Stem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation - PubMed (original) (raw)
. 2015 Feb 27;347(6225):1002-6.
doi: 10.1126/science.1261417. Epub 2015 Jan 1.
Sharon Moshitch-Moshkovitz 2, Dan Dominissini 3, Abed AlFatah Mansour 1, Nitzan Kol 2, Mali Salmon-Divon 2, Vera Hershkovitz 2, Eyal Peer 2, Nofar Mor 1, Yair S Manor 1, Moshe Shay Ben-Haim 2, Eran Eyal 2, Sharon Yunger 2, Yishay Pinto 4, Diego Adhemar Jaitin 5, Sergey Viukov 1, Yoach Rais 1, Vladislav Krupalnik 1, Elad Chomsky 1, Mirie Zerbib 1, Itay Maza 1, Yoav Rechavi 1, Rada Massarwa 1, Suhair Hanna 6, Ido Amit 5, Erez Y Levanon 4, Ninette Amariglio 7, Noam Stern-Ginossar 1, Noa Novershtern 8, Gideon Rechavi 9, Jacob H Hanna 8
Affiliations
- PMID: 25569111
- DOI: 10.1126/science.1261417
Stem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation
Shay Geula et al. Science. 2015.
Abstract
Naïve and primed pluripotent states retain distinct molecular properties, yet limited knowledge exists on how their state transitions are regulated. Here, we identify Mettl3, an N(6)-methyladenosine (m(6)A) transferase, as a regulator for terminating murine naïve pluripotency. Mettl3 knockout preimplantation epiblasts and naïve embryonic stem cells are depleted for m(6)A in mRNAs, yet are viable. However, they fail to adequately terminate their naïve state and, subsequently, undergo aberrant and restricted lineage priming at the postimplantation stage, which leads to early embryonic lethality. m(6)A predominantly and directly reduces mRNA stability, including that of key naïve pluripotency-promoting transcripts. This study highlights a critical role for an mRNA epigenetic modification in vivo and identifies regulatory modules that functionally influence naïve and primed pluripotency in an opposing manner.
Copyright © 2015, American Association for the Advancement of Science.
Similar articles
- Fate by RNA methylation: m6A steers stem cell pluripotency.
Zhao BS, He C. Zhao BS, et al. Genome Biol. 2015 Feb 22;16(1):43. doi: 10.1186/s13059-015-0609-1. Genome Biol. 2015. PMID: 25723450 Free PMC article. Review. - N(6)-Methyladenosine Methyltransferases and Demethylases: New Regulators of Stem Cell Pluripotency and Differentiation.
Wu Y, Zhang S, Yuan Q. Wu Y, et al. Stem Cells Dev. 2016 Jul 15;25(14):1050-9. doi: 10.1089/scd.2016.0062. Epub 2016 Jun 27. Stem Cells Dev. 2016. PMID: 27216987 Review. - The SMAD2/3 interactome reveals that TGFβ controls m6A mRNA methylation in pluripotency.
Bertero A, Brown S, Madrigal P, Osnato A, Ortmann D, Yiangou L, Kadiwala J, Hubner NC, de Los Mozos IR, Sadée C, Lenaerts AS, Nakanoh S, Grandy R, Farnell E, Ule J, Stunnenberg HG, Mendjan S, Vallier L. Bertero A, et al. Nature. 2018 Mar 8;555(7695):256-259. doi: 10.1038/nature25784. Epub 2018 Feb 28. Nature. 2018. PMID: 29489750 Free PMC article. - m6A methylation controls pluripotency of porcine induced pluripotent stem cells by targeting SOCS3/JAK2/STAT3 pathway in a YTHDF1/YTHDF2-orchestrated manner.
Wu R, Liu Y, Zhao Y, Bi Z, Yao Y, Liu Q, Wang F, Wang Y, Wang X. Wu R, et al. Cell Death Dis. 2019 Feb 20;10(3):171. doi: 10.1038/s41419-019-1417-4. Cell Death Dis. 2019. PMID: 30787270 Free PMC article. - METTL3 inhibits hepatic insulin sensitivity via N6-methyladenosine modification of Fasn mRNA and promoting fatty acid metabolism.
Xie W, Ma LL, Xu YQ, Wang BH, Li SM. Xie W, et al. Biochem Biophys Res Commun. 2019 Oct 8;518(1):120-126. doi: 10.1016/j.bbrc.2019.08.018. Epub 2019 Aug 10. Biochem Biophys Res Commun. 2019. PMID: 31405565
Cited by
- Genome-wide detection of high abundance N6-methyladenosine sites by microarray.
Li Y, Wang Y, Zhang Z, Zamudio AV, Zhao JC. Li Y, et al. RNA. 2015 Aug;21(8):1511-8. doi: 10.1261/rna.051474.115. Epub 2015 Jun 19. RNA. 2015. PMID: 26092943 Free PMC article. - Fate by RNA methylation: m6A steers stem cell pluripotency.
Zhao BS, He C. Zhao BS, et al. Genome Biol. 2015 Feb 22;16(1):43. doi: 10.1186/s13059-015-0609-1. Genome Biol. 2015. PMID: 25723450 Free PMC article. Review. - Exploring glioblastoma stem cell heterogeneity: Immune microenvironment modulation and therapeutic opportunities.
Johnson AL, Laterra J, Lopez-Bertoni H. Johnson AL, et al. Front Oncol. 2022 Sep 21;12:995498. doi: 10.3389/fonc.2022.995498. eCollection 2022. Front Oncol. 2022. PMID: 36212415 Free PMC article. Review. - WTAP Function in Sertoli Cells Is Essential for Sustaining the Spermatogonial Stem Cell Niche.
Jia GX, Lin Z, Yan RG, Wang GW, Zhang XN, Li C, Tong MH, Yang QE. Jia GX, et al. Stem Cell Reports. 2020 Oct 13;15(4):968-982. doi: 10.1016/j.stemcr.2020.09.001. Stem Cell Reports. 2020. PMID: 33053361 Free PMC article. - YTHDF2 Regulates Macrophage Polarization through NF-_κ_B and MAPK Signaling Pathway Inhibition or p53 Degradation.
Cai L, Li D, Feng Z, Gu X, Xu Q, Li Q. Cai L, et al. Dis Markers. 2022 Oct 12;2022:3153362. doi: 10.1155/2022/3153362. eCollection 2022. Dis Markers. 2022. PMID: 36277978 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials