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雌性缺失决定雌性疟蚊的性别决定和剂量补偿途径。

femaleless Controls Sex Determination and Dosage Compensation Pathways in Females of Anopheles Mosquitoes.

机构信息

The Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.

Big Data Institute, Nuffield Department of Medicine, University of Oxford, Old Road Campus, Oxford OX3 7LF, UK.

出版信息

Curr Biol. 2021 Mar 8;31(5):1084-1091.e4. doi: 10.1016/j.cub.2020.12.014. Epub 2021 Jan 7.

Abstract

The insect sex determination and the intimately linked dosage compensation pathways represent a challenging evolutionary puzzle that has been solved only in Drosophila melanogaster. Analyses of orthologs of the Drosophila genes identified in non-drosophilid taxa revealed that evolution of sex determination pathways is consistent with a bottom-up mode, where only the terminal genes within the pathway are well conserved. doublesex (dsx), occupying a bottom-most position and encoding sex-specific proteins orchestrating downstream sexual differentiation processes, is an ancient sex-determining gene present in all studied species. With the exception of lepidopterans, its female-specific splicing is known to be regulated by transformer (tra) and its co-factor transformer-2 (tra2). Here we show that in the African malaria mosquito Anopheles gambiae, a gene, which likely arose in the Anopheles lineage and which we call femaleless (fle), controls sex determination in females by regulating splicing of dsx and fruitless (fru; another terminal gene within a branch of the sex determination pathway). Moreover, fle represents a novel molecular link between the sex determination and dosage compensation pathways. It is necessary to suppress activation of dosage compensation in females, as demonstrated by the significant upregulation of the female X chromosome genes and a correlated female-specific lethality, but no negative effect on males, in response to fle knockdown. This unexpected property, combined with a high level of conservation in sequence and function in anopheline mosquitoes, makes fle an excellent target for genetic control of all major vectors of human malaria.

摘要

昆虫性别决定和与之密切相关的剂量补偿途径是一个具有挑战性的进化难题,仅在黑腹果蝇中得到了解决。对非果蝇分类群中鉴定的果蝇基因的同源物的分析表明,性别决定途径的进化与自下而上的模式一致,只有途径中的末端基因得到了很好的保守。双倍性别(dsx)占据最底层的位置,编码性别特异性蛋白质,协调下游的性分化过程,是所有研究物种中存在的古老性别决定基因。除鳞翅目昆虫外,其雌性特异性剪接被认为是由transformer(tra)及其辅助因子 transformer-2(tra2)调控的。在这里,我们表明在非洲疟蚊 Anopheles gambiae 中,一个可能在 Anopheles 谱系中出现的基因,我们称之为无雌性(fle),通过调节 dsx 和 fru(性别决定途径分支中的另一个末端基因)的剪接来控制雌性的性别决定。此外,fle 代表了性别决定和剂量补偿途径之间的一个新的分子联系。需要抑制雌性中剂量补偿的激活,正如 fle 敲低导致雌性 X 染色体基因的显著上调和相关的雌性特异性致死所证明的那样,但对雄性没有负面影响。这种出乎意料的特性,加上在按蚊中序列和功能的高度保守性,使得 fle 成为控制人类疟疾所有主要传播媒介的遗传控制的一个极好的靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b3c/7955153/303d56ddbb51/gr1.jpg

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