TABLE 1.
Functions of m6A modification-related proteins.
Type | Genetic name | Function | References |
---|---|---|---|
m 6 A writer | METTL3 | Identify the conservative base sequence of m6A, catalytic methylation modification | Geula et al. (2015) |
METTL14 | Assist METTL3 to catalytic methylation modifications | Wang et al. (2016) | |
WTAP | Promote METTL3 and METTL14 heterogeneous dilate | Agarwala et al. (2012) | |
VIRMA | Special modification of the 3′UTR region | Yue et al. (2018) | |
RBM15 | Combined with the m6A complex and recruit it to a special RNA site | Patil et al. (2016) | |
ZC3H13 | Connect to WTAP to mRNA binding factor Nito | Wen et al. (2018) | |
METTL16 | Catalytic methylation modification | Pendleton et al. (2017) | |
m 6 A eraser | FTO | Delete methylation modification | Jia et al. (2011) |
ALKBH5 | Delete methylation modification | Zheng et al. (2013) | |
m 6 A reader | YTHDC1 | Recruit splicing factors to splicing target mRNAs, promoting mRNA output degradation and specific transcription | (Xiao et al., 2016; Roundtree et al., 2017; Shima et al., 2017) |
YTHDC2 | Adjust the stability and translation of mRNA | Hsu et al. (2017) | |
YTHDF1 | Recruit translation start factor to promote the translation of mRNA | Wang et al. (2015) | |
YTHDF2 | Combined with m6A modifiers to recruit CCR4-NOT deadenylase complex acceleration destination mRNA degradation | Du et al. (2016) | |
YTHDF3 | Promote mRNA degradation or medium translation | (Li et al., 2017a; Shi et al., 2017) | |
HNRNPA2B1 | Promote primary microRNA processing | Wu et al. (2018) | |
HNRNPC/G | Mediate mRNA splicing | (Liu et al., 2015; Wang et al., 2015) | |
IGF2BP1/2/3 | Improve the stability of mRNA | Huang et al. (2018) | |
eIF3 | Combined with m6A to start translation | Meyer et al. (2015) | |
FMRP | Adjust the stability, translation and nuclear output of mRNA | Santoro et al. (2012) | |
Prrc2A | Improve the stability of mRNA | Wu et al. (2019) |