Roles of N6-Methyladenosine (m6A) in Stem Cell Fate Decisions and Early Embryonic Development in Mammals

被引:70
作者
Zhang, Meng [1 ]
Zhai, Yanhui [1 ]
Zhang, Sheng [1 ]
Dai, Xiangpeng [1 ]
Li, Ziyi [1 ]
机构
[1] First Hosp Jilin Univ, Key Lab Organ Regenerat & Transplantat, Minist Educ, Changchun, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
N6-methyladenosine; RNA metabolism; stem cell fate; cell reprogramming; embryonic development; MESSENGER-RNA METHYLATION; NUCLEAR-RNA; REGULATES PLURIPOTENCY; HEMATOPOIETIC STEM; READER YTHDF2; N-6-METHYLADENOSINE; DIFFERENTIATION; TRANSLATION; REVEALS; PROTEIN;
D O I
10.3389/fcell.2020.00782
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
N6-methyladenosine (m(6)A) is one of the most abundant internal mRNA modifications, and it affects multiple biological processes related to eukaryotic mRNA. The majority of m(6)A sites are located in stop codons and 3 ' UTR regions of mRNAs. m(6)A regulates RNA metabolism, including alternative splicing (AS), alternative polyadenylation (APA), mRNA export, decay, stabilization, and translation. The m(6)A metabolic pathway is regulated by a series of m(6)A writers, erasers and readers. Recent studies indicate that m(6)A is essential for the regulation of gene expression, tumor formation, stem cell fate, gametogenesis, and animal development. In this systematic review, we summarized the recent advances in newly identified m(6)A effectors and the effects of m(6)A on RNA metabolism. Subsequently, we reviewed the functional roles of RNA m(6)A modification in diverse cellular bioprocesses, such as stem cell fate decisions, cell reprogramming and early embryonic development, and we discussed the potential of m(6)A modification to be applied to regenerative medicine, disease treatment, organ transplantation, and animal reproduction.
引用
收藏
页数:15
相关论文
共 123 条
[41]  
Jia GF, 2011, NAT CHEM BIOL, V7, P885, DOI [10.1038/NCHEMBIO.687, 10.1038/nchembio.687]
[42]   Nuclear m6A reader YTHDC1 regulates alternative polyadenylation and splicing during mouse oocyte development [J].
Kasowitz, Seth D. ;
Ma, Jun ;
Anderson, Stephen J. ;
Leu, N. Adrian ;
Xu, Yang ;
Gregory, Brian D. ;
Schultz, Richard M. ;
Wang, P. Jeremy .
PLOS GENETICS, 2018, 14 (05)
[43]   A majority of m6A residues are in the last exons, allowing the potential for 3′ UTR regulation [J].
Ke, Shengdong ;
Alemu, Endalkachew A. ;
Mertens, Claudia ;
Gantman, Emily Conn ;
Fak, John J. ;
Mele, Aldo ;
Haripal, Bhagwattie ;
Zucker-Scharff, Ilana ;
Moore, Michael J. ;
Park, Christopher Y. ;
Vagbo, Cathrine Broberg ;
Kusnierczyk, Anna ;
Klungland, Arne ;
Darnell, James E., Jr. ;
Darnell, Robert B. .
GENES & DEVELOPMENT, 2015, 29 (19) :2037-2053
[44]   Chromatin modifications and their function [J].
Kouzarides, Tony .
CELL, 2007, 128 (04) :693-705
[45]   Stage-specific requirement for Mettl3-dependent m6A mRNA methylation during haematopoietic stem cell differentiation [J].
Lee, Heather ;
Bao, Suying ;
Qian, Yingzhi ;
Geula, Shay ;
Leslie, Juliana ;
Zhang, Chaolin ;
Hanna, Jacob H. ;
Ding, Lei .
NATURE CELL BIOLOGY, 2019, 21 (06) :700-+
[46]   Cytoplasmic m6A reader YTHDF3 promotes mRNA translation [J].
Li, Ang ;
Chen, Yu-Sheng ;
Ping, Xiao-Li ;
Yang, Xin ;
Xiao, Wen ;
Yang, Ying ;
Sun, Hui-Ying ;
Zhu, Qin ;
Baidya, Poonam ;
Wang, Xing ;
Bhattarai, Devi Prasad ;
Zhao, Yong-Liang ;
Sun, Bao-Fa ;
Yang, Yun-Gui .
CELL RESEARCH, 2017, 27 (03) :444-447
[47]   Targeted mRNA demethylation using an engineered dCas13b-ALKBH5 fusion protein [J].
Li, Jiexin ;
Chen, Zhuojia ;
Chen, Feng ;
Xie, Guoyou ;
Ling, Yuyi ;
Peng, Yanxi ;
Lin, Yu ;
Luo, Nan ;
Chiang, Cheng-Ming ;
Wang, Hongsheng .
NUCLEIC ACIDS RESEARCH, 2020, 48 (10) :5684-5694
[48]   Suppression of m6A reader Ythdf2 promotes hematopoietic stem cell expansion [J].
Li, Zhenrui ;
Qian, Pengxu ;
Shao, Wanqing ;
Shi, Hailing ;
He, Xi C. ;
Gogol, Madelaine ;
Yu, Zulin ;
Wang, Yongfu ;
Qi, Meijie ;
Zhu, Yunfei ;
Perry, John M. ;
Zhang, Kai ;
Tao, Fang ;
Zhou, Kun ;
Hu, Deqing ;
Han, Yingli ;
Zhao, Chongbei ;
Alexander, Richard ;
Xu, Hanzhang ;
Chen, Shiyuan ;
Peak, Allison ;
Hall, Kathyrn ;
Peterson, Michael ;
Perera, Anoja ;
Haug, Jeffrey S. ;
Parmely, Tari ;
Li, Hua ;
Shen, Bin ;
Zeitlinger, Julia ;
He, Chuan ;
Li, Linheng .
CELL RESEARCH, 2018, 28 (09) :904-917
[49]   The m6A Methyltransferase METTL3 Promotes Translation in Human Cancer Cells [J].
Lin, Shuibin ;
Choe, Junho ;
Du, Peng ;
Triboulet, Robinson ;
Gregory, Richard I. .
MOLECULAR CELL, 2016, 62 (03) :335-345
[50]   Mettl3-/Mettl14-mediated mRNA N6-methyladenosine modulates murine spermatogenesis [J].
Lin, Zhen ;
Hsu, Phillip J. ;
Xing, Xudong ;
Fang, Jianhuo ;
Lu, Zhike ;
Zou, Qin ;
Zhang, Ke-Jia ;
Zhang, Xiao ;
Zhou, Yuchuan ;
Zhang, Teng ;
Zhang, Youcheng ;
Song, Wanlu ;
Jia, Guifang ;
Yang, Xuerui ;
He, Chuan ;
Tong, Ming-Han .
CELL RESEARCH, 2017, 27 (10) :1216-1230