hydrogen sulfide increases thermotolerance and lifespan in Caenorhabditis elegans. Proc. Natl Acad. Sci. USA 104, 20618–20622 (2007).
Hine, C. et al. Endogenous hydrogen sulfide production is essential for dietary restriction benefits. Cell 160, 132–144 (2015).
Hammers, M. D. et al. A bright fluorescent probe for H2S enables analyte-responsive, 3D imaging in live zebrafish using light sheet fluorescence microscopy. J. Am. Chem. Soc. 137, 10216–10223 (2015).
Zivanovic, J. et al. Selective persulfide detection reveals evolutionarily conserved antiaging effects of s-sulfhydration. Cell Metab. 30, 1152–1170 (2019). e1113.
Paul, B. D. & Snyder, S. H. H2S: a novel gasotransmitter that signals by sulfhydration. Trends Biochem Sci. 40, 687–700 (2015).
Meng, J. et al. Global profiling of distinct cysteine redox forms reveals wide-ranging redox regulation in C. elegans. Nat. Commun. 12, 1415 (2021).
Molenaars, M. et al. A conserved mito-cytosolic translational balance links two longevity pathways. Cell Metab. 31, 549–563 (2020). e547.
Wei, Y. & Kenyon, C. Roles for ROS and hydrogen sulfide in the longevity response to germline loss in Caenorhabditis elegans. Proc. Natl Acad. Sci. USA 113, E2832–E2841 (2016).
Akaike, T. et al. Cysteinyl-tRNA synthetase governs cysteine polysulfidation and mitochondrial bioenergetics. Nat. Commun. 8, 1177 (2017).
Valvezan, A. J. & Manning, B. D. Molecular logic of mTORC1 signalling as a metabolic rheostat. Nat. Metab. 1, 321–333 (2019).
Zinzalla, V., Stracka, D., Oppliger, W. & Hall, M. N. Activation of mTORC2 by association with the ribosome. Cell 144, 757–768 (2011).
Sarbassov, D. D. et al. Prolonged rapamycin treatment inhibits mTORC2 assembly and Akt/PKB. Mol. Cell 22, 159–168 (2006).
Lamming, D. W. et al. Rapamycin-induced insulin resistance is mediated by mTORC2 loss and uncoupled from longevity. Science 335, 1638–1643 (2012).
Rogers, A. N. et al. Life span extension via eIF4G inhibition is mediated by posttranscriptional remodeling of stress response gene expression in C. elegans. Cell Metab. 14, 55–66 (2011).
Li, W., Li, X. & Miller, R. A. ATF4 activity: a common feature shared by many kinds of slow-aging mice. Aging Cell 13, 1012–1018 (2014).
Li, W. & Miller, R. A. Elevated ATF4 function in fibroblasts and liver of slow-aging mutant mice. J. Gerontol. A Biol. Sci. Med Sci. 70, 263–272 (2015).
Hine, C., Zhu, Y., Hollenberg, A. N. & Mitchell, J. R. Dietary and endocrine regulation of endogenous hydrogen sulfide production: implications for longevity. Antioxid. Redox Signal 28, 1483–1502 (2018).
Heintz, C. et al. Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans. Nature 541, 102–106 (2017).
Lee, G. et al. Post-transcriptional regulation of de novo lipogenesis by mTORC1-S6K1-SRPK2 signaling. Cell 171, 1545–1558.e18 (2017).
Paul, B. D. & Snyder, S. H. H2S signalling through protein sulfhydration and beyond. Nat. Rev. Mol. Cell Biol. 13, 499–507 (2012).
Filipovic, M. R., Zivanovic, J., Alvarez, B. & Banerjee, R. Chemical biology of H2S signaling through persulfidation. Chem. Rev. 118, 1253–1337 (2018).
Longchamp, A. et al. Amino acid restriction triggers angiogenesis via GCN2/ATF4 regulation of VEGF and H2S production. Cell 173, 117–129 (2018). e114.
Islam, K. N., Polhemus, D. J., Donnarumma, E., Brewster, L. P. & Lefer, D. J. Hydrogen sulfide levels and nuclear factor-erythroid 2-related factor 2 (NRF2) activity are attenuated in the setting of critical limb ischemia (CLI). J. Am. Heart Assoc. 4, https://doi.org/10.1161/JAHA.115.001986 (2015).
Venz, R., Korosteleva, A., Jongsma, E. & Ewald, C. Y. Combining auxin-induced degradation and RNAi screening identifies novel genes involved in lipid bilayer stress sensing in Caenorhabditis elegans. G3 (Bethesda) 10, 3921–3928 (2020).
Ewald, C. Y. et al. NADPH oxidase-mediated redox signaling promotes oxidative stress resistance and longevity through memo-1 in C. elegans. Elife 6, https://doi.org/10.7554/eLife.19493 (2017).
Schmidt, E. K., Clavarino, G., Ceppi, M. & Pierre, P. SUnSET, a nonradioactive method to monitor protein synthesis. Nat. Methods 6, 275–277 (2009).
Steinbaugh, M. J. et al. Lipid-mediated regulation of SKN-1/Nrf in response to germ cell absence. Elife 4, https://doi.org/10.7554/eLife.07836 (2015).
Kim, W., Underwood, R. S., Greenwald, I. & Shaye, D. D. OrthoList 2: a new comparative genomic analysis of human and Caenorhabditis elegans genes. Genetics 210, 445–461 (2018).
Patro, R., Duggal, G., Love, M. I., Irizarry, R. A. & Kingsford, C. Salmon provides fast and bias-aware quantification of transcript expression. Nat. Methods 14, 417–419 (2017).
Stroustrup, N. et al. The Caenorhabditis elegans lifespan machine. Nat. Methods 10, 665–670 (2013).
Gentleman, R. Ia. R. R: a language for data analysis and graphics. J. Computat. Graph. Stat. 5, 299–314 (1996).
Ewald, C. Y., Hourihan, J. M. & Blackwell, T. K. Oxidative Stress Assays (arsenite and tBHP) in Caenorhabditis elegans. Bio. Protoc. 7, https://doi.org/10.21769/BioProtoc.2365 (2017).
Takai, Y. & Asami, T. Formation of methyl mercaptan in paddy soils I. Soil Sci. Plant Nutr. 8, 40–44 (1962).
Farbood, M. I. & MacNEIL, J. H. Limitations of lead acetate for separation of methanethiol and hydrogen sulfide from food systems. J. Food Sci. 43, 139–140 (1978).
Dateo, G. P., Clapp, R. C., Mackey, D. A. M., Hewitt, E. J. & Hasselstrom, T. Identification of the volatile sulfur components of cooked cabbage and the nature of the precursors in the fresh vegetable. J. Food Sci. 22, 440–447 (1957).
Teuscher, A. C. & Ewald, C. Y. Overcoming autofluorescence to assess GFP expression during normal physiology and aging in Caenorhabditis elegans. Bio. Protoc. 8, https://doi.org/10.21769/BioProtoc.2940 (2018).
Hourihan, J. M., Moronetti Mazzeo, L. E., Fernandez-Cardenas, L. P. & Blackwell, T. K. Cysteine sulfenylation directs IRE-1 to activate the SKN-1/Nrf2 antioxidant response. Mol. Cell 63, 553–566 (2016).
Stadler, M., Artiles, K., Pak, J. & Fire, A. Contributions of mRNA abundance, ribosome loading, and post- or peri-translational effects to temporal repression of C. elegans heterochronic miRNA targets. Genome Res. 22, 2418–2426 (2012).
We thank Alex Hofer, Anita Goyala, Sara Schütze, Carolin Imse, Julia Rogers, and Lorenza E. Moronetti Mazzeo for help with scoring lifespan, stress, and GFP assays, Michael Steinbaugh for help with the initial analysis of the RNA sequencing data, Stephanie Lin for contributing to earlier stages of this work, S. Mitani and the National BioResource Project for the atf-4(tm4212 and tm4397) alleles, Mike Crowder for the rars-1(gc47) allele, Chi Yun and David Ron for the Patf-4(uORF)::GFP reporter strain, WormBase for curated gene and phenotype information, Jay Mitchell and Nancy Pohl for comments on the manuscript, and Spalentor and Michael Hall for inspiration. Some strains were provided by the CGC, which is funded by the NIH Office of Research Infrastructure Programs (P40 OD010440). Portions of this research were conducted on the Orchestra High Performance Computer Cluster at Harvard Medical School (NCRR 1S10RR028832-01). Supported by funding from the Swiss National Science Foundation PBSKP3_140135, P300P3_154633, and PP00P3_163898 to C.Y.E. and C.S., and PZ00P3-185927 to A.L., the Leenaards and Novartis Foundation to A.L., ETH Research Grant (ETH-30-16-2) to R.V., the Iacocca Family Foundation to J.M., and the NIH to T.K.B. (R35 GM122610), along with a DRC grant from the NIDDK (P30 DK036836). MRF and DP were funded by the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (Grant Agreement No. 864921). Part of this research was conducted while Collin Y. Ewald was an Ellison Medical Foundation/AFAR Postdoctoral Fellow.
The authors declare no competing interests.
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Statzer, C., Meng, J., Venz, R. et al. ATF-4 and hydrogen sulfide signalling mediate longevity in response to inhibition of translation or mTORC1. Nat Commun 13, 967 (2022). https://doi.org/10.1038/s41467-022-28599-9
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