果蝇幼虫聚集行为的遗传结构。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Journal of neurogenetics Pub Date : 2021-09-01 Epub Date: 2021-02-25 DOI:10.1080/01677063.2021.1887174
Ross M McKinney, Ryan Valdez, Yehuda Ben-Shahar
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引用次数: 5

摘要

许多昆虫都表现出聚集等基础社会行为,这在它们的觅食和交配生态中起着重要作用。然而,调节昆虫聚集的进化、遗传和生理机制对大多数物种来说仍然是未知的。在这里,我们使用黑腹果蝇的自然种群来确定驱动幼虫聚集摄食行为的遗传结构。通过使用定量和反向遗传方法,我们已经确定了一个复杂的神经遗传网络,在调节幼虫的决定中起作用,无论是单独进食还是作为一个群体。单基因rnai敲低实验结果表明,鉴定出的几个基因代表了遗传网络中的关键节点,决定了进食时的聚集水平。此外,研究人员发现,基因CG14205(一种假定的酰基转移酶)的一个非编码变异与mRNA表达减少和聚集形成增加相关,这表明它在抑制聚集行为中具有特定作用。我们的研究结果首次确定了相互作用的遗传成分,以调节黑腹天鼠幼虫自然发生的聚集水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The genetic architecture of larval aggregation behavior in Drosophila.

Many insect species exhibit basal social behaviors such as aggregation, which play important roles in their feeding and mating ecologies. However, the evolutionary, genetic, and physiological mechanisms that regulate insect aggregation remain unknown for most species. Here, we used natural populations of Drosophila melanogaster to identify the genetic architecture that drives larval aggregation feeding behavior. By using quantitative and reverse genetic approaches, we have identified a complex neurogenetic network that plays a role in regulating the decision of larvae to feed in either solitude or as a group. Results from single gene, RNAi-knockdown experiments show that several of the identified genes represent key nodes in the genetic network that determines the level of aggregation while feeding. Furthermore, we show that a single non-coding variant in the gene CG14205, a putative acyltransferase, is associated with both decreased mRNA expression and increased aggregate formation, which suggests that it has a specific role in inhibiting aggregation behavior. Our results identify, for the first time, the genetic components which interact to regulate naturally occurring levels of aggregation in D. melanogaster larvae.

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来源期刊
Journal of neurogenetics
Journal of neurogenetics 医学-神经科学
CiteScore
4.40
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms
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