卵巢外甾体生物合成与女性生殖系干细胞。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Fly Pub Date : 2017-07-03 Epub Date: 2017-02-08 DOI:10.1080/19336934.2017.1291472
Tomotsune Ameku, Yuto Yoshinari, Ruriko Fukuda, Ryusuke Niwa
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引用次数: 30

摘要

生殖系干细胞(GSCs)在整个成年期的配子发生中起着至关重要的作用。干细胞的身份是由来自称为生态位的特殊微环境的局部信号维持的。然而,目前尚不清楚系统信号如何调节干细胞对环境信号的反应。在我们之前的文章中,我们报道了交配刺激雌性果蝇的GSC增殖。交配诱导的GSC增殖是由卵巢外甾体介导的,其生物合成受性肽信号的正调控。在此,我们研究了卵巢中编码卵巢甾体生成酶的基因在羽化后和交配后的表达模式。我们进一步研究了卵巢外甾体激素在维持雌性雌性生殖系统中的生物合成功能。我们还简要讨论了体外甾体生成酶编码基因的调控以及随后在成年果蝇卵巢中体外甾体的生物合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Ovarian ecdysteroid biosynthesis and female germline stem cells.

The germline stem cells (GSCs) are critical for gametogenesis throughout the adult life. Stem cell identity is maintained by local signals from a specialized microenvironment called the niche. However, it is unclear how systemic signals regulate stem cell activity in response to environmental cues. In our previous article, we reported that mating stimulates GSC proliferation in female Drosophila. The mating-induced GSC proliferation is mediated by ovarian ecdysteroids, whose biosynthesis is positively controlled by Sex peptide signaling. Here, we characterized the post-eclosion and post-mating expression pattern of the genes encoding the ecdysteroidogenic enzymes in the ovary. We further investigated the biosynthetic functions of the ovarian ecdysteroid in GSC maintenance in the mated females. We also briefly discuss the regulation of the ecdysteroidogenic enzyme-encoding genes and the subsequent ecdysteroid biosynthesis in the ovary of the adult Drosophila.

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来源期刊
Fly
Fly 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
>12 weeks
期刊介绍: Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions. Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.
期刊最新文献
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