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核基因与线粒体翻译:一类新型遗传病

Nuclear genes and mitochondrial translation: a new class of genetic disease.

作者信息

Jacobs Howard T, Turnbull Douglass M

机构信息

Institute of Medical Technology and Tampere University Hospital, FI-33014 University of Tampere, Finland.

出版信息

Trends Genet. 2005 Jun;21(6):312-4. doi: 10.1016/j.tig.2005.04.003.

Abstract

Mitochondria contain a separate protein-synthesis machinery to produce the polypeptides encoded in mitochondrial DNA (mtDNA), and many mtDNA disease mutations affect this machinery. In humans, the mitochondrial rRNAs and tRNAs are encoded by mtDNA, whereas all proteins involved in mitochondrial translation are encoded by nuclear genes. Recently, several articles have discussed the identification of pathological mutations in nuclear genes encoding components of this protein-synthesis machinery, suggesting that these types of mutation are a frequent cause of human genetic diseases.

摘要

线粒体含有一套独立的蛋白质合成机制,用于产生线粒体DNA(mtDNA)编码的多肽,许多mtDNA疾病突变会影响这一机制。在人类中,线粒体rRNA和tRNA由mtDNA编码,而参与线粒体翻译的所有蛋白质均由核基因编码。最近,几篇文章讨论了编码这种蛋白质合成机制组分的核基因中病理性突变的鉴定,表明这些类型的突变是人类遗传病的常见病因。

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