黑腹果蝇候选蜕皮激素激酶的遗传特征。

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2024-11-06 DOI:10.1093/g3journal/jkae204
Jack L Scanlan, Charles Robin
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引用次数: 0

摘要

蜕皮激素是昆虫体内的主要激素,控制着蜕皮、生长、繁殖、生理和行为。蜕皮激素(如从食物固醇中提取的 20-hydroxyecdysone (20E))的生物合成过程已被很好地描述,但蜕皮激素的分解过程却鲜为人知。蜕皮甾醇激酶(EcKs)介导蜕皮甾醇的可逆磷酸化,这与各种昆虫胚胎发育和繁殖过程中的蜕皮甾醇循环有关。然而,迄今为止只在家蚕和冈比亚按蚊中发现了两个编码 EcK 的基因。此前,我们在模式果蝇黑腹果蝇中发现了两个类蜕皮激素激酶(EcKL)基因--墙花(Wall)和平克曼(pkm),它们是蜕皮激素 22 激酶基因 BmEc22K 的直向同源物。在这里,我们利用基因敲除、基因剔除和错误表达等方法,探讨了Wall和pkm的可能功能,并对它们编码蜕皮激素激酶的假说进行了基因测试。Wall和pkm的空突变体可以存活和繁殖,这表明它们对发育或繁殖并不重要,而RNAi和体细胞CRISPR产生的表型似乎来自于脱靶效应或其他假象。然而,Wall 的误表达会导致显著的表型,包括发育停滞以及气管、角质层和色素沉着缺陷。Wall的误表达不能表征通过误表达Cyp18a1而导致的不可逆蜕皮激素分解,这表明Wall并不直接使20E失活。此外,在 Cyp18a1 突变体中,Wall 的误表达表型并没有减弱,这强烈表明 Wall 并非蜕皮激素 26 激酶。我们推测,在这次误表达实验中,Wall 的底物可能是一种未知的非典型蜕皮激素,它在果蝇的发育过程中发挥着重要作用,并可能突显昆虫内分泌学中尚未定性的方面。我们还提供了初步证据,证明 CG5644 编码的蜕皮激素 22- 激酶在双翅目昆虫中是保守的。
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Genetic characterization of candidate ecdysteroid kinases in Drosophila melanogaster.

Ecdysteroids are major hormones in insects and control molting, growth, reproduction, physiology, and behavior. The biosynthesis of ecdysteroids such as 20-hydroxyecdysone (20E) from dietary sterols is well characterized, but ecdysteroid catabolism is poorly understood. Ecdysteroid kinases (EcKs) mediate the reversible phosphorylation of ecdysteroids, which has been implicated in ecdysteroid recycling during embryogenesis and reproduction in various insects. However, to date, only 2 EcK-encoding genes have been identified, in the silkworm Bombyx mori and the mosquito Anopheles gambiae. Previously, we identified 2 ecdysteroid kinase-like (EcKL) genes-Wallflower (Wall) and Pinkman (pkm)-in the model fruit fly Drosophila melanogaster that are orthologs of the ecdysteroid 22-kinase gene BmEc22K. Here, using gene knockdown, knockout, and misexpression, we explore Wall and pkm's possible functions and genetically test the hypothesis that they encode EcKs. Wall and pkm null mutants are viable and fertile, suggesting that they are not essential for development or reproduction, whereas phenotypes arising from RNAi and somatic CRISPR appear to derive from off-target effects or other artifacts. However, misexpression of Wall results in dramatic phenotypes, including developmental arrest, and defects in trachea, cuticle, and pigmentation. Wall misexpression fails to phenocopy irreversible ecdysteroid catabolism through misexpression of Cyp18a1, suggesting that Wall does not directly inactivate 20E. Additionally, Wall misexpression phenotypes are not attenuated in Cyp18a1 mutants, strongly suggesting that Wall is not an ecdysteroid 26-kinase. We hypothesize that the substrate of Wall in this misexpression experiment and possibly generally is an unknown, atypical ecdysteroid that plays essential roles in Drosophila development, and may highlight aspects of insect endocrinology that are as-yet uncharacterized. We also provide preliminary evidence that CG5644 encodes an ecdysteroid 22-kinase conserved across Diptera.

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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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