PTBP1 and PTBP2 Serve Both Specific and Redundant Functions in Neuronal Pre-mRNA Splicing

被引:86
|
作者
Vuong, John K. [1 ]
Lin, Chia-Ho [2 ]
Zhang, Min [1 ]
Chen, Liang [3 ]
Black, Douglas L. [2 ]
Zheng, Sika [1 ]
机构
[1] Univ Calif Riverside, Div Biomed Sci, Riverside, CA 92521 USA
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Southern Calif, Dept Biol Sci, Div Mol & Computat Biol, Los Angeles, CA 90089 USA
来源
CELL REPORTS | 2016年 / 17卷 / 10期
关键词
TRACT-BINDING-PROTEINS; BRAIN; DIFFERENTIATION; REPRESSION; INSIGHTS; CELLS; SEQ;
D O I
10.1016/j.celrep.2016.11.034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Families of alternative splicing regulators often contain multiple paralogs presumed to fulfill different functions. Polypyrimidine tract binding proteins PTBP1 and PTBP2 reprogram developmental pre-mRNA splicing in neurons, but how their regulatory networks differ is not understood. To compare their targeting, we generated a knockin allele that conditionally expresses PTBP1. Bred to a Ptbp2 knockout, the transgene allowed us to compare the developmental and molecular phenotypes of mice expressing only PTBP1, only PTBP2, or neither protein in the brain. This knockin Ptbp1 rescued a forebrain-specific, but not a pan-neuronal, Ptbp2 knockout, demonstrating both redundant and distinct roles for the proteins. Many developmentally regulated exons exhibited different sensitivities to PTBP1 and PTBP2. Nevertheless, the two paralogs displayed similar RNA binding across the transcriptome, indicating that their differential targeting does not derive from their RNA interactions, but from possible different cofactor interactions.
引用
收藏
页码:2766 / 2775
页数:10
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