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首页> 外文期刊>Eukaryotic cell >Identification of New Kinetoplast DNA Replication Proteins in Trypanosomatids Based on Predicted S-Phase Expression and Mitochondrial Targeting
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Identification of New Kinetoplast DNA Replication Proteins in Trypanosomatids Based on Predicted S-Phase Expression and Mitochondrial Targeting

机译:基于预测的S期表达和线粒体靶向鉴定锥虫中的新的Kinetoplast DNA复制蛋白。

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Trypanosomatid parasites contain an unusual form of mitochondrial DNA (kinetoplast DNA [kDNA]) consisting of a catenated network of several thousand minicircles and a smaller number of maxicircles. Many of the proteins involved in the replication and division of kDNA are likely to have no counterparts in other organisms and would not be identified by similarity to known replication proteins in other organisms. A new kDNA replication protein conserved in kinetoplastids has been identified based on the presence of posttranscriptional regulatory sequences associated with S-phase gene expression and predicted mitochondrial targeting. The Leishmania major protein P105 (LmP105) and Trypanosoma brucei protein P93 (TbP93) localize to antipodal sites flanking the kDNA disk, where several other replication proteins and nascent minicircles have been localized. Like some of these kDNA replication proteins, the LmP105 protein is only present at the antipodal sites during S phase. RNA interference (RNAi) of TbP93 expression resulted in a cessation of cell growth and the loss of kDNA. Nicked/gapped forms of minicircles, the products of minicircle replication, were preferentially lost from the population of free minicircles during RNAi, suggesting involvement of TbP93 in minicircle replication. This approach should allow the identification of other novel proteins involved in the duplication of kDNA.
机译:锥虫寄生虫包含一种不寻常形式的线粒体DNA(运动塑料DNA [kDNA]),由几千个小圆和少量的大圆的链状网络组成。与kDNA复制和分裂有关的许多蛋白质在其他生物中可能没有对应物,因此无法通过与其他生物中已知的复制蛋白的相似性进行鉴定。基于与S期基因表达和预测的线粒体靶向相关的转录后调控序列的存在,已经确定了一种在动素体中保守的新的kDNA复制蛋白。 主要利什曼原虫蛋白P105( Lm P105)和布鲁氏锥虫蛋白P93( Tb P93)定位于对立位点在kDNA盘的侧面,其中还定位了其他几种复制蛋白和新生的小圆圈。像其中一些kDNA复制蛋白一样, Lm P105蛋白仅在S期出现在反足位点。 Tb P93表达的RNA干扰(RNAi)导致细胞生长停止和kDNA丢失。小切口的缺口/缺口形式(小切口复制的产物)在RNAi期间优先从自由小切口种群中丢失,表明 Tb P93参与小切口复制。这种方法应允许鉴定与kDNA复制有关的其他新型蛋白质。

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