Zhang Ling, Li Wei, Ni Jin, Wu Jinghua, Liu Junping, Zhang Zhengang, Zhang Yong, Li Hongfei, Shi Yuqin, Teves Maria E, Song Shizheng, Strauss Jerome F, Zhang Zhibing
School of Public Health, Wuhan University of Science and Technology, Wuhan, Hubei, China.
Department of Obstetrics & Gynecology, Virginia Commonwealth University, Richmond, Virginia.
Cytoskeleton (Hoboken). 2015 Apr;72(4):171-81. doi: 10.1002/cm.21214. Epub 2015 Apr 29.
RC/BTB2 is a binding partner of sperm associated antigen 16S (SPAG16S), which is a regulator of spermiogenesis in mice, a process during which sperm flagella are formed. The expression of Rc/btb2 is also regulated by multicilin, a protein that controls ciliogenesis. Given that mouse Rc/btb2 mRNA is not only expressed in tissues bearing motile cilia, but also in tissues without motile cilia, we investigated whether RC/BTB2 plays a role in the general process of ciliogenesis by studying two cell lines that have primary cilia, NIH3T3, and IMCD3. We discovered that the subcellular localization of RC/BTB2 in the NIH3T3 and IMCD3 cells encompasses the pathway for ciliogenesis. RC/BTB2 was found in the Golgi bodies and centrosomes, two key structures essential for normal ciliogenesis. Knockdown of Rc/btb2 gene expression in these cell lines disrupted ciliogenesis. The percentage of cells with primary cilia was significantly reduced in stable cell lines transduced with specific Rc/btb2 shRNA viruses as compared to the control cells. When cilia were formed in the knockdown cells, they were significantly shorter than those in the control cells. Knockdown of Rc/btb2 expression did not affect cell proliferation and the cell cycle. Exogenous expression of RC/BTB2 in these stable knockdown cells restored ciliogenesis. These findings suggest that RC/BTB2 is a necessary component of the process of formation of primary cilia in somatic cells, perhaps through the transportation of cargos from Golgi bodies to centrosomes for cilia assembling.
RC/BTB2是精子相关抗原16S(SPAG16S)的结合伴侣,SPAG16S是小鼠精子发生过程中的一种调节因子,精子鞭毛在这一过程中形成。Rc/btb2的表达也受多纤毛蛋白调控,多纤毛蛋白是一种控制纤毛发生的蛋白质。鉴于小鼠Rc/btb2 mRNA不仅在具有运动性纤毛的组织中表达,还在没有运动性纤毛的组织中表达,我们通过研究两种具有初级纤毛的细胞系NIH3T3和IMCD3,来探究RC/BTB2是否在纤毛发生的一般过程中发挥作用。我们发现RC/BTB2在NIH3T3和IMCD3细胞中的亚细胞定位涵盖了纤毛发生途径。在高尔基体和中心体中发现了RC/BTB2,这是正常纤毛发生必不可少的两个关键结构。在这些细胞系中敲低Rc/btb2基因表达会破坏纤毛发生。与对照细胞相比,用特异性Rc/btb2 shRNA病毒转导的稳定细胞系中具有初级纤毛的细胞百分比显著降低。当在敲低细胞中形成纤毛时,它们明显比对照细胞中的纤毛短。敲低Rc/btb2表达不影响细胞增殖和细胞周期。在这些稳定的敲低细胞中外源表达RC/BTB2可恢复纤毛发生。这些发现表明,RC/BTB2可能是体细胞中初级纤毛形成过程的必要组成部分,也许是通过将货物从高尔基体运输到中心体进行纤毛组装。