%0 Journal Article
%T A novel m6A reader Prrc2a controls oligodendroglial specification and myelination
%A Ang Li
%A Baofa Sun
%A Fengchao Wang
%A Hai-Lin Wang
%A Jian-Guang Sun
%A Jinhua Zhang
%A Jun Ma
%A Qingyang Zhang
%A Rong Wu
%A Shukun Wang
%A Ting Zhang
%A Wei-Yi Lai
%A Xiaolong Qi
%A Xin Yang
%A Yajin Liao
%A Yousheng Shu
%A Yuhao Gao
%A Yujie Xiao
%A Yun-Gui Yang
%A Yusheng Chen
%A Zengqiang Yuan
%J Archive of "Cell Research".
%D 2019
%R 10.1038/s41422-018-0113-8
%X Prrc2a is a novel m6A reader. a Schematic illustration of m6A binding protein screening. b Scatter plot of proteins bound to Oligo-m6A vs Oligo-A RNA oligos. The plot was based on the average peptide numbers of proteins detected in two replicates. Enriched Prrc2a, Prrc2c, and YTH-domain containing proteins were highlighted (see also Supplementary information, Table S1). c Western blotting showing Ythdf1 and Prrc2a pulled down with an m6A-containing RNA probe. d Pie chart depicting the distribution of Prrc2a-binding peaks. e Binding motif identified by HOMER with Prrc2a-binding peaks (p£¿=£¿1e-46). f Overlap of Prrc2a-binding peaks and m6A-containing peaks. g Distribution of m6A-containing Prrc2a peaks across the length of mRNA. 5¡ä UTR, CDS, and 3¡ä UTR were each binned into regions spanning 1% of their total length, and the percentages of m6A-containing Prrc2a peaks that fall within each bin were determined. The moving averages of m6A-containing Prrc2a peak percentage are shown. h Representative Gene Ontology (GO) terms of the biological process categories enriched in transcripts with both Prrc2a-binding and m6A peaks. Gene ontology (GO) analysis was performed using the DAVID bioinformatics database. GO classification for cellular component, biological process, and molecular function were performed with default setting
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318280/