Regulation of oxytocin receptor gene expression in sheep: tissue specificity, multiple transcripts and mRNA editing.

H. C. Feng, M. Bhave, R. Fairclough
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引用次数: 9

Abstract

The increase in uterine oxytocin receptor concentrations over the late luteal phase of the oestrous cycle in sheep is thought to play an important role in the regulation of the duration of the cycle by facilitating the effect of oxytocin on uterine prostaglandin release. Experiments indicated that oxytocin receptor mRNA expression in the endometrium was high at oestrus compared with at days 2, 7 and 12 of the oestrous cycle. The amount of oxytocin receptor mRNA expression in the pituitary gland did not show any significant differences during the oestrous cycle. Oxytocin receptor cDNA was obtained and characterized from ovine uterine endometrium on day 15 of the oestrous cycle, using RT-PCR techniques, to study the mechanisms underlying the resolution of oxytocin receptor expression. The cDNA sequence for the oxytocin receptor gene in sheep was found to be similar to that described previously, except for a difference of seven nucleotides. These nucleotide differences resulted in changes in four of the deduced amino acids in the oxytocin receptor sequence. The heterogeneity of the different sized oxytocin receptor transcripts in sheep is due, at least in part, to the alternative use of polyadenylation sites. Northern hybridization confirmed that the oxytocin receptor gene is expressed in ovine corpus luteum. The investigations on oxytocin receptor gene expression indicate that the patten of oxytocin receptor gene expression in sheep is not only tissue-specific, but also highly function-related. Evidence was obtained of mRNA editing in both the coding and the 3'-untranslated (3'UTR) regions of oxytocin receptor gene transcripts in ovine endometrium; this was the first demonstration of this phenomenon for oxytocin receptor mRNA. The present results indicate that the observed differences in oxytocin receptor mRNA sequences for the different oxytocin receptor populations in endometrium are due to mRNA editing. mRNA editing of oxytocin receptor transcripts may be reflected in changes in the amino acid composition of the carboxyl terminus of the receptor, which would explain the differences in the observed responses to an oxytocin challenge.
绵羊催产素受体基因表达调控:组织特异性、多转录本和mRNA编辑。
在绵羊发情周期的黄体晚期,子宫催产素受体浓度的增加被认为通过促进催产素对子宫前列腺素释放的影响,在周期持续时间的调节中发挥重要作用。实验表明,与发情周期的第2、7和12天相比,子宫内膜中催产素受体mRNA的表达在发情时较高。脑垂体中催产素受体mRNA的表达量在发情周期内无显著差异。本研究采用RT-PCR技术,于发情周期第15天从绵羊子宫内膜中获得催产素受体cDNA,并对其进行鉴定,探讨催产素受体表达的解析机制。绵羊催产素受体基因的cDNA序列被发现与之前描述的相似,除了七个核苷酸的差异。这些核苷酸的差异导致了催产素受体序列中四个推断出的氨基酸的变化。绵羊中不同大小的催产素受体转录本的异质性至少部分是由于多聚腺苷化位点的替代使用。Northern杂交证实了催产素受体基因在羊黄体中有表达。对绵羊催产素受体基因表达的研究表明,绵羊催产素受体基因的表达模式不仅具有组织特异性,而且具有高度的功能相关性。在绵羊子宫内膜中获得了催产素受体基因转录本编码区和3'-非翻译区(3' utr) mRNA编辑的证据;这是催产素受体mRNA首次出现这种现象。目前的结果表明,子宫内膜中不同催产素受体群体的催产素受体mRNA序列的差异是由于mRNA编辑所致。催产素受体转录本的mRNA编辑可能反映在受体羧基端氨基酸组成的变化中,这可以解释观察到的催产素挑战反应的差异。
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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