Fan N C, Peng C, Krisinger J, Leung P C
Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada.
Mol Cell Endocrinol. 1995 Feb;107(2):R1-8. doi: 10.1016/0303-7207(94)03460-b.
The interaction of gonadotropin-releasing hormone and its receptor is a critical event in the endocrine regulation of reproduction. We have recently cloned the gene encoding for the human gonadotropin-releasing hormone receptor (hGnRHR). Partial sequence analysis revealed a structural organization consisting of three exons and two introns. Exon II contains only 219 bp and the remainder of the approximately 5 kb transcript is distributed between exons I and III. The complete coding region for the hGnRHR represented only 987 bp leaving an extensive 5' and 3' non-translated region and potentially additional exons unaccounted for. This report provides the complete sequence of exon I and III and demonstrates that further exons are unlikely to be contained within this gene. Sequencing of the 5' end of the gene revealed the presence of five consensus TATA sequences distributed within a 700 nucleotide region. Primer extension analysis detected multiple transcription initiation sites associated with this cluster of TATA sequences. Transcription of this region up to the most 5' initiation site was demonstrated by the reverse transcription-polymerase chain reaction (RT-PCR) method. The 5' non-translated region stretches between 703 and 1393 bp, depending on which initiation site is used. Several consensus cis-acting regulatory sequences were identified within the 5' end. These include, among others, sites for PEA-3, AP-1, and Pit-1. In addition, cAMP response element (CRE)-like and glucocorticoid/progesterone response element (GRE/PRE)-like sequences were found.(ABSTRACT TRUNCATED AT 250 WORDS)
促性腺激素释放激素与其受体的相互作用是生殖内分泌调节中的关键事件。我们最近克隆了编码人促性腺激素释放激素受体(hGnRHR)的基因。部分序列分析揭示了一个由三个外显子和两个内含子组成的结构组织。外显子II仅包含219 bp,其余约5 kb的转录本分布在外显子I和III之间。hGnRHR的完整编码区仅为987 bp,留下了广泛的5'和3'非翻译区以及可能未被解释的其他外显子。本报告提供了外显子I和III的完整序列,并证明该基因不太可能包含其他外显子。对该基因5'端的测序揭示了在700个核苷酸区域内分布的五个共有TATA序列。引物延伸分析检测到与该TATA序列簇相关的多个转录起始位点。通过逆转录-聚合酶链反应(RT-PCR)方法证实了该区域直至最5'起始位点的转录。5'非翻译区根据所使用的起始位点在703至1393 bp之间延伸。在5'端鉴定出了几个共有顺式作用调节序列。其中包括PEA-3、AP-1和Pit-1的位点。此外,还发现了类似cAMP反应元件(CRE)和糖皮质激素/孕酮反应元件(GRE/PRE)的序列。(摘要截短于250字)