Cui Yong-Ping, Wang Jian-Bo, Zhang Xin-Yu, Bi Mei-Xia, Guo Li-Ping, Lu Shih-Hsin
Department of Etiology and Carcinogenesis, Tumor Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China.
World J Gastroenterol. 2003 Sep;9(9):1892-6. doi: 10.3748/wjg.v9.i9.1892.
To identify esophageal cancer related gene2 (ECRG2) associated proteins and their possible interactions with ECRG2 gene.
In the yeast forward two-hybrid system, ECRG2 was fused with the DNA-binding domain (DBD) of Gal4 and human fetal liver cDNA library was fused with the transcriptional activation domain (AD) of Gal4. We performed a high-stringency scale procedure to screen ECRG2 against human fetal liver cDNA library and characterized positives by sequence analysis.
We found the following 9 putatively associated proteins. They were metallothionein2A, metallothionein1H, metallothionein1G, ferritin, erythrocyte membrane protein band4.2, mitochondrial ribosomal protein S12, hypothetical protein FLJ10101, and a novel gene whose cDNA was found to have no strong homology to any other previously characterized gene whose DDBJ/EMBL/GenBank accession number is AF422192 mapped to human chromosome 14q31.
MT, a potential interaction partner for ECRG2, might be involved in the regulation of cell proliferation and apoptosis, and in various physiological processes. Determination of a reliability score for each single protein-protein interaction, especially interaction of ECRG2 and MT, permits the assignment of ECRG2 and unannotated proteins to biological pathways. A further understanding of the association between ECRG2 and MT should facilitate the functions of ECRG2 gene.
鉴定与食管癌相关基因2(ECRG2)相互作用的蛋白及其与ECRG2基因可能的相互作用关系。
在酵母正向双杂交系统中,将ECRG2与Gal4的DNA结合结构域(DBD)融合,将人胎肝cDNA文库与Gal4的转录激活结构域(AD)融合。采用高严谨度筛选程序,以人胎肝cDNA文库为对象筛选与ECRG2相互作用的蛋白,并通过序列分析对阳性克隆进行鉴定。
发现9种可能与之相互作用的蛋白,分别为金属硫蛋白2A、金属硫蛋白1H、金属硫蛋白1G、铁蛋白、红细胞膜带4.2蛋白、线粒体核糖体蛋白S12、假定蛋白FLJ10101,以及一个新基因,其cDNA与其他已知基因无明显同源性,其DDBJ/EMBL/GenBank登录号为AF422192,定位于人染色体14q31。
金属硫蛋白(MT)作为ECRG2潜在的相互作用伙伴,可能参与细胞增殖、凋亡调控及多种生理过程。确定每个蛋白-蛋白相互作用的可靠性评分,尤其是ECRG2与MT的相互作用评分,有助于将ECRG2及未注释蛋白归入生物学途径。进一步了解ECRG2与MT之间的关系将有助于明确ECRG2基因的功能。