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Toxic PR Poly-Dipeptides Encoded by the C9orf72 Repeat Expansion Target LC Domain Polymers

机译:C9orf72重复扩增目标LC域聚合物编码的有毒PR多肽

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摘要

Two complementary approaches were used in search of the intracellular targets of the toxic PR poly-dipeptide encoded by the repeat sequences expanded in the C9orf72 form of amyotrophic lateral sclerosis. The top categories of PRn-bound proteins include constituents of non-membrane invested cellular organelles and intermediate filaments. PRn targets are enriched for the inclusion of low complexity (LC) sequences. Evidence is presented indicating that LC sequences represent the direct target of PRn binding and that interaction between the PRn poly-dipeptide and LC domains is polymer-dependent. These studies indicate that PRn-mediated toxicity may result from broad impediments to the dynamics of cell structure and information flow from gene to message to protein.
机译:使用两种互补的方法来搜索由肌萎缩性侧索硬化症的C9orf72形式扩展的重复序列编码的有毒PR多肽的细胞内靶标。 PRn结合蛋白的顶级类别包括非膜投入的细胞器和中间丝。 PRn靶标丰富了低复杂度(LC)序列。提供的证据表明,LC序列代表PRn结合的直接目标,并且PRn多肽和LC结构域之间的相互作用是聚合物依赖性的。这些研究表明PRn介导的毒性可能是由于广泛阻碍细胞结构动力学以及信息从基因到信息再到蛋白质的流动所致。

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