Department of Developmental Biology, Sloan-Kettering Institute, New York, NY 10065, USA.
Department of Developmental Biology, Sloan-Kettering Institute, New York, NY 10065, USA.
Dev Cell. 2020 Aug 10;54(3):410-423.e4. doi: 10.1016/j.devcel.2020.06.004. Epub 2020 Jun 23.
How are diverse regulatory strategies integrated to impose appropriately patterned gene expression that underlie in vivo phenotypes? Here, we reveal how coordinated miRNA regulation and neural-specific alternative polyadenylation (APA) of a single locus controls complex behaviors. Our entry was the unexpected observation that deletion of Bithorax complex (BX-C) miRNAs converts virgin female flies into a subjective post-mated behavioral state, normally induced by seminal proteins following copulation. Strikingly, this behavioral switch is directly attributable to misregulation of homothorax (hth). We localize specific CNS abdominal neurons where de-repressed Hth compromises virgin behavior in BX-C miRNA mutants. Moreover, we use genome engineering to demonstrate that precise mutation of hth 3' UTR sites for BX-C miRNAs or deletion of its neural 3' UTR extension containing most of these sites both induce post-mated behaviors in virgins. Thus, facilitation of miRNA-mediated repression by neural APA is required for virgin females to execute behaviors appropriate to their internal state.
不同的调控策略是如何整合起来,以实现对体内表型有基础作用的基因表达模式的适当施加呢?在这里,我们揭示了单一基因座的协调 miRNA 调控和神经特异性可变多聚腺苷酸化(APA)如何控制复杂行为。我们的切入点是一个意外的观察结果,即 Bithorax complex(BX-C)miRNAs 的缺失将处女蝇转化为一种主观的交配后行为状态,这种行为通常是由交配后精液蛋白诱导的。引人注目的是,这种行为转变直接归因于同源异型盒(hth)的错误调控。我们定位到特定的中枢神经系统腹部神经元,其中去抑制的 Hth 会破坏 BX-C miRNA 突变体中的处女行为。此外,我们利用基因组工程技术证明,BX-C miRNAs 对 hth 3'UTR 位点的精确突变或删除其包含大多数这些位点的神经 3'UTR 延伸都能诱导处女产生交配后的行为。因此,神经 APA 促进 miRNA 介导的抑制作用,对于处女蝇执行与其内部状态相适应的行为是必需的。