From: Crosstalk between m6A modification and autophagy in cancer
Type | Regulator | Function | References |
---|---|---|---|
“Writer” | METTL3 | Binds to METTL14 to form a stable heterodimer that acts as a catalytic core | [49] |
METTL14 | Binds to METTL3 to form a stable heterodimer that serves as a structural support for binding to RNA | [49] | |
WTAP | Ensure that the METTL3-METTL14 heterodimer is localized in the nuclear speckle | ||
RBM15 | Binds the m6A complex and recruits it to specific RNA sites | ||
VIRMA, KIAA1429 | Regulation of regioselective methylation by recruitment of MTCs | [53] | |
METTL16 | Catalytic m6A modification of U6-snRNA involved in pre-RNA splicing | [40] | |
ZC3H13 | Enhancement of m6A by ligating WTAP to the mRNA binding factor Nito | [54] | |
“Erasers” | FTO | Remove m6A modifier | |
ALKBH5 | Remove m6A modifier | [55] | |
“Readers” | YTHDF1 | Enhancement of m6A mRNA translation by promoting ribosome assembly and interaction with initiation factors | [56] |
YTHDF2 | Selective binding and recruitment of m6A-modified mRNAs to mRNA decay sites induces transcript degradation | [57] | |
YTHDF3 | Interaction with YTHDF1 promotes RNA translation and interaction with YTHDF2 promotes RNA degradation | ||
YTHDC1 | Involved in RNA splicing and export | ||
YTHDC2 | Increased translation efficiency but reduced abundance of target mRNAs | ||
IGF2BPs | Enhanced mRNA stability and translation | [48] | |
EIF3 | Promote mRNA translation | [64] |