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日本鳗鲡精子发生过程中Spo11的分子克隆与基因表达

Molecular cloning and gene expression of Spo11 during spermatogenesis in the Japanese eel, Anguilla japonica.

作者信息

Ozaki Yuichi, Miura Chiemi, Miura Takeshi

机构信息

PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2006 Mar;143(3):309-14. doi: 10.1016/j.cbpb.2005.12.008. Epub 2006 Jan 19.

Abstract

Spo11 is a protein involved specifically in the meiotic recombination in several species, however, it is little characterized in lower vertebrates. We identified a cDNA encoding Spo11 from the testis of Japanese eel, Anguilla japonica. The deduced amino acid sequence of eel Spo11 was more than 60% identical with human and mouse Spo11s. In order to examine changes in the expression and localization of Spo11 during spermatogenesis induced by the injection of human chorionic gonadotropin (hCG) and to compare with those of Dmc1, we generated specific antibodies against the eel Spo11 and Dmc1. In general, it is believed that Dmc1 is a meiosis-specific protein, and the localization of Dmc1 in spermatocytes was confirmed also in Japanese eel. Spo11 transcripts were slightly detected in the testis after 1 day post-hCG injection by Northern blot analysis. Western blot analysis also indicated that Spo11 production began at day 1 after hCG injection. However, immunohistochemical observations showed that Spo11 was localized only in spermatocytes. In contrast, Dmc1 transcripts and the protein production were first detected at day 6 after hCG injection and increased along with the increment of spermatocytes. These results suggested that Spo11 was expressed in spermatogonia proliferated toward meiosis at quite low level that could not induce meiotic recombination, thereafter Spo11 expression increased and Dmc1 expression was initiated in early meiotic prophase. Hence, the antibodies against eel Spo11 and Dmc1 generated in the present study can be use to detect germ cells in early meiotic prophase immunohistochemically. Importantly, it is suggested that germ cells, which are in quite earlier stage during meiotic prophase, can be detected by Spo11.

摘要

Spo11是一种专门参与多种物种减数分裂重组的蛋白质,然而,在低等脊椎动物中对其研究甚少。我们从日本鳗鲡(Anguilla japonica)的睾丸中鉴定出一个编码Spo11的cDNA。鳗鲡Spo11推导的氨基酸序列与人类和小鼠的Spo11有60%以上的同源性。为了检测注射人绒毛膜促性腺激素(hCG)诱导精子发生过程中Spo11的表达和定位变化,并与Dmc1进行比较,我们制备了针对鳗鲡Spo11和Dmc1的特异性抗体。一般认为,Dmc1是一种减数分裂特异性蛋白,在日本鳗鲡的精母细胞中也证实了Dmc1的定位。通过Northern印迹分析,在hCG注射后1天的睾丸中可轻微检测到Spo11转录本。蛋白质印迹分析也表明,hCG注射后第1天开始产生Spo11。然而,免疫组织化学观察显示,Spo11仅定位于精母细胞中。相反,Dmc1转录本和蛋白质产物在hCG注射后第6天首次检测到,并随着精母细胞数量的增加而增加。这些结果表明,Spo11在向减数分裂增殖的精原细胞中以相当低的水平表达,这种水平不能诱导减数分裂重组,此后Spo11表达增加,Dmc1表达在减数分裂前期早期开始。因此,本研究中制备的针对鳗鲡Spo11和Dmc1的抗体可用于免疫组织化学检测减数分裂前期早期的生殖细胞。重要的是,提示Spo11可检测到减数分裂前期相当早期阶段的生殖细胞。

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