Literature DB >> 25028417

Mitochondrial genetics and disease.

Estela Area-Gomez1, Eric A Schon2.   

Abstract

Mitochondrial disease resulting in reduced bioenergetic output can be due to mutations in either nuclear DNA-encoded or mitochondrial DNA-encoded gene products. We summarize some of the underlying principles of mitochondrial genetics that impact the diagnosis and pathogenesis of mitochondrial disorders. In addition, we present a brief overview of a new frontier in the field, namely, mitochondrial "dynamics," which controls organellar fusion, fission, trafficking, and positioning, and exerts mitochondrial "quality control" by maintaining organellar integrity and viability. Analysis of mutations in gene products associated with this latter area has opened up new vistas in the study of disorders associated with compromised energy production.
© The Author(s) 2014.

Entities:  

Keywords:  mitodynamics; mtDNA; oxidative phosphorylation; respiratory chain

Mesh:

Substances:

Year:  2014        PMID: 25028417     DOI: 10.1177/0883073814539561

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  16 in total

1.  Pathological ribonuclease H1 causes R-loop depletion and aberrant DNA segregation in mitochondria.

Authors:  Gokhan Akman; Radha Desai; Laura J Bailey; Takehiro Yasukawa; Ilaria Dalla Rosa; Romina Durigon; J Bradley Holmes; Chloe F Moss; Mara Mennuni; Henry Houlden; Robert J Crouch; Michael G Hanna; Robert D S Pitceathly; Antonella Spinazzola; Ian J Holt
Journal:  Proc Natl Acad Sci U S A       Date:  2016-07-08       Impact factor: 11.205

Review 2.  Mitochondria-associated ER membranes and Alzheimer disease.

Authors:  Estela Area-Gomez; Eric A Schon
Journal:  Curr Opin Genet Dev       Date:  2016-05-25       Impact factor: 5.578

Review 3.  Role of the mitochondrial stress response in human cancer progression.

Authors:  Sheng-Fan Wang; Shiuan Chen; Ling-Ming Tseng; Hsin-Chen Lee
Journal:  Exp Biol Med (Maywood)       Date:  2020-04-23

4.  Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutation.

Authors:  Shasha Gong; Xiaoqiong Wang; Feilong Meng; Limei Cui; Qiuzi Yi; Qiong Zhao; Xiaohui Cang; Zhiyi Cai; Jun Qin Mo; Yong Liang; Min-Xin Guan
Journal:  J Biol Chem       Date:  2019-12-09       Impact factor: 5.157

5.  Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy.

Authors:  Tamar Harel; Gozde Yesil; Yavuz Bayram; Zeynep Coban-Akdemir; Wu-Lin Charng; Ender Karaca; Ali Al Asmari; Mohammad K Eldomery; Jill V Hunter; Shalini N Jhangiani; Jill A Rosenfeld; Davut Pehlivan; Ayman W El-Hattab; Mohammed A Saleh; Charles A LeDuc; Donna Muzny; Eric Boerwinkle; Richard A Gibbs; Wendy K Chung; Yaping Yang; John W Belmont; James R Lupski
Journal:  Am J Hum Genet       Date:  2016-03-03       Impact factor: 11.025

Review 6.  Mitochondrial Lon protease in human disease and aging: Including an etiologic classification of Lon-related diseases and disorders.

Authors:  Daniela A Bota; Kelvin J A Davies
Journal:  Free Radic Biol Med       Date:  2016-07-05       Impact factor: 7.376

7.  A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.

Authors:  Meng Wang; Yanyan Peng; Jing Zheng; Binjiao Zheng; Xiaofen Jin; Hao Liu; Yong Wang; Xiaowen Tang; Taosheng Huang; Pingping Jiang; Min-Xin Guan
Journal:  Nucleic Acids Res       Date:  2016-08-17       Impact factor: 16.971

8.  ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism.

Authors:  Radha Desai; Ann E Frazier; Romina Durigon; Harshil Patel; Aleck W Jones; Ilaria Dalla Rosa; Nicole J Lake; Alison G Compton; Hayley S Mountford; Elena J Tucker; Alice L R Mitchell; Deborah Jackson; Abdul Sesay; Miriam Di Re; Lambert P van den Heuvel; Derek Burke; David Francis; Sebastian Lunke; George McGillivray; Simone Mandelstam; Fanny Mochel; Boris Keren; Claude Jardel; Anne M Turner; P Ian Andrews; Jan Smeitink; Johannes N Spelbrink; Simon J Heales; Masakazu Kohda; Akira Ohtake; Kei Murayama; Yasushi Okazaki; Anne Lombès; Ian J Holt; David R Thorburn; Antonella Spinazzola
Journal:  Brain       Date:  2017-06-01       Impact factor: 13.501

9.  Multi-omics identify xanthine as a pro-survival metabolite for nematodes with mitochondrial dysfunction.

Authors:  Anna Gioran; Antonia Piazzesi; Fabio Bertan; Jonas Schroer; Lena Wischhof; Pierluigi Nicotera; Daniele Bano
Journal:  EMBO J       Date:  2019-02-22       Impact factor: 11.598

10.  Imaging Patterns Characterizing Mitochondrial Leukodystrophies.

Authors:  S D Roosendaal; T van de Brug; C A P F Alves; S Blaser; A Vanderver; N I Wolf; M S van der Knaap
Journal:  AJNR Am J Neuroradiol       Date:  2021-04-01       Impact factor: 4.966

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