ZHANG CUI-LI, YANG XIAO-MING, CHENG HAI-EN, et al. Isolation and identification of NR4A1 interacting with Smac/DIABLO. [J]. Journal of army medical university, 2007, 29(6): 482-485.
ZHANG CUI-LI, YANG XIAO-MING, CHENG HAI-EN, et al. Isolation and identification of NR4A1 interacting with Smac/DIABLO. [J]. Journal of army medical university, 2007, 29(6): 482-485.DOI:
Western blot检测融合蛋白在酵母中的正确表达,自激活作用的检测并确定抑制His基础表达的3AT浓度。③对成人肝cDNA文库的筛选。选择能同时激活His、Ura、LacZ 3个报告基因的克隆为阳性,利用回转实验和GST-pull down 对阳性克隆进行鉴定。 结果 成功构建pDBLeu-Smac/DIABLO载体,转化酵母细胞MaV203,无细胞毒性,无自激活作用,3AT浓度为25 mmol/L。 经回转实验和GST-pull down证实了线粒体促凋亡因子Smac/DIABLO与核受体NR4A1之间具有相互作用。 结论 Smac/DIABLO可能通过与核受体NR4A1的相互作用来影响核受体NR4A1对细胞生存或者凋亡的调控。
Abstract
Objective To screen proteins in human adult liver cDNA library interacting with Smac/DIABLO with yeast two-hybrid technique. Methods The wild Smac/DIABLO was amplified with PCR in human adult liver cDNA library. The recombinant vector pDBLeu-Smac/DIABLO was constructed and transformed into yeast MaV203
and the expression of GAL4 BD-Smac/DIABLO fusion protein was dectected by Western blotting. The self-activation was examined
and 3-Amino-1
2
4-Triazole (3AT) concentration required to titrate basal HIS expression levels was determined. The human adult liver cDNA library was screened sequentially. The clones that grew on SC-Leu-Trp-His-Ura plates was employed to test if they could activate His
Ura and LacZ report genes. The plasmids from those clones that could activate the 3 report genes were isolated
then cotransformed with pDBLeu-Smac/DIABLO
and verified with GST-pull down after sequencing. Results The bait vector pDBLeu-Smac/DIABLO was successfully constructed and expressed correctly in MaV203. One clone nuclear receptor subfamily 4
group A
member 1 (NR4A1) was obtained and could interact with wild Smac/DIABLO via cotransformation and GST-pull down. Conclusion Smac/DIABLO may interact with NR4A1 and affect its function on cell growth and apoptosis.