Literature DB >> 20576512

Mitochondrial helicases and mitochondrial genome maintenance.

Nadja C de Souza-Pinto1, Maria D Aamann, Tomasz Kulikowicz, Tinna V Stevnsner, Vilhelm A Bohr.   

Abstract

Helicases are essential enzymes that utilize the energy of nucleotide hydrolysis to drive unwinding of nucleic acid duplexes. Helicases play roles in all aspects of DNA metabolism including DNA repair, DNA replication and transcription. The subcellular locations and functions of several helicases have been studied in detail; however, the roles of specific helicases in mitochondrial biology remain poorly characterized. This review presents important recent advances in identifying and characterizing mitochondrial helicases, some of which also operate in the nucleus. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh：

Substances：

Year:  2010        PMID： 20576512      PMCID： PMC2933315          DOI： 10.1016/j.mad.2010.04.009

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN： 0047-6374            Impact factor:   5.432


  83 in total

Review 1.  DNA replication and transcription in mammalian mitochondria.

Authors:  Maria Falkenberg; Nils-Göran Larsson; Claes M Gustafsson
Journal:  Annu Rev Biochem       Date:  2007       Impact factor: 23.643

2.  The transcriptional regulatory protein, YB-1, promotes single-stranded regions in the DRA promoter.

Authors:  G H MacDonald; Y Itoh-Lindstrom; J P Ting
Journal:  J Biol Chem       Date:  1995-02-24       Impact factor: 5.157

3.  Characterization of the enzymatic properties of the yeast dna2 Helicase/endonuclease suggests a new model for Okazaki fragment processing.

Authors:  S H Bae; Y S Seo
Journal:  J Biol Chem       Date:  2000-12-01       Impact factor: 5.157

4.  Down-regulation of human RNA/DNA helicase SUV3 induces apoptosis by a caspase- and AIF-dependent pathway.

Authors:  Roman J Szczesny; Helene Obriot; Aleksandra Paczkowska; Robert Jedrzejczak; Aleksandra Dmochowska; Ewa Bartnik; Pierre Formstecher; Renata Polakowska; Piotr P Stepien
Journal:  Biol Cell       Date:  2007-06       Impact factor: 4.458

5.  Mitochondrial and nuclear localization of human Pif1 helicase.

Authors:  Kazunobu Futami; Akira Shimamoto; Yasuhiro Furuichi
Journal:  Biol Pharm Bull       Date:  2007-09       Impact factor: 2.233

6.  Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria.

Authors:  Pingfang Liu; Limin Qian; Jung-Suk Sung; Nadja C de Souza-Pinto; Li Zheng; Daniel F Bogenhagen; Vilhelm A Bohr; David M Wilson; Binghui Shen; Bruce Demple
Journal:  Mol Cell Biol       Date:  2008-06-09       Impact factor: 4.272

Review 7.  What causes mitochondrial DNA deletions in human cells?

Authors:  Kim J Krishnan; Amy K Reeve; David C Samuels; Patrick F Chinnery; John K Blackwood; Robert W Taylor; Sjoerd Wanrooij; Johannes N Spelbrink; Robert N Lightowlers; Doug M Turnbull
Journal:  Nat Genet       Date:  2008-03       Impact factor: 38.330

8.  Human mitochondrial RNA turnover caught in flagranti: involvement of hSuv3p helicase in RNA surveillance.

Authors:  Roman J Szczesny; Lukasz S Borowski; Lien K Brzezniak; Aleksandra Dmochowska; Kamil Gewartowski; Ewa Bartnik; Piotr P Stepien
Journal:  Nucleic Acids Res       Date:  2009-10-28       Impact factor: 16.971

9.  The human Bloom syndrome gene suppresses the DNA replication and repair defects of yeast dna2 mutants.

Authors:  Osamu Imamura; Judith L Campbell
Journal:  Proc Natl Acad Sci U S A       Date:  2003-06-25       Impact factor: 12.779

10.  Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling.

Authors:  Steffi Goffart; Helen M Cooper; Henna Tyynismaa; Sjoerd Wanrooij; Anu Suomalainen; Johannes N Spelbrink
Journal:  Hum Mol Genet       Date:  2008-10-29       Impact factor: 6.150
View more
  6 in total

Review 1.  Mechanism of homologous recombination and implications for aging-related deletions in mitochondrial DNA.

Authors:  Xin Jie Chen
Journal:  Microbiol Mol Biol Rev       Date:  2013-09       Impact factor: 11.056

2.  Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice.

Authors:  Sylvie Bannwarth; Laetitia Berg-Alonso; Gaëlle Augé; Konstantina Fragaki; Jill E Kolesar; Françoise Lespinasse; Sandra Lacas-Gervais; Fanny Burel-Vandenbos; Elodie Villa; Frances Belmonte; Jean-François Michiels; Jean-Ehrland Ricci; Romain Gherardi; Lea Harrington; Brett A Kaufman; Véronique Paquis-Flucklinger
Journal:  Mitochondrion       Date:  2016-02-24       Impact factor: 4.160

Review 3.  Helicase-inactivating mutations as a basis for dominant negative phenotypes.

Authors:  Yuliang Wu; Robert M Brosh
Journal:  Cell Cycle       Date:  2010-10-15       Impact factor: 4.534

4.  Impaired p32 regulation caused by the lymphoma-prone RECQ4 mutation drives mitochondrial dysfunction.

Authors:  Jiin-Tarng Wang; Xiaohua Xu; Aileen Y Alontaga; Yuan Chen; Yilun Liu
Journal:  Cell Rep       Date:  2014-04-17       Impact factor: 9.423

Review 5.  The Similarities between Human Mitochondria and Bacteria in the Context of Structure, Genome, and Base Excision Repair System.

Authors:  Karolina Boguszewska; Michał Szewczuk; Julia Kaźmierczak-Barańska; Bolesław T Karwowski
Journal:  Molecules       Date:  2020-06-21       Impact factor: 4.411

Review 6.  TWINKLE and Other Human Mitochondrial DNA Helicases: Structure, Function and Disease.

Authors:  Bradley Peter; Maria Falkenberg
Journal:  Genes (Basel)       Date:  2020-04-09       Impact factor: 4.096
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.