Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT05495
[1]
m6A modification miR-133a miR-133a IGF2BP2 : m6A sites Direct Enhancement Non-coding RNA miR-133a AGO2  lncRNA       miRNA   circRNA
m6A Modification:
m6A Regulator Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) READER
m6A Target miR-133a
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Non-coding RNA (ncRNA)
Epigenetic Regulator hsa-miR-133a-3p microRNA View Details
Regulated Target Protein argonaute-2 (AGO2) View Details
Crosstalk Relationship m6A  →  ncRNA Enhancement
Crosstalk Mechanism m6A regulators directly modulate the functionality of ncRNAs through specific targeting ncRNA
Crosstalk Summary IGF2BP2 physically interacted with Protein argonaute-2 (AGO2) and increased more miR-133a accumulation on its target site.m6A modification promoted the repression of specific miRNA during heart development and hypertrophy.
Responsed Disease Cardiomegaly ICD-11: BC45
Cell Process Cell proliferation
In-vitro Model
CM Pancreatic insulinoma Homo sapiens CVCL_H246
In-vivo Model Neonatal mouse cardiomyocytes (CMs) were blinded to isolate from 7-10 cases of postnatal 1-day old wildtype C57/B mice and cultured using Pierce Primary Cardi Page 10.omyocyte Isolation Kit (Thermo Fisher Scientific) as the manufacturer's instructions.
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
BC45: Cardiomegaly 1 Compound(s) Regulating the Disease Click to Show/Hide the Full List
 Compound Name UK-356202 Clinical trial [2]
Synonyms
compound 13j [PMID: 15149680]; UK-356,202
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External Link
References
Ref 1 m6A modification promotes miR-133a repression during cardiac development and hypertrophy via IGF2BP2. Cell Death Discov. 2021 Jun 26;7(1):157. doi: 10.1038/s41420-021-00552-7.
Ref 2 Selective urokinase-type plasminogen activator (uPA) inhibitors. Part 3: 1-isoquinolinylguanidines. Bioorg Med Chem Lett. 2004 Jun 21;14(12):3227-30. doi: 10.1016/j.bmcl.2004.03.094.