Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT03216
[1]
Histone modification H3K4me3 MLL1 RBM15 Direct Enhancement m6A modification TRIM72 TRIM72 RBM15 Methylation : m6A sites
m6A Modification:
m6A Regulator RNA-binding motif protein 15 (RBM15) WRITER
m6A Target Tripartite motif-containing protein 72 (TRIM72)
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Histone modification (HistMod)
Epigenetic Regulator Histone-lysine N-methyltransferase 2A (KMT2A) WRITER View Details
Regulated Target Histone H3 lysine 4 trimethylation (H3K4me3) View Details
Downstream Gene RBM15 View Details
Crosstalk Relationship Histone modification  →  m6A Enhancement
Crosstalk Mechanism histone modification directly impacts m6A modification through modulating the level of m6A regulator
Crosstalk Summary KMT2A elevated RBM15 expression by increasing Histone H3 lysine 4 trimethylation (H3K4me3) on RBM15 promoter. RBM15 promoted the binding of Tripartite motif-containing protein 72 (TRIM72) to YTHDF2 by enhancing m6A modification on TRIM72 mRNA, thereby repressing TRIM72 expression. TRIM72 bound to ADAM9 and ubiquitinated it for degradation.
Responsed Disease Preeclampsia ICD-11: JA23
Responsed Drug Actinomycin D
In-vitro Model
HTR-8/SVneo Normal Homo sapiens CVCL_7162
References
Ref 1 MLL1 promotes placental trophoblast ferroptosis and aggravates preeclampsia symptoms through epigenetic regulation of RBM15/TRIM72/ADAM9 axis. Biol Direct. 2024 Dec 22;19(1):133. doi: 10.1186/s13062-024-00572-0.