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日本鳗鲡中HCG诱导精子发生过程中表达的阶段特异性基因的cDNA克隆。

cDNA cloning of a stage-specific gene expressed during HCG-induced spermatogenesis in the Japanese eel.

作者信息

Miura C, Miura T, Kudo N, Yamashita M, Yamauchi K

机构信息

Department of Biology, Faculty of Fisheries, Hokkaido University, Hakodate, Japan.

出版信息

Dev Growth Differ. 1999 Aug;41(4):463-71. doi: 10.1046/j.1440-169x.1999.00445.x.

Abstract

A single injection of human chorionic gonadotropin (HCG) can induce complete spermatogenesis in immature Japanese eel (Anguilla japonica) testes consisting of only premitotic spermatogonia. Proliferation of spermatogonia, meiosis and spermiogenesis begin on 3, 12 and 18 days after HCG injection, respectively. To isolate the genes responsible for regulating the initiation of meiosis, differential mRNA display using poly (A)+ RNA extracted from testes of eels at different times after HCG treatment was carried out. Five cDNA clones in which expression was initiated before the onset of meiosis were obtained. Northern blot analysis showed that one clone, which encoded activin betaB subunit, was expressed in the initial phase of spermatogenesis (1-6 days after HCG treatment), in agreement with the previous suggestion that activin B induces the initiation of spermatogenesis in the Japanese eel. The remaining four were expressed in the testes during the following time frames: 3-18 days (two clones), 6-18 days (one clone) and 9-18 days (one clone) after HCG treatment. One of the two clones expressed on day 3 exhibited strong expression on days 12 and 15, just at the initiation period of meiosis. This clone was selected as a candidate gene responsible for initiating meiosis, and its full-length cDNA isolated. The cDNA contained an open reading frame of 1571 nucleotides encoding a protein of 260 amino acid residues, which showed high homology with the proliferating cell nuclear antigen (PCNA) of human, mouse and Xenopus. Northern blot analysis using eel PCNA cDNA showed that a 1.6 kb transcript first appeared on day 3 and became abundant, reaching maximum levels on days 12-15. In situ hybridization analysis revealed that PCNA mRNA was expressed strongly in late type B spermatogonia before the sixth mitotic division. It has already been shown that spermatogonia have a regulatory point to enter meiosis between the fifth and sixth mitotic division. The coincidence of PCNA expression and this regulatory point suggests an involvement of PCNA in the progression of mitotic germ cells into meiosis during HCG-induced spermatogenesis in the eel.

摘要

单次注射人绒毛膜促性腺激素(HCG)可诱导仅由有丝分裂前精原细胞组成的未成熟日本鳗鲡(Anguilla japonica)睾丸产生完全的精子发生。精原细胞增殖、减数分裂和精子形成分别在HCG注射后3天、12天和18天开始。为了分离负责调节减数分裂起始的基因,利用从HCG处理后不同时间的鳗鲡睾丸中提取的聚腺苷酸加尾RNA(poly (A)+ RNA)进行了差异mRNA展示。获得了5个在减数分裂开始前开始表达的cDNA克隆。Northern印迹分析表明,一个编码激活素βB亚基的克隆在精子发生的初始阶段(HCG处理后1 - 6天)表达,这与之前激活素B诱导日本鳗鲡精子发生起始的观点一致。其余4个在以下时间框架内在睾丸中表达:HCG处理后3 - 18天(2个克隆)、6 - 18天(1个克隆)和9 - 18天(1个克隆)。在第3天表达的2个克隆中的一个在第12天和15天,即减数分裂起始期,表现出强烈表达。这个克隆被选为负责启动减数分裂的候选基因,并分离出其全长cDNA。该cDNA包含一个1571个核苷酸的开放阅读框,编码一个260个氨基酸残基的蛋白质,该蛋白质与人、小鼠和非洲爪蟾的增殖细胞核抗原(PCNA)具有高度同源性。使用鳗鲡PCNA cDNA进行的Northern印迹分析表明,一个1.6 kb的转录本首先在第3天出现并变得丰富,在第12 - 15天达到最高水平。原位杂交分析显示,PCNA mRNA在第6次有丝分裂之前在晚期B型精原细胞中强烈表达。已经表明精原细胞在第5次和第6次有丝分裂之间有一个进入减数分裂的调控点。PCNA表达与这个调控点的重合表明PCNA在鳗鲡HCG诱导的精子发生过程中参与有丝分裂生殖细胞向减数分裂的进程。

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