Literature DB >> 22406627

Effect of mtDNA point mutations on cellular bioenergetics.

Joanna Szczepanowska1, Dominika Malinska, Mariusz R Wieckowski, Jerzy Duszynski.   

Abstract

This overview discusses the results of research on the effects of most frequent mtDNA point mutations on cellular bioenergetics. Thirteen proteins coded by mtDNA are crucial for oxidative phosphorylation, 11 of them constitute key components of the respiratory chain complexes I, III and IV and 2 of mitochondrial ATP synthase. Moreover, pathogenic point mutations in mitochondrial tRNAs and rRNAs generate abnormal synthesis of the mtDNA coded proteins. Thus, pathogenic point mutations in mtDNA usually disturb the level of key parameter of the oxidative phosphorylation, i.e. the electric potential on the inner mitochondrial membrane (Δψ), and in a consequence calcium signalling and mitochondrial dynamics in the cell. Mitochondrial generation of reactive oxygen species is also modified in the mutated cells. The results obtained with cultured cells and describing biochemical consequences of mtDNA point mutations are full of contradictions. Still they help elucidate the biochemical basis of pathologies and provide a valuable tool for finding remedies in the future. This article is part of a Special Issue entitled: 17th European Bioenergetics Conference (EBEC 2012).
Copyright © 2012 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22406627     DOI: 10.1016/j.bbabio.2012.02.028

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  23 in total

1.  Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.

Authors:  Yanchun Ji; Juanjuan Zhang; Yuanyuan Lu; Qiuzi Yi; Mengquan Chen; Shipeng Xie; Xiaoting Mao; Yun Xiao; Feilong Meng; Minglian Zhang; Rulai Yang; Min-Xin Guan
Journal:  J Biol Chem       Date:  2020-07-28       Impact factor: 5.157

2.  Reduced mitochondrial activity in colonocytes facilitates AMPKα2-dependent inflammation.

Authors:  Sandra Heller; Harrison M Penrose; Chloe Cable; Debjani Biswas; Hani Nakhoul; Melody Baddoo; Erik Flemington; Susan E Crawford; Suzana D Savkovic
Journal:  FASEB J       Date:  2017-02-09       Impact factor: 5.191

3.  A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).

Authors:  Mi Zhou; Meng Wang; Ling Xue; Zhi Lin; Qiufen He; Wenwen Shi; Yaru Chen; Xiaofen Jin; Haiying Li; Pingping Jiang; Min-Xin Guan
Journal:  J Biol Chem       Date:  2017-07-05       Impact factor: 5.157

4.  ANKRD49 inhibits etoposide-induced intrinsic apoptosis of GC-1 cells by modulating NF-κB signaling.

Authors:  Xia Zhou; Wen-Tao Wang; Jia Sun; Hong-Yan Liu; Xin-Yan Bai; Juan-Juan Liu; Bao-Feng Yu; Rui Guo; Hai-Long Wang
Journal:  Mol Cell Biochem       Date:  2019-02-23       Impact factor: 3.396

5.  Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma.

Authors:  Ji-Hong Wu; Sheng-Hai Zhang; John M Nickerson; Feng-Juan Gao; Zhongmou Sun; Xin-Ya Chen; Shu-Jie Zhang; Feng Gao; Jun-Yi Chen; Yi Luo; Yan Wang; Xing-Huai Sun
Journal:  Neurobiol Dis       Date:  2014-12-03       Impact factor: 5.996

6.  Silybin regulates P450s activity by attenuating endoplasmic reticulum stress in mouse nonalcoholic fatty liver disease.

Authors:  Jing Wu; Yun-Ge Lou; Xu-le Yang; Rui Wang; Ran Zhang; Ji-Ye Aa; Guang-Ji Wang; Yuan Xie
Journal:  Acta Pharmacol Sin       Date:  2022-06-15       Impact factor: 6.150

7.  Analysis of the entire mitochondrial genome reveals Leber's hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis.

Authors:  Ghada Al-Kafaji; Maram A Alharbi; Hasan Alkandari; Abdel Halim Salem; Moiz Bakhiet
Journal:  Sci Rep       Date:  2022-06-30       Impact factor: 4.996

8.  Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.

Authors:  Pingping Jiang; Min Liang; Chaofan Zhang; Xiaoxu Zhao; Qiufen He; Limei Cui; Xiaoling Liu; Yan-Hong Sun; Qun Fu; Yanchun Ji; Yidong Bai; Taosheng Huang; Min-Xin Guan
Journal:  Hum Mol Genet       Date:  2016-07-17       Impact factor: 6.150

9.  A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.

Authors:  Meng Wang; Hao Liu; Jing Zheng; Bobei Chen; Mi Zhou; Wenlu Fan; Hen Wang; Xiaoyang Liang; Xiaolong Zhou; Gilbert Eriani; Pingping Jiang; Min-Xin Guan
Journal:  J Biol Chem       Date:  2016-08-12       Impact factor: 5.157

10.  Mitochondrial gene mutations in pediatric septic shock.

Authors:  Junsung Park; Eunju Kang; Seoon Kang; Deokhoon Kim; Dahyun Kim; Seong Jong Park; Won Kyoung Jhang
Journal:  Pediatr Res       Date:  2021-01-27       Impact factor: 3.756

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.