Literature DB >> 19348897

Chapter 18 Analysis of respiratory chain complex assembly with radiolabeled nuclear- and mitochondrial-encoded subunits.

Matthew McKenzie1, Michael Lazarou, Michael T Ryan.   

Abstract

The mitochondrial respiratory chain is composed of individual complexes that range widely in terms of size and subunit composition. For example, whereas complex II is approximately 260 kDa and is composed of 4 subunits, complex I is almost 1 MDa and contains 45 different subunits. Furthermore, complexes I, III, IV, and V harbor additional complexity, because their subunits are encoded by both nuclear and mitochondrial DNA. Subunits that are encoded by nuclear genes must be imported into mitochondria before undergoing processing, folding, and assembly with other subunits that are synthesized within the organelle. This process requires the coordinated action of assembly factors with the integration of subunits into intermediate assembly complexes. Recent studies have used various techniques to analyze subunit assembly to gain information into the biogenesis of these respiratory chain complexes and to understand how defects in assembly lead to disease. Here we describe methods to monitor the assembly of newly synthesized subunits encoded by mitochondrial DNA from cultured mammalian cells, as well as the import and assembly of individual subunits encoded by nuclear DNA.

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Year:  2009        PMID: 19348897     DOI: 10.1016/S0076-6879(08)04418-2

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  17 in total

1.  Mitochondrial OXPHOS genes provides insights into genetics basis of hypoxia adaptation in anchialine cave shrimps.

Authors:  Huayun Guo; Hao Yang; Yitao Tao; Dan Tang; Qiong Wu; Zhengfei Wang; Boping Tang
Journal:  Genes Genomics       Date:  2018-03-06       Impact factor: 1.839

2.  Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I).

Authors:  Sze Chern Lim; Kirstyn T Carey; Matthew McKenzie
Journal:  Am J Cancer Res       Date:  2015-01-15       Impact factor: 6.166

3.  Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome.

Authors:  Lisa G Riley; Sandra Cooper; Peter Hickey; Joëlle Rudinger-Thirion; Matthew McKenzie; Alison Compton; Sze Chern Lim; David Thorburn; Michael T Ryan; Richard Giegé; Melanie Bahlo; John Christodoulou
Journal:  Am J Hum Genet       Date:  2010-07-09       Impact factor: 11.025

4.  Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.

Authors:  Elena J Tucker; Steven G Hershman; Caroline Köhrer; Casey A Belcher-Timme; Jinal Patel; Olga A Goldberger; John Christodoulou; Jonathon M Silberstein; Matthew McKenzie; Michael T Ryan; Alison G Compton; Jacob D Jaffe; Steven A Carr; Sarah E Calvo; Uttam L RajBhandary; David R Thorburn; Vamsi K Mootha
Journal:  Cell Metab       Date:  2011-09-07       Impact factor: 27.287

5.  A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndrome.

Authors:  Sze Chern Lim; Katherine R Smith; David A Stroud; Alison G Compton; Elena J Tucker; Ayan Dasvarma; Luke C Gandolfo; Justine E Marum; Matthew McKenzie; Heidi L Peters; David Mowat; Peter G Procopis; Bridget Wilcken; John Christodoulou; Garry K Brown; Michael T Ryan; Melanie Bahlo; David R Thorburn
Journal:  Am J Hum Genet       Date:  2014-01-23       Impact factor: 11.025

6.  Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome.

Authors:  Nurun Nahar Borna; Yoshihito Kishita; Masakazu Kohda; Sze Chern Lim; Masaru Shimura; Yibo Wu; Kaoru Mogushi; Yukiko Yatsuka; Hiroko Harashima; Yuichiro Hisatomi; Takuya Fushimi; Keiko Ichimoto; Kei Murayama; Akira Ohtake; Yasushi Okazaki
Journal:  Neurogenetics       Date:  2019-01-03       Impact factor: 2.660

7.  LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure.

Authors:  Lisa G Riley; Joëlle Rudinger-Thirion; Klaus Schmitz-Abe; David R Thorburn; Ryan L Davis; Juliana Teo; Susan Arbuckle; Sandra T Cooper; Dean R Campagna; Magali Frugier; Kyriacos Markianos; Carolyn M Sue; Mark D Fleming; John Christodoulou
Journal:  JIMD Rep       Date:  2015-11-05

8.  The effects of nuclear reprogramming on mitochondrial DNA replication.

Authors:  Richard D W Kelly; Huseyin Sumer; Matthew McKenzie; Joao Facucho-Oliveira; Ian A Trounce; Paul J Verma; Justin C St John
Journal:  Stem Cell Rev Rep       Date:  2013-02       Impact factor: 5.739

9.  Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression.

Authors:  Elena J Tucker; Bas F J Wanschers; Radek Szklarczyk; Hayley S Mountford; Xiaonan W Wijeyeratne; Mariël A M van den Brand; Anne M Leenders; Richard J Rodenburg; Boris Reljić; Alison G Compton; Ann E Frazier; Damien L Bruno; John Christodoulou; Hitoshi Endo; Michael T Ryan; Leo G Nijtmans; Martijn A Huynen; David R Thorburn
Journal:  PLoS Genet       Date:  2013-12-26       Impact factor: 5.917

10.  Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease.

Authors:  Ahmad Alodaib; Nara Sobreira; Wendy A Gold; Lisa G Riley; Nicole J Van Bergen; Meredith J Wilson; Bruce Bennetts; David R Thorburn; Corinne Boehm; John Christodoulou
Journal:  Eur J Hum Genet       Date:  2016-10-19       Impact factor: 5.351

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