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促凋亡Bcl-2相关蛋白Bim的基因结构、可变剪接及染色体定位

Gene structure alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim.

作者信息

Bouillet P, Zhang L C, Huang D C, Webb G C, Bottema C D, Shore P, Eyre H J, Sutherland G R, Adams J M

机构信息

The Walter and Eliza Hall Institute of Medical Research, The Royal Melbourne Hospital, Parkville, Victoria, Australia.

出版信息

Mamm Genome. 2001 Feb;12(2):163-8. doi: 10.1007/s003350010242.

Abstract

Bim is a proapoptotic protein of the Bcl-2 family that shares only the short BH3 domain with other members. It has three isoforms, apparently produced by alternative splicing. The demonstration that Bim is essential for certain apoptotic responses and to prevent overproduction of hematopoietic cells suggests that it may be a tumor suppressor. We have, therefore, investigated the organization of the mouse Bim gene, delineating its promoter and splicing, and positioned the gene on both mouse and human chromosomes. Bim has six exons, but the third is a facultative intron that is spliced out in the mRNAs for the smaller isoforms (BimL and BimS), but not that encoding the largest isoform (BimEL). The 0.8-kb region 5' to exon 1, which contains a TATA-less promoter and binding sites for several transcription factors, can drive expression of a reporter gene. Mouse Bim localizes to the distal third of Chromosome (Chr) 2, near the F-G boundary, and its human counterpart to Chr 2q12 or q13. Deletions of these bands have been reported in ten tumors (eight hematopoietic), reinforcing the possibility that Bim is a tumor suppressor. These findings should help to clarify the regulation of Bim expression and to assess whether mutations involving Bim contribute to neoplastic and other diseases.

摘要

Bim是Bcl-2家族的一种促凋亡蛋白,它与其他成员仅共享短的BH3结构域。它有三种异构体,显然是由可变剪接产生的。有证据表明,Bim对于某些凋亡反应以及防止造血细胞过度增殖至关重要,这表明它可能是一种肿瘤抑制因子。因此,我们研究了小鼠Bim基因的结构,确定了其启动子和剪接方式,并将该基因定位在小鼠和人类染色体上。Bim有六个外显子,但第三个是一个选择性内含子,在较小异构体(BimL和BimS)的mRNA中被剪接掉,但在编码最大异构体(BimEL)的mRNA中不被剪接。外显子1上游0.8 kb的区域,包含一个无TATA框的启动子和几个转录因子的结合位点,能够驱动报告基因的表达。小鼠Bim定位于2号染色体(Chr)远端的三分之一处,靠近F-G边界,其人类对应物定位于2q12或q13。在十种肿瘤(八种造血系统肿瘤)中报道了这些带的缺失,这增加了Bim是肿瘤抑制因子的可能性。这些发现应有助于阐明Bim表达的调控,并评估涉及Bim的突变是否会导致肿瘤及其他疾病。

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