Iriarte Lucrecia S, Midlej Victor, Frontera Lorena S, Moros Duarte Daniel, Barbeito Claudio G, de Souza Wanderley, Benchimol Marlene, de Miguel Natalia, Coceres Veronica M
Laboratorio de Parásitos Anaerobios, Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico Chascomús (IIB-INTECH), CONICET-UNSAM, Chascomús, B7130IWA, Argentina.
Laboratorio de Ultraestrutura Celular Hertha Meyer, Centro de Ciências da Saúde, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Cidade Universitaria, Av. Carlos Chagas Filho, 373 - G1-019 - Ilha do Fundão, Rio de Janeiro, RJ, 21941-902, Brazil.
J Eukaryot Microbiol. 2018 Jan;65(1):28-37. doi: 10.1111/jeu.12424. Epub 2017 Jun 7.
The flagellated protist Tritrichomonas foetus is a parasite that causes bovine trichomonosis, a major sexually transmitted disease in cattle. Cell division has been described as a key player in controlling cell survival in other cells, including parasites but there is no information on the regulation of this process in T. foetus. The regulation of cytokinetic abscission, the final stage of cell division, is mediated by members of the ESCRT (endosomal sorting complex required for transport) machinery. VPS32 is a subunit within the ESCRTIII complex and here, we report that TfVPS32 is localized on cytoplasmic vesicles and a redistribution of the protein to the midbody is observed during the cellular division. In concordance with its localization, deletion of TfVPS32 C-terminal alpha helices (α5 helix and/or α4-5 helix) leads to abnormal T. foetus growth, an increase in the percentage of multinucleated parasites and cell cycle arrest at G2/M phase. Together, these results indicate a role of this protein in controlling normal cell division.
具鞭毛的原生生物胎儿三毛滴虫是一种寄生虫,可引发牛毛滴虫病,这是牛群中一种主要的性传播疾病。细胞分裂在包括寄生虫在内的其他细胞的细胞存活控制中被描述为关键因素,但关于胎儿三毛滴虫中这一过程的调控尚无相关信息。细胞分裂的最后阶段——细胞动力分离的调控由ESCRT(运输所需的内体分选复合体)机制的成员介导。VPS32是ESCRTIII复合体中的一个亚基,在此我们报告,TfVPS32定位于细胞质囊泡上,并且在细胞分裂期间观察到该蛋白重新分布至中体。与其定位一致,TfVPS32 C末端α螺旋(α5螺旋和/或α4 - 5螺旋)的缺失导致胎儿三毛滴虫生长异常、多核寄生虫百分比增加以及细胞周期在G2/M期停滞。这些结果共同表明该蛋白在控制正常细胞分裂中发挥作用。