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从人类Y染色体上分离并鉴定一个表达基因

Molecular isolation and characterization of an expressed gene from the human Y chromosome.

作者信息

Zhang J S, Yang-Feng T L, Muller U, Mohandas T K, de Jong P J, Lau Y F

机构信息

Division of Cell and Developmental Genetics, VA Medical Center, University of California, San Francisco 94121.

出版信息

Hum Mol Genet. 1992 Dec;1(9):717-26. doi: 10.1093/hmg/1.9.717.

Abstract

Using a positional cloning approach, we have isolated an expressed gene from a flow-sorted Y chromosome cosmid library. The isolation of this gene was based on the identification of the Y-231 cosmid that contains CpG rich sequences (HTF islands) in its human insert. The Y-231 cosmid was capable of detecting a 1.3 kb transcript in poly (A)+ RNA samples from human testis. Several cDNA clones were isolated from a human testis cDNA library constructed in lambda gt10. In addition, DNA-mediated gene transfer and restriction enzyme mapping experiments demonstrated that two functional transcriptional units are present within the Y-231 cosmid. DNA sequencing analysis showed that the largest cDNA clone contains 1075 bp of unique sequence and a poly (A) track at the 3' end of the corresponding mRNA. An open reading frame of 762 bp that encodes a predicted protein of 253 amino acids with a calculated molecular weight of 28.9 kD was identified. The Y-231 structural gene encompasses approximately 2.7 kb of genomic sequence and contains six exons that are interrupted by five introns. The Y-231 gene shares very high (97%) identity at the DNA level to a previously described Y-specific gene, testis specific protein Y-encoded (TSPY) gene, suggesting the possibility that these two genes are related, if not identical. However, the TSPY gene has been postulated to be intronless. Further PCR and RT-PCR analyses of these two genes and their transcripts have provided evidence supporting the hypothesis that they are the same gene and are members of a Y-specific repeated gene family containing intronic sequences. The Y-231 (TSPY) gene is conserved in the male genome and expressed in the testis of the chimpanzee, suggesting that it may play an important role in the physiology of this organ in man and the great ape.

摘要

我们采用定位克隆方法,从经流式细胞仪分选的Y染色体黏粒文库中分离出一个表达基因。该基因的分离基于对Y-231黏粒的鉴定,其人类插入片段中含有富含CpG的序列(HTF岛)。Y-231黏粒能够在来自人类睾丸的聚腺苷酸(poly(A)+)RNA样本中检测到一个1.3 kb的转录本。从构建于λgt10的人类睾丸cDNA文库中分离出了几个cDNA克隆。此外,DNA介导的基因转移和限制性内切酶图谱分析表明,Y-231黏粒中存在两个功能性转录单元。DNA测序分析显示,最大的cDNA克隆包含1075 bp的独特序列以及相应mRNA 3'端的一个聚腺苷酸尾。鉴定出一个762 bp的开放阅读框,其编码一个预测的含253个氨基酸、计算分子量为28.9 kD的蛋白质。Y-231结构基因包含约2.7 kb的基因组序列,含有六个外显子,被五个内含子隔开。Y-231基因在DNA水平上与先前描述的Y特异性基因——睾丸特异性蛋白Y编码(TSPY)基因具有非常高(97%)的同一性,这表明这两个基因即便不是完全相同,也有可能相关。然而,TSPY基因被推测为无内含子。对这两个基因及其转录本进行的进一步PCR和RT-PCR分析提供了证据,支持它们是同一基因且是包含内含子序列的Y特异性重复基因家族成员的假说。Y-231(TSPY)基因在雄性基因组中保守,并在黑猩猩的睾丸中表达,这表明它可能在人类和大猩猩该器官的生理学中发挥重要作用。

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