School of Biomedical Sciences, Faculty of Medicine, The University of Queensland, Brisbane, Queensland 4072, Australia.
Sci Adv. 2019 Jan 16;5(1):eaav1678. doi: 10.1126/sciadv.aav1678. eCollection 2019 Jan.
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 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 alternative splicing. Mbl represses isoform A and promotes the selection of isoform B. mutants exhibit phenotypes also observed in flies engineered to express a single isoform. Consistent with this, 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.
可变剪接增加了蛋白质组的多样性,这对建立数十亿个神经元之间复杂的电路至关重要。然而,为了使每个细胞具有不同的蛋白质同工型库,这个过程必须受到调节。以前,我们发现产生具有独特结合特性的两种同工型(A 和 B)的相互排斥的可变剪接。这种剪接事件是细胞类型特异性的,它产生的跨膜蛋白对轴突、树突和突触的发育至关重要。在这里,我们表明肌肉盲蛋白 (Mbl) 控制着的可变剪接。Mbl 抑制同工型 A 并促进同工型 B 的选择。突变体表现出也在表达单一同工型的果蝇中观察到的表型。与此一致,的表达是细胞类型特异性的,并与同工型 B 的剪接相关。我们的研究表明,剪接因子的表达如何受到调节,足以使神经元获得对发育至关重要的独特蛋白质同工型。