Shen Enzhi, Lei Yan, Liu Qian, Zheng Yanbo, Song Chunqing, Marc Jan, Wang Yongchao, Sun Le, Liang Qianjin
Key Laboratory of Cell Proliferation and Regulation Biology of Ministry of Education, College of Life Sciences, Beijing Normal University, Beijing 100875, PR China.
Exp Cell Res. 2009 Apr 15;315(7):1100-16. doi: 10.1016/j.yexcr.2009.01.022. Epub 2009 Feb 3.
A novel protein that associates with interphase nucleus and mitotic apparatus (INMAP) was identified by screening HeLa cDNA expression library with an autoimmune serum followed by tandem mass spectrometry. Its complete cDNA sequence of 1.818 kb encodes 343 amino acids with predicted molecular mass of 38.2 kDa and numerous phosphorylation sites. The sequence is identical with nucleotides 1-1800 bp of an unnamed gene (GenBank accession no. 7022388) and highly homologous with the 3'-terminal sequence of POLR3B. A monoclonal antibody against INMAP reacted with similar proteins in S. cerevisiae, Mel and HeLa cells, suggesting that it is a conserved protein. Confocal microscopy using either GFP-INMAP fusion protein or labeling with the monoclonal antibody revealed that the protein localizes as distinct dots in the interphase nucleus, but during mitosis associates closely with the spindle. Double immunolabeling using specific antibodies showed that the INMAP co-localizes with alpha-tubulin, gamma-tubulin, and NuMA. INMAP also co-immunoprecipitated with these proteins in their native state. Stable overexpression of INMAP in HeLa cell lines leads to defects in the spindle, mitotic arrest, formation of polycentrosomal and multinuclear cells, inhibition of growth, and apoptosis. We propose that INMAP is a novel protein that plays essential role in spindle formation and cell-cycle progression.
通过用自身免疫血清筛选HeLa cDNA表达文库,随后进行串联质谱分析,鉴定出一种与间期细胞核和有丝分裂装置相关的新型蛋白质(INMAP)。其1.818 kb的完整cDNA序列编码343个氨基酸,预测分子量为38.2 kDa,并有许多磷酸化位点。该序列与一个未命名基因(GenBank登录号7022388)的1 - 1800 bp核苷酸相同,且与POLR3B的3'末端序列高度同源。一种抗INMAP的单克隆抗体与酿酒酵母、Mel和HeLa细胞中的类似蛋白质发生反应,表明它是一种保守蛋白。使用GFP - INMAP融合蛋白或用单克隆抗体标记的共聚焦显微镜显示,该蛋白在间期细胞核中定位为不同的点,但在有丝分裂期间与纺锤体紧密结合。使用特异性抗体的双重免疫标记显示,INMAP与α - 微管蛋白、γ - 微管蛋白和NuMA共定位。INMAP在其天然状态下也与这些蛋白质进行共免疫沉淀。在HeLa细胞系中稳定过表达INMAP会导致纺锤体缺陷、有丝分裂停滞、多中心体和多核细胞形成、生长抑制以及细胞凋亡。我们提出INMAP是一种在纺锤体形成和细胞周期进程中起重要作用的新型蛋白质。