Gao Yanhong, Yue Wen, Zhang Peng, Li Li, Xie Xiaoyan, Yuan Hongfeng, Chen Lin, Liu Daqing, Yan Fang, Pei Xuetao
Laboratory of Stem Cell Biology, Beijing Institute of Transfusion Medicine, 27 Taiping Road, Beijing 100850, PR China.
Biochem Biophys Res Commun. 2005 Sep 23;335(2):343-50. doi: 10.1016/j.bbrc.2005.07.087.
spindlin1, a novel human gene recently isolated by our laboratory, is highly homologous to mouse spindlin gene. In this study, we cloned cDNA full-length of this novel gene and send it to GenBank database as spindlin1 (Homo sapiens spindlin1) with Accession No. AF317228. In order to investigate the function of spindlin1, we studied further the subcellular localization of Spindlin1 protein and the effects of spindlin1 overexpression in NIH3T3 cells. The results showed that the fusion protein pEGFP-N1-spindlin1 was located in the nucleus and the C-terminal is correlated with nuclear localization of Spindlin1 protein. NIH3T3 cells which could stably express spindlin1 as a result of RT-PCR analysis compared with the control cells displayed a complete morphological change; made cell growth faster; and increased the percentage of cells in G2/M and S phase. Furthermore, overexpressed spindlin1 cells formed colonies in soft agar in vitro and formed tumors in nude mice. Our findings provide direct evidence that spindlin1 gene may contribute to tumorigenesis.
Spindlin1是我们实验室最近分离出的一个新的人类基因,与小鼠Spindlin基因高度同源。在本研究中,我们克隆了该新基因的cDNA全长,并将其作为Spindlin1(智人Spindlin1)提交至GenBank数据库,登录号为AF317228。为了研究Spindlin1的功能,我们进一步研究了Spindlin1蛋白的亚细胞定位以及Spindlin1在NIH3T3细胞中过表达的影响。结果显示,融合蛋白pEGFP-N1-Spindlin1定位于细胞核,且C末端与Spindlin1蛋白的核定位相关。RT-PCR分析结果表明,与对照细胞相比,能够稳定表达Spindlin1的NIH3T3细胞呈现出完全的形态变化;细胞生长加快;G2/M期和S期细胞百分比增加。此外,过表达Spindlin1的细胞在体外软琼脂中形成集落,并在裸鼠体内形成肿瘤。我们的研究结果提供了直接证据,表明Spindlin1基因可能与肿瘤发生有关。