Wang Qingqing, Taliaferro J Matthew, Klibaite Ugne, Hilgers Valérie, Shaevitz Joshua W, Rio Donald C
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720; Center for RNA Systems Biology, University of California, Berkeley, CA 94720; California Institute for Quantitative Biosciences (QB3), University of California, Berkeley, CA 94720;
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720;
Proc Natl Acad Sci U S A. 2016 May 10;113(19):5269-74. doi: 10.1073/pnas.1600936113. Epub 2016 Apr 25.
Alternative pre-mRNA splicing (AS) is a critical regulatory mechanism that operates extensively in the nervous system to produce diverse protein isoforms. Fruitless AS isoforms have been shown to influence male courtship behavior, but the underlying mechanisms are unknown. Using genome-wide approaches and quantitative behavioral assays, we show that the P-element somatic inhibitor (PSI) and its interaction with the U1 small nuclear ribonucleoprotein complex (snRNP) control male courtship behavior. PSI mutants lacking the U1 snRNP-interacting domain (PSIΔAB mutant) exhibit extended but futile mating attempts. The PSIΔAB mutant results in significant changes in the AS patterns of ∼1,200 genes in the Drosophila brain, many of which have been implicated in the regulation of male courtship behavior. PSI directly regulates the AS of at least one-third of these transcripts, suggesting that PSI-U1 snRNP interactions coordinate the behavioral network underlying courtship behavior. Importantly, one of these direct targets is fruitless, the master regulator of courtship. Thus, PSI imposes a specific mode of regulatory control within the neuronal circuit controlling courtship, even though it is broadly expressed in the fly nervous system. This study reinforces the importance of AS in the control of gene activity in neurons and integrated neuronal circuits, and provides a surprising link between a pleiotropic pre-mRNA splicing pathway and the precise control of successful male mating behavior.
可变前体mRNA剪接(AS)是一种关键的调控机制,在神经系统中广泛发挥作用,以产生多种蛋白质异构体。无果AS异构体已被证明会影响雄性求偶行为,但其潜在机制尚不清楚。通过全基因组方法和定量行为分析,我们发现P因子体细胞抑制剂(PSI)及其与U1小核核糖核蛋白复合体(snRNP)的相互作用控制着雄性求偶行为。缺乏U1 snRNP相互作用结构域的PSI突变体(PSIΔAB突变体)表现出延长但徒劳的交配尝试。PSIΔAB突变体导致果蝇大脑中约1200个基因的AS模式发生显著变化,其中许多基因与雄性求偶行为的调控有关。PSI直接调控这些转录本中至少三分之一的AS,这表明PSI-U1 snRNP相互作用协调了求偶行为背后的行为网络。重要的是,这些直接靶点之一是无果基因,它是求偶行为的主要调节因子。因此,尽管PSI在果蝇神经系统中广泛表达,但它在控制求偶行为的神经元回路中施加了一种特定的调控模式。这项研究强化了AS在控制神经元和整合神经元回路中基因活性方面的重要性,并在多效性前体mRNA剪接途径与成功雄性交配行为的精确控制之间建立了一个惊人的联系。