Liu Jun-Wei, Chandra Dhyan, Tang Shao-Hua, Chopra Dharam, Tang Dean G
Department of Carcinogenesis, the University of Texas M. D. Anderson Cancer Center, Science Park Research Division, Park Road 1C, Smithville, TX 78957, USA.
Cancer Res. 2002 May 15;62(10):2976-81.
BH3 (Bcl-2 homology 3)-only proteins of the Bcl-2 family play an essential role in apoptosis. In this study, a novel human BH3-only protein, Bcl-2-interacting mediator (Bim)gamma, was identified during our study of regulation of prostate cancer cell death by Bcl-2 family proteins. Bimgamma shares the highest amino acid sequence homology to BimEL and BimL, two proapoptotic BH3-only Bcl-2 proteins derived from alternative mRNA splicing. Genomic studies indicate that Bimgamma is a novel splice variant of Bim and is generated as a result of the retention of a 126-bp intron of the bim gene. Bimgamma mRNA displays a tissue-specific expression pattern distinct from those of the other Bim isoforms. Subcellular fractionation studies indicate that Bimgamma is localized both in intracellular membranes and cytosol. Interestingly, Bimgamma mRNA, similar to the BimEL protein, is up-regulated in the majority of the prostate cancer cell lines studied, whereas several other proapoptotic Bcl-2 proteins, including Bax, Bak, and Bad, are down-regulated in prostate cancer cells. Functional studies indicate that Bimgamma inhibits clonal growth in prostate cancer cells and promotes apoptosis, which is inhibited by overexpressing Bcl-2. Because both Bimgamma and BimEL are proapoptotic BH3-only proteins and both are up-regulated in prostate cancer cells, they may play a unique role in prostate cancer development.
Bcl-2家族中仅含BH3(Bcl-2同源结构域3)的蛋白质在细胞凋亡中起重要作用。在本研究中,我们在研究Bcl-2家族蛋白对前列腺癌细胞死亡的调控过程中,鉴定出一种新型的人类仅含BH3的蛋白质——Bcl-2相互作用介质(Bim)γ。Bimγ与BimEL和BimL的氨基酸序列同源性最高,BimEL和BimL是通过选择性mRNA剪接产生的两种促凋亡的仅含BH3的Bcl-2蛋白。基因组研究表明,Bimγ是Bim的一种新型剪接变体,是由于bim基因的一个126bp内含子保留而产生的。Bimγ mRNA表现出与其他Bim亚型不同的组织特异性表达模式。亚细胞分级分离研究表明,Bimγ定位于细胞内膜和细胞质中。有趣的是,与BimEL蛋白类似,Bimγ mRNA在所研究的大多数前列腺癌细胞系中上调,而其他几种促凋亡的Bcl-2蛋白,包括Bax、Bak和Bad,在前列腺癌细胞中下调。功能研究表明,Bimγ抑制前列腺癌细胞的克隆生长并促进细胞凋亡,而过表达Bcl-2可抑制这种作用。由于Bimγ和BimEL都是促凋亡的仅含BH3的蛋白,且在前列腺癌细胞中均上调,它们可能在前列腺癌的发展中发挥独特作用。