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人类促凋亡基因Bik的结构分析:染色体定位、基因组组织及启动子序列定位

Structural analysis of the human pro-apoptotic gene Bik: chromosomal localization, genomic organization and localization of promoter sequences.

作者信息

Verma S, Budarf M L, Emanuel B S, Chinnadurai G

机构信息

Institute for Molecular Virology, St. Louis University Health Sciences Center, 3681 Park Avenue, St. Louis, MO 63110, USA.

出版信息

Gene. 2000 Aug 22;254(1-2):157-62. doi: 10.1016/s0378-1119(00)00276-6.

Abstract

The human Bik gene codes for a strong pro-apoptotic protein BIK. We have used fluorescent in-situ hybridization to establish the chromosomal localization of the Bik gene to 22q13.3. Genomic clones of the Bik gene were identified from a cosmid library of chromosome 22. Detailed analysis of the Bik gene revealed that it spans a region of about 19kb and comprises of five exons. Sequence analysis indicated that the 5' flanking region of Bik lacks canonical TATA and CAAT boxes but directs transcriptional initiation from a single site. A 1.9kb region containing the promoter elements of the Bik gene was identified and was found to direct expression of the reporter cat gene in transient transfection studies. By mutational analysis, the minimal Bik promoter was localized to a region between -211 to +153. Northern blot analysis showed a ubiquitous expression profile of the Bik mRNA with elevated levels of expression in heart and skeletal muscle.

摘要

人类Bik基因编码一种强效促凋亡蛋白BIK。我们利用荧光原位杂交技术将Bik基因定位于22q13.3染色体上。从22号染色体的黏粒文库中鉴定出Bik基因的基因组克隆。对Bik基因的详细分析表明,它跨越约19kb的区域,由五个外显子组成。序列分析表明,Bik基因的5'侧翼区域缺乏典型的TATA和CAAT框,但从单个位点指导转录起始。鉴定出一个包含Bik基因启动子元件的1.9kb区域,并发现它在瞬时转染研究中指导报告基因cat的表达。通过突变分析,将最小的Bik启动子定位于-211至+153之间的区域。Northern印迹分析显示Bik mRNA具有普遍的表达谱,在心脏和骨骼肌中的表达水平升高。

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