Methylation Modifications in Eukaryotic Messenger RNA

被引:110
作者
Liu, Jun [1 ]
Jia, Guifang [1 ]
机构
[1] Peking Univ, Synthet & Funct Biomol Ctr, Beijing Natl Lab Mol Sci, Dept Chem Biol,Coll Chem & Mol Engn, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA methylation; N-7-methylguanosine (m(7)G); N-6-methyladenosine (m(6)A); 5-methylcytosine (m(5)C); HETEROGENEOUS NUCLEAR-RNA; SACCHAROMYCES-CEREVISIAE; CAP METHYLTRANSFERASE; FTO GENE; MOUSE; DNA; OBESITY; IDENTIFICATION; NUCLEOSIDES; SEQUENCES;
D O I
10.1016/j.jgg.2013.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA methylation modifications have been found for decades of years, which occur at different RNA types of numerous species, and their distribution is species-specific. However, people rarely know their biological functions. There are several identified methylation modifications in eukaryotic messenger RNA (mRNA), such as N-7-methylguanosine (m(7)G) at the cap, N-6-methyl-2'-O-methyladenosine (m(6)A(m)), 2'-O-methylation (N-m) within the cap and the internal positions, and internal N-6-methyladenosine (m(6)A) and 5-methylcytosine (m(5)C). Among them, m(7)G cap was studied more clearly and found to have vital roles in several important mRNA processes like mRNA translation, stability and nuclear export. m(6)A as the most abundant modification in mRNA was found in the 1970s and has been proposed to function in mRNA splicing, translation, stability, transport and so on. m(6)A has been discovered as the first RNA reversible modification which is demethylated directly by human fat mass and obesity associated protein (FTO) and its homolog protein, alkylation repair homolog 5 (ALKBH5). FTO has a special demethylation mechanism that demethylases m(6)A to A through two over-oxidative intermediate states: N-6-hydroxymethyladenosine (hm(6)A) and N-6-formyladenosine (f(6)A). The two newly discovered m(6)A demethylases, FTO and ALKBH5, significantly control energy homeostasis and spermatogenesis, respectively, indicating that the dynamic and reversible m(6)A, analogous to DNA and histone modifications, plays broad roles in biological kingdoms and brings us an emerging field "RNA Epigenetics". 5-methylcytosine (5mC) as an epigenetic mark in DNA has been studied widely, but m(5)C in mRNA is seldom explored. The bisulfide sequencing showed m(5)C is another abundant modification in mRNA, suggesting that it might be another RNA epigenetic mark. This review focuses on the main methylation modifications in mRNA to describe their formation, distribution, function and demethylation from the current knowledge and to provide future perspectives on functional studies.
引用
收藏
页码:21 / 33
页数:13
相关论文
共 109 条
[91]   Human mRNA cap methyltransferase: Alternative nuclear localization signal motifs ensure nuclear localization required for viability [J].
Shafer, B ;
Chu, C ;
Shatkin, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (07) :2644-2649
[92]   The Centrality of RNA [J].
Sharp, Phillip A. .
CELL, 2009, 136 (04) :577-580
[93]   CAPPING OF EUKARYOTIC MESSENGER-RNAS [J].
SHATKIN, AJ .
CELL, 1976, 9 (04) :645-653
[94]   What messenger RNA capping tells us about eukaryotic evolution [J].
Shuman, S .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (08) :619-625
[95]   METHYLATION OF ADENOVIRUS-SPECIFIC NUCLEAR AND CYTOPLASMIC RNA [J].
SOMMER, S ;
SALDITTGEORGIEFF, M ;
BACHENHEIMER, S ;
DARNELL, JE ;
FURUICHI, Y ;
MORGAN, M ;
SHATKIN, AJ .
NUCLEIC ACIDS RESEARCH, 1976, 3 (03) :749-765
[96]   Re-programming of translation following cell stress allows IRES-mediated translation to predominate [J].
Spriggs, Keith A. ;
Stoneley, Mark ;
Bushell, Martin ;
Willis, Anne E. .
BIOLOGY OF THE CELL, 2008, 100 (01) :27-38
[97]   Widespread occurrence of 5-methylcytosine in human coding and non-coding RNA [J].
Squires, Jeffrey E. ;
Patel, Hardip R. ;
Nousch, Marco ;
Sibbritt, Tennille ;
Humphreys, David T. ;
Parker, Brian J. ;
Suter, Catherine M. ;
Preiss, Thomas .
NUCLEIC ACIDS RESEARCH, 2012, 40 (11) :5023-5033
[98]   Cloning and characterization of three human cDNAs encoding mRNA (guanine-7-)-methyltransferase, an mRNA cap methylase [J].
Tsukamoto, T ;
Shibagaki, Y ;
Niikura, Y ;
Mizumoto, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 251 (01) :27-34
[99]  
VENMURTHY MR, 1982, J NEUROCHEM, V38, P28
[100]   Cysteine of sequence motif VI is essential for nucleophilic catalysis by yeast tRNA m5C methyltransferase [J].
Walbott, Helene ;
Husson, Clotilde ;
Auxilien, Sylvie ;
Golinelli-Pimpaneau, Beatrice .
RNA, 2007, 13 (07) :967-973