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Driving ribosome assembly.

机译:驱动核糖体装配。

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摘要

Ribosome biogenesis is a fundamental process that provides cells with the molecular factories for cellular protein production. Accordingly, its misregulation lies at the heart of several hereditary diseases (e.g., Diamond-Blackfan anemia). The process of ribosome assembly comprises the processing and folding of the pre-rRNA and its concomitant assembly with the ribosomal proteins. Eukaryotic ribosome biogenesis relies on a large number (>200) of non-ribosomal factors, which confer directionality and accuracy to this process. Many of these non-ribosomal factors fall into different families of energy-consuming enzymes, notably including ATP-dependent RNA helicases, AAA-ATPases, GTPases, and kinases. Ribosome biogenesis is highly conserved within eukaryotic organisms; however, due to the combination of powerful genetic and biochemical methods, it is best studied in the yeast Saccharomyces cerevisiae. This review summarizes our current knowledge on eukaryotic ribosome assembly, with particular focus on the molecular role of the involved energy-consuming enzymes.
机译:核糖体生物发生是为细胞提供细胞蛋白质生产分子工厂的基本过程。因此,其调节失调是几种遗传性疾病(例如,钻石-黑范氏贫血)的核心。核糖体装配的过程包括前rRNA的加工和折叠及其与核糖体蛋白的伴随装配。真核生物核糖体的生物发生依赖于大量(> 200)非核糖体因子,这些因子赋予该过程方向性和准确性。这些非核糖体因子中有许多属于能量消耗酶的不同家族,特别是包括ATP依赖性RNA解旋酶,AAA-ATPase,GTPase和激酶。核糖体的生物发生在真核生物中高度保守。但是,由于强大的遗传和生化方法的结合,最好在酿酒酵母中进行研究。这篇综述总结了我们目前在真核生物核糖体组装方面的知识,特别关注所涉及的耗能酶的分子作用。

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