首页> 外文期刊>Proceedings of the Japan Academy, Series B. Physical and Biological Sciences >Unique features of animal mitochondrial translation systems - The non-universal genetic code, unusual features of the translational apparatus and their relevance to human mitochondrial diseases
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Unique features of animal mitochondrial translation systems - The non-universal genetic code, unusual features of the translational apparatus and their relevance to human mitochondrial diseases

机译:动物线粒体翻译系统的独特特征-非通用的遗传密码,翻译装置的异常特征及其与人类线粒体疾病的相关性

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摘要

In animal mitochondria, several codons are non-universal and their meanings differ depending on the species. In addition, the tRNA structures that decipher codons are sometimes unusually truncated. These features seem to be related to the shortening of mitochondrial (mt) genomes, which occurred during the evolution of mitochondria. These organelles probably originated from the endosymbiosis of an aerobic eubacterium into an ancestral enkaryote. It is plausible that these events brought about the various characteristic features of animal mt translation systems, such as genetic code variations, unusually truncated tRNA and rRNA structures, unilateral tRNA recognition mechanisms by aminoacyl-tRNA synthetases, elongation factors and ribosomes, and compensation for RNA deficits by enlarged proteins. In this article, we discuss molecular mechanisms for these phenomena. Finally, we describe human mt disease that are caused by modification defects in mt tRNAs.
机译:在动物线粒体中,几个密码子不是通用的,其含义因物种而异。另外,破译密码子的tRNA结构有时会被截短。这些特征似乎与线粒体(mt)基因组的缩短有关,线粒体(mt)基因组的发生在线粒体的进化过程中。这些细胞器可能起源于好氧真细菌的共生作用,成为祖先的真核生物。可能是这些事件带来了动物mt翻译系统的各种特征,例如遗传密码变异,异常截断的tRNA和rRNA结构,氨酰基tRNA合成酶的单侧tRNA识别机制,延伸因子和核糖体以及RNA补偿蛋白质增加造成的缺陷。在本文中,我们讨论了这些现象的分子机制。最后,我们描述了由mt tRNA修饰缺陷引起的人类mt疾病。

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