Transposons are generally kept silent by epigenetic mechanisms including DNA methylation. Here, we identified a pair of H arbinger transposon-derived proteins (HDPs), HDP1 and HDP2, as anti-silencing factors in Arabidopsis. hdp1 and hdp2 mutants displayed an enhanced silencing of transgenes and some transposons. Phylogenetic analyses revealed that HDP1 and HDP2 were co-domesticated from the Harbinger transposon-encoded transposase and DNA-binding protein, respectively. HDP1 interacts with HDP2 in the nucleus, analogous to their transposon counterparts. Moreover, HDP1 and HDP2 are associated with IDM1, IDM2, IDM3 and MBD7 that constitute a histone acetyltransferase complex functioning in DNA demethylation. HDP2 and the methyl-DNA-binding protein MBD7 share a large set of common genomic binding sites, indicating that they jointly determine the target specificity of the histone acetyltransferase complex. Thus, our data revealed that HDP1 and HDP2 constitute a functional module that has been recruited to a histone acetyltransferase complex to prevent DNA hypermethylation and epigenetic silencing.
Transposable elements (TEs) are mobile, repetitive genetic elements that represent large portions of eukaryote genomes1,2. Transposons are generally viewed as “selfish” DNA or “parasitic” elements due to the deleterious effects on host genomes. However, emerging evidence suggests that TEs play key roles in the evolution of gene function and regulation2,3,4. Moreover, an increasing number of host genes that are derived or “domesticated” from transposons have been uncovered5. The identification of these genes and elucidation of their functions in host genomes are of great interest for understanding how transposons contribute to host adaptation.
In plants, TEs are regulated by epigenetic silencing mechanisms, including DNA methylation and histone modifications6,7. DNA methylation plays important roles in multiple processes, including genome stability, cell responses to environmental stimuli and organ development6,7,8,9. DNA methylation levels and patterns are dynamic and determined by two reversible reactions: DNA methylation and demethylation8,10. DNA demethylation can occur through passive or active pathways, or a combination of both. In comparison with passive DNA demethylation, specific enzymatic reactions are required for active DNA demethylation8. In Arabidopsis, active DNA demethylation is carried out by a family of bifunctional DNA glycosylases/lyases, including ROS1, Demeter (DME), DME-like 2 (DML2) and DML3. Loss-of-function mutations in ROS1 cause DNA hypermethylation and enhanced transcriptional gene silencing (TGS) of transgenes and endogenous genes and TEs8,11,12,13. However, how the active DNA demethylation machinery is recruited to specific genomic loci is poorly understood in plants and animals. Increased DNA Methylation 1 (IDM1), a histone acetyltransferase, is required for a subset of ROS1-mediated DNA demethylation13. Recently, IDM1 was shown to be in a complex with IDM2, IDM3 and a methyl-DNA-binding protein, MBD713,14,15,16. Mutations of any components in this IDM complex result in enhanced transgene silencing and DNA hypermethylation of specific genomic regions including TEs. MBD7 recognizes densely methylated CpG regions and contributes to the recruitment of IDM1 to specific genomic loci14. However, MBD7 alone cannot determine the target specificity of IDM1 since the complex does not associate with all genomic regions that have high DNA methylation14. Therefore, there are likely additional components in the IDM complex that may determine the targeting specificity of the complex jointly with MBD7.
Harbinger transposons are DNA transposons which usually encode a DDE transposase and a SANT/Myb/trihelix domain-containing DNA-binding protein17,18. Domestications of Harbinger transposons have been reported in mammals, Drosophila and Arabidopsis17,19,20, suggesting their evolutionary importance. However, their biological functions are unclear. Here, using a forward genetic screen, we identified a pair of Harbinger transposon-derived anti-silencing factors, HDP1 and HDP2 in Arabidopsis. Loss-of-function mutations in these two genes not only triggered enhanced silencing of transgenes and some endogenous TEs, but also increased DNA methylation. Analogous to their Harbinger transposon counterparts, HDP1 interacts with HDP2 in the nucleus. We provide evidence that HDP1 and HDP2 are new components of the previously identified IDM histone acetyltransferase complex in which IDM1, IDM2, IDM3 and MBD7 are included. Our results suggest that HDP1 and HDP2 are required for IDM1 histone acetyltransferase activity at tested loci. Moreover, HDP2 and MBD7 share a large set of common genomic regions of chromatin association. Thus, our data revealed that HDP1 and HDP2 constitute a functional module from ancient Harbinger transposon which has been recruited to function in a host histone acetyltransferase complex. The HDP1 and HDP2 module is important in determining the target specificity of the histone acetyltransferase complex to facilitate DNA demethylation and to prevent epigenetic silencing.
HDP1 and HDP2 prevent transcriptional gene silencing of transgenes
We previously established a transgene reporter system in Arabidopsis in which expression of the 35S promoter-driven SUC2 transgene (35S::SUC2) causes a short-root phenotype on sucrose medium (Figure 1A). This phenotype requires the ROS1-dependent DNA demethylation pathway21. From an EMS mutagenesis screen, we identified three recessive mutants, hdp1-1, hdp1-2 (which are allelic) and hdp2-1, that display normal root length and 35S::SUC2, 35S::NPTII (neomycin phosphotransferase II) transgene silencing phenotype (Figure 1A, 1B and Supplementary information, Figure S1). Map-based cloning followed by whole-genome resequencing revealed that both hdp1 mutants had nonsense mutations in AT1G72270 and hdp2-1 had a nonsense mutation in AT4G31270 (Figure 1C and 1D). The two nonsense mutations within AT1G72270 both occur in the short transcript annotation and our RNA-seq data show transcripts only from this short form region, suggesting that the short transcript is the functional unit. Genetic complementation of hdp1-1 and hdp2-1 with genomic DNA, including upstream 2 kb native promoters, confirmed that the mutations in AT1G72270 and AT4G31270 caused the transgene silencing (Figure 1A and 1B).
To test whether DNA methylation plays a role in the transgene silencing in hdp1 and hdp2 mutants, we treated these mutants with the DNA methylation inhibitor 5′Aza-2′-deoxycytidine (5′Aza). 5′Aza treatment restored kanamycin resistance to hdp1 and hdp2 mutants (Supplementary information, Figure S1A) and increased the relative expression of transgenes compared to 35S::SUC2 plants (Supplementary information, Figure S1B), suggesting that the transgene silencing in the mutants may be caused by increased DNA methylation. Moreover, transgene silencing is likely to be at the transcriptional level, as chromatin immunoprecipitation (ChIP) assays showed that there were depletion of pol II occupancy, decreased H3K4 tri-methylation, an active histone modification, and increased H3K9 di-methylation, a repressive histone modification, at transgene promoters. 5′Aza treatment counteracted the chromatin alterations caused by hdp1 and hdp2 mutations (Supplementary information, Figure S1C). These results suggest that loss of HDP1 and HDP2 leads to increased DNA methylation levels, altered histone modifications and depleted Pol II at transgene promoters, resulting in decreased transcription of transgenes.
HDP1 and HDP2 prevent DNA hypermethylation and transcriptional silencing of TEs
Next, we performed whole-genome bisulfite sequencing (WGBS) using genomic DNA from 35S::SUC2, hdp1-1 and hdp2-1 seedlings. We first evaluated DNA methylation levels at the transgene promoters. We found that DNA methylation levels at region B of the 35S promoters are increased in hdp1-1 and hdp2-1 relative to 35S::SUC2 plants (Figure 2A), suggesting that the transgene silencing may be caused by increased DNA methylation. We also evaluated the methylation levels of four additional endogenous ROS1 targets by DNA methylation-sensitive PCR (chop-PCR). Similar to a ros1 mutant, DNA methylation levels at these loci were increased in hdp1 and hdp2 mutants relative to the 35S::SUC2 tester line (Figure 2B). To further confirm the methylation phenotype, we employed CRISPR/Cas9-based genome editing to generate hdp1-3, hdp1-4 and hdp2-2 mutants in the Col-0 background (Figure 1C and 1D). Chop-PCR again showed increased DNA methylation levels at the four tested loci (Figure 2B), confirming that HDP1 and HDP2 repress DNA methylation at the tested ROS1 target loci.
We then evaluated the DNA methylation change on a genome-wide level in hdp1 and hdp2 mutants. WGBS identified 1 243 and 2 768 hyper-differentially methylated regions (hyper-DMRs) in hdp1-1 and hdp2-1 mutants, respectively (Supplementary information, Table S1). Venn diagram shows that about 43.3% hyper-DMRs of hdp1-1 overlap with that of hdp2-1 (Figure 2C, upper panel). Moreover, box plot shows that even for those hyper-DMRs that appear specific for hdp1-1 and hdp2-1 in the Venn diagram, the average DNA methylation levels are still increased in hdp2-1 and hdp1-1 mutants compared to 35S::SUC2 plants (Figure 2C, lower panel), supporting that HDP1 and HDP2 function to prevent DNA hypermethylation of similar genomic loci. In addition, we found that most of the hyper-DMRs are mapped to TE regions (Figure 2D), suggesting that HDP1 and HDP2 may prevent TEs from silencing.
Next we profiled the transcriptomes of hdp1-1 and hdp2-1 by mRNA-Seq. We did not observe significant differences in gene expression between 35S::SUC2 and hdp1-1 or hdp2-1 plants (Supplementary information, Figure S2). TEs and repetitive sequences are the primary targets of the silencing machinery, including DNA methylation and repressive histone modifications6,9,22, and are transcribed at low levels, therefore the effects of HDP1 and HDP2 dysfunction in further reducing TE expression may not be detected by mRNA-Seq. Thus, we analyzed three TE loci, AT1TE46455, AT1TE36115 and AT1TE35325, which had increased DNA methylation in hdp1-1 and hdp2-1 mutants (Figure 2E) by RT-qPCR. We found that the expression of all three TEs was significantly reduced in hdp1 and hdp2 mutants compared to control (Figure 2E). These results suggest that HDP1 and HDP2 function in the anti-silencing of endogenous TEs in plants.
HDP1 is a Harbinger transposon-derived host protein in Arabidopsis
HDP1 protein has an annotated “Harbinger transposase-derived nuclease domain” (InterPro accession: IPR027806)23, suggesting that it may be a “domesticated” protein from Harbinger transposase (Figure 3A). The derivation of host protein-coding genes from Harbinger transposons has previously been reported in human, Drosophila and Arabidopsis17,20,24. A BLASTP search using the Harbinger transposon database (Repbase)25 revealed that HDP1 shares about 30% identity with some Harbinger transposase sequences (Supplementary information, Table S2). The Harbinger transposases belong to the “DDE” superfamily endonucleases, which contain a conserved catalytic triad of amino acid sequence “DDE”26. However, the alignment of HDP1 with selected transposases revealed that the triad is not completely conserved in HDP1 (Figure 3A, red arrows), suggesting that HDP1 probably has lost the nuclease activity. It is noteworthy that HDP1 is not a transposon remnant since, despite the homology to Harbinger transposase, it lacks transposon characteristics such as terminal inverted repeat (TIR) and target site duplication (TSD).
To determine the phylogenetic relationship between HDP1 and its homologous transposases, HDP1 homologous sequences retrieved from the Harbinger transposon database and various plant species, zebrafish and human in NCBI non-redundant (nr) protein database were used to construct a phylogenetic tree (Figure 3B). HDP1 is located in a clade consisting of sequences from all selected angiosperm species (bright green clade, at1g72270 is HDP1), indicating that HDP1 has orthologues in these selected angiosperm species as the gene tree and species tree are consistent. The phylogenetic tree shows that several host protein clades, including the one which contains HDP1, are intermingled with clades consisting of transposase sequences (Figure 3B). These intermingled host proteins may share a common ancestor with the transposases that are located in their sister clusters. The phylogenetic tree reveals that HDP1 originated from Harbinger transposons and that the derivation of HDP1 had likely happened before the emergence of angiosperms.
Besides the HDP1 clade, five more orthologous clusters (clades colored in yellow, red, purple, orange and grey) containing Arabidopsis protein sequences and a group of non-transposon-encoded sequences are present in the phylogenetic tree (Figure 3B). Notably, the six orthologous clusters containing Arabidopsis sequences were not all within a single larger clade that lacks transposase sequences. Rather, two transposase clades are intermingled with the clades of orthologous angiosperm proteins. This topology suggests that the multiple Arabidopsis sequences were derived from independent “domestication” of harbinger-encoded sequences instead of solely from gene duplication after a single “domestication” event. Similarly, the Harbinger transposon-derived HARBI1 in human (homo_gi|767965708) is located in its own orthologous cluster which also has a sister transposase clade27, indicating that HARBI1 in human does not share a common “domestication” event with Harbinger-derived proteins in plants. Collectively, our results show that Harbinger transposons have been repeatedly “domesticated” into host proteins in species from different kingdoms, suggesting its functional importance during evolution.
HDP2 is a DNA-binding protein derived from Harbinger transposons
HDP2 protein contains a SANT/Myb/trihelix DNA-binding motif (Figure 4A). Interestingly, besides the canonical transposase, Harbinger transposons usually have a second ORF which encodes this motif17,28. The alignment of the SANT/Myb/trihelix domains from HDP2 and from Harbinger transposon-encoded proteins shows that three tryptophan residues critical for DNA binding are conserved between HDP2 and Harbinger proteins from Arabidopsis lyrata (Figure 4A, red stars). However, a search of Repbase with the protein sequence of HDP2 identified only one significant hit (E-value < 0.01; Supplementary information, Table S2). Notably, it has been suggested that the Myb-like proteins encoded by Harbinger transposons were significantly more divergent than the transposase18, therefore it may be difficult to track the phylogenetic history of HDP2. Nevertheless, when we combined Harbinger transposon-encoded Myb-like proteins from Repbase and HDP2 homologous sequences from the NCBI nr database to construct the phylogenetic tree of HDP2, we observed intermingled clades of HDP2 homologous proteins and clades of transposon proteins (Supplementary information, Figure S3). The clade containing HDP2, like HDP1, shows agreement between genes and the taxa that they are sampled from, indicating derivation from a Harbinger transposon before the diversification of angiosperms.
The DNA-binding activity of HDP2 is required to prevent transgene silencing
Next, we tested the DNA-binding activity of HDP2 by electrophoretic mobility shift assay (EMSA) with recombinant maltose-binding protein (MBP)-tagged HDP2. It was reported that the Harbinger transposon-derived human NAIF1 protein binds to the TIR region of zebrafish Harbinger3N_DR transposon DNA27. We selected four double-stranded DNA probes in Harbinger3N_DR TIR region to test whether HDP2 may have DNA-binding activity. We found that MBP-HDP2 can bind to two of the DNA probes (Figure 4B and Supplementary information, Figure S4A), suggesting that HDP2 has DNA-binding activity but is not a ubiquitous DNA-binding protein. Moreover, HDP2 displayed similar DNA-binding activities to methylated and unmethylated 35S-1 DNA fragments from the 35S::SUC2 transgene promoter (Supplementary information, Figure S4B and Figure 2A), suggesting that HDP2 does not discriminate the methylation state of its target DNA.
Further, we found that mutation of each of the three conserved tryptophan residues eliminated (W19R, W48R) or reduced (W71R) the DNA-binding activity of HDP2 (Figure 4C), consistent with the observation that W71 is less conserved than W19 and W48 within this DNA binding motif29. Thus, the DNA-binding activity of HDP2 requires these three conserved tryptophan residues. Consistent with the in vitro binding assays, transgenic hdp2-1 plants expressing HDP2W19R or HDP2W48R failed to rescue the long root, transcriptional transgene silencing and DNA hypermethylation phenotypes caused by hdp2-1 mutation (Figure 4D, 4E and Supplementary information, Figure S4C). Although HDP2W71R did recover the long root mutant phenotype to shorter roots, they were not as short as transgenic mutant plants expressing wild-type HDP2 (Figure 4D). These results indicate that the DNA-binding activity of HDP2 is required to prevent transgene silencing. In addition, we tested whether HDP2 can bind to the transgene promoters in vivo by performing ChIP assay in HDP2 transgenic plants. We found that wild-type and W71R mutated form of HDP2, but not the W19R and W48R mutated forms of HDP2, were enriched at the 35S promoter regions of the SUC2, HPTII and NPTII transgenes relative to the “no antibody” and 35S::SUC2 controls, but not at the ACTIN7 promoter (Figure 4F and Supplementary information, Figure S4D). Thus, HDP2 binds specifically to the transgene promoter, and the DNA-binding activity is required for full function of HDP2 in vivo.
HDP1 and HDP2 interact in the nucleus
Transposition by the Harbinger transposon is facilitated by an interaction between the DNA-binding protein and the transposase27. The observation that both HDP1 and HDP2 may be domesticated from the Harbinger transposon prompted us to investigate whether a physical interaction between these two proteins has been conserved. We performed a yeast two-hybrid (Y2H) assay and found that HDP1 and HDP2 can directly interact (Figure 5A). The interaction was also confirmed by a split luciferase assay in Arabidopsis protoplasts (Figure 5B). To further test whether HDP1 and HDP2 interact in vivo, we performed a co-immunoprecipitation assay using hybrid plants generated from HDP1-4MYC/hdp1-1 and 3FH-HDP2/hdp2-1. Col-0 and 3FH-HDP2/hdp2-1 plants served as controls. We found that HDP1-4MYC co-immunoprecipitated with 3FH-HDP2 from hybrid plants (Figure 5C), suggesting their interaction in vivo. To map the domains required for the interaction, we evaluated two truncated forms of HDP1 and HDP2 in the Y2H assay. We found that the N-terminal region (amino acid 1-225) of HDP1 and the C-terminal region (amino acid 151-259) of HDP2 are required for the interaction of HDP1 and HDP2 (Supplementary information, Figure S5A). Collectively, these findings strongly suggest that HDP1 and HDP2 interact in vivo.
To investigate the subcellular localizations of HDP1 and HDP2, we first transiently expressed 35S promoter-driven HDP1- and HDP2-YFP fusion proteins in tobacco leaves and Arabidopsis protoplasts. We found that both HDP1-YFP and HDP2-YFP were localized mainly to nuclei (Figure 5D). To further confirm that their interaction occurs in the nucleus, we performed bimolecular fluorescence complementation (BiFC) in tobacco leaves. We found that YFP fluorescence was restored mostly in the nuclei expressing both HDP1-YFPN and HDP2-YFPC, or both HDP1-YFPC and HDP2-YFPN (Supplementary information, Figure S5B), suggesting that HDP1 and HDP2 interact in the nucleus. We then examined co-localization of HDP1 and HDP2 at subnuclear level by immunostaining. HDP1-4MYC and 3FH-HDP2 were detected by anti-MYC and anti-FLAG antibodies, respectively. Co-staining of HDP1 and HDP2 in the same nuclei revealed many yellow foci (Figure 5E), indicating the co-localization of HDP1-4MYC and 3FH-HDP2 at the subnuclear level. Collectively, these data demonstrate that HDP1 and HDP2 physically interact in the nucleus to function in the epigenetic anti-silencing pathway.
HDP1 and HDP2 are new components of the IDM complex and are required for IDM1 histone acetyltransferase activity at tested loci
To better understand the mechanism of functions of HDP1 and HDP2, we attempted to identify HDP1- and HDP2-interacting proteins using immunoprecipitation followed by mass spectrometry (IP-MS) analysis in transgenic plants expressing native promoter-driven epitope-tagged proteins. We immunoprecipitated HDP1-4MYC and 3FH-HDP2 with anti-MYC and anti-FLAG antibodies, respectively. 35S::SUC2 plants were used as negative controls. Consistent with the interaction between HDP1 and HDP2 (Figure 5), both HDP1 and HDP2 proteins were present in their reciprocal IP products, but not in control IP (Figure 6A and Supplementary information, Table S4). Interestingly, from both HDP1 and HDP2 IP samples, but not the control, four other anti-silencing factors, including IDM1 and its associating proteins IDM2, IDM3 and MBD7, were identified. To verify the association of these six proteins, we performed IP-MS experiments with IDM1-YFP-HA, IDM2-HA, IDM3-3FLAG-3HA and MBD7-4MYC transgenic plants. The results showed that HDP1, HDP2, IDM1, IDM2, IDM3 and MBD7 were always co-purified together, with the exception that the IDM2-HA purification did not yield MBD7 (Figure 6A and Supplementary information, Table S4). The results support that the six proteins form a protein complex in vivo, which is referred to hereafter as the IDM complex since it contains the IDM1 histone acetyltransferase and dysfunction of any of its components causes the IDM (Increased DNA Methylation) phenotype. To further confirm the formation of IDM complex, protein gel filtration assays were performed using epitope-tagged transgenic plants. The results show that the tested components co-eluted in the same fractions (Figure 6B), supporting that a complex is formed in vivo. The molecular weight of the protein complex was estimated to be ∼350 kDa. Considering the molecular weight of the protein tag, the estimated size is very close to the sum (∼339 kDa) of the molecular weights of the six subunits at 1:1:1:1:1:1 stoichiometry.
To identify direct interactions within the IDM complex, we tested pairwise interactions between each component with Y2H assays. We found that HDP1, but not HDP2, can directly interact with IDM1 (Figure 6C). The N-terminal domain (amino acid residues 1-592) of IDM1 is required for its interaction with HDP1 (Supplementary information, Figure S6A). No interaction between IDM1 and truncated HDP1 proteins was observed (Supplementary information, Figure S6B), indicating that full-length HDP1 is required for its interaction with IDM1. The interaction between IDM1 and HDP1 was further verified by split luciferase assays in tobacco leaves (Figure 6C). In addition, neither HDP1 nor HDP2 showed any interaction with IDM2, IDM3 or MBD7 in either Y2H or split luciferase assays (Supplementary information, Figure S6C and S6D). Our previous report has shown that MBD7 can directly interact with IDM2 and IDM3, and IDM2 and IDM3 can directly interact with IDM114. Taken together, these results suggest that the IDM complex has two DNA-binding components, HDP2 and MBD7, and that HDP1 and IDM2/IDM3 mediate their associations with the enzymatic core IDM1, respectively.
IDM1 can acetylate histone H3 at lysine 18 (H3K18) and idm1 mutant shows reduced H3K18Ac levels at 35S promoter regions13,14,15. We next tested whether H3K18Ac level is also affected in hdp1 and hdp2 mutants. ChIP-qPCR showed that the level of H3K18Ac was reduced in both hdp1 and hdp2 mutants at the 35S promoters and an endogenous IDM1-dependent locus tested (Figure 6D). The reduction was comparable to that in idm1 mutant, supporting that HDP1 and HDP2 are required for the IDM1 histone acetyltransferase activity at the tested loci. Since IDM1-mediated histone acetylation is required for DNA demethylation at specific genomic regions13,14, we investigated whether mutations in HDP1 and HDP2 may cause similar DNA hypermethylation phenotypes as observed in idm1 mutant. We performed WGBS in hdp1-1, hdp2-1 and idm1-9 mutants (all in the 35S::SUC2 background). We identified 1 243, 2 768 and 1 612 hyper-DMRs in hdp1-1, hdp2-1 and idm1-9 mutants, respectively (Supplementary information, Table S1). By intersecting the identified hyper-DMRs, we found that idm1-9 mutant shares 416 and 562 out of its 1 612 identified hyper-DMRs with hdp1 and hdp2 mutants, respectively (Supplementary information, Figure S7A). We then plotted the DNA methylation levels of wild type, hdp1, hdp2 and idm1 mutants at the hyper-DMRs identified from the idm1-9 mutant. The plots show that the DNA methylation levels in hpd1 and hdp2 mutants are increased compared to wild type in all cytosine contexts (CG, CHG and CHH) at the idm1 hyper-DMRs (Figure 6E), suggesting that HDP1 and HDP2 affect DNA methylation at common genomic regions with IDM1. As both HDP2 and MBD7 are DNA-binding proteins and the increase of DNA methylation in hdp2 mutant is less than that of idm1 mutant, we also performed WGBS using mbd7-1 and hdp2-1mbd7-1 mutants to see whether HDP2 and MBD7 may have functional redundancy (Figure 6E). The results show that the hdp2mbd7 double mutant has a similar level of DNA methylation increase to either single mutant. It is likely that there are other functionally redundant proteins to the HDPs and MBD7, and IDM1 may also function independently of the complex. Taken together, our results suggest that HDP1 and HDP2 are required for full IDM1 function in vivo, which is consistent with their associations in the same protein complex.
HDP2 and MBD7 bind to similar genomic regions for DNA demethylation
To determine the role of HDP2 in the IDM complex, we investigated the in vivo binding sites of HDP2 by performing ChIP-Seq using 3FH-HDP2/hdp2-1 transgenic plants. There were 2 354 common HDP2 binding sites identified from two biological replicates (Figure 7A). MBD7 was previously shown to bind densely methylated CpG regions and mediate the recruitment of IDM114. As HDP2 is in the same complex with MBD7, we compared the binding sites of HDP2 with those of MBD7. We found that 1 360 out of the 2 354 (58%) HDP2-enriched regions overlap with MBD7-enriched regions (Figure 7A). Similarly, 1 144 out of the 2 181 (52%) MBD7-enriched regions (common peaks from two replicates) overlap with HDP2-enriched regions (Figure 7A). In addition, we plotted ChIP signals of HDP2, MBD7 and control (ChIP signals for randomly selected regions) over MBD7 peak regions and HDP2 peak regions, respectively (Figure 7B). The distribution shows that both HDP2 and MBD7, but not the control, were enriched over the peak regions of each other, with the highest ChIP signal at the center of identified peaks. Taken together, our results show that HDP2 and MBD7 target a common set of genomic regions.
Next, we sought to determine the relationship between the roles of HDP2 and MBD7 in affecting DNA methylation and their genomic binding sites. The numbers of differentially methylated cytosines (DMCs) identified in hdp1-3, hdp2-2, idm1-1 and mbd7-2 mutants14 in every 2-kb genomic regions were plotted against the corresponding ChIP signals of HDP2 and MBD7. We found that there were positive correlations between the ChIP signal and the numbers of hyper DMCs in regions where ChIP signals were high (Figure 7C). These results suggest that the enrichments of HDP2 and MBD7 at genomic regions correlate with the role of IDM complex in DNA demethylation.
Although many transposon-derived proteins have been reported, only a few are functionally characterized. Here, we show that HDP1 and HDP2 are derived from the two proteins in Harbinger transposons and are present in the same complex, indicating that the components of Harbinger transposons can be “co-domesticated” to function in the same pathway. Although the catalytically important “DDE” triad is not conserved in HDP1, HDP2 retains the DNA binding activity. The DNA-binding protein in transposons can recognize specific sequence for transposition; however, due to the weak conservation of the SANT/Myb/trihelix domain, HDP2 may have gained new specificity beyond Harbinger terminal sequences. The function of animal HARBI1 and NAIF1 proteins, which were also derived from the Harbinger transposase and SANT/Myb/trihelix domain protein, respectively, is unclear27. We predict that HARBI1 and NAIF1 in animals may also be involved in epigenetic regulation.
The “domestication” of Harbinger transposons into host proteins shows a convergent evolution pattern. Recently, another Harbinger transposon-derived protein, ALP1, was found to associate with Arabidopsis Polycomb Repressive Complex 2 (PRC2)30. ALP1 is present in a different orthologous clade from HDP1 in the phylogenetic tree (Figure 3B), which is consistent with their different functions and suggests that they are from independent “domestications”. Previously, multiple “domestication” events of Harbinger transposons were also reported in Drosophila19. Our findings and others suggest that the Harbinger transposons have been repeatedly “co-opted” into host proteins17,19,20. This phenomenon has also been shown for the “domestication” of pogo-like transposases into CENP-B-related proteins24,31. The convergent “domestication” pattern suggests their importance during evolution and that there may be additional Harbinger transposon-derived chromatin regulators.
Histone modifying enzymes are usually found in large protein complexes which, in addition to the enzymes, contains DNA- or chromatin-binding proteins, chaperone proteins and scaffold/hinge proteins32. Multiple DNA-binding proteins may cooperate to determine the target specificity of the complex33. Here, for the IDM complex, we propose that MBD7 and HDP2 jointly determine the genomic targeting of IDM1 (Supplementary information, Figure S7). MBD7 binds to methylated CpG sites, ensuring that the IDM complex is targeted to heavily methylated genomic region14. In addition, as a transcription factor-like protein, HDP2 would enable the IDM complex to target regulatory sequences. In support of this notion, we found that hyper-DMRs in hdp2-1 mutant are enriched over promoters (1 kb upstream) of genes and TEs (Supplementary information, Table S5). Together, MBD7 and HDP2 ensure that the IDM complex is targeted only to highly methylated regulatory sequences, where active DNA demethylation is required for expression. HDP1, IDM2 and IDM3 proteins likely function to connect the DNA recognition components to the core enzyme, IDM1. However, HDP1 may also participate in helping HDP2 for target specificity or play a role in target recognition itself. In addition, IDM2 and IDM3 may also function as chaperone proteins to ensure IDM1 activity, since IDM2 and IDM3 belong to the family of α-crystallin domain proteins, most of which are small heat shock proteins that function as protein chaperones34. How IDM1-catalyzed histone acetylation is connected to the recruitment of the DNA demethylase ROS1 to mediate DNA demethylation is unclear and will require future investigation.
In plants and animals, the expression and activity of TEs and other repetitive sequences are regulated by host epigenetic mechanisms, including DNA methylation and histone modifications6. The current work shows that transposon-derived proteins may be components of this regulatory system and this may be one possible mechanism how the epigenetic machinery primarily targets transposons. A transposon-encoded protein in maize was reported previously to also participate in DNA demethylation, although the underlying mechanism was not clear4. Our findings uncovered a mechanism for the regulation of TEs in which transposon-derived HDP1 and HDP2 are recruited to a host histone acetyltransferase complex to protect transposons and some endogenous genes from epigenetic silencing.
Materials and Methods
Plant materials and growth conditions
All plants were grown under a long day photoperiod (16-h light/8-h dark). For 35S::SUC2 background plants, 1/2-strength Murashige and Skoog (MS) medium containing 1% sucrose was used to observe the root phenotype and 1% glucose-containing 1/2 MS medium was used for all other experiments. For kanamycin sensitivity experiment, 50 mg/L of kanamycin was used. For DNA methylation inhibitor treatment, 5′Aza-2′-deoxycytidine (Sigma) was added into 1/2 MS medium at the concentration of 5 μM and DMSO was used as negative control. All seedlings on 1/2 MS media were photographed 14 days after germination.
The knockout mutants of HDP1 and HDP2 by CRISPR/Cas9 were generated as reported previously35.
DNA methylation analysis
For DNA methylation-sensitive chop-PCR and WGBS, genomic DNA was extracted from 2-week-old seedlings using DNeasy Plant Mini Kit (Qiagen). Chop-PCR was performed as reported previously36. DMRs were identified according to Duan et al.37. In brief, a sliding-window approach with a 200-bp window sliding at 50-bp intervals was used to identify DMRs. Fisher's exact test was performed for methylated versus unmethylated cytosines for each context, within each window, with FDRs estimated using a Benjamini-Hochberg adjustment of Fisher's P-values calculated in the R environment. Windows with an FDR ≤ 0.05 were considered for further analysis, and windows within 100 bp of each other were condensed to larger regions. Regions were then adjusted to extend to DMC at each border. A cytosine was considered differentially methylated if it showed at least a 2-fold change in methylation percentage in the mutant. The regions were then filtered to include only those with at least 10 DMCs and with at least an average of a 2-fold change in methylation percentage per cytosine. The 35S::SUC2 BS-data is from Lang et al.14.
Protein interaction analysis
For the Y2H assay, the full-length and truncated coding regions of HDP1, HDP2, IDM1, IDM2, IDM3 and MBD7 were directly cloned into the pGADT7 (AD) and pGBKT7 (BD) vectors. For the split luciferase assay, protein coding sequences were first cloned into entry vector pENTR/D-TOPO (Invitrogen) and then into modified pEarleyGate vectors14, which bear split luciferase coding sequence, by Gateway LR Clonase II-mediated recombination reaction (Invitrogen). For split luciferase assay, the constructs fused with split luciferase were co-transfected into Arabidopsis protoplast (Col-0) for overnight incubation. Arabidopsis protoplast was prepared as previously reported38. The luciferase activity was determined using CCD camera equipped with Winview software (Princeton instruments). For co-immunoprecipitation assay, the inflorescence tissues from hybrid plants crossed from 3FH-HDP2/hdp2-1 and HDP1-4myc/hdp1-1 were collected for total protein extraction using a previously reported method36. Total proteins extracted from Col-0 and 3FH-HDP2/hdp2-1 plants were used as controls. Total proteins were then precipitated by agarose-conjugated anti-MYC antibody for 2 h at 4 °C. After washing 5 times with protein extraction buffer, the precipitated proteins were separated on 12% SDS-PAGE gel together with input proteins for immunoblot.
Multiple sequence alignment and phylogenetic tree construction
HDP1 protein sequence was used as the query for BLASTP search with NCBI nr protein database. Searched species include Amborella trichopoda, Glycine max, Populus trichocarpa, Brassica rapa, Arabidopsis thaliana, Selaginella moellendorffii, Zea mays, Brachypodium distachyon, Oryza stiva, Danio rerio and Homo sapiens. Top 250 protein sequences except sequences longer than 2 000 amino acids were used for protein alignment and phylogenetic tree construction. For multiple sequence alignment (MSA; Figure 3A), transposase sequences used include Harbinger-2_Ami_1p, from Alligator mississippiensis, Harbinger-2G_CPB_1p and Harbinger-4_CPB_1p, from Chrysemys picta bellii. From the phylogenetic tree, we selected a subtree which includes all Arabidopsis protein sequences present in the tree and extracted all sequences with the subtree. The resulted list has 123 sequence entries. HDP2 protein sequence was also used as query for BLASTP search with all available Harbinger transposon sequences in Repbase. Top 50 hits based on E-value were selected together with the 123 sequences from NCBI nr database for the final phylogenetic tree construction. Command line version ClustalW39 2.1 was used for MSA and phylogenetic tree construction of selected protein sequence.
See Supplementary information, Data S1 for more details.
The hdp1-1 and hdp2-1 WGBS data have been deposited to NCBI's Gene Expression Omnibus (GSE85060). The 35S::SUC2 BS-data (GSE58787) was from Lang et al.14. The WGBS data of the hdp1 and hdp2 mutants in Col-0 background, the ChIP-Seq and mRNA-Seq data have been deposited to NCBI's Gene Expression Omnibus (GSE89320).
C-G D, XW and J-K Z designed the study. C-G D, XW, LP, DM, C-C H, ML, YZ, Y-J H, ZW, ZZ, S-K M, HX and HZ conducted the experiments. SX and KT analyzed the whole-genome sequencing data. C-G D, XW, W-A T, BD and J-K Z wrote the paper.
Competing Financial Interests
The authors declare no competing financial interests.
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This work was supported by the Chinese Academy of Sciences and by National Institutes of Health (R01GM070795) to J-K Z.
( Supplementary information is linked to the online version of the paper on the Cell Research website.)
DNA methylation inhibitor 5′AZA treatment released the transcriptional silencing of SUC2 and NPTII transgenes. (PDF 225 kb)
Pearson's coefficient plots for RNA-Seq of 35S::SUC2, hdp1-1 and hdp2-1. (PDF 105 kb)
The phylogenetic analysis of HDP2. (PDF 1039 kb)
DNA-binding activity of HDP2 and its role in anti-silencing and DNA demethylation. (PDF 277 kb)
The domain requirement of HDP1 and HDP2 interaction. (PDF 86 kb)
The N-terminal domain of IDM1 is responsible for its interaction with HDP1 but not HDP2. (PDF 101 kb)
A working model for the derivation of HDP1 and HDP2 and their role in the IDM complex. (PDF 390 kb)
The hyper-DMR list identified from hdp1-1 and hdp2-1 mutants in comparison to 35S::SUC2 plants. Related to Figure 2 (XLSX 124 kb)
The primers and oligos used in this study (XLSX 14 kb)
The Mass-spectrometry list identified from co-immunoprecipitation assays. Related to Figure 6. (XLSX 1096 kb)
Fisher's exact test on weather hper-DMRs in hdp mutant are enriched in regulatory regions (promoters). (PDF 41 kb)
Materials and Methods (PDF 51 kb)
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Cite this article
Duan, CG., Wang, X., Xie, S. et al. A pair of transposon-derived proteins function in a histone acetyltransferase complex for active DNA demethylation. Cell Res 27, 226–240 (2017). https://doi.org/10.1038/cr.2016.147
- DNA demethylation
- histone acetylation
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