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Trypanosoma brucei RNA Editing Complex

机译:布氏锥虫RNA编辑复合体

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摘要

Maturation of Trypanosoma brucei mitochondrial mRNA involves massive posttranscriptional insertion and deletion of uridine residues. This RNA editing utilizes an enzymatic complex with seven major proteins, band I through band VII. We here use RNA interference (RNAi) to examine the band II and band V proteins. Band II is found essential for viability; it is needed to maintain the normal structure of the editing complex and to retain the band V ligase protein. Previously, band III was found essential for certain activities, including maintenance of the editing complex and retention of the band IV ligase protein. Thus, band II and band V form a protein pair with features analogous to the band III/band IV ligase pair. Since band V is specific for U insertion and since band IV is needed for U deletion, their parallel organization suggests that the editing complex has a pseudosymmetry. However, unlike the essential band IV ligase, RNAi to band V has only a morphological but no growth rate effect, suggesting that it is stimulatory but nonessential. Indeed, in vitro analysis of band V RNAi cell extract demonstrates that band IV can seal U insertion when band V is lacking. Thus, band IV ligase is the first activity of the basic editing complex shown able to serve in both forms of editing. Our studies also indicate that the U insertional portion may be less central in the editing complex than the corresponding U deletional portion.
机译:布鲁氏锥虫线粒体mRNA的成熟涉及大量转录后插入和尿苷残基的删除。这种RNA编辑利用了一种酶复合物,该复合物具有七个主要蛋白,从I带到VII带。我们在这里使用RNA干扰(RNAi)检查II带和V带蛋白。乐队II被认为对生存能力至关重要;需要维持编辑复合物的正常结构并保留条带V连接酶蛋白。以前,发现III带对于某些活动至关重要,包括维持编辑复合体和保留IV带连接酶蛋白。因此,条带II和条带V形成具有类似于条带III /条带IV连接酶对的特征的蛋白质对。由于V带是U插入特有的,并且IV带是U删除所必需的,因此它们的平行组织表明编辑复合体具有伪对称性。但是,与必需的IV带连接酶不同,V带的RNAi仅具有形态学作用,而没有生长速率效应,表明它是刺激性的,而不是必需的。实际上,对V带RNAi细胞提取物的体外分析表明,当缺少V带时,IV带可以密封U插入。因此,IV带连接酶是基本编辑复合体的第一个活动,显示为可同时用于两种编辑形式。我们的研究还表明,与相应的U缺失部分相比,U插入部分在编辑复合体中的中心位置可能更低。

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