Kage-Nakadai Eriko, Sun Simo, Iwata Satoru, Yoshina Sawako, Nishikawa Yoshikazu, Mitani Shohei
Department of Physiology, Tokyo Women's Medical University School of Medicine, 8-1, Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.
Graduate School of Human Life Science, Osaka City University, Osaka, 558-8585, Japan.
J Physiol Sci. 2019 Jan;69(1):47-56. doi: 10.1007/s12576-018-0617-5. Epub 2018 Apr 27.
The membrane trafficking events that regulate unicellular tube formation and maintenance are not well understood. Here, using an RNAi screen, we identified the small GTPase ARF1 homolog ARF-1.2 as a regulator of excretory tube formation in Caenorhabditis elegans. RNAi-mediated knockdown and knockout of the arf-1.2 gene resulted in the formation of large intracellular vacuoles at the growth sites (varicosities) of the excretory canals. arf-1.2 mutant animals were sensitive to hyperosmotic conditions. arf-1.2 RNAi affected the localization of the anion transporter SULP-8, which is expressed in the basal plasma membrane of the excretory canals, but did not affect the expression of SULP-4, which is expressed in the apical membrane. The phenotype of arf-1.2 mutants was suppressed by mutation of the small Rho GTPase CDC-42, a regulator of apical/basal traffic balance. These results suggest that ARF-1.2 plays an essential role in basal membrane traffic to regulate the formation of the unicellular excretory tube.
调节单细胞管形成和维持的膜运输事件尚未得到充分了解。在这里,我们通过RNA干扰筛选,鉴定出小GTP酶ARF1同源物ARF-1.2是秀丽隐杆线虫排泄管形成的调节因子。RNA干扰介导的arf-1.2基因敲低和敲除导致排泄管生长部位(静脉曲张)形成大的细胞内液泡。arf-1.2突变动物对高渗条件敏感。arf-1.2 RNA干扰影响排泄管基底质膜中表达的阴离子转运蛋白SULP-8的定位,但不影响顶端膜中表达的SULP-4的表达。小Rho GTP酶CDC-42(顶端/基底运输平衡的调节因子)的突变抑制了arf-1.2突变体的表型。这些结果表明,ARF-1.2在基底膜运输中起重要作用,以调节单细胞排泄管的形成。