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Protein & Cell

ISSN 1674-800X

ISSN 1674-8018(Online)

CN 11-5886/Q

Postal Subscription Code 80-984

2018 Impact Factor: 7.575

Protein Cell    2021, Vol. 12 Issue (6) : 455-474    https://doi.org/10.1007/s13238-021-00837-8
RESEARCH ARTICLE
Nuclear m6A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos
Chuan Chen1, Wenqiang Liu2, Jiayin Guo3, Yuanyuan Liu3, Xuelian Liu1, Jun Liu4,5, Xiaoyang Dou6,7, Rongrong Le1, Yixin Huang1, Chong Li2, Lingyue Yang2, Xiaochen Kou1, Yanhong Zhao1, You Wu1, Jiayu Chen2, Hong Wang2, Bin Shen3(), Yawei Gao1(), Shaorong Gao1,2()
1. Institute for Regenerative Medicine, Shanghai East Hospital, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai 200120, China
2. Clinical and Translation Research Center of Shanghai First Maternity & Infant Hospital, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai 200092, China
3. State Key Laboratory of Reproductive Medicine, Department of Prenatal Diagnosis, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing Medical University, Nanjing 211166, China
4. School of Life Sciences, Peking University, Beijing 100871, China
5. Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China
6. Department of Chemistry and Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA
7. Howard Hughes Medical Institute, Chicago, IL 60637, USA
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Abstract

N6-methyladenosine (m6A) on chromosome-associated regulatory RNAs (carRNAs), including repeat RNAs, plays important roles in tuning the chromatin state and transcription, but the intrinsic mechanism remains unclear. Here, we report that YTHDC1 plays indispensable roles in the self-renewal and differentiation potency of mouse embryonic stem cells (ESCs), which highly depends on the m6A-binding ability. Ythdc1 is required for sufficient rRNA synthesis and repression of the 2-cell (2C) transcriptional program in ESCs, which recapitulates the transcriptome regulation by the LINE1 scaffold. Detailed analyses revealed that YTHDC1 recognizes m6A on LINE1 RNAs in the nucleus and regulates the formation of the LINE1-NCL partnership and the chromatin recruitment of KAP1. Moreover, the establishment of H3K9me3 on 2C-related retrotransposons is interrupted in Ythdc1-depleted ESCs and inner cell mass (ICM) cells, which consequently increases the transcriptional activities. Our study reveals a role of m6A in regulating the RNA scaffold, providing a new model for the RNA-chromatin cross-talk.

Keywords YTHDC1      LINE1-scaffold complex      2-cell      retrotransposons      H3K9me3     
Corresponding Author(s): Bin Shen,Yawei Gao,Shaorong Gao   
Online First Date: 21 May 2021    Issue Date: 14 July 2021
 Cite this article:   
Chuan Chen,Wenqiang Liu,Jiayin Guo, et al. Nuclear m6A reader YTHDC1 regulates the scaffold function of LINE1 RNA in mouse ESCs and early embryos[J]. Protein Cell, 2021, 12(6): 455-474.
 URL:  
https://academic.hep.com.cn/pac/EN/10.1007/s13238-021-00837-8
https://academic.hep.com.cn/pac/EN/Y2021/V12/I6/455
1 PJ Batista, B Molinie, J Wang, K Qu, J Zhang, L Li, DM Bouley, E Lujan, B Haddad, K Daneshvaret al. (2014) m(6)A RNA modification controls cell fate transition in mammalian embryonic stem cells. Cell Stem Cell 15:707–719
https://doi.org/10.1016/j.stem.2014.09.019
2 J Brind’Amour, S Liu, M Hudson, C Chen, MM Karimi, MC Lorincz (2015) An ultra-low-input native ChIP-seq protocol for genomewide profiling of rare cell populations. Nat Commun 6:6033
https://doi.org/10.1038/ncomms7033
3 T Chelmicki, E Roger, A Teissandier, M Dura, L Bonneville, S Rucli, F Dossin, C Fouassier, S, Lameiras D Bourc’his (2021) m(6)A RNA methylation regulates the fate of endogenous retroviruses. Nature 591(7849):312–316
https://doi.org/10.1038/s41586-020-03135-1
4 T Chen, YJ Hao, Y, Zhang MM Li, M Wang, W Han, Y Wu, Y, Lv J Hao, L Wanget al. (2015) m(6)A RNA methylation is regulated by microRNAs and promotes reprogramming to pluripotency. Cell Stem Cell 16:289–301
https://doi.org/10.1016/j.stem.2015.01.016
5 A De Iaco, E Planet, A Coluccio, S Verp, J, Duc D Trono (2017) DUX-family transcription factors regulate zygotic genome activation in placental mammals. Nat Genet 49:941–945
https://doi.org/10.1038/ng.3858
6 D Dominissini, S Moshitch-Moshkovitz, S, Schwartz M Salmon-Divon, L Ungar, S Osenberg, K Cesarkas, J, Jacob-Hirsch N Amariglio, M Kupiecet al. (2012) Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq. Nature 485:201–206
https://doi.org/10.1038/nature11112
7 S Geula, S Moshitch-Moshkovitz, D Dominissiniet al. (2015) m(6)A mRNA methylation facilitates resolution of naive pluripotency toward differentiation. Science 347:1002–1006
https://doi.org/10.1126/science.1261417
8 S Heinz, C Benner, N Spann, E Bertolino, YC Lin, P Laslo, JX Cheng, C Murre, H Singh, CK Glass (2010) Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. Mol Cell 38:576–589
https://doi.org/10.1016/j.molcel.2010.05.004
9 I Ivanova, C Much, M Di Giacomo, C Azzi, M Morgan, PN Moreira, J Monahan, C Carrieri, AJ Enright, D O’Carroll (2017) The RNA m (6)A reader YTHDF2 is essential for the post-transcriptional regulation of the maternal transcriptome and oocyte competence. Mol Cell 67(1059–1067):
https://doi.org/10.1016/j.molcel.2017.08.003
10 S Iyengar, AV Ivanov, VX Jinet al. (2011) Functional analysis of KAP1 genomic recruitment. Mol Cell Biol 31:1833–1847
https://doi.org/10.1128/MCB.01331-10
11 JW Jachowicz, X Bing, J Pontabry, A Boskovic, OJ Rando, ME Torres- Padilla (2017) LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo. Nat Genet 49:1502–1510
https://doi.org/10.1038/ng.3945
12 SD Kasowitz, J Ma, SJ Anderson, NA Leu, Y Xu, BD Gregory, RM Schultz, PJ Wang (2018) Nuclear m6A reader YTHDC1 regulates alternative polyadenylation and splicing during mouse oocyte development. PLoS Genet 14:
https://doi.org/10.1371/journal.pgen.1007412
13 WJ Kent, AS Zweig, G, Barber AS Hinrichs, D Karolchik (2010) BigWig and BigBed: enabling browsing of large distributed datasets. Bioinformatics 26:2204–2207
https://doi.org/10.1093/bioinformatics/btq351
14 B Langmead, SL Salzberg (2012) Fast gapped-read alignment with Bowtie 2. Nat Methods 9:357–359
https://doi.org/10.1038/nmeth.1923
15 X Li, XD Fu (2019) Chromatin-associated RNAs as facilitators of functional genomic interactions. Nat Rev Genet 20:503–519
https://doi.org/10.1038/s41576-019-0135-1
16 H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, G, Abecasis R Durbin, S Genome Project Data Processing, (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25:2078–2079
https://doi.org/10.1093/bioinformatics/btp352
17 Y, Li L Xia, K Tan, X, Ye Z, Zuo M Li, R Xiao, Z, Wang X, Liu M Denget al. (2020) N(6)-Methyladenosine co-transcriptionally directs the demethylation of histone H3K9me2. Nat Genet 52:870–877
https://doi.org/10.1038/s41588-020-0677-3
18 X, Liu C Wang, W Liu, J Li, C Li, X Kou, J, Chen Y Zhao, H Gao, H Wanget al. (2016) Distinct features of H3K4me3 and H3K27me3 chromatin domains in pre-implantation embryos. Nature 537:558–562
https://doi.org/10.1038/nature19362
19 J Liu, X, Dou C Chen, C, Chen C Liu, MM Xu, S Zhao, B Shen, Y, Gao D Hanet al. (2020) N (6)-methyladenosine of chromosomeassociated regulatory RNA regulates chromatin state and transcription. Science 367:580–586
https://doi.org/10.1126/science.aay6018
20 JD Liu, MW Gao, JP He, KX Wu, SY Lin, LM Jin, YP Chen, H Liu, JJ Shi, XW Wanget al. (2021) The RNA m(6)A reader YTHDC1 silences retrotransposons and guards ES cell identity. Nature
https://doi.org/10.1038/s41586-021-03313-9
21 JY Lu, W Shao, L Chang, Y Yin, T Li, H Zhang, Y Hong, M Percharde, L Guo, Z Wuet al. (2020) Genomic repeats categorize genes with distinct functions for orchestrated regulation. Cell Rep 30(3296–3311):
https://doi.org/10.1016/j.celrep.2020.02.048
22 TS Macfarlan, WD Gifford, S Driscoll, K Lettieri, HM Rowe, D Bonanomi, A Firth, O Singer, D Trono, SL Pfaff (2012) Embryonic stem cell potency fluctuates with endogenous retrovirus activity. Nature 487:57–63
https://doi.org/10.1038/nature11244
23 IA Maksakova, PJ Thompson, P, Goyal SJ Jones, PB Singh, MM Karimi, MC Lorincz (2013) Distinct roles of KAP1, HP1 and G9a/ GLP in silencing of the two-cell-specific retrotransposon MERVL in mouse ES cells. Epigenet Chromatin 6:15
https://doi.org/10.1186/1756-8935-6-15
24 T Matsui, D Leung, H Miyashita, IA Maksakova, H Miyachi, H Kimura, M, Tachibana MC Lorincz, Y Shinkai(2010) Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET. Nature 464:927–931
https://doi.org/10.1038/nature08858
25 M Mendel, KM Chen, D Homolka, P, Gos RR Pandey, AA McCarthy, RS Pillai (2018) Methylation of structured RNA by the m(6)A writer METTL16 is essential for mouse embryonic development. Mol Cell 71:986
https://doi.org/10.1016/j.molcel.2018.08.004
26 KD Meyer, Y Saletore, P Zumbo, O Elemento, CE Mason, SR Jaffrey (2012) Comprehensive analysis of mRNA methylation reveals enrichment in 3’ UTRs and near stop codons. Cell 149:1635–1646
https://doi.org/10.1016/j.cell.2012.05.003
27 O Nayler, AM Hartmann, S Stamm (2000) The ER repeat protein YT521-B localizes to a novel subnuclear compartment. J Cell Biol 150:949–962
https://doi.org/10.1083/jcb.150.5.949
28 DP Patil, CK Chen, BF Pickering, A Chow, C, Jackson M Guttman, SR Jaffrey (2016) m(6)A RNA methylation promotes XISTmediated transcriptional repression. Nature 537:369–373
https://doi.org/10.1038/nature19342
29 M Percharde, CJ Lin, Y Yin, J Guan, GA Peixoto, A Bulut-Karslioglu, S, Biechele B, Huang X Shen, M Ramalho-Santos(2018) A LINE1-nucleolin Partnership Regulates Early Development and ESC identity. Cell 174(391–405):
https://doi.org/10.1016/j.cell.2018.05.043
30 AR Quinlan (2014) BEDTools: the swiss-army tool for genome feature analysis. Curr Protoc Bioinform 47:11–12
https://doi.org/10.1002/0471250953.bi1112s47
31 D Rodriguez-Terrones, X Gaume, T, Ishiuchi A Weiss, A Kopp, K Kruse, A Penning, JM Vaquerizas, L, Brino ME Torres-Padilla (2018) A molecular roadmap for the emergence of early-embryonic- like cells in culture. Nat Genet 50:106–119
https://doi.org/10.1038/s41588-017-0016-5
32 IA Roundtree, ME Evans, T Pan, C He (2017a) Dynamic RNA modifications in gene expression regulation. Cell 169:1187–1200
https://doi.org/10.1016/j.cell.2017.05.045
33 IA Roundtree, Z Zhang GZ Luo, X Wang, T Zhou, Y Cui, J Sha, X Huang, L Guerrero, P Xieet al. (2017b) YTHDC1 mediates nuclear export of N(6)-methyladenosine methylated mRNAs. Elife 6:
https://doi.org/10.7554/eLife.31311
34 HM Rowe, J Jakobsson, D Mesnard, J Rougemont, S Reynard, T Aktas, PV Maillard, H Layard-Liesching, S, Verp J Marquiset al. (2010) KAP1 controls endogenous retroviruses in embryonic stem cells. Nature 463:237–240
https://doi.org/10.1038/nature08674
35 S Schafer, K Miao, CC Benson, M Heinig, SA Cook, N Hubner (2015) Alternative splicing signatures in RNA-seq data: percent spliced in (PSI). Curr Protoc Hum Genet 87:11–16
https://doi.org/10.1002/0471142905.hg1116s87
36 H Shi, X Wang, Z Lu, BS Zhao, H Ma, PJ Hsu, C Liu, C He (2017) YTHDF3 facilitates translation and decay of N(6)-methyladenosine- modified RNA. Cell Res 27:315–328
https://doi.org/10.1038/cr.2017.15
37 Y Su, K Sugiura, F Sunet al. (2012) MARF1 regulates essential oogenic processes in mice. Science 335:1496–1499
https://doi.org/10.1126/science.1214680
38 A Subramanian, P Tamayo, VK Mootha, S Mukherjee, BL Ebert, MA Gillette, A Paulovich, SL Pomeroy, TR Golub, ES Landeret al. (2005) Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci USA 102:15545–15550
https://doi.org/10.1073/pnas.0506580102
39 H Thorvaldsdottir, JT Robinson, JP Mesirov (2013) Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration. Brief Bioinform 14:178–192
https://doi.org/10.1093/bib/bbs017
40 C Trapnell, L Pachter, SL Salzberg (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25:1105–1111
https://doi.org/10.1093/bioinformatics/btp120
41 C Trapnell, BA Williams, G Pertea, A Mortazavi, G Kwan, MJ van Baren, SL Salzberg, BJ Wold, L Pachter (2010) Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol 28:511–515
https://doi.org/10.1038/nbt.1621
42 X Wang, Z Lu, A Gomez, GC Hon, Y Yue, D Han, Y Fu, M Parisien, Q Dai, G Jiaet al. (2014) N6-methyladenosine-dependent regulation of messenger RNA stability. Nature 505:117–120
https://doi.org/10.1038/nature12730
43 X Wang, BS Zhao, IA Roundtree, Z Lu, D Han, H Ma, X Weng, K Chen, H Shi, C He (2015) N(6)-methyladenosine modulates messenger RNA translation efficiency. Cell 161:1388–1399
https://doi.org/10.1016/j.cell.2015.05.014
44 AS Warda, J Kretschmer, P Hackert, C Lenz, H Urlaub, C Hobartner, KE Sloan, MT Bohnsack (2017) Human METTL16 is a N-6-methyladenosine (m(6)A) methyltransferase that targets premRNAs and various non-coding RNAs. Embo Rep 18:2004–2014
https://doi.org/10.15252/embr.201744940
45 W Xiao, S Adhikari, U Dahal, YS Chen, YJ Hao, BF Sun, HY Sun, A Li, XL Ping, WY Laiet al. (2016) Nuclear m(6)A reader YTHDC1 regulates mRNA splicing. Mol Cell 61:507–519
https://doi.org/10.1016/j.molcel.2016.01.012
46 WQ Xu, JH Li, CX He, J Wen, HH Ma, BW Rong, JB Diao, LY Wang, JH Wang, FZ Wuet al. (2021) METTL3 regulates heterochromatin in mouse embryonic stem cells. Nature. 591(7849):317–321
https://doi.org/10.1038/s41586-021-03210-1
47 S Zaccara, SR Jaffrey (2020) A unified model for the function of YTHDF proteins in regulating m(6)A-modified mRNA. Cell 181 (1582–1595):
https://doi.org/10.1016/j.cell.2020.05.012
48 Y Zhang, T Liu, CA Meyer, J Eeckhoute, DS Johnson, BE Bernstein, C Nusbaum, RM Myers, M Brown, W Liet al. (2008) Model-based analysis of ChIP-Seq (MACS). Genome Biol 9:R137
https://doi.org/10.1186/gb-2008-9-9-r137
49 BS Zhao, X Wang, AV Beadell, Z Lu, H Shi, A Kuuspalu, RK Ho, C He (2017) m(6)A-dependent maternal mRNA clearance facilitates zebrafish maternal-to-zygotic transition. Nature 542:475–478
https://doi.org/10.1038/nature21355
50 J, Zhou J Wan, X, Gao X Zhang, SR Jaffrey, SB Qian (2015) Dynamic m(6)A mRNA methylation directs translational control of heat shock response. Nature 526:591–594
https://doi.org/10.1038/nature15377
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