首页> 美国卫生研究院文献>American Journal of Human Genetics >Identification of the transcriptional unit structural organization and promoter sequence of the human sex-determining region Y (SRY) gene using a reverse genetic approach.
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Identification of the transcriptional unit structural organization and promoter sequence of the human sex-determining region Y (SRY) gene using a reverse genetic approach.

机译:使用反向遗传方法鉴定人类性别决定区Y(SRY)基因的转录单位结构组织和启动子序列。

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摘要

Using a simple strategy involving cosmid-mediated gene transfer, cDNA library construction, and molecular characterization techniques, we have determined the transcriptional unit, structural organization, and promoter sequence of the human sex-determining region Y (SRY) gene, the putative testis-determining factor (TDF) gene on the human Y chromosome. By this approach, a recombinant cosmid harboring the human SRY sequence was isolated and transfected to appropriate tissue-cultured cells. Recombinant cDNA clones were isolated from a cDNA library constructed from poly (A) + RNA of the transfected cells. Comparative studies between the respective cDNAs and the genomic cosmid have provided information regarding the organization of the SRY gene and its mRNAs. The results indicate that the human SRY gene is an intronless gene, produces transcripts of 1.1 kb, and possesses promoter activities in the transfected cells at approximately 310 bp of its upstream sequences.
机译:使用涉及粘粒介导的基因转移,cDNA文库构建和分子表征技术的简单策略,我们确定了人类性别决定区Y(SRY)基因(假定的睾丸)的转录单位,结构组织和启动子序列。人Y染色体上的决定因子(TDF)基因。通过这种方法,分离出具有人SRY序列的重组粘粒并将其转染到合适的组织培养细胞中。从由转染细胞的poly(A)+ RNA构建的cDNA文库中分离重组cDNA克隆。各个cDNA与基因组粘粒的比较研究提供了有关SRY基因及其mRNA的组织信息。结果表明,人SRY基因是无内含子基因,产生1.1kb的转录本,并在其上游序列的大约310bp处的转染细胞中具有启动子活性。

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