Literature DB >> 15922826

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

Howard T Jacobs1, Douglass M Turnbull.   

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.

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Year:  2005        PMID: 15922826     DOI: 10.1016/j.tig.2005.04.003

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  43 in total

Review 1.  Protective effects and mechanisms of sirtuins in the nervous system.

Authors:  Feng Zhang; Suping Wang; Li Gan; Peter S Vosler; Yanqin Gao; Michael J Zigmond; Jun Chen
Journal:  Prog Neurobiol       Date:  2011-09-10       Impact factor: 11.685

2.  eIF2B Mutations Cause Mitochondrial Malfunction in Oligodendrocytes.

Authors:  Melisa Herrero; Shir Mandelboum; Orna Elroy-Stein
Journal:  Neuromolecular Med       Date:  2019-05-27       Impact factor: 3.843

3.  A history of mitochondrial diseases.

Authors:  Salvatore Dimauro
Journal:  J Inherit Metab Dis       Date:  2010-05-21       Impact factor: 4.982

4.  Mitochondrial encephalomyopathies--fifty years on: the Robert Wartenberg Lecture.

Authors:  Salvatore DiMauro
Journal:  Neurology       Date:  2013-07-16       Impact factor: 9.910

5.  Long-term consequences of radiation-induced bystander effects depend on radiation quality and dose and correlate with oxidative stress.

Authors:  Manuela Buonanno; Sonia M de Toledo; Debkumar Pain; Edouard I Azzam
Journal:  Radiat Res       Date:  2011-02-14       Impact factor: 2.841

Review 6.  Mitochondrial ribosome assembly in health and disease.

Authors:  Dasmanthie De Silva; Ya-Ting Tu; Alexey Amunts; Flavia Fontanesi; Antoni Barrientos
Journal:  Cell Cycle       Date:  2015-06-01       Impact factor: 4.534

7.  Purification, crystallization and preliminary X-ray characterization of a human mitochondrial phenylalanyl-tRNA synthetase.

Authors:  Inna Levin; Naama Kessler; Nina Moor; Liron Klipcan; Emine Koc; Paul Templeton; Linda Spremulli; Mark Safro
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-08-25

8.  Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome.

Authors:  Jiqiang Ling; Hervé Roy; Daoming Qin; Mary Anne T Rubio; Juan D Alfonzo; Kurt Fredrick; Michael Ibba
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-18       Impact factor: 11.205

9.  Expression and maintenance of mitochondrial DNA: new insights into human disease pathology.

Authors:  Gerald S Shadel
Journal:  Am J Pathol       Date:  2008-05-05       Impact factor: 4.307

10.  Tinkering evolution of post-transcriptional RNA regulons: puf3p in fungi as an example.

Authors:  Huifeng Jiang; Wenjun Guan; Zhenglong Gu
Journal:  PLoS Genet       Date:  2010-07-22       Impact factor: 5.917

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