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即早基因X-1与调节细胞凋亡的蛋白质相互作用。

Immediate early gene X-1 interacts with proteins that modulate apoptosis.

作者信息

Kumar Rajiv, Lutz Ward, Frank Elena, Im Hee-Jeong

机构信息

Division of Nephrology and Hypertension, Department of Internal Medicine, Mayo Clinic and Foundation, Rochester, MN 55905, USA.

出版信息

Biochem Biophys Res Commun. 2004 Oct 29;323(4):1293-8. doi: 10.1016/j.bbrc.2004.09.006.

Abstract

Immediate early gene X-1 (IEX-1) modulates apoptosis, cellular growth, mechanical strain-induced cardiac hypertrophy, and vascular intimal hyperplasia. To determine how IEX-1 alters apoptosis, we performed yeast two-hybrid studies using IEX-1 as the "bait" protein, and examined interactions between IEX-1 and proteins expressed by a human kidney cDNA expression library. We found that IEX-1 interacts with several proteins of which at least four are known to play a role in the regulation of apoptosis: (1) calcium-modulating cyclophilin ligand; (2) tumor necrosis factor-related apoptosis-inducing ligand (tumor necrosis factor superfamily, member 10); (3) ML-1 myeloid cell leukemia gene encoded protein; and (4) BAT3, a gene present in the major histo-compatibility complex. Our data suggest that IEX-1 may regulate apoptosis by directly interacting with various proteins involved in the control of apoptotic pathways.

摘要

即刻早期基因X-1(IEX-1)可调节细胞凋亡、细胞生长、机械应变诱导的心肌肥大以及血管内膜增生。为了确定IEX-1如何改变细胞凋亡,我们以IEX-1作为“诱饵”蛋白进行了酵母双杂交研究,并检测了IEX-1与人类肾脏cDNA表达文库所表达蛋白之间的相互作用。我们发现IEX-1与几种蛋白相互作用,其中至少有四种蛋白已知在细胞凋亡调节中发挥作用:(1)钙调节亲环蛋白配体;(2)肿瘤坏死因子相关凋亡诱导配体(肿瘤坏死因子超家族,成员10);(3)ML-1髓样细胞白血病基因编码蛋白;(4)BAT3,一种存在于主要组织相容性复合体中的基因。我们的数据表明,IEX-1可能通过与参与凋亡途径控制的各种蛋白直接相互作用来调节细胞凋亡。

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