Suppr超能文献

鉴定人同源盒基因 NKX3.1 启动子区的 Sp1 元件。

Identification of Sp1-elements in the promoter region of human homeobox gene NKX3.1.

机构信息

Department of Endocrinology, Provincial Hospital affiliated to Shandong University, 250021 Jinan, People's Republic of China.

出版信息

Mol Biol Rep. 2009 Nov;36(8):2353-60. doi: 10.1007/s11033-009-9457-y. Epub 2009 Mar 5.

Abstract

NKX3.1 is a prostate-specific homeobox gene related strongly to prostate development and prostate cancer. However, little is known about the mechanism for regulation of NKX3.1 in prostate cancer. With RT-PCR and western blot, we found that NKX3.1 expression was enhanced by over-expression of Sp1 at both the mRNA and protein levels in prostate cancer LNCaP cells. To identify the Sp1-elements in the promoter region of NKX3.1, a 521 bp-promoter of human NKX3.1 gene containing three possible Sp1-elements was cloned into the upstream of the luciferase reporter gene in pGL(3)-basic plasmid. With deletion mutation analysis, plasmid construction, EMSA and oligonucleotide decoy technique, two Sp1-elements which located between ?29 to ?43 and -60 to -46 of NKX3.1 gene were identified and proven to be functional elements. It will be important to further study on the functions and the regulatory mechanisms of Sp1 element in NKX3.1 gene expression.

摘要

NKX3.1 是一种前列腺特异性同源盒基因,与前列腺发育和前列腺癌密切相关。然而,对于 NKX3.1 在前列腺癌中的调控机制知之甚少。通过 RT-PCR 和 Western blot,我们发现 Sp1 的过表达可增强前列腺癌细胞系 LNCaP 中 NKX3.1 的 mRNA 和蛋白水平的表达。为了鉴定 NKX3.1 启动子区中的 Sp1 元件,我们克隆了包含三个可能的 Sp1 元件的人 NKX3.1 基因的 521bp 启动子,将其插入 pGL(3)-basic 质粒的荧光素酶报告基因上游。通过缺失突变分析、质粒构建、EMSA 和寡核苷酸诱饵技术,鉴定并证实了位于 NKX3.1 基因 -29 到 -43 和 -60 到 -46 之间的两个 Sp1 元件是具有功能的元件。进一步研究 Sp1 元件在 NKX3.1 基因表达中的功能和调控机制将非常重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验