Literature DB >> 3368459

Spectrum of spontaneous mutation at the APRT locus of Chinese hamster ovary cells: an analysis at the DNA sequence level.

P J de Jong1, A J Grosovsky, B W Glickman.   

Abstract

The spectrum of spontaneous mutation of an endogenous mammalian cell gene has been determined at the DNA sequence level. Thirty independent spontaneous APRT- mutations were cloned and subsequently completely sequenced. Twenty-seven contained single base substitutions. Of these, 22 were G.C to A.T transitions, suggesting a major role for the deamination of cytosine in spontaneous mutagenesis of Chinese hamster ovary cells. The remaining mutants included a tandem double substitution, a -1 frameshift, and a 17-base-pair deletion flanked by a 2-base-pair direct repeat. Many of the independently recovered mutants were clustered at sites of multiple occurrence (hot spots). One site accounted for greater than 25% of all independently recovered events. Mutations were generally located within the coding sequence, although two mutations occurred within the consensus sequence for a 3' splice site.

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Year:  1988        PMID: 3368459      PMCID: PMC280239          DOI: 10.1073/pnas.85.10.3499

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  41 in total

1.  A shuttle vector plasmid for studying carcinogen-induced point mutations in mammalian cells.

Authors:  M M Seidman; K Dixon; A Razzaque; R J Zagursky; M L Berman
Journal:  Gene       Date:  1985       Impact factor: 3.688

2.  Genetic studies of the lac repressor. VII. On the molecular nature of spontaneous hotspots in the lacI gene of Escherichia coli.

Authors:  P J Farabaugh; U Schmeissner; M Hofer; J H Miller
Journal:  J Mol Biol       Date:  1978-12-25       Impact factor: 5.469

3.  Mutations affecting adenine phosphoribosyl transferase activity in Chinese hamster cells.

Authors:  L A Chasin
Journal:  Cell       Date:  1974-05       Impact factor: 41.582

4.  Mutagenic specificity of ultraviolet light.

Authors:  J H Miller
Journal:  J Mol Biol       Date:  1985-03-05       Impact factor: 5.469

5.  Nucleotide sequence of hamster adenine phosphoribosyl transferase (aprt) gene.

Authors:  J Nalbantoglu; G A Phear; M Meuth
Journal:  Nucleic Acids Res       Date:  1986-02-25       Impact factor: 16.971

6.  Variance estimation in single-cell mutation assays: comparison to experimental observations in human lymphoblasts at 4 gene loci.

Authors:  P M Leong; W G Thilly; S Morgenthaler
Journal:  Mutat Res       Date:  1985 Jun-Jul       Impact factor: 2.433

7.  Nonrandomness of point mutation as reflected in nucleotide substitutions in pseudogenes and its evolutionary implications.

Authors:  W H Li; C I Wu; C C Luo
Journal:  J Mol Evol       Date:  1984       Impact factor: 2.395

8.  High mutation frequency in DNA transfected into mammalian cells.

Authors:  M P Calos; J S Lebkowski; M R Botchan
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

9.  DNA methylation and the frequency of CpG in animal DNA.

Authors:  A P Bird
Journal:  Nucleic Acids Res       Date:  1980-04-11       Impact factor: 16.971

10.  Intron sequences involved in lariat formation during pre-mRNA splicing.

Authors:  R Reed; T Maniatis
Journal:  Cell       Date:  1985-05       Impact factor: 41.582

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  23 in total

1.  Mouse transgenes in human cells detect specific base substitutions.

Authors:  D A Schaff; R A Jarrett; S R Dlouhy; S Ponniah; M Stockelman; P J Stambrook; J A Tischfield
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

2.  Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.

Authors:  D Papadopoulo; C Guillouf; H Mohrenweiser; E Moustacchi
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

3.  Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment.

Authors:  M Krawczak; D N Cooper
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

4.  A DNA polymerase alpha pause site is a hot spot for nucleotide misinsertion.

Authors:  M Fry; L A Loeb
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-15       Impact factor: 11.205

5.  Molecular analysis of two mouse dilute locus deletion mutations: spontaneous dilute lethal20J and radiation-induced dilute prenatal lethal Aa2 alleles.

Authors:  M C Strobel; P K Seperack; N G Copeland; N A Jenkins
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

6.  Mutator phenotype induced by aberrant replication.

Authors:  V F Liu; D Bhaumik; T S Wang
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

Review 7.  The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions.

Authors:  D N Cooper; M Krawczak
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

8.  Broad spectrum of in vivo forward mutations, hypermutations, and mutational hotspots in a retroviral shuttle vector after a single replication cycle: deletions and deletions with insertions.

Authors:  V K Pathak; H M Temin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205

9.  Respective roles of pyrimidine dimer and pyrimidine (6-4) pyrimidone photoproducts in UV mutagenesis of simian virus 40 DNA in mammalian cells.

Authors:  F Bourre; A Benoit; A Sarasin
Journal:  J Virol       Date:  1989-11       Impact factor: 5.103

10.  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

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