Telomerase deficiency leads to age-related diseases and shorter lifespans. Inhibition of the mechanistic target of rapamycin (mTOR) delays aging and age-related pathologies. Here, we show that telomerase deficient mice with short telomeres (G2-Terc−/−) have an hyper-activated mTOR pathway with increased levels of phosphorylated ribosomal S6 protein in liver, skeletal muscle and heart, a target of mTORC1. Transcriptional profiling confirms mTOR activation in G2-Terc−/− livers. Treatment of G2-Terc−/− mice with rapamycin, an inhibitor of mTORC1, decreases survival, in contrast to lifespan extension in wild-type controls. Deletion of mTORC1 downstream S6 kinase 1 in G3-Terc−/− mice also decreases longevity, in contrast to lifespan extension in single S6K1−/− female mice. These findings demonstrate that mTOR is important for survival in the context of short telomeres, and that its inhibition is deleterious in this setting. These results are of clinical interest in the case of human syndromes characterized by critically short telomeres.
Telomeres are nucleoprotein structures that protect the ends of chromosomes from being recognized as DNA breaks1,2. Mammalian telomeres are composed of repeats of the TTAGGG DNA sequence bound by a six-protein complex termed shelterin2. Owing to the end-replication problem3 telomeres shorten with each cell division leading to progressive telomere attrition, which is considered one of the mechanisms underlying organismal ageing4,5. When telomeres become critically short, they trigger a persistent DNA damage response (DDR) at the chromosome ends6, chromosomal end-to-end fusions as well as cellular senescence and/or apoptosis, eventually compromising the regenerative capacity of tissues7. Telomerase is a reverse transcriptase capable of synthesizing telomeric repeats de novo, thus elongating telomeres8. Telomerase is composed of a catalytic subunit (TERT) and an associated RNA component (Terc), which serves as a template for the synthesis of TTAGGG repeats8. Telomerase is inactive in adult tissues with the exception of some stem cells compartments; however, this is not sufficient to prevent telomere attrition with age in tissues4,7,9. In contrast, cancer cells aberrantly reactivate telomerase to maintain telomeres and divide indefinitely10. Indeed, TERT is one of the most mutated genes in human cancers11.
Mice genetically deficient for the RNA component of telomerase (Terc−/−) show accelerated telomere shortening and decreased lifespan owing to premature development of age-associated pathologies, being intestinal atrophy the most prevalent12,13,14. These pathologies are anticipated with increasing generations of telomerase-deficient mice owing to inheritance of progressively shorter telomeres with each mouse generation12,13,14. Owing to the fact that telomere maintenance by telomerase is essential for tumor growth, telomerase-deficient mice with short telomeres are cancer resistant, except when in the absence of p53, a potent inducer of cell cycle arrest and/or apoptosis in response to telomere DNA damage15,16.
There are a number of human diseases, known as telomere syndromes, that are characterized by the presence of abnormally short telomeres caused by mutations in telomerase and other telomere genes17,18. These diseases include cases of Dyskeratosis congenita, aplastic anemia, as well as pulmonary and liver fibrosis among other degenerative diseases. Unfortunately, there are no effective therapeutic strategies for the treatment of these diseases in the clinic.
Inhibition of the nutrient sensing pathway regulated by the mechanistic target of rapamycin (mTOR) is considered a therapeutic target to delay aging and age-related pathologies. mTOR is a serine/threonin protein kinase of the PI3K-related family that is part of the PI3K/AKT signaling pathway, and that regulated cell growth and metabolism in response to nutrient availability and hormonal cues19,20. mTOR exists in two distinct complexes, mTORC1 and mTORC2, each with different substrates and activities21,22. mTORC1 downstream targets include ribosomal protein S6 kinase (S6K), eukaryotic initiation factor 4E binding protein-1 (4EBP1), and unc-51 like kinase (ULK1)21,22. mTORC2 downstream substrates include the protein kinase AKT, serum- and glucocorticoid-induced kinase (SGK), and protein kinase C (PKCα)21,22. Of these two complexes, mTORC1 is the only one sensitive to acute rapamycin treatment19,20,23. However, prolonged rapamycin treatment has also been shown to inhibit mTORC2 activity24,25.
Genetic or pharmacological inhibition of mTORC1 with rapamycin, or with rapamycin-derived compounds known as rapalogs, delays aging and can increase the lifespan of yeast, flies, worms, and mice26,27,28,29,30. In mice, rapamycin treatment can increase longevity even in the case of outbreed mouse strains29,30,31. Similarly, deletion of the ribosomal S6 protein kinase 1 (S6K1), a downstream effector of mTORC1, can also increase lifespan in female mice32. Furthermore, evidence suggests that lifespan extension by dietary restriction may also be partly due to inhibition of the mTORC1 function33,34. Rapamycin has also been shown to significantly decrease cancer incidence in wild-type mice as well as to have immunosuppressant properties35,36.
In light of all these beneficial effects of inhibition of the mTORC1 pathway in extending longevity, here we set to address whether rapamycin treatment could also ameliorate the premature aging phenotypes and the decreased longevity of telomerase-deficient mice with short telomeres. This is of relevance as mTOR inhibitors could represent potential treatments for human patients suffering from telomere syndromes.
Here we find that the mTOR pathway is upregulated in telomerase-deficient mice with short telomeres. Unexpectedly, inhibition of the mTOR pathway both by chronic rapamycin treatment and by genetic means decreases longevity of Terc−/− mice, in marked contrast to lifespan extension in similarly treated wild-type mice. Together, these findings demonstrate that hyperactivation of the mTOR pathway in the context of telomerase deficiency and short telomeres is acting as a survival pathway, and that inhibition of this pathway has deleterious effects in this condition.
Chronic rapamycin diet decreases lifespan of Terc −/− mice
To address whether rapamycin treatment could ameliorate premature aging pathologies and decreased longevity in mice with short telomeres, 3-month-old wild type and second-generation telomerase-deficient mice (G2 Terc−/−) in a C57BL/6 genetic background14 were fed with either control chow or chow-containing encapsulated rapamycin at 42 ppm (mg of drug per kg of food)31. Mouse cohorts were followed until the humanitarian endpoint to determine both median and maximum longevity (Fig. 1a). We found that rapamycin treatment increased median longevity of wild-type mice (Terc+/+) by 39%, resulting in a median longevity of 26.5 months in rapamycin-fed Terc+/+ mice compared to only 19 months in the control-fed cohorts (Fig. 1b). This was increased to 58% when considering tumor-free survival (Fig. 1c). In addition, maximum lifespan (mean lifespan of the 10% oldest individuals within each cohort) was also significantly increased, reaching 32 months in the case of rapamycin-fed Terc+/+ mice compared to 29.25 months in control diet-fed Terc+/+ mice (Fig. 1b). When survival curves were separated by sex, rapamycin-fed Terc+/+ females showed an increase in median lifespan of 23% compared to control diet-fed females, while the increase was of 43% in the case of the rapamycin-fed males compared to control-diet Terc+/+ males (Supplementary Fig. 1A, B). We observed similar increases in longevity when considering tumor-free survival (Supplementary Fig. 1C, D).
In contrast to the observed lifespan extension in rapamycin-fed wild-type mice, rapamycin-fed telomerase-deficient mice showed the opposite effect, with a significantly decreased longevity upon rapamycin treatment (Fig. 1b, c). In particular, rapamycin-fed G2 Terc−/− mice showed a 16% decrease in median lifespan compared to control fed G2 Terc−/− mice (Fig. 1b). When G2 Terc−/− mice were separated by sex, median survival was decreased by 19% in the rapamycin-fed G2 Terc−/− males compared to control-fed males, while no changes in median survival were observed between the rapamycin-fed G2 Terc−/− females and the G2 Terc−/− controls (Supplementary Fig. 1A, B). We obtained similar results when considering tumor-free survival (Supplementary Fig. 1C, D). These findings suggest that lifespan extension by rapamycin is abrogated in the context of telomerase deficiency and presence of short telomeres.
One of the main phenotypes of chronic rapamycin treatment in mice is a significant decrease in body weight owing to the known effects of rapamycin on metabolism30. In agreement with this, rapamycin-fed Terc+/+ male and female mice showed a decrease in body weight compared to control diet-fed counterparts (Fig. 1d, e). G2 Terc−/− mice of both sexes started off with smaller body weights compared to wild-type mice (Fig. 1d, e)14. Rapamycin treatment did not further decrease body weight of G2 Terc−/− mice, suggesting that this phenotype associated to rapamycin was abolished in G2 Terc−/− mice (Fig. 1d, e). To study whether G2 Terc−/− mice had upregulated the xenobiotic response pathway resulting in degradation of the rapamycin in the liver and thereby blocking its effects on survival, we measured the rapamycin levels in fed male and female liver samples as well as in fasted and fed male plasma samples (Supplementary Fig. 2A, B). We found similar liver rapamycin levels in Terc+/+ and G2 Terc−/− males and females (Supplementary Fig. 2A). We also detected similar rapamycin plasma levels in Terc+/+ and G2 Terc−/− samples in both nutritional conditions, fasted and fed (Supplementary Fig. 2B). These observations rule out a telomerase-dependent degradation of rapamycin.
Cancer and aging pathologies in rapamycin-fed Terc −/− mice
To further investigate the higher mortality of rapamycin-fed G2 Terc−/− mice, we performed a full histopathological analysis at death point in all mouse cohorts. As expected37, rapamycin-fed wild-type mice showed significantly decreased lymphoma incidence (Fig. 1f), although the incidence of sarcoma was not affected by rapamycin (Fig. 1g). Terc−/− mice are reported to be cancer resistant owing to a tumor suppressive role of short telomeres, with the exception of p53-deficiency16. In agreement with this, control diet-fed G2 Terc−/− mice did not show tumors at their time of death and this was not modified by rapamycin treatment (Fig. 1f, g), thus ruling out that the decreased survival of rapamycin-treated G2 Terc−/− mice was due to loss of the tumor suppressor effect of short telomeres15,16. In agreement with this, the tumor-free survival curves of wild type and G2 Terc−/− mice showed the same trends than the overall survival curves (Fig. 1b, c), also when separated by sex (Supplementary Fig. 1C,D).
We next addressed whether rapamycin treatment could be aggravating one of the main causes of death of G2 Terc−/− mice, i.e., intestinal atrophy14. To this end, we classified the intestinal pathologies present at the mouse endpoint in mild, medium, or severe according to the pathological findings. Mild intestinal lesions are characterized by multifocal epithelia and glandular atrophy that affect up to 20% of the tissue. Medium and severe intestinal lesions show multifocal areas in the mucosa lacking glands and the presence of degenerative epithelial and glandular cystic hyperplasia that affect between 21% and 60% or >61% of the tissue, respectively. We found that 100% of G2 Terc−/− mice presented intestinal atrophy at their endpoint in contrast to the absence of this pathology in wild-type cohorts independently of the diet (Fig. 1h). Rapamycin-fed G2 Terc−/− mice showed less severe intestinal atrophies compared to the control diet cohorts (Fig. 1h). In particular, while 50% of control diet G2 Terc−/− mice presented severe intestinal atrophy, 80% of rapamycin-fed G2 Terc−/− mice showed mild atrophy (Fig. 1h). Although these findings may suggest that rapamycin treatment ameliorates intestinal atrophy in telomerase-deficient mice, the fact that rapamycin-treated G2 Terc−/− mice died at an earlier timepoint (2 months earlier) compared to the control diet cohorts (Fig. 1i) may also explain the lower severity of intestinal atrophy. This notion is supported by the fact that, when we separated mice by sex, only rapamycin-treated G2 Terc−/− males but not females showed significantly decreased severe intestinal lesions (Supplementary Fig. 2C, D), in agreement with the fact that only rapamycin-treated males showed a significantly decreased longevity compared to G2 Terc−/− controls (see Supplementary Figs. 1B and 2C, D).
Together, these findings show that the negative effects of rapamycin treatment on telomerase-deficient mice are not due to increased cancer or to an aggravation of the degenerative pathologies associated to telomerase deficiency and the presence of short telomeres.
Rapamycin treatment does not affect telomere length
The finding that lifespan extension by rapamycin does not occur in telomerase-deficient mice may suggest that the underlying mechanism of lifespan extension by rapamycin may require of telomere maintenance by telomerase, a possibility that has not been addressed before. To address this, we measured telomere length in Terc+/+ and G2 Terc−/− female cohorts subjected either to control or rapamycin diet by performing quantitative telomere fluorescence in situ hybridization (Q-FISH) analysis in mice at the human endpoint. To avoid age-related variations in telomere length within each experimental group, we compared untreated and rapamycin-treated wild type and G2 Terc−/− female mice that died at same age, namely 2 years old in the case of wild-type mice and 6 months old in the case of Terc−/− mice. Telomere length was determined in tissue sections from a highly proliferative tissue such as the intestine and a non-proliferative post-mitotic tissue such as the liver. As expected, G2 Terc−/− mice showed significantly shorter telomeres than the Terc+/+ controls in both tissues. Rapamycin treatment of wild type and G2 Terc−/− mice did not result in significant changes in telomere length in both tissues compared to the control diet-fed cohorts (Fig. 2a, b). Thus, the opposite effects on longevity of the rapamycin diet in wild type and G2 Terc−/− mice cannot be attributed to telomere length changes. To further rule out any potential effects of rapamycin on telomere length, we determined telomere length in a longitudinal manner in several of the individual mice included in the study. To this end, we obtained white blood cells from mice of both genotypes at different time points during treatment (i.e., at 4.5, 6–7, 12–15 and 15–20 months of age, as well as at their endpoint) and measured telomere length by high throughput Q-FISH (HT Q-FISH)38. As expected, Terc−/− mice under a control diet showed a faster rate of telomere shortening in peripheral blood than similarly fed wild-type mice (Fig. 2C). Rapamycin treatment did not alter the rate of telomere shortening in wild-type and telomerase-deficient mice with aging (Fig. 2c). Thus, the increased longevity of rapamycin-treated wild-type mice is not due to a better preservation of telomere length during aging. Similarly, rapamycin treatment did not aggravate telomere shortening in the context of the telomerase-deficient mice.
Rapamycin treatment increases replicative damage
Short telomeres have been previously shown to induce a persistent DDR at chromosome ends, which in turn can trigger senescence and/or apoptosis and limit the regenerative capacity of tissues39. To address whether rapamycin treatment increases DNA damage or exacerbates the proliferative defects in the context of telomerase deficiency, we next studied expression of the DNA damage marker γH2AX, of the senescence markers p53 and p21, and of the apoptosis marker active caspase 3 (AC3) in both Terc+/+ and G2 Terc−/− intestines at the human endpoint. As expected, G2 Terc−/− mice showed more cells positive for these markers in the intestine compared to the wild-type controls (Supplementary Fig. 3A–D). The number of telomere-induced DNA damage foci (TIFs), indicative of telomere damage, was also higher in G2 Terc−/− intestines compared to wild-type mice although the difference did not reach statistical significance (Supplementary Fig. 3E). Rapamycin treatment did not alter the number of cells positive for these markers in the intestines of wild type or G2 Terc−/− mice (Supplementary Fig. 3A–E). We also analyzed the levels of γH2AX, p53, p19, and the mitotic marker pH3 in both Terc+/+ and G2 Terc−/− intestines of healthy young mice subjected to rapamycin treatment for 2 months (Supplementary Fig. 3F–I). Again, we did not find significant differences as the consequence of rapamycin treatment (Supplementary Fig. 3F–I). These results were also confirmed in a non-proliferative tissue such as skeletal muscle in mice treated with rapamycin for 2 months (Supplementary Fig. 3J–L).
Critically short-uncapped telomeres can lead to chromosomal aberrations, including end-to-end chromosome fusions12. We next determined whether rapamycin treatment could affect the occurrence of chromosomal aberrations. For that, we treated both Terc+/+ and G2 Terc−/− mouse embryonic fibroblasts (MEFs) with rapamycin (1 μM, for 24 h) and then performed telomere-FISH analysis. We observed that G2 Terc−/− MEFs showed significantly higher numbers of chromosome fusion events per metaphase compared to wild-type MEFs, and this was not aggravated by rapamycin treatment (Supplementary Fig. 4A, C). One type of telomere aberration are the so-called multitelomeric signals (MTS), i.e. presence of chromosome ends with more than 1 telomere signal, that are associated with telomere fragility owing to DNA replication problems at telomeres40,41. Rapamycin treatment of wild-type MEFs resulted in a significant increase in the MTS frequency (Supplementary Fig. 4B, C), suggestive of increased replicative damage at telomeres. Untreated G2 Terc−/− MEFs showed an already elevated frequency of MTSs; however, this was not further aggravated by rapamycin treatment (Supplementary Fig. 4B, C). These findings suggest that rapamycin treatment increases replicative stress in wild-type MEFs but not in telomerase-deficient MEFs. In support of rapamycin treatment causing increased replicative damage in wild-type cells, we observed that rapamycin-treated wild-type mice showed increased numbers of cells positive for phosphorylated RPA (pRPA) in the intestine, a known marker of replicative stress42,43 (Supplementary Fig. 4D, E). Again, telomerase-deficient mice subjected to a control diet already showed higher pRPA levels in the intestine and this was not further aggravated by rapamycin treatment (Supplementary Fig. 4D, E). Previous in vitro work with human cells showed that rapamycin does not impact on senescence mediated pathways but supress the pro-inflammatory phenotype of senescence cells (SASP) by reducing cytokine expression and IL-6 secretion44. We measured IL-6 plasma levels in our mouse cohorts at the human endpoint and found elevated IL-6 levels in G2 Terc−/− mice compared to wild-type mice, in agreement with a higher number of senescent cells in mice with short telomeres. However, rapamycin treatment did not alter IL-6 plasma levels in either genotype (Supplementary Fig. 4F). Together, these findings suggest that the lower survival of telomerase-deficient mice subjected to a rapamycin diet cannot be attributed to increased levels of global and telomeric DNA damage and increased senescence or apoptosis.
Persistent S6 phosphorylation in Terc −/− mice
As the effects of rapamycin treatment in modulating lifespan seem to be independent of telomere length and of cellular DNA damage, we set to address whether telomerase deficiency may have an impact on the regulation of the mTOR pathway per se. It is well known that the rapamycin-mediated lifespan extension in wild-type mice occurs concomitantly with the downregulation of the mTOR signaling pathway29. To analyze the downregulation levels of mTORC1 signaling by rapamycin, we measured the hepatic levels of the phosphorylated ribosomal protein S6 (pS6), a downstream target of mTORC1, in both Terc+/+ and G2 Terc−/− mice sacrificed at the humane endpoint. As expected, rapamycin-treated Terc+/+ livers showed significantly lower levels of pS6 than the untreated controls (Fig. 3a, b). Strikingly, pS6 levels were not decreased in rapamycin-treated G2 Terc−/− livers compared to the control diet cohorts (Fig. 3a, b). Thus, the ability of rapamycin to inhibit the mTOR pathway is lost or compensated in the context of telomerase-deficient mice.
As the above results were obtained at the mouse endpoint, next, we set out to analyze the mTORC1 pathway activity in young, healthy mice under similar nutritional conditions. To this end, a group of adult (2–6 months old) Terc+/+ and G2 Terc−/− mice fed with rapamycin or control diet were sacrificed after 2 months of treatment (Fig. 3C). To ensure that all mice were in the same nutritional conditions at the time of sacrifice, we fasted them overnight and refed them for 3 h before sacrifice. We analyzed the pS6 levels in the liver, skeletal muscle, and heart by immunohistochemistry. We found that rapamycin-treated wild-type mice showed significant lower pS6 levels compared to control fed counterparts in the three tissues (Fig. 3D–I). Again, rapamycin-fed G2 Terc−/− mice did not show inhibition of pS6 levels in the liver, skeletal muscle, or in the heart compared to control-fed mice (Fig. 3d–i), suggesting that chronic rapamycin treatment does not inhibit mTORC1 in the context of Terc−/− mice.
Inhibition of the mTOR pathway results in glucose intolerance, insulin resistance, and downregulates glycolysis, leading to a reduction in ATP levels25,31,45,46. To address the rapamycin effects on the response to glucose and insulin we performed a glucose (GTT) and insulin (ITT) tolerance tests on these mouse cohorts. We found that wild-type mice treated with rapamycin are more glucose intolerant compared to untreated wild-type mice but this was not seen in G2 Terc−/− (Supplementary Fig. 5A–B). Rapamycin treatment however did not affect the response to exogenously administered insulin in any of the genotypes (Supplementary Fig. 5C). Plasma IGF1 levels were not altered by rapamycin in either wild type or G2 Terc−/− mice (Supplementary Fig. 5D).
mTOR has been shown to impact on mitochondrial biogenesis/autophagy47. Since Terc−/− mice have a decreased mitochondrial function48, we set to address whether rapamycin treatment could be aggravating this phenotype. To this end, we analyzed the mitochondrial content and the ratio of LC3-II/LC3-I as a readout of autophagy47 (Fig. 4). We found that mTORC1 inhibition by chronic rapamycin treatment induces autophagy in wild-type mice but does not alter autophagy levels in the G2 Terc−/− mice, again indicating a lack of effect of chronic rapamycin in mice with short telomeres (Fig. 4a). As expected48, control diet-fed G2 Terc−/− mice presented reduced mtDNA copy number in liver and muscle compared to wild-type controls indicating worsened mitochondrial biogenesis in Terc−/− mice (Fig. 4b, c). Rapamycin treatment led to a decrease in the mtDNA copy number in wild-type liver and muscle samples while no effects were seen in G2 Terc−/− mice (Fig. 4b, c). We also analyzed by western blot the levels of ATP5A, UQCRC2, MTCO1 and SDHB, components of mitochondrial complex V, III, IV, and II, respectively, in liver samples. The results confirmed decreased mitochondria in wild type treated with rapamycin and in G2 Terc−/− mice compared to wild-type control samples and no differences between untreated and rapamycin-treated G2 Terc−/− samples (Fig. 4d). We measured the hepatic levels of ATP after 2 months of rapamycin treatment. In agreement with reduced number of mitochondria, rapamycin-treated Terc+/+ livers showed lower levels of ATP than the untreated controls (Supplementary Fig. 5E). However, no differences in hepatic ATP levels were observed between rapamycin-treated and control-fed G2 Terc−/− mice (Supplementary Fig. 5E), further suggesting that inhibition of the mTOR pathway seemed to be lost or compensated in the context of telomerase-deficient mice under a chronic rapamycin treatment.
To distinguish between these two possibilities, we first tested whether G2 Terc−/− mice were able to inhibit mTORC1 in response to an acute rapamycin treatment. To this end, we performed an acute inhibition of the mTOR pathway by intraperitoneal injection (i.p.) of rapamycin (2 mg/kg body weight) in 4–6 months old Terc+/+ and G2 Terc−/− males followed by mouse sacrifice 2 h later. We found that rapamycin was able to inhibit mTORC1 activity in both Terc+/+ and G2 Terc−/− mice, as indicated by phosphorylation of its downstream target S6 in the liver by western blot (Supplementary Fig. 6). This result indicates that the lack of inhibition of mTORC1 in G2 Terc−/− mice under a chronic rapamycin diet is not due to a failure of rapamycin to directly inhibit mTORC1. Instead, these findings suggest that G2 Terc−/− mice subjected to a chronic rapamycin treatment may be compensating/over-activating the mTORC1 pathway to minimize deleterious effects of rapamycin treatment in the context of short telomeres, such as the decreased survival observed in rapamycin-treated G2 Terc−/− mice (Fig. 1b).
Further supporting this possibility, we observed significantly higher hepatic levels of pS6 in G2 Terc−/− mice compared to wild-type mice even under a control diet (Fig. 3d, e). Similarly, in the acute rapamycin treatment experiment, control 4–6 months old G2 Terc−/− mice showed significantly higher hepatic pS6 levels than wild-type mice in the absence of rapamycin treatment (Supplementary Fig. 6), further supporting the notion that telomerase-deficient mice have an hyperactivated mTORC1 pathway. These unexpected findings open the interesting possibility that Terc−/− mice have a hyperactivated mTORC1 pathway in response to short telomeres and that this activation is acting as a survival pathway since inhibition of mTORC1 by chronic rapamycin treatment results in decreased longevity.
Hyperactivation of mTOR in Terc −/− mice
To address whether Terc−/− mice had a hyperactivated mTOR pathway, we performed RNA sequencing to analyze gene expression profiles in the liver of adult (2–6 months old) Terc+/+ and G2 Terc−/− male mice fed with either rapamycin or control diet during 2 months (Fig. 3c; GEO database GSE127475). Gene-set enrichment analysis (GSEA) of control fed G2 Terc−/− versus control fed Terc+/+ confirmed that the mTOR pathway is upregulated in telomerase-deficient mice compared to wild-type mice (Fig. 5a; Supplementary Table 1), in agreement with higher hepatic levels of pS6 in G2 Terc−/− mice (Fig. 3d, e; Supplementary Fig. 6). In addition, we found that other metabolic pathways related to the mTOR pathway22 were also upregulated in G2 Terc−/− mice compared to wild-type mice, including insulin signaling, cholesterol and fatty acid biosynthesis, PPAR signaling, apoptosis, peroxisome, pyruvate metabolism, the PI3K–AKT pathway, glycolysis, lysosome, as well as the RAS and HIF-1 signaling pathways (Fig. 5a, b; Supplementary Table 1).
Further supporting hyperactivation of the mTOR pathway in Terc−/− mice, GSEA analysis of rapamycin-treated G2 Terc−/− versus rapamycin-treated Terc+/+ also showed upregulation of the mTOR pathway in the telomerase-deficient mice compared to wild-type mice, even under the rapamycin treatment (Fig. 5c; Supplementary Table 2).
Next, we compared all pathways (KEGG database) found upregulated in control fed G2 Terc−/− versus control fed Terc+/+ to all the pathways found downregulated both in rapamycin-treated G2 Terc−/− versus control-fed G2 Terc−/− and in rapamycin-treated wild type versus control-fed wild-type (Fig. 6a). We detected a total of 22 common pathways at the intersection of these comparisons, including several mTOR-related pathways (Fig. 6a; Supplementary Tables 1–4). Interestingly, GSEA analysis showed that control fed G2 Terc−/− also had a significant upregulation of the mTOR upstream regulator pathways PI3K–AKT and Ras signaling compared to wild-type controls (Fig. 6a–c; Supplementary Table 1)22,49,50,51,52, further supporting hyperactivation of the mTOR pathway in Terc−/− mice. Furthermore, GSEA analysis showed that control fed G2 Terc−/− also had a significant upregulation of the mTOR downstream PPAR signaling pathway compared to the wild-type controls (Fig. 6a, d; Supplementary Table 1)53,54,55,56.
Interestingly, rapamycin treatment leads to downregulation of PI3K–AKT, Ras and PPAR signaling pathways in both G2 Terc−/− and Terc+/+ compared to control-fed counterparts (Fig. 6a, e–j; Supplementary Tables 3 and 4).
Together, these results demonstrate that Terc−/− mice with short telomeres have higher basal activation levels of the mTOR pathway, as well as other related metabolic pathways, suggesting an increased metabolism. In turn, this increased metabolism might be a survival response to telomerase deficiency and presence of short telomeres, as supported by the fact that inhibition of these metabolic routes by rapamycin negatively impacts in the survival of telomerase-deficient mice.
Reduced survival in Terc −/− S6K1 −/− mice
Our results suggest a previously unnoticed role of the mTOR pathway in promoting organismal survival in the absence of telomerase activity and in the presence of short telomeres. To further demonstrate this notion using mouse genetics, we deleted the downstream target of mTOR, the ribosomal protein S6 kinase 1 (S6K1), known to positively regulate protein synthesis and cell growth57,58. We generated a double-knockout mouse model for S6k1 and Terc by crossing S6k1−/− mice59 with Terc+/− heterozygous mice14 to obtain G1 Terc−/− S6k1−/− and G1 Terc−/− S6k1+/+. Successive Terc−/− S6k1+/− intercrosses generated the G2–G3 Terc−/− S6k1−/− and G2–G3 Terc−/− S6k1+/+ experimental groups.
Deletion of S6k1 was previously known to lead to a 19% increase in median longevity in female mice32. In agreement with this, we observed an 8% increase in median survival of Terc+/+ S6k1−/− females compared to wild-type counterparts (Fig. 7a), while no differences in longevity were found between the Terc+/+ S6k1−/− and Terc+/+ S6k1+/+ males (Fig. 7b) or when considering both sexes together (Fig. 7c). With increasing generations of Terc−/− we observed a negative effect of S6K1 abrogation, and G3 Terc−/− S6k1−/− female mice showed a significant 20% decrease in median lifespan compared to G3 Terc−/− S6k1+/+ counterparts (Fig. 7a). A similar trend was observed in male mice although the difference did not reach statistical significance (Fig. 7b). These findings demonstrate that S6K1 is a survival signal in the context of telomerase deficiency as S6k1 deficiency further decreases longevity in G3 Terc−/− females. The fact that the decreased survival was observed with increasing mouse generations of Terc−/− mice indicates that it is the presence of short telomeres what causes deleterious effects of S6K1 inhibition in these mice.
We analyzed the levels of pS6 in the livers of these mouse cohorts. In agreement with previous work, S6K1 deficiency does not affect the pS6 levels in either Terc+/+ or in G2 Terc−/− backgrounds (Supplementary Fig. 7A)59,60. To address whether the effect of S6K1 deficiency on mouse survival was dependent on telomere maintenance, we measured telomere length in these mouse cohorts by performing Q-FISH analysis in mice at the human endpoint. To avoid age-related variations in telomere length within each experimental group, we compared S6k1+/+ and S6k1−/− within each Terc−/− generation groups that died at same age, namely 22–26 months old in the case of Terc+/+ mice, 13–18 month old in G2 Terc−/− mice, and 12–14 month old in the case of G3 Terc−/− mice. Telomere length was determined in tissue sections from the intestine and the liver (Supplementary Fig. 7B–C). The results show that S6K1 deficiency does not affect mean telomere length neither in a highly proliferative tissue as the intestine nor in a post-mitotic tissue such as the liver, indicating that S6K1 function in mouse survival is independent of telomere maintenance. As expected, successive generations of Terc−/− mice present progressively shorter telomeres (Supplementary Fig. 7B, C). These findings demonstrate that the increased longevity of S6k1−/−Terc+/+ female mice is not due to a better preservation of telomere length during aging mediated by telomerase. Similarly, we did not see that S6K1 deficiency aggravated telomere shortening in the context of Terc−/− mice (Supplementary Fig. 7B, C). Histopathological analysis at human endpoint of the different mouse cohorts showed a decreased lymphoma incidence in S6k1−/−Terc+/+ mice compared to S6k1+/+Terc+/+ mice while no difference was observed in the frequency of sarcoma (Supplementary Fig. 7D–E). These results are in agreement with the reduced lymphoma observed in Terc+/+ mice treated with rapamycin (Fig. 1f), confirming a protective role of mTORC1 pathway inhibition in lymphoma development. We did not observe significant difference in the incidence of intestinal degenerative pathologies developed by late generation (G2–G3) Terc−/− mice independently of S6K1 status (Supplementary Fig. 7F), also in agreement with the results obtained in rapamycin-treated G2 Terc−/− (Fig. 1h).
In summary, these findings provide genetic support for our observation that chronic rapamycin treatment has deleterious effects in the context of telomerase deficiency and presence of short telomeres.
Telomerase deficiency and presence of telomeres shorter than normal have been shown to induce premature loss of the regenerative capacity of tissues and premature aging pathologies both in mice and humans17,18. In humans, mutations in telomerase or telomere-maintenance genes are at the origin of the so-called telomere syndromes, which are characterized by the presence of critically short telomeres. These diseases include Hoyeral–Hreidarsson syndrome, dyskeratosis congenita, pulmonary fibrosis, aplastic anemia, and liver fibrosis17,18. Although telomerase-activation strategies are being studied as potential treatment for these diseases61,62,63, currently there are still no curative therapeutic options for these patients.
The mechanistic target of rapamycin or mTOR is a serine/threonine protein kinase of the PI3K family that functions as a master regulator of cell growth and metabolism in response to nutrients and hormonal cues. Inhibition of mTOR pathway has been shown to extend lifespan and delay age-related pathologies across many different species, from yeast to mice64. Rapamycin is the first mTOR inhibitor to be isolated and has extensively been studied in its ability to extend lifespan, decrease cancer, and have immunosuppressant effects29,30,35.
Here, we set to address a functional interaction between the mTOR pathway and telomeres, by testing whether mTOR inhibition could also extend the lifespan of telomerase-deficient mice with short telomeres29,30,31,65 as this could serve as a proof of principle that inhibition of the mTOR pathway may be a therapeutic approach for the so-called telomere syndromes. Unexpectedly, we found that rapamycin treatment decreases the longevity of telomerase-deficient mice with short telomeres, in marked contrast to very significant lifespan extension in the case of wild-type controls. Of interest, wild-type mice treated with rapamycin showed an increase that is higher than that reported by other authors using the same diet in genetically heterogeneous mice31. These discrepancies may be due to different genetic backgrounds or to different housing conditions66 and/or to the fact that we initiated the rapamycin treatment at 3 months of age instead of 9 months of age31.
We rule out here that decreased survival of rapamycin-fed Terc−/− mice is due to effects of rapamycin aggravating telomere shortening or telomere aberrations in the absence of telomerase. Intriguingly, we found that rapamycin increased telomere fragility in wild-type mice, which could be suggestive of increased replicative stress associated to rapamycin treatment, an observation which warrants future research.
The fact that rapamycin treatment was deleterious in the context of short telomeres and telomerase deficiency suggests that the mTOR pathway maybe acting as a pro-survival pathway in this setting. In support of this, we find that Terc−/− mice show a hyperactivated mTORC1 pathway. RNA sequencing further demonstrated hyperactivation of the mTOR pathway and of related metabolic pathways in Terc−/− mice. Among the upregulated pathways, we find insulin signaling, cholesterol and fatty acid biosynthesis, PPAR signaling, peroxisome, pyruvate metabolism, the PI3K–AKT pathway, glycolysis, lysosome, RAS signaling, and HIF-1 signaling pathway. Of interest, we also previously observed upregulation of the PI3K/AKT pathway in the skin of Terc−/− mice with extremely short telomeres67. Upregulation of these pathways in mice with short telomeres is consistent with the need of higher energy consumption in these mice, lower mitochondria content48, and the notion that they are acting as survival pathways in the context of telomerase deficiency and presence of short telomeres (see model in Fig. 8). Indeed, rapamycin treatment significantly inhibited the PI3K/AKT and Ras pathways upstream of mTOR in both wild type and telomerase-deficient mice, indicating that the inhibition of these survival pathways is underlying the detrimental effects of rapamycin treatment in the setting of short telomeres (see model in Fig. 8).
We further validate this notion using mouse genetics, and demonstrate here that female mice doubly deficient in telomerase and S6 kinase 1 of third generation (G3) also show a decreased survival in contrast to increased survival of S6K1-deficient females compared to wild-type controls (see model in Fig. 8). The fact that the decreased survival was only observed in the third generation of the telomerase-deficient mice indicates that it is not the lack of active telomerase but the presence of very short telomeres what causes the synthetic lethality with S6K1 deficiency. While chronic rapamycin affects negatively already in G2 Terc−/−, the effects of S6K1 deficiency become apparent in G3. This discrepancy might be explained by different telomere length due to different genetic backgrounds of both mouse colonies and by the fact that S6K1 and S6K2 present functional compensation and redundancy59,60.
Finally, the fact that mTORC1 activity has been found elevated in the livers of old mice68 suggests that this may be a general phenomenon associated not only with telomere-induced aging but also with physiological aging.
Mice, husbandry, and diet preparation
All mice were generated and maintained at the Animal Facility of the Spanish National Cancer Research Centre (CNIO) under specific pathogen-free conditions in accordance with the recommendation of the Federation of European Laboratory Animal Science Associations (FELASA). C57BL/6 Terc+/− heterozygous female and male mice14 were intercrossed to obtain Terc+/+ and first-generation (G1) Terc−/− litters. G1 Terc−/− mice were then intercrossed to obtain second-generation (G2) Terc−/− offspring. All the mice included in survival studies were fed control chow from the weaning onwards. At 3 months of age, mice were divided in two groups, one of them continued with control chow and the other were changed to chow-containing encapsulated rapamycin at 42 ppm (mg of drug per kg of food). All mice were followed until their endpoint. Rapamycin was microencapsulated by Rapamycin Holdings Inc. (San Antonio, Texas) using a spinning disk atomization coating process with the enteric coating material Eudragit S100 (Rohm Pharma)31. This coating material increases the fraction of rapamycin that survives the food preparation process; moreover, being water soluble only, it allows the drug to be released in the small intestine rather than in the stomach, then increasing its absorption. Encapsulated rapamycin was then incorporated into 5LG6 mouse chow (TestDiet, London, UK). Food and water were provided ad libitum and measurements of the body weight were performed monthly.
For studying the molecular hepatic response to chronic rapamycin treatment in healthy young mice, male and female Terc+/+ and G2 Terc−/− mice were given rapamycin diet or control diet and sacrificed after the time indicated. To ensure that all mice were in the same nutritional conditions at the time of sacrifice, we fasted them overnight and refed them (ad libitum, rapamycin or control chow) for 3 h before sacrifice.
The response to an acute rapamycin treatment was performed by intraperitoneal injection (i.p.) of rapamycin (2 mg/kg body weight) in 4–6 months old Terc+/+ and G2 Terc−/− males followed by mouse sacrifice 2 h later. To measure the basal activation of the mTOR pathway in absence of treatment, these mice were fasted overnight and refed for 1 h (ad libitum) before sacrifice, to ensure similar nutritional conditions.
To generate double-knockout mice for S6k1 and Terc, S6k1−/− mice59 were first crossed with Terc+/− heterozygous mice14 to obtain G1 Terc−/− S6k1+/+, G1 Terc−/− S6k1+/−, and G1 Terc−/− S6k1−/− litters. G1 Terc−/− S6k1+/− mice were then intercrossed to generate G2 Terc−/− S6k1+/+, G2 Terc−/− S6k1+/−, and G2 Terc−/− S6k1−/− litters. G3 Terc−/− S6k1+/+ and G3 Terc−/− S6k1−/− mice were then obtained by mating G2 Terc−/− S6k1+/− female and male mice. Food (Harlan Laboratories) and water were provided ad libitum.
All animal experiments were approved by the Ethical Committee (CEIyBA) (IACUC.040-2014, CBA_20_2014) and performed in accordance with the guidelines stated in the International Guiding Principles for Biomedical Research Involving Animals, developed by the Council for International Organizations of Medical Sciences (CIOMS).
Tissue samples were fixed in 10% buffered formalin, dehydrated, embedded in paraffin wax, and sectioned at 2.5 mm. Tissue sections were deparaffinized in xylene and re-hydrated through a series of graded ethanol until water and then stained with hematoxylin and eosin for pathological examination. The classification of the intestinal pathologies was performed by a trained pathologist in a blinded manner. Mild intestinal lesions are characterized by multifocal epithelia and glandular atrophy that affect up to 20% of the tissue. Medium and severe intestinal lesions show multifocal areas in the mucosa lacking glands and the presence of degenerative epithelial and glandular cystic hyperplasia that affect between 21% and 60% or > 61% of the tissue, respectively.
Immunohistochemistry was performed on deparaffinized tissue sections processed with 10 mM sodium citrate (pH 6.5) cooked under pressure for 2 min. Slides were washed in water, then in Buffer TBS-0.5% Tween 20, blocked with peroxidase, washed with TBS-0.5% Tween 20, and blocked with fetal bovine serum. Intestine or skeletal muscle sections were incubated with the following primary antibodies: mouse monoclonal to phospho-histone H2AX (ser139) (1:15,000; JBW301, Millipore, Cat#05-636), rat monoclonal to p21 (1:10; 291H/B5), rat monoclonal to p53 (1:100; POE316 A/E9), rabbit polyclonal to phospho-histone H3 (1:500; Abcam, Cat#ab5168), rat monoclonal to p19 ARF (1:50; 5-C3-1, Santa Cruz Biotechnology, Cat#sc-32748), or rabbit polyclonal to AC3 cleaved-caspase 3 (Asp175) (1:300; Cell Signaling Technology, Cat#9661). Liver, heart, and skeletal muscle sections were incubated with a rabbit polyclonal anti-phospho-S6 ribosomal protein (Ser240/244) (1:500; Cell Signaling Technology, Cat#2215). Slides were then incubated with secondary antibodies conjugated with peroxidase from DAKO. Sections were lightly counterstained with hematoxylin and analyzed by light microscopy. The number of positive cells for phospho-H2AX, p21, p53, and AC3 was quantified by eye using an Olympus AX70 microscope. The percentage of tissue area positive for phospho-S6 was quantified with the AxioVision microscope software from Carl Zeiss.
Immunofluorescence analyzes on tissue sections
For immunofluorescence analyzes, intestine sections were fixed in 10% buffered formalin (Sigma) and embedded in paraffin. After deparaffinization and citrate antigen retrieval, sections were permeabilized with 0.5% Triton in PBS and blocked with 1% BSA and 10% Australian FBS (GENYCELL) in PBS. The antibodies were applied overnight in antibody diluents with background reducing agents (Invitrogen). Intestinal foci of replication protein A (RPA) were detected using a rat polyclonal antibody anti-RPA 32 (1:200; 4E4 Cell Signaling Technology) and further incubated with 555 Alexa Fluor goat anti-rat antibody. A double immunofluorescence using primary antibodies against 53BP1 (1:500; Novus Biologicals) and TRF1 (1:500; homemade rat monoclonal) was performed to assay for telomeric DNA damage. Slides were then incubated with 488 Alexa Fluor goat anti-rabbit and 555 Alexa Fluor goat anti-rat secondary antibodies. Immunofluorescence images were obtained using a confocal ultraspectral microscope (Leica TCS-SP5). Quantifications were performed with Definiens software.
Rapamycin quantification in liver and blood samples
Liver samples were mechanically homogenized in water with 2.8 mm ceramic bead in a Precellys® Tissue Homogenizer. Homogenate was incubated in ultrasonic bath 10 min and centrifuged at 15,000g for 5 min. Blood samples were centrifuged twice at 500g for 10 min. The supernatants were placed into a 96-well solid phase extraction plate and proteins were precipitated with 4 volumes of 0.1% formic acid/acetonitrile. Vacuum was applied and sample recovered into a 96-well plate and analyzed by specific LC-MS/MS method in MRM mode. MS analysis was conducted using a Qtrap 5500 mass spectrometer (AB Sciex). The turboionspray source (TIS) was operated in positive ionization mode. Instrument control and data analysis were performed using Analyst® 1.6.2 application software from Applied Biosystems. Mass spectrometry parameters optimization of rapamycin was carried out by a standard stock dilution (100.0 ng/mL) in methanol through direct infusion into the mass spectrometer. Data from rapamycin were first acquired in full scan from the range between m/z 50 and 1000 in order to identify the most suitable parent ion for MS/MS experiments. The sodium adduct [M+Na]+ at m/z 936.348 was selected as the parent ion for rapamycin and fragmented. The MS/MS parent ion was still preserved as a parent in the MS2 spectrum and it was together with two other daughter ions at m/z 409.300 and 453.300. Chromatographic separation was carried out on an Agilent 1100 series LC system consisting of a G1312A binary pump, a G1379A degasser, and an ALSG1330B refrigerated autosampler. Isocratic mobile phase composed of 80% acetonitrile in water mixture containing 0.1% of formic acid at a flow rate of 0.6 mL/min was used. As sample injection volume of 20.0 μL was used, and total analytical run time was 6.0 min. LC-MS/MS chromatographic separation was achieved on a Phenomenex Gemini 3 µm C18 110 Å analytical column. The column oven temperature was maintained at 40 °C. Twenty microliters were injected on LC-MS/MS. Ionspray source temperature 350 °C and ionspray voltages 5500 V were optimized. Mass spectrometry data were acquired in positive ion mode and processed using Analyst software (version 1.6.2, AB Sciex). An LC-MS/MS analysis, rapamycin was eluted at retention time 3.2 min. The curtain gas (CUR) was at 40.0 psi, the nebulizer source gas 1 at 40.0 psi, and the turbo ion source gas 2 at 45.0 psi was utilized. Declustering potential 105.0 V and entrance potential 10.0 V were optimized. The collision gas pressure was medium. The collision energy 75.0 V for rapamycin and the collision cell exit potential 10.0 V. Known concentration standards were prepared by spiking control liver and plasma homogenates with the rapamycin at different concentrations.
To perform GTT and ITT, mice were i.p. injected with 2 g of glucose/kg of body weight and 0.75 U insulin/kg of body weight (Eli Lilly; Humalog Insulin), respectively. In the case of GTT mice were previously fasted for 16 h. Blood glucose levels were measured with the StatStrip® glucose meters from Nova biomedical at the indicated times after injection. Plasma IGF1, insulin, and IL-6 levels were determined by ELISA with m/rIGF-1 ELISA mediagnost; Ultra Sensitive Mouse Insulin ELISA kit (Crystal Chem) and Quantikine ELISA, mouse IL-6 (R&D systems), respectively. ATP levels in liver lysates were measured by colorimetric assay (OD 570 nm) with the ATP Assay Kit (Abcam, ab83355).
Mitochondrial copy number
Relative mtDNA content were obtained by the comparative Ct method48. Briefly, we measured by qPCR the mtDNA genes Cytb and Nd1 and the nuclear DNA (nucDNA) gene H19. The mtDNA averaged Ct values were subtracted from the nucDNA averaged Ct values obtaining the ΔCt (ΔCt = nucDNA Ct−mtDNA Ct). The relative mitochondrial DNA content was calculated by raising 2 to the power of ΔCt and then multiplying by 2 (mtDNA copy number = 2 × 2ΔCt). Primers were used as follows: CYTB-F 5′-ATTCCTTCATGTCGGACGAG-3′, CYTB-R 5′-ACTGAGAAGCCCCCTCAAAT-3′, ND1-F 5′-AATCGCCATAGCCTTCCTAACAT-3′, ND1-R 5′-GGCGTCTGCAAATGGTTGTAA-3′, H19-F 5′-GTACCCACCTGTCGTCC-3′, H19-R 5′-GTCCACGAGACCAATGACTG-3′.
Quantitative fluorescence in situ hybridization (Q-FISH) in tissue samples
For Q-FISH, paraffin-embedded intestine or liver sections were deparaffinized and fixed with 4% formaldehyde, followed by digestion with pepsine/HCl and a second fixation with 4% formaldehyde. Slides were dehydrated with increasing concentrations of EtOH (70%, 90%, 100%) and incubated with the telomeric (TTAGGG) probe labeled with Cy3 at 85 °C for 3 min followed by 2 h at room temperature in a wet chamber. The slides were extensively washed with 50% formamide and 0.08% TBS-Tween 20 (ref. 9). Confocal microscopy was performed at room temperature with a laser-scanning microscope (TSC SP5) using a Plan Apo 63Å-1.40 NA oil immersion objective (HCX). Maximal projection of z-stack images generated using advanced fluorescence software (LAS) were analyzed with Definiens XD software package. The DAPI images were used to detect telomeric signals inside each nucleus.
To analyze telomere length in a longitudinal manner in individual mice, white blood cells were obtained from mice of both genotypes at different time points during treatment (4.5, 6–7, 12–15, and 15–20 months of age, as well as at their endpoint). High throughput (HT)-Q-FISH on peripheral blood leukocytes was done using 120–150 μL of blood as described above38. Confocal images were captured using the Opera High-Content Screening system (Perkin Elmer). Telomere length values were analyzed using individual telomere spots (>10,000 telomere spots per sample).
Fluorescence in situ hybridization in primary MEFs
Primary embryonic fibroblasts (MEFs) were isolated from 13.5-day-old wild type or G2 Terc−/− embryos according to standard protocols. Briefly, after removal of the head and organs the whole embryo was minced and rinsed in ice-cold PBS, incubated in trypsin/EDTA (Gibco, Grand Island, NY) before dissociating in complete medium. Cells were plated in 10 cm plates containing DMEM plus 10% FBS and incubated at 37 °C. Colcemide (Gibco) was added at a concentration of 0.1 µg/mL during the last 4 h and cells were harvested by centrifugation. After hypotonic swelling in sodium citrate (0.03 M) for 25 min at 37 °C, the cells were fixed in methanol:acetic acid (3:1). After two additional changes of fixative, the cell suspension was dropped on wet, clean slides and dried overnight. FISH was performed as described above69. Metaphases images were captured with the Leica LAS-X software (3.4.2. version). The incidence of chromosomal aberrations per metaphase was determined by eye.
Protein extracts were obtained using Nuclear Cytosolic Fractionation Kit (Biovision) or RIPA extraction buffer and protein concentration was determined using the Bio-Rad DC Protein Assay (Bio-Rad). Up to 20 μg of protein per extract were separated in SDS–polyacrylamide gels by electrophoresis. After protein transfer onto nitrocellulose membrane (Whatman), the membranes were incubated with the following primary antibodies: anti-S6 ribosomal protein (1:1000; Cell Signaling Technology, Cat#2217), anti-phospho-S6 ribosomal protein (Ser 240/244) (1:1000; Cell Signaling Technology, Cat#2215), anti LC3 (1:500; Cell Signaling Technology, Cat#2775), anti-β-actin (Sigma), anti-SMC1 (1:2000; Bethyl), anti-total OXPHOS (1:500; Total OXPHOS Rodent WB Antibody Cocktail, Cell Signaling Technology, Cat#110413). Antibody binding was detected after incubation with a secondary antibody coupled to horseradish peroxidase using chemiluminescence with ECL detection KIT (GE Healthcare). Protein-band intensities were measured with ImageJ software.
Gene expression analysis
Total RNA was extracted from liver of Terc+/+ and G2 Terc−/− male mice fed rapamycin or control diet during 2 months. RNA samples from three independent mice per condition were analyzed. Total RNA (1 µg) was used for the RNAseq experiment. The PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA, and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters with the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, Cat. No. E7760). This kit incorporates dUTP during second-strand cDNA synthesis and therefore only the cDNA strand generated during first-strand synthesis is sequenced. Adapter-ligated library was completed by PCR with Illumina PE primers. The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina sequencer (HiSeq Sequencing v4 Chemistry). Single-end sequenced reads were analyzed with the nextpresso pipeline70. Briefly, sequencing quality was checked with FastQC v0.11.7 (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/), reads were aligned to the mouse reference genome (NCBI37/mm9, https://ccb.jhu.edu/software/tophat/igenomes.shtml) with TopHat-2.0.10 (ref. 71) using Bowtie 1.0.0 (ref. 72) and Samtools 0.1.19 (ref. 73), allowing two mismatches and 20 multihits. Read counts were obtained with HTSeq-count v0.6.1 (ref. 74), using the mouse NCBI37/mm9 gene annotation from https://ccb.jhu.edu/software/tophat/igenomes.shtml. Differential expression was performed with DESeq2 (ref. 75), using a 0.05 FDR. GSEAPreranked76 was used to perform gene set enrichment analysis for several gene signatures on a pre-ranked gene list, setting 1000 gene set permutations. Only those gene sets with significant enrichment levels (FDR q-value <0.25) were considered.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Blackburn, E. H. Structure and function of telomeres. Nature 350, 569–573 (1991).
De Lange, T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes Dev. 19, 2100–2110 (2005).
Watson, J. D. Origin of concatemeric T7 DNA. Nat. N. Biol. 239, 197–201 (1972).
Harley, C. B., Futcher, A. B. & Greider, C. W. Telomeres shorten during ageing of human fibroblasts. Nature 345, 458–460 (1990).
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M. & Kroemer, G. The hallmarks of aging. Cell https://doi.org/10.1016/j.cell.2013.05.039 (2013).
D’Adda Di Fagagna, F. et al. A DNA damage checkpoint response in telomere-initiated senescence. Nature https://doi.org/10.1038/nature02118 (2003).
Blasco, M. A. A. Telomere length, stem cells and aging. Nat. Chem. Biol. https://doi.org/10.1038/nchembio.2007.38 (2007).
Greider, C. W. & Blackburn, E. H. Identification of a specific telomere terminal transferase activity in tetrahymena extracts. Cell 43, 405–413 (1985).
Flores, I. et al. The longest telomeres: a general signature of adult stem cell compartments. Genes Dev. 22, 654–667 (2008).
Shay, J. W. & Wright, W. E. Telomerase therapeutics for cancer: challenges and new directions. Nat. Rev. Drug Discov. https://doi.org/10.1038/nrd2081 (2006).
Vinagre, J. et al. Frequency of TERT promoter mutations in human cancers. Nat. Commun. https://doi.org/10.1038/ncomms3185 (2013).
Blasco, M. A. et al. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell 91, 25–34 (1997).
Lee, H. W. et al. Essential role of mouse telomerase in highly proliferative organs. Nature 392, 569–574 (1998).
Herrera, E. et al. Disease states associated with telomerase deficiency appear earlier in mice with short telomeres. EMBO J. 18, 2950–2960 (1999).
Chin, L. et al. p53 deficiency rescues the adverse effects of telomere loss and cooperates with telomere dysfunction to accelerate carcinogenesis. Cell 97, 527–538 (1999).
Gonzalez-Suarez, E., Samper, E., Flores, J. M. & Blasco, M. A. Telomerase-deficient mice with short telomeres are resistant to skin tumorigenesis. Nat. Genet. 26, 114–117 (2000).
Armanios, M. & Blackburn, E. H. The telomere syndromes. Nat. Rev. Genet. 13, 693–704 (2012).
Martínez, P. & Blasco, M. A. Telomere-driven diseases and telomere-targeting therapies. J. Cell Biol. https://doi.org/10.1083/jcb.201610111 (2017).
Brown, E. J. et al. A mammalian protein targeted by G1-arresting rapamycin-receptor complex. Nature https://doi.org/10.1038/369756a0 (1994).
Sabatini, D. M., Erdjument-Bromage, H., Lui, M., Tempst, P. & Snyder, S. H. RAFT1: a mammalian protein that binds to FKBP12 in a rapamycin-dependent fashion and is homologous to yeast TORs. Cell https://doi.org/10.1016/0092-8674(94)90570-3 (1994).
Laplante, M. & Sabatini, D. M. MTOR signaling in growth control and disease. Cell https://doi.org/10.1016/j.cell.2012.03.017 (2012).
Saxton, R. A. & Sabatini, D. M. mTOR signaling in growth, metabolism, and fisease. Cell https://doi.org/10.1016/j.cell.2017.02.004 (2017).
Dos, D. S. et al. Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton. Curr. Biol. https://doi.org/10.1016/j.cub.2004.06.054 (2004).
Sarbassov, D. D. et al. Prolonged Rapamycin Treatment Inhibits mTORC2 Assembly and Akt/PKB. Mol. Cell https://doi.org/10.1016/j.molcel.2006.03.029 (2006).
Lamming, D. W. et al. Rapamycin-induced insulin resistance is mediated by mTORC2 loss and uncoupled from longevity. Science. https://doi.org/10.1126/science.1215135 (2012)
Vellai, T. et al. Influence of TOR kinase on lifespan in C. elegans. Nature https://doi.org/10.1038/426620a (2003).
Kapahi, P. et al. Regulation of lifespan in Drosophila by modulation of genes in the TOR signaling pathway. Curr. Biol. https://doi.org/10.1016/j.cub.2004.03.059 (2004).
Matt Kaeberlein et al. Regulation of yeast replicative life span by TOR and Sch9 in response to nutrients. Science https://doi.org/10.1126/science.1115535 (2012).
Harrison, D. E. E. et al. Rapamycin fed late in life extends lifespan in genetically heterogeneous mice. Nature 460, 392–395 (2009).
Miller, R. A. et al. Rapamycin, but not resveratrol or simvastatin, extends life span of genetically heterogeneous mice. J. Gerontol. Ser. A Biol. Sci. Med. Sci. https://doi.org/10.1093/gerona/glq178 (2011).
Miller, R. A. et al. Rapamycin-mediated lifespan increase in mice is dose and sex dependent and metabolically distinct from dietary restriction. Aging Cell https://doi.org/10.1111/acel.12194 (2014).
Selman, C. et al. Ribosomal protein S6 kinase 1 signaling regulates mammalian life span. Science https://doi.org/10.1126/science.1177221 (2009).
Kaeberlein, M. & Kennedy, B. K. Ageing: A midlife longevity drug? Nature https://doi.org/10.1038/460331a (2009).
Sun, L., Sadighi Akha, A. A., Miller, R. A. & Harper, J. M. Life-span extension in mice by preweaning food restriction and by methionine restriction in middle age. J. Gerontol. Ser. A Biol. Sci. Med. Sci. https://doi.org/10.1093/gerona/glp051 (2009).
Martel, R. R., Klicius, J. & Galet, S. Inhibition of the immune response by rapamycin, a new antifungal antibiotic. Can. J. Physiol. Pharmacol. https://doi.org/10.1139/y77-007 (1977).
Garber, K. Rapamycin’s resurrection: a new way to target the cancer cell cycle. J. Natl. Cancer Inst. https://doi.org/10.1093/jnci/93.20.1517 (2001).
Lorberg, A. & Hall, M. N. TOR: the first 10 years. Curr. Top. Microbiol. Immunol. 279, 1–18 (2004).
Canela, A., Vera, E., Klatt, P. & Blasco, M. A. High-throughput telomere length quantification by FISH and its application to human population studies. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.0609367104 (2007).
Martínez, P. & Blasco, M. A. Telomeric and extra-telomeric roles for telomerase and the telomere-binding proteins. Nat. Rev. Cancer 11, 161–176 (2011).
Martínez, P. et al. Increased telomere fragility and fusions resulting from TRF1 deficiency lead to degenerative pathologies and increased cancer in mice. Genes Dev. 23, 2060–2075 (2009).
Sfeir, A. et al. Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication. Cell 138, 90–103 (2009).
Cortez, D., Guntuku, S., Qin, J. & Elledge, S. J. ATR and ATRIP: partners in checkpoint signaling. Science https://doi.org/10.1126/science.1065521 (2001).
Zou, L. & Elledge, S. J. Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes. Science https://doi.org/10.1126/science.1083430 (2003).
Laberge, R. M. et al. MTOR regulates the pro-tumorigenic senescence-associated secretory phenotype by promoting IL1A translation. Nat. Cell Biol. https://doi.org/10.1038/ncb3195 (2015).
Schieke, S. M. et al. The mammalian target of rapamycin (mTOR) pathway regulates mitochondrial oxygen consumption and oxidative capacity. J. Biol. Chem. https://doi.org/10.1074/jbc.M603536200 (2006).
Sun, Q. et al. Mammalian target of rapamycin up-regulation of pyruvate kinase isoenzyme type M2 is critical for aerobic glycolysis and tumor growth. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.1014769108 (2011).
Bartolomé, A. et al. MTORC1 regulates both general autophagy and mitophagy induction after oxidative phosphorylation uncoupling. Mol. Cell. Biol. https://doi.org/10.1128/mcb.00441-17 (2017).
Missios, P. et al. Glucose substitution prolongs maintenance of energy homeostasis and lifespan of telomere dysfunctional mice. Nat. Commun. https://doi.org/10.1038/ncomms5924 (2014).
Inoki, K., Li, Y., Zhu, T., Wu, J. & Guan, K. L. TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling. Nat. Cell Biol. https://doi.org/10.1038/ncb839 (2002).
Manning, B. D., Tee, A. R., Logsdon, M. N., Blenis, J. & Cantley, L. C. Identification of the tuberous sclerosis complex-2 tumor suppressor gene product tuberin as a target of the phosphoinositide 3-kinase/Akt pathway. Mol. Cell https://doi.org/10.1016/S1097-2765(02)00568-3 (2002).
Ballif, B. A., Blenis, J., Roux, P. P., Anjum, R. & Gygi, S. P. Tumor-promoting phorbol esters and activated Ras inactivate the tuberous sclerosis tumor suppressor complex via p90 ribosomal S6 kinase. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.0405659101 (2004).
Ma, L., Chen, Z., Erdjument-Bromage, H., Tempst, P. & Pandolfi, P. P. Phosphorylation and functional inactivation of TSC2 by Erk: implications for tuberous sclerosis and cancer pathogenesis. Cell https://doi.org/10.1016/j.cell.2005.02.031 (2005).
Kim, J. E. & Chen, J. Regulation of peroxisome proliferator-activated receptor-γ activity by mammalian target of rapamycin and amino acids in adipogenesis. Diabetes https://doi.org/10.2337/diabetes.53.11.2748 (2004).
Zhang, H. H. et al. Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway. PLoS ONE https://doi.org/10.1371/journal.pone.0006189 (2009).
Rosen, E. D. & MacDougald, O. A. Adipocyte differentiation from the inside out. Nat. Rev. Mol. Cell Biol. https://doi.org/10.1038/nrm2066 (2006).
Laplante, M. & Sabatini, D. M. Regulation of mTORC1 and its impact on gene expression at a glance. J. Cell Sci. https://doi.org/10.1242/jcs.125773 (2013).
Hara, K. et al. Amino acid sufficiency and mTOR regulate p70 S6 kinase and eIF-4E BP1 through a common effector mechanism. J. Biol. Chem. https://doi.org/10.1074/jbc.273.23.14484 (1998).
Fingar, D. C., Salama, S., Tsou, C., Harlow, E. & Blenis, J. Mammalian cell size is controlled by mTOR and its downstream targets S6K1 and 4EBP1/eIF4E. Genes Dev. https://doi.org/10.1101/gad.995802 (2002).
Shima, H. Disruption of the p70s6k/p85s6k gene reveals a small mouse phenotype and a new functional S6 kinase. EMBO J. https://doi.org/10.1093/emboj/17.22.6649 (2002).
Pende, M. et al. S6K1−/−/S6K2−/− Mice exhibit perinatal lethality and rapamycin-sensitive 5’-terminal oligopyrimidine mRNA translation and reveal a mitogen-activated protein kinase-dependent S6 kinase pathway. Mol. Cell. Biol. https://doi.org/10.1128/mcb.24.8.3112-3124.2004 (2004).
Bernardes de Jesus, B. et al. Telomerase gene therapy in adult and old mice delays aging and increases longevity without increasing cancer. EMBO Mol. Med. 4, 691–704 (2012).
Bär, C. et al. Telomerase expression confers cardioprotection in the adult mouse heart after acute myocardial infarction. Nat. Commun. https://doi.org/10.1038/ncomms6863 (2014).
Povedano, J. M. et al. Therapeutic effects of telomerase in mice with pulmonary fibrosis induced by damage to the lungs and short telomeres. Elife https://doi.org/10.7554/eLife.31299 (2018).
Johnson, S. C., Rabinovitch, P. S. & Kaeberlein, M. MTOR is a key modulator of ageing and age-related disease. Nature https://doi.org/10.1038/nature11861 (2013).
Wilkinson, J. E. et al. Rapamycin slows aging in mice. Aging Cell https://doi.org/10.1111/j.1474-9726.2012.00832.x (2012).
Brust, V., Schindler, P. M. & Lewejohann, L. Lifetime development of behavioural phenotype in the house mouse (Mus musculus). Front. Zool. https://doi.org/10.1186/1742-9994-12-S1-S17 (2015).
Schoeftner, S. et al. Telomere shortening relaxes X chromosome inactivation and forces global transcriptome alterations. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.0909265106 (2009).
Sengupta, S., Peterson, T. R., Laplante, M., Oh, S. & Sabatini, D. M. MTORC1 controls fasting-induced ketogenesis and its modulation by ageing. Nature https://doi.org/10.1038/nature09584 (2010).
Samper, E., Goytisolo, F. A., Slijepcevic, P., Van Buul, P. P. W. & Blasco, M. A. Mammalian Ku86 protein prevents telomeric fusions independently of the length of TTAGGG repeats and the G-strand overhang. EMBO Rep. https://doi.org/10.1093/embo-reports/kvd051 (2000).
Pisano, D. G., Graña, O., Glez-Peña, D., Rubio-Camarillo, M. & Fdez-Riverola, F. Nextpresso: next generation sequencing expression analysis pipeline. Curr. Bioinform. 13, 583–591 (2017).
Trapnell, C. et al. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nat. Protoc. https://doi.org/10.1038/nprot.2012.016 (2012).
Langmead, B., Trapnell, C., Pop, M. & Salzberg, S. L. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. https://doi.org/10.1186/gb-2009-10-3-r25 (2009).
Li, H. et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics https://doi.org/10.1093/bioinformatics/btp352 (2009).
Anders, S., Pyl, P. T. & Huber, W. HTSeq-A Python framework to work with high-throughput sequencing data. Bioinformatics https://doi.org/10.1093/bioinformatics/btu638 (2015).
Love, M. I., Huber, W. & Anders, S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. https://doi.org/10.1186/s13059-014-0550-8 (2014).
Subramanian, A. et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.0506580102 (2005).
We thank Sara Kozma for kindly sharing the S6K1−/− mouse. We thank A. Efeyan and A. Ortega for helpful discussions. We are indebted to D. Megias for confocal microscopy analysis. Research in the Blasco Lab is funded by the Spanish Ministry of Economy and Competitiveness Projects (SAF2013-45111-R and SAF2015-72455-EXP), the Comunidad de Madrid Project (S2017/BMD-3770), the World Cancer Research (WCR) Project (16-1177), and the Fundación Botín (Spain).
The authors declare no competing interests.
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Ferrara-Romeo, I., Martinez, P., Saraswati, S. et al. The mTOR pathway is necessary for survival of mice with short telomeres. Nat Commun 11, 1168 (2020). https://doi.org/10.1038/s41467-020-14962-1
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