Literature DB >> 22215550

Radioactive labeling of mitochondrial translation products in cultured cells.

Florin Sasarman1, Eric A Shoubridge.   

Abstract

The mammalian mitochondrial genome contains 37 genes, 13 of which encode polypeptide subunits in the enzyme complexes of the oxidative phosphorylation system. The other genes encode the rRNAs and tRNAs necessary for their translation. The mitochondrial translation machinery is located in the mitochondrial matrix, and is exclusively dedicated to the synthesis of these 13 enzyme subunits. Mitochondrial disease in humans is often associated with defects in mitochondrial translation. This can manifest as a global decrease in the rate of mitochondrial protein synthesis, a decrease in the synthesis of specific polypeptides, the synthesis of abnormal polypeptides, or in altered stability of specific translation products. All of these changes in the normal pattern of mitochondrial translation can be assessed by a straightforward technique that takes advantage of the insensitivity of the mitochondrial translation machinery to antibiotics that completely inhibit cytoplasmic translation. Thus, specific radioactive labeling of the mitochondrial translation products can be achieved in cultured cells, and the results can be visualized on gradient gels. The analysis of mitochondrial translation in cells cultured from patient biopsies is useful in the study of disease-causing mutations in both the mitochondrial and the nuclear genomes.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22215550     DOI: 10.1007/978-1-61779-504-6_14

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  28 in total

1.  Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome.

Authors:  Nicole J Lake; Bryn D Webb; David A Stroud; Tara R Richman; Benedetta Ruzzenente; Alison G Compton; Hayley S Mountford; Juliette Pulman; Coralie Zangarelli; Marlene Rio; Nathalie Boddaert; Zahra Assouline; Mingma D Sherpa; Eric E Schadt; Sander M Houten; James Byrnes; Elizabeth M McCormick; Zarazuela Zolkipli-Cunningham; Katrina Haude; Zhancheng Zhang; Kyle Retterer; Renkui Bai; Sarah E Calvo; Vamsi K Mootha; John Christodoulou; Agnes Rötig; Aleksandra Filipovska; Ingrid Cristian; Marni J Falk; Metodi D Metodiev; David R Thorburn
Journal:  Am J Hum Genet       Date:  2017-08-03       Impact factor: 11.025

2.  Early complex I assembly defects result in rapid turnover of the ND1 subunit.

Authors:  Olga Zurita Rendón; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2012-05-31       Impact factor: 6.150

3.  A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability.

Authors:  Hana Antonicka; Karine Choquet; Zhen-Yuan Lin; Anne-Claude Gingras; Claudia L Kleinman; Eric A Shoubridge
Journal:  EMBO Rep       Date:  2016-12-14       Impact factor: 8.807

4.  LONP1 Is Required for Maturation of a Subset of Mitochondrial Proteins, and Its Loss Elicits an Integrated Stress Response.

Authors:  Olga Zurita Rendón; Eric A Shoubridge
Journal:  Mol Cell Biol       Date:  2018-09-28       Impact factor: 4.272

5.  An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect.

Authors:  Alexandre Janer; Hana Antonicka; Emilie Lalonde; Tamiko Nishimura; Florin Sasarman; Garry K Brown; Ruth M Brown; Jacek Majewski; Eric A Shoubridge
Journal:  Am J Hum Genet       Date:  2012-09-27       Impact factor: 11.025

6.  The arginine methyltransferase NDUFAF7 is essential for complex I assembly and early vertebrate embryogenesis.

Authors:  Olga Zurita Rendón; Lissiene Silva Neiva; Florin Sasarman; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2014-05-16       Impact factor: 6.150

7.  TRMT1-Catalyzed tRNA Modifications Are Required for Redox Homeostasis To Ensure Proper Cellular Proliferation and Oxidative Stress Survival.

Authors:  Joshua M Dewe; Benjamin L Fuller; Jenna M Lentini; Stefanie M Kellner; Dragony Fu
Journal:  Mol Cell Biol       Date:  2017-10-13       Impact factor: 4.272

8.  Pathogenic variants in NUBPL result in failure to assemble the matrix arm of complex I and cause a complex leukoencephalopathy with thalamic involvement.

Authors:  Marisa W Friederich; Francisco A Perez; Kaz M Knight; Roxanne A Van Hove; Samuel P Yang; Russell P Saneto; Johan L K Van Hove
Journal:  Mol Genet Metab       Date:  2019-12-30       Impact factor: 4.797

9.  An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.

Authors:  Reetta Hinttala; Florin Sasarman; Tamiko Nishimura; Hana Antonicka; Catherine Brunel-Guitton; Jeremy Schwartzentruber; Somayyeh Fahiminiya; Jacek Majewski; Denis Faubert; Elsebet Ostergaard; Jan A Smeitink; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2015-04-24       Impact factor: 6.150

10.  Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome.

Authors:  Florin Sasarman; Tamiko Nishimura; Hana Antonicka; Woranontee Weraarpachai; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2014-09-11       Impact factor: 6.150

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.