Literature DB >> 12110180

Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. implications for Cockayne syndrome.

Sung-Keun Lee1, Sung-Lim Yu, Louise Prakash, Satya Prakash.   

Abstract

In addition to xeroderma pigmentosum, mutations in the human XPG gene cause early onset Cockayne syndrome (CS). Here, we provide evidence for the involvement of RAD2, the S. cerevisiae counterpart of XPG, in promoting efficient RNA polymerase II transcription. Inactivation of RAD26, the S. cerevisiae counterpart of the human CSB gene, also causes a deficiency in transcription, and a synergistic decline in transcription occurs in the absence of both the RAD2 and RAD26 genes. Growth is also retarded in the rad2 Delta and rad26 Delta single mutant strains, and a very severe growth inhibition is seen in the rad2 Delta rad26 Delta double mutant. From these and other observations presented here, we suggest that transcriptional defects are the underlying cause of CS.

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Year:  2002        PMID: 12110180     DOI: 10.1016/s0092-8674(02)00795-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  35 in total

1.  Association between the XPG gene rs2094258 polymorphism and risk of gastric cancer.

Authors:  Zhe Zhang; Jiefeng Yin; Qi Xu; Jianfeng Shi
Journal:  J Clin Lab Anal       Date:  2018-05-07       Impact factor: 2.352

2.  Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage.

Authors:  Fabrizio Thorel; Angelos Constantinou; Isabelle Dunand-Sauthier; Thierry Nouspikel; Philippe Lalle; Anja Raams; Nicolaas G J Jaspers; Wim Vermeulen; Mahmud K K Shivji; Richard D Wood; Stuart G Clarkson
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

3.  Homologous recombination is involved in transcription-coupled repair of UV damage in Saccharomyces cerevisiae.

Authors:  Abdelilah Aboussekhra; Ibtehaj S Al-Sharif
Journal:  EMBO J       Date:  2005-05-19       Impact factor: 11.598

4.  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

5.  H2A.Z has a function reminiscent of an activator required for preferential binding to intergenic DNA.

Authors:  Marc Larochelle; Luc Gaudreau
Journal:  EMBO J       Date:  2003-09-01       Impact factor: 11.598

Review 6.  Hot topics in DNA repair: the molecular basis for different disease states caused by mutations in TFIIH and XPG.

Authors:  Orlando D Schärer
Journal:  DNA Repair (Amst)       Date:  2008-02-01

7.  Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method.

Authors:  Naoko Shiomi; Seiji Kito; Masaki Oyama; Tsukasa Matsunaga; Yoshi-Nobu Harada; Masahito Ikawa; Masaru Okabe; Tadahiro Shiomi
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

8.  Cdt2-mediated XPG degradation promotes gap-filling DNA synthesis in nucleotide excision repair.

Authors:  Chunhua Han; Gulzar Wani; Ran Zhao; Jiang Qian; Nidhi Sharma; Jinshan He; Qianzheng Zhu; Qi-En Wang; Altaf A Wani
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

Review 9.  XPG: its products and biological roles.

Authors:  Orlando D Schärer
Journal:  Adv Exp Med Biol       Date:  2008       Impact factor: 2.622

10.  Dissociation of CAK from core TFIIH reveals a functional link between XP-G/CS and the TFIIH disassembly state.

Authors:  Hany H Arab; Gulzar Wani; Alo Ray; Zubair I Shah; Qianzheng Zhu; Altaf A Wani
Journal:  PLoS One       Date:  2010-06-08       Impact factor: 3.240

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