PRMT1 regulates astrocytic differentiation of embryonic neural stem/precursor cells.
Mizuki HondaKinichi NakashimaSayako KatadaPublished in: Journal of neurochemistry (2017)
Arginine methylation is a post-translational modification which is catalyzed by protein arginine methyltransferases (PRMTs). Here, we report that PRMT1 is highly expressed in neural stem/precursor cells (NS/PCs) of mouse embryos, and knockdown of PRMT1 in NS/PCs suppresses the generation of astrocytes. The luciferase assay demonstrated that knockdown of PRMT1 inhibits activation of the promoter of a typical astrocytic marker gene, glial fibrillary acidic protein (Gfap), in NS/PCs. The transcription factor signal transducer and activator of transcription 3 (STAT3) is known to generally be critical for astrocytic differentiation of NS/PCs. We found that PRMT1 methylates arginine residue(s) of STAT3 to regulate its activity positively, resulting in the promotion of astrocytic differentiation of NS/PCs.
Keyphrases
- dengue virus
- transcription factor
- induced apoptosis
- amino acid
- nitric oxide
- cell cycle arrest
- zika virus
- dna methylation
- genome wide
- cell proliferation
- signaling pathway
- gene expression
- oxidative stress
- high throughput
- endoplasmic reticulum stress
- dna binding
- binding protein
- cell death
- inflammatory response
- small molecule
- ionic liquid
- room temperature
- toll like receptor
- spinal cord
- nuclear factor