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Alternatively spliced mRNA transcripts encoding the extracellular domain of the FSH receptor gene. Expression in the mouse ovary during the ovulatory cycle.

机译:编码FSH受体基因的胞外域的剪接的mRNA转录物。在排卵周期中在小鼠卵巢中表达。

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摘要

OBJECTIVE: To evaluate regulation of follicle-stimulating hormone (FSH) receptor expression in the mouse ovary during different stages of an artificially induced ovulatory cycle. STUDY DESIGN: Follicular maturation was achieved in pubertal female mice by pregnant mares' serum gonadotropin (PMSG). Ovulation was induced 48 hours later by human chorionic gonadotropin (hCG). Ovaries were harvested before treatment, at 24 and 48 hours after PMSG and at 3, 9 and 12 hours after hCG. RNA was extracted using a single-step isolation method and used for reverse transcription. The cDNA was amplified by polymerase chain reaction (PCR) using primers designed to amplify a 512-basepair product corresponding to the extracellular fragment of the FSH receptor. RESULTS: PCR products, resolved by electrophoresis on agarose gels, showed four bands corresponding to four discrete, alternatively spliced forms of the FSH receptor. Expression of the various transcripts varied at different stages of the ovulatory cycle such that the larger transcripts increased up to 48 hours following PMSG and began to decrease thereafter, reaching a trough 12 hours following hCG administration. Conversely, a smaller transcript reached a peak 9 hours following hCG administration and decreased thereafter. CONCLUSION: The various transcripts represent different FSH receptor mRNA splicing and may mediate changes in receptor function. Since these alternative spliced forms encode different portions of the extracellular domain, it is possible that they have altered hormone-binding affinity serving a regulatory purpose, such as decreasing hormone binding affinity.
机译:目的:评估人工诱导排卵周期不同阶段小鼠卵巢中促卵泡激素(FSH)受体表达的调节。研究设计:青春期雌性小鼠的母马的血清促性腺激素(PMSG)使卵泡成熟。 48小时后,人绒毛膜促性腺激素(hCG)诱导排卵。在治疗前,PMSG治疗后24和48小时以及hCG治疗后3、9和12小时收获卵巢。使用单步分离方法提取RNA,并将其用于逆转录。使用设计用于扩增对应于FSH受体胞外片段的512个碱基对产物的引物,通过聚合酶链反应(PCR)扩增cDNA。结果:通过琼脂糖凝胶电泳分离的PCR产物显示出四个条带,分别对应于FSH受体的四个离散或剪接形式。各种转录物的表达在排卵周期的不同阶段变化,使得较大的转录物在PMSG后长达48小时增加并在此后开始减少,在hCG施用后12小时达到谷底。相反,较小的转录本在hCG施用后9小时达到峰值,此后降低。结论:各种转录本代表不同的FSH受体mRNA剪接,并可能介导受体功能的变化。由于这些替代的剪接形式编码细胞外结构域的不同部分,因此它们有可能改变了荷尔蒙结合亲和力,从而达到调节目的,例如降低了荷尔蒙结合亲和力。

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