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Image Search Results
Journal: Frontiers in Veterinary Science
Article Title: MEF2C Expression Is Regulated by the Post-transcriptional Activation of the METTL3-m 6 A-YTHDF1 Axis in Myoblast Differentiation
doi: 10.3389/fvets.2022.900924
Figure Lengend Snippet: The protein expression of MEF2C is regulated by m6A modification. (A,B) MEF2C and FTO protein levels after FTO knockdown and overexpression on the 4th day after differentiation. (C,D) MEF2C and METTL3 protein levels after METTL3 knockdown and overexpression for 4th day post differentiation. (E,F) Treatment with a global methylation inhibitor, 3-Deazaadenosine (DAA), for 24 and 48 h led to the downregulation of the MEF2C protein levels in bovine skeletal myoblasts. The results are presented as the means ± SD (* p < 0.05, ** p < 0.01, *** p < 0.001, siNC vs. siRNA samples and DMSO vs. DAA at 24h; # p < 0.05, # # # p < 0.001, empty vector vs. overexpression plasmid samples and DMSO vs. DAA at 48h), using Student's t test.
Article Snippet: Additionally, MEF2C protein level was substantially decreased after 24 and 48 h of treatment with a
Techniques: Expressing, Modification, Knockdown, Over Expression, Methylation, Plasmid Preparation
Journal: Frontiers in Veterinary Science
Article Title: MEF2C Expression Is Regulated by the Post-transcriptional Activation of the METTL3-m 6 A-YTHDF1 Axis in Myoblast Differentiation
doi: 10.3389/fvets.2022.900924
Figure Lengend Snippet: MEF2C promotes the differentiation of bovine myoblasts by posttranscriptional activation of the METTL3-m 6 A-YTHDF1 axis. METTL3 catalyzes the N 6 -methylation of MEF2C mRNA, and YTHDF1 recognizes this modification site to promote the translation of MEF2C. Then, MEF2C can directly bind to the promoter region of METTL3 to activate its expression, suggesting that there is a positive feedback loop underlying the process of bovine skeletal myoblast differentiation.
Article Snippet: Additionally, MEF2C protein level was substantially decreased after 24 and 48 h of treatment with a
Techniques: Activation Assay, Methylation, Modification, Expressing