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鉴定人类促性腺激素释放激素基因在生殖组织和细胞系中使用的一个主要上游转录起始位点。

Identification of a major up-stream transcription start site for the human progonadotropin-releasing hormone gene used in reproductive tissues and cell lines.

作者信息

Dong K W, Yu K L, Roberts J L

机构信息

Research Center for Neurobiology, Mount Sinai School of Medicine, New York, New York 10029.

出版信息

Mol Endocrinol. 1993 Dec;7(12):1654-66. doi: 10.1210/mend.7.12.8145771.

Abstract

Previous studies suggested that GnRH gene transcripts in human tissues may be derived from an upstream transcriptional start site in addition to the well characterized hypothalamic start site. To resolve this issue we characterized the transcriptional start sites of the human GnRH gene in a human placental tumor cell line (JEG) and a human breast tumor cell line (MDA). Using primer extension and reverse transcription-polymerase chain reaction (RT-PCR) assay, we identified a discrete upstream transcriptional start site 579 bases up-stream from the hypothalamic site in both JEG and MDA cell lines. The up-stream start site lacks the TATA and CAAT elements often present in RNA polymerase-II promoters, but contains the sequence GGTCTTGCT located 84 bases 5' to the up-stream start site similar to other genes that lack TATA/CAAT boxes. RT-PCR quantitation shows that the up-stream start site is the major transcriptional start site, representing 74% of the cytoplasmic transcripts in JEG cells and 67% in MDA cells. Supporting this observation, transfection assay using a human GnRH promoter/luciferase reporter gene construct containing only the up-stream transcription start site has a higher level of transcriptional activity than the human GnRH promoter/luciferase reporter construct containing only the down-stream start site. A high relative abundance (approximately 45%) of total GnRH mRNAs were also found in the nucleus of both cell lines, which did not appear to be a consequence of the nuclear/cytoplasmic fractionation procedure. To determine if this upstream start site was used in normal GnRH-expressing human tissues, we analyzed RNA from a variety of postmortem/surgical procedure tissue samples. RT-PCR analysis together with Southern blot analysis demonstrated the presence of GnRH mRNA in human pituitary, cerebral cortex, testes, ovary, and mammary gland for the first time as well as verified GnRH gene expression in hypothalamus and placenta. The up-stream transcriptional start site is used only in reproductive tissues, such as placenta, testes, ovary, and mammary gland, suggesting tissue-specific regulation at this site.

摘要

以往研究表明,除了已充分表征的下丘脑起始位点外,人类组织中的促性腺激素释放激素(GnRH)基因转录本可能还源自一个上游转录起始位点。为解决这一问题,我们对人胎盘肿瘤细胞系(JEG)和人乳腺肿瘤细胞系(MDA)中的人类GnRH基因转录起始位点进行了表征。通过引物延伸和逆转录-聚合酶链反应(RT-PCR)分析,我们在JEG和MDA细胞系中均鉴定出一个位于下丘脑位点上游579个碱基处的离散上游转录起始位点。该上游起始位点缺乏RNA聚合酶II启动子中常见的TATA和CAAT元件,但在其上游起始位点5'端84个碱基处含有序列GGTCTTGCT,这与其他缺乏TATA/CAAT框的基因相似。RT-PCR定量分析表明,上游起始位点是主要的转录起始位点,在JEG细胞的细胞质转录本中占74%,在MDA细胞中占67%。支持这一观察结果的是,使用仅包含上游转录起始位点的人GnRH启动子/荧光素酶报告基因构建体的转染分析显示,其转录活性水平高于仅包含下游起始位点的人GnRH启动子/荧光素酶报告构建体。在这两种细胞系的细胞核中还发现了相对丰度较高(约45%)的总GnRH mRNA,这似乎不是核/细胞质分级分离过程的结果。为了确定该上游起始位点是否在正常表达GnRH的人类组织中被使用,我们分析了来自各种尸检/手术组织样本的RNA。RT-PCR分析以及Southern印迹分析首次证明了GnRH mRNA在人垂体、大脑皮层、睾丸、卵巢和乳腺中的存在,并验证了下丘脑和胎盘中GnRH基因的表达。上游转录起始位点仅在胎盘、睾丸、卵巢和乳腺等生殖组织中被使用,表明该位点存在组织特异性调控。

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