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在果蝇胚胎原始生殖细胞中与Sxl蛋白免疫沉淀的转录本。

Transcripts immunoprecipitated with Sxl protein in primordial germ cells of Drosophila embryos.

作者信息

Ota Ryoma, Morita Shumpei, Sato Masanao, Shigenobu Shuji, Hayashi Makoto, Kobayashi Satoru

机构信息

Life Science Center of Tsukuba Advanced Research Alliance (TARA Center), University of Tsukuba, Tsukuba, 305-8577, Japan.

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, 305-8572, Japan.

出版信息

Dev Growth Differ. 2017 Dec;59(9):713-723. doi: 10.1111/dgd.12408. Epub 2017 Nov 10.

Abstract

In Drosophila, Sex lethal (Sxl), an RNA binding protein, is required for induction of female sexual identity in both somatic and germline cells. Although the Sxl-dependent feminizing pathway in the soma was previously elucidated, the downstream targets for Sxl in the germline remained elusive. To identify these target genes, we selected transcripts associated with Sxl in primordial germ cells (PGCs) of embryos using RNA immunoprecipitation coupled to sequencing (RIP-seq) analysis. A total of 308 transcripts encoded by 282 genes were obtained. Seven of these genes, expressed at higher levels in PGCs as determined by microarray and in situ hybridization analyses, were subjected to RNAi-mediated functional analyses. Knockdown of Neos, Kap-alpha3, and CG32075 throughout germline development caused gonadal dysgenesis in a sex-dependent manner, and Su(var)2-10 knockdown caused gonadal dysgenesis in both sexes. Moreover, as with knockdown of Sxl, knockdown of Su(var)2-10 in PGCs gave rise to a tumorous phenotype of germline cells in ovaries. Because this phenotype indicates loss of female identity of germline cells, we consider Su(var)2-10 to be a strong candidate target of Sxl in PGCs. Our results represent a first step toward elucidating the Sxl-dependent feminizing pathway in the germline.

摘要

在果蝇中,RNA结合蛋白性致死基因(Sex lethal,Sxl)是体细胞和生殖细胞中诱导雌性性别特征所必需的。尽管之前已经阐明了体细胞中依赖Sxl的雌性化途径,但Sxl在生殖细胞中的下游靶点仍然不清楚。为了鉴定这些靶基因,我们使用RNA免疫沉淀结合测序(RIP-seq)分析,在胚胎的原始生殖细胞(PGC)中选择了与Sxl相关的转录本。共获得了由282个基因编码的308个转录本。通过微阵列和原位杂交分析确定,其中7个基因在PGC中表达水平较高,并对其进行了RNAi介导的功能分析。在整个生殖系发育过程中敲低Neos、Kap-alpha3和CG32075会以性别依赖的方式导致性腺发育不全,敲低Su(var)2-10会导致两性性腺发育不全。此外,与敲低Sxl一样,在PGC中敲低Su(var)2-10会导致卵巢中生殖细胞出现肿瘤样表型。由于这种表型表明生殖细胞丧失了雌性特征,我们认为Su(var)2-10是PGC中Sxl的一个强有力的候选靶标。我们的结果代表了阐明生殖系中依赖Sxl的雌性化途径的第一步。

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