Literature DB >> 9268290

Yeast Rad7-Rad16 complex, specific for the nucleotide excision repair of the nontranscribed DNA strand, is an ATP-dependent DNA damage sensor.

S N Guzder1, P Sung, L Prakash, S Prakash.   

Abstract

In eukaryotes, nucleotide excision repair of ultraviolet light-damaged DNA is a highly intricate process that requires a large number of evolutionarily conserved protein factors. Genetic studies in the yeast Saccharomyces cerevisiae have indicated a specific role of the RAD7 and RAD16 genes in the repair of transcriptionally inactive DNA. Here we show that the RAD7- and RAD16-encoded products exist as a complex of 1:1 stoichiometry, exhibiting an apparent dissociation constant (Kd) of <4 x 10(-10) M. The Rad7-Rad16 complex has been purified to near homogeneity in this study and is shown to bind, in an ATP-dependent manner and with high specificity, to DNA damaged by ultraviolet light. Importantly, inclusion of the Rad7-Rad16 complex in the in vitro nucleotide excision repair system that consists entirely of purified components results in a marked stimulation of damage specific incision. Thus, Rad7-Rad16 complex is the ATP-dependent DNA damage sensor that specifically functions with the ensemble of nucleotide excision repair factor (NEF) 1, NEF2, NEF3, and replication protein A in the repair of transcriptionally inactive DNA. We name this novel complex of Rad7 and Rad16 proteins NEF4.

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Year:  1997        PMID: 9268290     DOI: 10.1074/jbc.272.35.21665

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  26 in total

1.  Recruitment of the nucleotide excision repair endonuclease XPG to sites of UV-induced dna damage depends on functional TFIIH.

Authors:  Angelika Zotter; Martijn S Luijsterburg; Daniël O Warmerdam; Shehu Ibrahim; Alex Nigg; Wiggert A van Cappellen; Jan H J Hoeijmakers; Roel van Driel; Wim Vermeulen; Adriaan B Houtsmuller
Journal:  Mol Cell Biol       Date:  2006-09-25       Impact factor: 4.272

Review 2.  Mechanisms for ATP-dependent chromatin remodelling: the means to the end.

Authors:  Andrew Flaus; Tom Owen-Hughes
Journal:  FEBS J       Date:  2011-09-08       Impact factor: 5.542

Review 3.  Emerging roles for histone modifications in DNA excision repair.

Authors:  Peng Mao; John J Wyrick
Journal:  FEMS Yeast Res       Date:  2016-10-12       Impact factor: 2.796

Review 4.  DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae.

Authors:  Serge Boiteux; Sue Jinks-Robertson
Journal:  Genetics       Date:  2013-04       Impact factor: 4.562

5.  p53-mediated DNA repair responses to UV radiation: studies of mouse cells lacking p53, p21, and/or gadd45 genes.

Authors:  M L Smith; J M Ford; M C Hollander; R A Bortnick; S A Amundson; Y R Seo; C X Deng; P C Hanawalt; A J Fornace
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

6.  Evidence for the involvement of nucleotide excision repair in the removal of abasic sites in yeast.

Authors:  C A Torres-Ramos; R E Johnson; L Prakash; S Prakash
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

Review 7.  Metabolic Dysfunction in Parkinson's Disease: Bioenergetics, Redox Homeostasis and Central Carbon Metabolism.

Authors:  Annadurai Anandhan; Maria S Jacome; Shulei Lei; Pablo Hernandez-Franco; Aglaia Pappa; Mihalis I Panayiotidis; Robert Powers; Rodrigo Franco
Journal:  Brain Res Bull       Date:  2017-03-21       Impact factor: 4.077

8.  Spt4 modulates Rad26 requirement in transcription-coupled nucleotide excision repair.

Authors:  L E Jansen; H den Dulk; R M Brouns; M de Ruijter; J A Brandsma; J Brouwer
Journal:  EMBO J       Date:  2000-12-01       Impact factor: 11.598

9.  Saccharomyces cerevisiae Rad16 mediates ultraviolet-dependent histone H3 acetylation required for efficient global genome nucleotide-excision repair.

Authors:  Yumin Teng; Hairong Liu; Hefin W Gill; Yachuan Yu; Raymond Waters; Simon H Reed
Journal:  EMBO Rep       Date:  2007-11-09       Impact factor: 8.807

10.  Testing for DNA tracking by MOT1, a SNF2/SWI2 protein family member.

Authors:  D T Auble; S M Steggerda
Journal:  Mol Cell Biol       Date:  1999-01       Impact factor: 4.272

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