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Mitochondrial development during life cycle differentiation of African trypanosomes: Evidence for a kinetoplast-dependent differentiation control point

机译:非洲锥虫生命周期分化过程中的线粒体发育:依赖运动塑料的分化控制点的证据。

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Life cycle differentiation of African trypanosomes entails developmental regulation of mitochondrial activity. This requires regulation of the nuclear genome and the kinetoplast, the trypanosome's unusual mitochondrial genome. To investigate the potential cross talk between the nuclear and mitochondrial genome during the events of differentiation, we have 1) disrupted expression of a nuclear-encoded component of the cytochrome oxidase (COX) complex; and 2) generated dyskinetoplastid cells, which lack a mitochondrial genome. Using RNA interference (RNAi) and by disrupting the nuclear COX VI gene, we demonstrate independent regulation of COX component mRNAs encoded in the nucleus and kinetoplast. However, two independent approaches (acriflavine treatment and RNA interference ablation of mitochondrial topoisomerase II) failed to establish clonal lines of dyskinetoplastid bloodstream forms. Nevertheless, dyskinetoplastid forms generated in vivo could undergo two life cycle differentiation events: transition from bloodstream slender to stumpy forms and the initiation of transformation to procyclic forms. However, they subsequently arrested at a specific point in this developmental program before cell cycle reentry. These results provide strong evidence for a requirement for kinetoplast DNA in the bloodstream and for a kinetoplast-dependent control point during differentiation to procyclic forms. [References: 41]
机译:非洲锥虫的生命周期分化需要线粒体活性的发育调节。这需要调节核基因组和锥虫体不常见的线粒体基因组的动子体。为了研究分化过程中核和线粒体基因组之间的潜在串扰,我们有1)破坏了细胞色素氧化酶(COX)复合物的核编码成分的表达; 2)产生了缺乏线粒体基因组的动素体细胞。使用RNA干扰(RNAi)并通过破坏核COX VI基因,我们证明了在核和运动质体中编码的COX成分mRNA的独立调节。但是,两种独立的方法(a啶黄处理和线粒体拓扑异构酶II的RNA干扰消融)未能建立动植物体血流形式的克隆系。然而,体内产生的运动异常型可能会经历两个生命周期分化事件:从细长的血流向残端的转变以及向顺环型的转变的开始。然而,他们随后在细胞周期再进入之前在该发育计划的特定点被捕。这些结果提供了强有力的证据,证明血液中需要动塑料DNA,并且在分化为前环形式的过程中需要依赖动塑料的控制点。 [参考:41]

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