Deterministic splicing of Dscam2 is regulated by Muscleblind

被引:8
作者
Li, Joshua Shing Shun [1 ]
Millard, S. Sean [1 ]
机构
[1] Univ Queensland, Fac Med, Sch Biomed Sci, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
GENE-EXPRESSION; DROSOPHILA; PROTEINS; FAMILY; NETWORKS;
D O I
10.1126/sciadv.aav1678
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alternative splicing increases the proteome diversity crucial for establishing the complex circuitry between trillions of neurons. To provide individual cells with different repertoires of protein isoforms, however, this process must be regulated. Previously, we found that the mutually exclusive alternative splicing of Drosophila Dscam2 produces two isoforms (A and B) with unique binding properties. This splicing event is cell type specific, and the transmembrane proteins that it generates are crucial for the development of axons, dendrites, and synapses. Here, we show that Muscleblind (Mbl) controls Dscam2 alternative splicing. Mbl represses isoform A and promotes the selection of isoform B. Mbl mutants exhibit phenotypes also observed in flies engineered to express a single Dscam2 isoform. Consistent with this, mbl expression is cell type specific and correlates with the splicing of isoform B. Our study demonstrates how the regulated expression of a splicing factor is sufficient to provide neurons with unique protein isoforms crucial for development.
引用
收藏
页数:10
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