Suppr超能文献

Chinmo 防止变压器可变剪接以维持雄性性别身份。

Chinmo prevents transformer alternative splicing to maintain male sex identity.

机构信息

Department of Biochemistry & Molecular Pharmacology, New York University School of Medicine, New York, New York, United States of America.

MRC Clinical Sciences Centre, Imperial College London, London, United Kingdom.

出版信息

PLoS Genet. 2018 Feb 1;14(2):e1007203. doi: 10.1371/journal.pgen.1007203. eCollection 2018 Feb.

Abstract

Reproduction in sexually dimorphic animals relies on successful gamete production, executed by the germline and aided by somatic support cells. Somatic sex identity in Drosophila is instructed by sex-specific isoforms of the DMRT1 ortholog Doublesex (Dsx). Female-specific expression of Sex-lethal (Sxl) causes alternative splicing of transformer (tra) to the female isoform traF. In turn, TraF alternatively splices dsx to the female isoform dsxF. Loss of the transcriptional repressor Chinmo in male somatic stem cells (CySCs) of the testis causes them to "feminize", resembling female somatic stem cells in the ovary. This somatic sex transformation causes a collapse of germline differentiation and male infertility. We demonstrate this feminization occurs by transcriptional and post-transcriptional regulation of traF. We find that chinmo-deficient CySCs upregulate tra mRNA as well as transcripts encoding tra-splice factors Virilizer (Vir) and Female lethal (2)d (Fl(2)d). traF splicing in chinmo-deficient CySCs leads to the production of DsxF at the expense of the male isoform DsxM, and both TraF and DsxF are required for CySC sex transformation. Surprisingly, CySC feminization upon loss of chinmo does not require Sxl but does require Vir and Fl(2)d. Consistent with this, we show that both Vir and Fl(2)d are required for tra alternative splicing in the female somatic gonad. Our work reveals the need for transcriptional regulation of tra in adult male stem cells and highlights a previously unobserved Sxl-independent mechanism of traF production in vivo. In sum, transcriptional control of the sex determination hierarchy by Chinmo is critical for sex maintenance in sexually dimorphic tissues and is vital in the preservation of fertility.

摘要

在有性二态动物中,生殖依赖于生殖细胞和体细胞支持细胞的成功配子产生。果蝇的体细胞性别身份由 DMRT1 直系同源物 Double-sex (Dsx) 的性别特异性同工型指导。Sex-lethal (Sxl) 的雌性特异性表达导致 transformer (tra) 向雌性同工型 traF 的选择性剪接。反过来,TraF 又将 dsx 选择性剪接为雌性同工型 dsxF。睾丸中雄性体细胞干细胞 (CySCs) 中的转录抑制因子 Chinmo 的缺失导致它们“雌性化”,类似于卵巢中的雌性体细胞干细胞。这种体细胞性别转化导致生殖细胞分化崩溃和雄性不育。我们证明这种雌性化是通过 traF 的转录和转录后调控发生的。我们发现 chinmo 缺陷的 CySCs 上调了 tra mRNA 以及编码 tra 剪接因子 Virilizer (Vir) 和 Female lethal (2)d (Fl(2)d) 的转录本。chinmo 缺陷的 CySCs 中的 traF 剪接导致 DsxF 的产生,而不是雄性同工型 DsxM,并且 TraF 和 DsxF 都需要 CySC 性别转化。令人惊讶的是,chinmo 缺失后 CySC 的雌性化不需要 Sxl,但需要 Vir 和 Fl(2)d。与之一致,我们表明,Vir 和 Fl(2)d 都需要 tra 在雌性体细胞生殖腺中的选择性剪接。我们的工作揭示了在成年雄性干细胞中 tra 的转录调控的必要性,并强调了体内以前未观察到的 traF 产生的 Sxl 独立机制。总之,Chinmo 对性别决定层次结构的转录调控对于有性二态组织中的性别维持至关重要,对于生育能力的维持至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f930/5811060/a381271ecb5d/pgen.1007203.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验