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Distinct Roles of a Mitogen-Activated Protein Kinase in Cytokinesis between Different Life Cycle Forms of Trypanosoma brucei

机译:丝裂原活化蛋白激酶在布鲁氏锥虫不同生命周期形式之间的胞质分裂中的不同作用。

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Mitogen-activated protein kinase (MAPK) modules are evolutionarily conserved signaling cascades that function in response to the environment and play crucial roles in intracellular signal transduction in eukaryotes. The involvement of a MAP kinase in regulating cytokinesis in yeast, animals, and plants has been reported, but the requirement for a MAP kinase for cytokinesis in the early-branching protozoa is not documented. Here, we show that a MAP kinase homolog (TbMAPK6) from Trypanosoma brucei plays distinct roles in cytokinesis in two life cycle forms of T. brucei. TbMAPK6 is distributed throughout the cytosol in the procyclic form but is localized in both the cytosol and the nucleus in the bloodstream form. RNA interference (RNAi) of TbMAPK6 results in moderate growth inhibition in the procyclic form but severe growth defects and rapid cell death in the bloodstream form. Moreover, TbMAPK6 appears to be implicated in furrow ingression and cytokinesis completion in the procyclic form but is essential for cytokinesis initiation in the bloodstream form. Despite the distinct defects in cytokinesis in the two forms, RNAi of TbMAPK6 also caused defective basal body duplication/segregation in a small cell population in both life cycle forms. Altogether, our results demonstrate the involvement of the TbMAPK6-mediated pathway in regulating cytokinesis in trypanosomes and suggest distinct roles of TbMAPK6 in cytokinesis between different life cycle stages of T. brucei.
机译:丝裂原激活的蛋白激酶(MAPK)模块是进化上保守的信号级联,其响应环境而起作用,并在真核生物的细胞内信号转导中起关键作用。已经报道了MAP激酶参与调节酵母,动物和植物中的胞质分裂,但是尚未记录早期分支原生动物对胞质分裂的MAP激酶的需求。在这里,我们显示了来自布鲁氏锥虫的MAP激酶同源物(TbMAPK6)在布鲁氏梭菌的两种生命周期形式中,在胞质分裂中起着独特的作用。 TbMAPK6以前环形式分布在整个细胞质中,但以血流形式定位在细胞质和细胞核中。 TbMAPK6的RNA干扰(RNAi)在前环形式中导致中等程度的生长抑制,但在血流形式中导致严重的生长缺陷和快速细胞死亡。此外,TbMAPK6似乎以前环形式参与沟进入和胞质分裂的完成,但对于血流形式的胞质分裂的启动是必不可少的。尽管两种形式的胞质分裂都有明显的缺陷,但TbMAPK6的RNAi在两种生命周期形式的小细胞群中也引起有缺陷的基体复制/分离。总而言之,我们的结果表明TbMAPK6介导的通路参与了锥虫体内胞质分裂的调控,并暗示了TbMAPK6在布鲁氏梭菌不同生命周期阶段之间的胞质分裂中的独特作用。

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