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首页> 外文期刊>Molecular and Cellular Endocrinology >Expression of follicle-stimulating hormone-receptor mRNA alternate transcripts in bovine granulosa cells during luteinization in vivo and in vitro.
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Expression of follicle-stimulating hormone-receptor mRNA alternate transcripts in bovine granulosa cells during luteinization in vivo and in vitro.

机译:黄体化过程中体内和体外牛颗粒细胞中促卵泡激素受体mRNA替代转录物的表达。

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摘要

In cattle, as in many other species, formation of the corpus luteum is associated with loss of sensitivity to FSH. To determine whether this is associated with changes in FSH-receptor mRNA levels or alternate splicing of the primary transcript, reverse transcription and the polymerase chain reaction (RT-PCR) were used to examine transcripts during granulosa cell luteinization in vivo and in vitro. Using RT-PCR and Southern blotting, three alternate transcripts of the FSH-receptor were found consistently in bovine granulosa cells. The largest transcript encoded the full-length receptor while the other transcripts lacked either exon 9 or exons 4, 5 and 9. One day after luteinization in vivo, full-length FSH-receptor mRNA was detectable at low levels in the newly-formed corpus luteum. By day 3, however, no full-length transcripts were detectable in the corpus luteum. In contrast, when primers were used which amplify only the extracellular domain, FSH-receptor transcripts were detectable in all corpora lutea tested up to mid-cycle. In granulosa cells, luteinized in vitro, there was a similar loss of full-length FSH-receptor transcripts after day 1 but continued expression of transcripts encoding the extracellular domain. Results show that granulosa cell luteinization in cattle is associated with a change in splicing of the FSH-receptor primary transcript such that after luteinization only shortened transcripts coding for the extracellular domain are detectable. This process resembles, in reverse, changes in FSH-receptor transcript splicing during development of the gonads.
机译:与许多其他物种一样,在牛中,黄体的形成与对FSH的敏感性降低有关。为了确定这是否与FSH受体mRNA水平的变化或初级转录物的可变剪接有关,在体内和体外使用颗粒细胞黄体化过程中,通过逆转录和聚合酶链反应(RT-PCR)来检查转录物。使用RT-PCR和Southern印迹,在牛颗粒细胞中一致地发现了FSH受体的三个替代转录物。最大的转录本编码全长受体,而其他转录本缺少外显子9或外显子4、5和9。外在黄体化后的一天,在新生体中可检测到低水平的全长FSH受体mRNA。黄体。然而,到第3天,在黄体中没有检测到全长转录本。相反,当使用仅扩增细胞外结构域的引物时,在测试至整个周期中期的所有语料库中均可检测到FSH受体转录物。在体外经黄素化处理的颗粒细胞中,第1天后全长FSH受体转录物丢失类似,但编码胞外域的转录物继续表达。结果表明,牛的颗粒细胞黄体化与FSH受体初级转录物的剪接变化有关,因此在黄化后,仅可检测到编码胞外域的缩短的转录物。相反,此过程类似于性腺发育过程中FSH受体转录剪接的变化。

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