Kim J K, Ryll R, Ishizuka Y, Kato S
Kato Cytoprotein Network Project, ERATO, Japan Science and Technology Corporation (JST), c/o Sagami Chemical Research Center, Nishi-Ohnuma 4-4-1, Sagamihara, 229-0012, Kanagawa, Japan.
Gene. 2000 Oct 31;257(2):327-34. doi: 10.1016/s0378-1119(00)00414-5.
Using a model system of young, senescent and SV40-immortalized WI-38 fibroblasts, we identified two mRNAs upregulated in immortalized cells (imup-1, immortalization-upregulated protein 1, and imup-2). Compared to normal tissues, both genes were more frequently expressed in cancer cells. The open reading frame of imup-1 spans 321bp, coding for a 10.9 kDa protein of 106 amino acids, while an insertion of 59bp in the otherwise identical mRNA of imup-2 leads to a frameshift, resulting in an 8.5 kDa protein of 85 amino acids. Database searches identified these genes on chromosome 19, which could account for the cloned imup-1 and imup-2 transcripts by alternative splicing. Southern blot analysis of digested genomic DNA confirmed that both transcripts are derived from a single locus. The expressed proteins IMUP-1 and IMUP-2 share 46 identical N-terminal amino acids, whereas the C-termini are unrelated. Green fluorescent protein-fusions of both IMUP-1 and IMUP-2 accumulated in the nucleus of HeLa cells. The C-terminus of IMUP-1 contains a bipartite nuclear localization signal, the deletion of which impaired nuclear translocation. In-vitro translated proteins bound to poly(rG), but did not interact with single-stranded DNA or double-stranded DNA. The nuclear localization of IMUP-1 and IMUP-2 as well as the upregulation of both underlying mRNAs in immortalized cells suggest a function in immortalization.
利用年轻、衰老和SV40永生化的WI-38成纤维细胞模型系统,我们鉴定出在永生化细胞中上调的两种mRNA(imup-1,永生化上调蛋白1和imup-2)。与正常组织相比,这两个基因在癌细胞中更频繁地表达。imup-1的开放阅读框跨度为321bp,编码一个106个氨基酸的10.9kDa蛋白质,而在imup-2的其他相同mRNA中插入59bp会导致移码,产生一个85个氨基酸的8.5kDa蛋白质。数据库搜索在19号染色体上鉴定出这些基因,这可以通过可变剪接来解释克隆的imup-1和imup-2转录本。对消化的基因组DNA进行的Southern印迹分析证实,这两种转录本均来自单个基因座。表达的蛋白质IMUP-1和IMUP-2共享46个相同的N端氨基酸,而C端则不相关。IMUP-1和IMUP-2与绿色荧光蛋白的融合体在HeLa细胞核中积累。IMUP-1的C端包含一个双分型核定位信号,缺失该信号会损害核转位。体外翻译的蛋白质与聚(rG)结合,但不与单链DNA或双链DNA相互作用。IMUP-1和IMUP-2的核定位以及永生化细胞中两种基础mRNA的上调表明它们在永生化过程中发挥作用。