首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning and characterization of TDD5 an androgen target gene that is differentially repressed by testosterone and dihydrotestosterone
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Cloning and characterization of TDD5 an androgen target gene that is differentially repressed by testosterone and dihydrotestosterone

机译:TDD5的克隆和鉴定TDD5是被睾丸激素和gene二氢睾丸激素差异抑制的雄激素靶基因

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摘要

By using mRNA polymerase chain reaction differential display technique (DDPCR), we have identified one early responsive cDNA fragment, TDD5, from a 5α-reductase-deficient T cell hybridoma. The DDPCR profiles of TDD5 suggest that its expression can be repressed by testosterone (T) within 2 hr. More importantly, both DDPCR and Northern blot analysis further demonstrated that the expression of TDD5 was differentially repressed by T and dihydrotestosterone (DHT) at the mRNA level. To our knowledge, this is the first androgen target gene to show a preference in response to T over DHT in cell culture. TDD5 is expressed in several tissues with particular abundance in kidney. Full-length TDD5 cDNA (2,916 bp) encodes a protein with a calculated molecular weight of 42,000. Finally, our animal studies further confirm that TDD5 mRNA levels can be repressed to the basal level 8 hr after DHT administration. The isolation and characterization of the early-responsive androgen target gene TDD5 and the fact that TDD5 mRNA level can be differentially regulated by T and DHT may provide a useful tool to study the molecular mechanism of androgen preference on target gene regulation.
机译:通过使用mRNA聚合酶链反应差异显示技术(DDPCR),我们从5α-还原酶缺陷型T细胞杂交瘤中鉴定了一个早期响应cDNA片段TDD5。 TDD5的DDPCR图谱表明,其表达可在2小时内被睾丸激素(T)抑制。更重要的是,DDPCR和Northern blot分析均进一步证明T和二氢睾丸激素(DHT)在mRNA水平上差异抑制了TDD5的表达。据我们所知,这是第一个在细胞培养中对T的反应优于DHT的雄激素靶基因。 TDD5在肾脏特别丰富的几种组织中表达。全长TDD5 cDNA(2,916 bp)编码一种蛋白质,计算的分子量为42,000。最后,我们的动物研究进一步证实,施用DHT后8小时,TDD5 mRNA水平可被抑制至基础水平。早期反应雄激素靶基因TDD5的分离和鉴定以及TD和DHT可以差异调节TDD5 mRNA水平这一事实可能为研究雄激素对靶基因调控的分子机制提供了有用的工具。

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