TY - JOUR
T1 - PRMT1 regulates astrocytic differentiation of embryonic neural stem/precursor cells
AU - Honda, Mizuki
AU - Nakashima, Kinichi
AU - Katada, Sayako
N1 - Funding Information:
MEXT of Japan (17H05647) to S.K. M.H. received funding from a Sasakawa Scientific Research Grant. The authors declare that they have no conflicts of interest.
Funding Information:
We thank Z. Zhou, M. E. Greenberg, and Fred H. Gage for sharing reagents, and all members of the Laboratory of Stem Cell Biology and Medicine in Kyushu University for valuable comments. This work was supported by funding from the Takeda Science Foundation, the Uehara Memorial Foundation, and Grant in Aid for Scientific Research on Innovative Areas ?Stem Cell Aging and Disease? from the MEXT of Japan (17H05647) to S.K. M.H. received funding from a Sasakawa Scientific Research Grant. The authors declare that they have no conflicts of interest. All experiments were conducted in compliance with the ARRIVE guidelines.
Funding Information:
We thank Z. Zhou, M. E. Greenberg, and Fred H. Gage for sharing reagents, and all members of the Laboratory of Stem Cell Biology and Medicine in Kyushu University for valuable comments. This work was supported by funding from the Takeda Science Foundation, the Uehara Memorial Foundation, and Grant in Aid for Scientific Research on Innovative Areas ‘Stem Cell Aging and Disease’ from the
Publisher Copyright:
© 2017 International Society for Neurochemistry
PY - 2017/9
Y1 - 2017/9
N2 - 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. (Figure presented.).
AB - 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. (Figure presented.).
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U2 - 10.1111/jnc.14123
DO - 10.1111/jnc.14123
M3 - Article
C2 - 28695568
AN - SCOPUS:85026676215
SN - 0022-3042
VL - 142
SP - 901
EP - 907
JO - Journal of Neurochemistry
JF - Journal of Neurochemistry
IS - 6
ER -