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大鼠联会复合体两个主要成分的组织分布

Tissue distribution of two major components of synaptonemal complexes of the rat.

作者信息

Offenberg H H, Dietrich A J, Heyting C

机构信息

Institute of Genetics, Agricultural University, Wageningen, The Netherlands.

出版信息

Chromosoma. 1991 Nov;101(2):83-91. doi: 10.1007/BF00357057.

Abstract

In this paper we describe an analysis of the tissue distribution of two recently identified components of synaptonemal complexes (SCs), an Mr 125,000 and an Mr 190,000 protein, in the male rat by immunoblot analysis and immunocytochemical techniques. We compared the tissue distribution of these antigens with that of two earlier identified SC components, an Mr 30,000 and an Mr 33,000 polypeptide. For this purpose we used monoclonal antibodies (Mabs) that react exclusively with SCs in lysed spermatocytes, and that recognize the above mentioned antigens specifically in immunoblots of SC proteins or of nuclear proteins from spermatocytes; these were Mab IX9D5 (anti-190,000), Mab IX5B2 (anti-125,000), Mab II52F10 (anti-30,000 + 33,000), and Mab IX8G9 (anti-30,000 + 33,000). In the immunoblot experiments, we could detect the Mr 190,000 and 125,000 antigens exclusively in blots of SC proteins or nuclear proteins from spermatocytes; these antigens were not detectable in blots of nuclear proteins from liver, brain, spermatogonia or spermatids or in blots of proteins from mitotic chromosomes or nuclear laminae. With the anti- 30,000 + 33,000 Mabs we obtained essentially the same result, except that Mab IX8G9, but not II52F10, recognizes a small amount of Mr 30,000 antigen in blots of nuclear proteins from spermatids and spermatogonia. Although this might be ascribed to contamination of the isolated spermatids and spermatogonia, we cannot exclude that a small amount of Mr 30,000 antigen is present in these cells. In the immunofluorescence analysis, the testis was the only tissue that reacted detectably with the above antibodies. Within the testis, spermatocytes and some early spermatids were the only cell types that contained detectable amounts of antigen.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本文中,我们描述了通过免疫印迹分析和免疫细胞化学技术,对雄性大鼠中最近鉴定出的联会复合体(SCs)的两种成分(一种分子量为125,000的蛋白质和一种分子量为190,000的蛋白质)进行组织分布分析。我们将这些抗原的组织分布与两种早期鉴定出的SCs成分(一种分子量为30,000的多肽和一种分子量为33,000的多肽)的组织分布进行了比较。为此,我们使用了单克隆抗体(Mabs),这些抗体仅与裂解的精母细胞中的SCs发生反应,并在SCs蛋白或精母细胞核蛋白的免疫印迹中特异性识别上述抗原;它们分别是Mab IX9D5(抗190,000)、Mab IX5B2(抗125,000)、Mab II52F10(抗30,000 + 33,000)和Mab IX8G9(抗30,000 + 33,000)。在免疫印迹实验中,我们仅能在精母细胞的SCs蛋白或核蛋白印迹中检测到分子量为190,000和125,000的抗原;在肝脏、大脑、精原细胞或精子细胞的核蛋白印迹中,以及有丝分裂染色体或核纤层蛋白的印迹中均未检测到这些抗原。使用抗30,000 + 33,000的单克隆抗体,我们得到了基本相同的结果,只是Mab IX8G9而非II52F10在精子细胞和精原细胞核蛋白印迹中识别出少量分子量为30,000的抗原。尽管这可能归因于分离的精子细胞和精原细胞的污染,但我们不能排除这些细胞中存在少量分子量为30,000的抗原。在免疫荧光分析中,睾丸是唯一能与上述抗体发生可检测反应的组织。在睾丸内,精母细胞和一些早期精子细胞是仅有的含有可检测量抗原的细胞类型。(摘要截短至250字)

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