Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT05084
[1]
Non-coding RNA FAS-AS1 FMR1  lncRNA       miRNA   circRNA Direct Enhancement m6A modification ADAM8 ADAM8 FMR1 : m6A sites
m6A Modification:
m6A Regulator Synaptic functional regulator FMR1 (FMR1) READER
m6A Target Disintegrin and metalloproteinase domain-containing protein 8 (ADAM8)
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Non-coding RNA (ncRNA)
Epigenetic Regulator FAS antisense RNA 1 (FAS-AS1) LncRNA View Details
Regulated Target Fragile X messenger ribonucleoprotein 1 (FMR1) View Details
Crosstalk Relationship ncRNA  →  m6A Enhancement
Crosstalk Mechanism ncRNAs directly impacts m6A modification through recruiting m6A regulator
Crosstalk Summary FAS-AS1 maintained the stability of Disintegrin and metalloproteinase domain-containing protein 8 (ADAM8) mRNA by recruiting FMR1. METTL14 knockdown repressed FAS-AS1 expression in an m6A-dependent manner. METTL14-mediated lncRNA-FAS-AS1 promotes osteoarthritis progression by up-regulating ADAM8
Responsed Disease Osteoarthritis ICD-11: FA05
References
Ref 1 METTL14-mediated lncRNA-FAS-AS1 promotes osteoarthritis progression by up-regulating ADAM8. Int J Rheum Dis. 2024 Sep;27(9):e15323. doi: 10.1111/1756-185X.15323.