Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT03236
[1]
m6A modification RBBP5 RBBP5 ALKBH5 Demethylation : m6A sites Direct Enhancement Histone modification H3K4me3 RBBP5 GATA4
m6A Modification:
m6A Regulator RNA demethylase ALKBH5 (ALKBH5) ERASER
m6A Target Retinoblastoma-binding protein 5 (RBBP5)
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Histone modification (HistMod)
Epigenetic Regulator Retinoblastoma-binding protein 5 (RBBP5) WRITER View Details
Regulated Target Histone H3 lysine 4 trimethylation (H3K4me3) View Details
Downstream Gene GATA4 View Details
Crosstalk Relationship m6A  →  Histone modification Enhancement
Crosstalk Mechanism m6A modification impacts directly histone modification through modulating the expression level of histone-associated enzymes
Crosstalk Summary KDM5B and Retinoblastoma-binding protein 5 (RBBP5), the components of H3K4 modifying enzyme complexes, are identified as downstream targets for ALKBH5 in cardiac-committed hESCs. Loss of function of ALKBH5 alters the expression of KDM5B and RBBP5 through impairing stability of their mRNAs, which in turn promotes the transcription of GATA4 by enhancing Histone H3 lysine 4 trimethylation (H3K4me3) at the promoter region of GATA4.
References
Ref 1 ALKBH5-mediated m(6)A mRNA methylation governs human embryonic stem cell cardiac commitment. Mol Ther Nucleic Acids. 2021 May 29;26:22-33. doi: 10.1016/j.omtn.2021.05.019. eCollection 2021 Dec 3.