Literature DB >> 1423294

Expression of the endogenous O6-methylguanine-DNA-methyltransferase protects Chinese hamster ovary cells from spontaneous G:C to A:T transitions.

G Aquilina1, R Biondo, E Dogliotti, M Meuth, M Bignami.   

Abstract

We have investigated whether the presence of a DNA repair enzyme, O6-methylguanine-DNA-methyltransferase (MGMT), affects the nature of spontaneous mutations in a mammalian cell line. We compared spontaneous mutations in the adenine phosphoribosyl transferase gene of a Chinese hamster ovary (CHO) cell line that expressed 14,000 MGMT molecules/cell with those in the parental CHO cells lacking this DNA repair activity. The mutation rate/cell/generation of the two CHO cell lines did not differ significantly. However, DNA sequence analysis of spontaneous mutations in the MGMT-proficient CHO cell line revealed a complex picture. No significant difference from the parental CHO cells was found in the number or type of deletions, frameshifts, multiple substitutions, or insertions. The frequency of G:C to T:A transversions was elevated in MGMT-proficient CHO cells. Expression of the enzyme considerably reduced G:C to A:T transitions (25% versus 8.3%). This latter result is the first evidence that this protein is active on an endogenous source of O6-methylguanine that is normally responsible for spontaneous G:C to A:T transition mutations.

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Year:  1992        PMID: 1423294

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  12 in total

1.  Lack of the DNA repair protein O6-methylguanine-DNA methyltransferase in histologically normal brain adjacent to primary human brain tumors.

Authors:  J R Silber; A Blank; M S Bobola; B A Mueller; D D Kolstoe; G A Ojemann; M S Berger
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-09       Impact factor: 11.205

Review 2.  DNA repair mechanisms in dividing and non-dividing cells.

Authors:  Teruaki Iyama; David M Wilson
Journal:  DNA Repair (Amst)       Date:  2013-05-16

3.  O(6)-methylguanine methyltransferase in colorectal cancers: detection of mutations, loss of expression, and weak association with G:C>A:T transitions.

Authors:  S Halford; A Rowan; E Sawyer; I Talbot; I Tomlinson
Journal:  Gut       Date:  2005-06       Impact factor: 23.059

4.  Polymorphisms of the DNA repair gene MGMT and risk and progression of head and neck cancer.

Authors:  Zhengdong Zhang; Luo Wang; Sheng Wei; Zhensheng Liu; Li-E Wang; Erich M Sturgis; Qingyi Wei
Journal:  DNA Repair (Amst)       Date:  2010-03-04

5.  Generation of an endogenous DNA-methylating agent by nitrosation in Escherichia coli.

Authors:  P Taverna; B Sedgwick
Journal:  J Bacteriol       Date:  1996-09       Impact factor: 3.490

6.  Molecular correlates with MGMT promoter methylation and silencing support CpG island methylator phenotype-low (CIMP-low) in colorectal cancer.

Authors:  Shuji Ogino; Takako Kawasaki; Gregory J Kirkner; Yuko Suemoto; Jeffrey A Meyerhardt; Charles S Fuchs
Journal:  Gut       Date:  2007-03-05       Impact factor: 23.059

7.  DNA alkylation repair limits spontaneous base substitution mutations in Escherichia coli.

Authors:  W J Mackay; S Han; L D Samson
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

8.  A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype.

Authors:  G Aquilina; P Hess; P Branch; C MacGeoch; I Casciano; P Karran; M Bignami
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

9.  Influence of alkyltransferase activity and chromosomal locus on mutational hotspots in Chinese hamster ovary cells.

Authors:  A Belouchi; M Ouimet; P Dion; N Gaudreault; W E Bradley
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-09       Impact factor: 11.205

10.  Methylation pattern of the O6-methylguanine-DNA methyltransferase gene in colon during progressive colorectal tumorigenesis.

Authors:  Takeshi Nagasaka; Ajay Goel; Kenji Notohara; Takaomi Takahata; Hiromi Sasamoto; Takuyuki Uchida; Naoshi Nishida; Noriaki Tanaka; Clement Richard Boland; Nagahide Matsubara
Journal:  Int J Cancer       Date:  2008-06-01       Impact factor: 7.396

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