| Literature DB >> 25762510 |
Ling Zhang1,2, Wei Li2, Jin Ni3, Jinghua Wu2, Junping Liu1,2, Zhengang Zhang4, Yong Zhang2,5, Hongfei Li2, Yuqin Shi1, Maria E Teves2, Shizheng Song1, Jerome F Strauss2, Zhibing Zhang1,2.
Abstract
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.Entities:
Keywords: Golgi body; RC/BTB2; centriole; ciliogenesis
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Year: 2015 PMID: 25762510 PMCID: PMC4758837 DOI: 10.1002/cm.21214
Source DB: PubMed Journal: Cytoskeleton (Hoboken) ISSN: 1949-3592