Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT05206
[1]
Non-coding RNA CircHIPK3 IGF2BP2  lncRNA       miRNA   circRNA Direct Enhancement m6A modification Krm1 Krm1 IGF2BP2 : m6A sites
m6A Modification:
m6A Regulator Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) READER
m6A Target Kremen protein 1 (KRM1)
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Non-coding RNA (ncRNA)
Epigenetic Regulator Circ_HIPK3 circRNA View Details
Regulated Target Insulin like growth factor 2 mRNA binding protein 2 (IGF2BP2) View Details
Crosstalk Relationship ncRNA  →  m6A Enhancement
Crosstalk Mechanism ncRNAs directly impacts m6A modification through recruiting m6A regulator
Crosstalk Summary m6A-modified circRNA was found to increase mRNA stability by functioning as a scaffold for the binding of IGF2BP2 and mRNA. This phenomenon was also observed in the present study, and we identified Kremen protein 1 (KRM1) as a target gene of the Circ_HIPK3/IGF2BP2 complex.
Responsed Disease Calcific aortic valve disease ICD-11: BB71
References
Ref 1 Noncoding RNA regulates the expression of Krm1 and Dkk2 to synergistically affect aortic valve lesions. Exp Mol Med. 2024 Jul;56(7):1560-1573. doi: 10.1038/s12276-024-01256-5. Epub 2024 Jul 1.