Hauge Helena, Patzke Sebastian, Aasheim Hans-Christian
Faculty of Medicine, University of Oslo, and Department of Immunology, Institute for Cancer Research, Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway.
Genomics. 2007 Jul;90(1):14-27. doi: 10.1016/j.ygeno.2007.03.002. Epub 2007 May 11.
We have previously characterized the centrosome/spindle pole-associated protein (CSPP) involved in cell cycle progression. The open reading frame C20orf55 was identified in a yeast two-hybrid screen in a search for CSPP-interacting proteins. A homology search revealed that C20orf55 belongs to a gene family consisting of three members that have not yet been described. The HUGO Nomenclature Committee has assigned these genes the names FAM110A-FAM110C. Studies of transfectants showed that the FAM110 proteins localized to centrosomes and accumulated at the microtubule organization center in interphase and at spindle poles in mitosis. In addition, overexpression of FAM110C induced microtubule aberrancies. Our data also indicated a cell cycle-regulated expression of FAM110A. Moreover, ectopic expression of FAM110B and FAM110C proteins impaired cell cycle progression in G1 phase. To summarize, we have characterized a novel family of genes encoding proteins with distinct conserved motifs, of which all members localize to centrosomes and spindle poles.
我们之前已对参与细胞周期进程的中心体/纺锤体极相关蛋白(CSPP)进行了表征。在酵母双杂交筛选中鉴定出开放阅读框C20orf55,以寻找与CSPP相互作用的蛋白。同源性搜索显示,C20orf55属于一个由三个尚未被描述的成员组成的基因家族。人类基因组组织命名委员会已将这些基因命名为FAM110A - FAM110C。对转染子的研究表明,FAM110蛋白定位于中心体,并在间期积累于微管组织中心,在有丝分裂时积累于纺锤体极。此外,FAM110C的过表达诱导微管异常。我们的数据还表明FAM110A的表达受细胞周期调控。而且,FAM110B和FAM110C蛋白的异位表达会损害G1期的细胞周期进程。总之,我们已表征了一个新的基因家族,其编码具有不同保守基序的蛋白,所有成员均定位于中心体和纺锤体极。