Isolation and characterization of cDNA clones for castration-induced mRNAs in the rat ventral prostate.

Y Hoshikawa, Y Satoh, S Ichii
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引用次数: 4

Abstract

To identify gene products involved in castration-induced involution of the rat ventral prostate, we constructed a subtraction cDNA library of the ventral prostate from rats castrated for 48 h. The library was screened with subtracted cDNA probes enriched for sequences with a low copy number expressed in intact or castrated rats. As a result of differential screening, 48 cDNA clones representing 10 different induced mRNAs were isolated. The time course of these mRNA inductions after castration was examined. Within the first 24 h after castration, the level of mRNAs for these cDNA clones was significantly increased and it reached its peak by 48-72 h after castration. Although mRNAs for these cDNA clones were expressed in various tissues from intact rats, an increase in mRNA as a response to castration was observed only in the ventral prostate. Partial sequence analyses of the 10 cDNA clones indicate that three cDNA clones represent rat glutathione S-transferase Yb-1, Yb-2 and Yb-3 subunit mRNA sequences, but for others respective homologues could not be found in a search of the GenBank database (release 67).

大鼠腹侧前列腺去势诱导mrna cDNA克隆的分离与鉴定。
为了鉴定与去势诱导的大鼠腹侧前列腺退化相关的基因产物,我们构建了一个去势48 h大鼠腹侧前列腺的减法cDNA文库。对文库进行筛选的减法cDNA探针富集了在完整或去势大鼠中表达的低拷贝数序列。通过差异筛选,分离到48个cDNA克隆,分别代表10种不同的诱导mrna。观察去势后这些mRNA诱导的时间过程。在去势后24 h内,这些cDNA克隆的mrna水平显著升高,在去势后48 ~ 72 h达到峰值。尽管这些cDNA克隆的mRNA在完整大鼠的各种组织中都有表达,但作为阉割的反应,mRNA的增加仅在前列腺腹侧观察到。对10个cDNA克隆的部分序列分析表明,其中3个cDNA克隆代表大鼠谷胱甘肽s -转移酶Yb-1、Yb-2和Yb-3亚基mRNA序列,而其他cDNA克隆在GenBank数据库(release 67)中搜索不到各自的同源物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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