Huang Xiaoyi, Shi Zhongcheng, Wang Wei, Bai Jing, Chen Zhenghua, Xu Jiujin, Zhang Dekai, Fu Songbin
Department of Medical Genetics, Harbin Medical University, Baojian Road, Harbin 150081, China.
Biochem Biophys Res Commun. 2007 Sep 21;361(2):287-93. doi: 10.1016/j.bbrc.2007.06.181. Epub 2007 Jul 16.
p16(INK4a) is a multiple tumor suppressor, playing an important role in proliferation and tumorigenesis. To screen the p16(INK4a)-associated proteins, we performed a yeast two-hybrid assay and identified a novel protein isochorismatase domain containing 2 (ISOC2). ISOC2 conserves in different species, and encodes 205 and 210 amino acids in human and mouse, respectively. The expression of ISOC2 in mouse is universal but predominantly in uterus, stomach, and urinary tract system. Interaction between ISOC2 and p16(INK4a) was verified using in vitro pull-down assays and in vivo co-immunoprecipitation. Confocal microscopy studies using green and cyan fluorescent fusion proteins determined that ISOC2 co-localizes with p16(INK4a). Over-expressed ISOC2 is able to inhibit p16(INK4a) in dose-dependent manner. Our data indicated that ISOC2 is a novel functional protein, which is able to bind and co-localize with a tumor suppressor gene p16(INK4a). Over-expressed ISOC2 inhibits the expression of p16(INK4a), suggesting that this novel gene may play a role during the tumor development by interacting with p16(INK4a).
p16(INK4a)是一种多重肿瘤抑制因子,在细胞增殖和肿瘤发生过程中发挥着重要作用。为了筛选与p16(INK4a)相关的蛋白,我们进行了酵母双杂交实验,并鉴定出一种含有异分支酸酶结构域2(ISOC2)的新型蛋白。ISOC2在不同物种中保守,在人和小鼠中分别编码205和210个氨基酸。ISOC2在小鼠中的表达具有普遍性,但主要集中在子宫、胃和泌尿系统。通过体外下拉实验和体内共免疫沉淀验证了ISOC2与p16(INK4a)之间的相互作用。使用绿色和青色荧光融合蛋白进行的共聚焦显微镜研究确定ISOC2与p16(INK4a)共定位。过表达的ISOC2能够以剂量依赖的方式抑制p16(INK4a)。我们的数据表明,ISOC2是一种新型功能蛋白,能够与肿瘤抑制基因p16(INK4a)结合并共定位。过表达的ISOC2抑制p16(INK4a)的表达,表明这个新基因可能通过与p16(INK4a)相互作用在肿瘤发生过程中发挥作用。