Literature DB >> 11018584

Characterization of the hOGG1 promoter and its expression during the cell cycle.

A Dhénaut1, S Boiteux, J P Radicella.   

Abstract

The human OGG1 gene codes for a 38kD protein with an antimutator activity related to its capacity to excise the mutagenic base 8-OH-Guanine from DNA. Mutant forms of this gene have been found in lung and kidney tumors. The determination of the start of transcription allowed the definition of the promoter sequences for the gene. By transient transfection and a luciferase reporter assay a 135 base pair region immediately upstream of the transcription start is shown to have full promoter activity. Two CpG islands and an Alu repeat were identified within the promoter and the 5' sequences of the transcribed region. The lack of TATA or CAAT boxes suggests that OGG1 is a housekeeping gene. Consistently, its expression, measured as the transcription from the promoter or as the enzymatic activity in cultured fibroblast cell lines, does not vary during the cell cycle.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11018584     DOI: 10.1016/s0921-8777(00)00042-2

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  26 in total

1.  hMYH cell cycle-dependent expression, subcellular localization and association with replication foci: evidence suggesting replication-coupled repair of adenine:8-oxoguanine mispairs.

Authors:  I Boldogh; D Milligan; M S Lee; H Bassett; R S Lloyd; A K McCullough
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

Review 2.  Regulation of DNA glycosylases and their role in limiting disease.

Authors:  Harini Sampath; Amanda K McCullough; R Stephen Lloyd
Journal:  Free Radic Res       Date:  2012-02-06

Review 3.  NRF2 and the Hallmarks of Cancer.

Authors:  Montserrat Rojo de la Vega; Eli Chapman; Donna D Zhang
Journal:  Cancer Cell       Date:  2018-05-03       Impact factor: 31.743

4.  Pro-oxidant induced DNA damage in human lymphoblastoid cells: homeostatic mechanisms of genotoxic tolerance.

Authors:  Anna L Seager; Ume-Kulsoom Shah; Jane M Mikhail; Bryant C Nelson; Bryce J Marquis; Shareen H Doak; George E Johnson; Sioned M Griffiths; Paul L Carmichael; Sharon J Scott; Andrew D Scott; Gareth J S Jenkins
Journal:  Toxicol Sci       Date:  2012-04-26       Impact factor: 4.849

5.  Genetic variation in the base excision repair pathway and bladder cancer risk.

Authors:  Jonine D Figueroa; Núria Malats; Francisco X Real; Debra Silverman; Manolis Kogevinas; Stephen Chanock; Robert Welch; Mustafa Dosemeci; Adonina Tardón; Consol Serra; Alfredo Carrato; Reina García-Closas; Gemma Castaño-Vinyals; Nathaniel Rothman; Montserrat García-Closas
Journal:  Hum Genet       Date:  2007-01-03       Impact factor: 4.132

6.  Identification and characterization of a human DNA glycosylase for repair of modified bases in oxidatively damaged DNA.

Authors:  Tapas K Hazra; Tadahide Izumi; Istvan Boldogh; Barry Imhoff; Yoke W Kow; Pawel Jaruga; Miral Dizdaroglu; Sankar Mitra
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

7.  Lung cancer risk and genetic polymorphisms in DNA repair pathways: a meta-analysis.

Authors:  Chikako Kiyohara; Koichi Takayama; Yoichi Nakanishi
Journal:  J Nucleic Acids       Date:  2010-10-14

8.  DNA base excision repair activities and pathway function in mitochondrial and cellular lysates from cells lacking mitochondrial DNA.

Authors:  J A Stuart; K Hashiguchi; D M Wilson; W C Copeland; N C Souza-Pinto; V A Bohr
Journal:  Nucleic Acids Res       Date:  2004-04-23       Impact factor: 16.971

9.  Insight into mechanism of oxidative DNA damage in angiomyolipomas from TSC patients.

Authors:  Samy L Habib
Journal:  Mol Cancer       Date:  2009-03-05       Impact factor: 27.401

10.  Molecular mechanism of regulation of OGG1: tuberin deficiency results in cytoplasmic redistribution of transcriptional factor NF-YA.

Authors:  Samy L Habib
Journal:  J Mol Signal       Date:  2009-12-29
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.