Zhao Xiaoyu, Jin Miaomiao, Wang Mengzhu, Sun Lili, Hong Xuejiao, Cao Ying, Wang Chunguang
a Department of Central Laboratory , Shanghai 10th People's Hospital, School of Life Sciences and Technology, Tongji University , Shanghai , China.
Cell Cycle. 2016 Sep;15(17):2367-75. doi: 10.1080/15384101.2016.1204059. Epub 2016 Jul 6.
Fidgetin-like 1 (FIGL-1) is a homolog of fidgetin, an AAA protein that was identified as the protein encoded by the gene mutated in fidget mice. Because the phenotypes of fidget mice are reminiscent of the phenotypes of ciliopathy diseases, and because fidgetin has microtubule-severing activity, we hypothesize that these proteins participate in cilia-related processes. Indeed, overexpression of FIGL-1 interfered with ciliogenesis in cultured cells. In particular, overexpressed FIGL-1 strongly accumulated at the centrosome, and, when highly expressed, perturbed the localization of centrosomal proteins such as pericentrin, CP110, and centrin. Using a polyclonal antibody against human FIGL-1, we found that endogenous FIGL-1 localized preferentially around the mother centriole. Consistently, depletion of FIGL-1 by shRNA treatment enhanced ciliogenesis in HEK293T cells. By checking the integrity of the cytoplasmic microtubule network in FIGL-1-overexpressing cells, we found that FIGL-1 probably has microtubule-severing activity, as suggested by its sequence homology with other microtubule-severing proteins. Furthermore, we showed that overexpression of FIGL-1 in zebrafish embryo decreased the length of cilia and perturbed the heart laterality. Taken together, these results demonstrate that FIGL-1 is a new centrosomal protein and inhibits ciliogenesis. These results extend the already long list of centrosomal proteins and provide new insights into the regulation of ciliogenesis.
类纤颤蛋白1(FIGL-1)是纤颤蛋白的同源物,纤颤蛋白是一种AAA蛋白,被确定为由在纤颤小鼠中发生突变的基因所编码的蛋白质。由于纤颤小鼠的表型让人联想到纤毛病疾病的表型,并且由于纤颤蛋白具有切断微管的活性,我们推测这些蛋白质参与与纤毛相关的过程。事实上,FIGL-1的过表达干扰了培养细胞中的纤毛发生。特别是,过表达的FIGL-1强烈聚集在中心体,并且在高表达时,扰乱了诸如中心体蛋白、中心粒外周蛋白、CP110和中心粒蛋白等中心体蛋白的定位。使用针对人FIGL-1的多克隆抗体,我们发现内源性FIGL-1优先定位于母中心粒周围。一致地,通过短发夹RNA处理耗尽FIGL-1可增强HEK293T细胞中的纤毛发生。通过检查FIGL-1过表达细胞中细胞质微管网络的完整性,我们发现FIGL-1可能具有切断微管的活性,正如其与其他切断微管蛋白的序列同源性所表明的那样。此外,我们表明在斑马鱼胚胎中过表达FIGL-1会缩短纤毛长度并扰乱心脏的左右不对称性。综上所述,这些结果表明FIGL-1是一种新的中心体蛋白并抑制纤毛发生。这些结果扩展了已经很长的中心体蛋白列表,并为纤毛发生的调控提供了新的见解。