大鼠精囊中与雄激素刺激mrna杂交的cDNA克隆pSv-1和pSv-2的核苷酸序列。

M Izawa
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引用次数: 3

摘要

为了进一步鉴定从完整大鼠精囊cDNA文库中新分离到的pSv-1和pSv-2克隆与雄激素刺激的mrna杂交,其长度分别约为1500和3500个核苷酸,我们测定了它们的全核苷酸序列。pSv-1和pSv-2的长度分别为1135和1819个核苷酸,似乎不包含与mrna对应的完整序列。用4种限制性内切酶酶切后的0.7 kb的pSv-1和1 kb的pSv-2的HindIII片段检测大鼠基因组DNA,结果显示存在多个与pSv-1相关的基因和一个与pSv-2相关的基因。这些结果表明,pSv-1和pSv-2不仅为进一步表征mrna编码产物提供了有用的探针,而且为研究雄激素依赖性基因在大鼠精囊中的生理作用提供了有用的探针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleotide sequences of cDNA clones, pSv-1 and pSv-2, hybridizing to androgen-stimulated mRNAs in rat seminal vesicles.

In order to further characterize the cDNA clones, pSv-1 and pSv-2, which had been newly isolated from a cDNA library of intact rat seminal vesicles as clones hybridizing to androgen-stimulated mRNAs of approximately 1,500 and 3,500 nucleotides in length, respectively, the whole nucleotide sequences were determined. The pSv-1 and pSv-2 were 1135 and 1819 nucleotides in length, respectively, and seemed not to contain entire sequences corresponding to the mRNAs. When the 0.7 kb HindIII fragments from pSv-1 and the 1 kb fragments from pSv-2 were used to probe rat genomic DNA that had been digested with four restriction enzymes, the Southern blots suggested the existence of multiple genes related to pSv-1 and a single gene related to pSv-2. These results suggest that pSv-1 and pSv-2 provide useful probes not only for further characterization of products encoded by the mRNAs, but also for the study on the physiological roles of androgen-dependent gene expression in rat seminal vesicles.

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