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Molecular and Cellular Biology, April 1999, p. 3177-3183, Vol. 19, No. 4
0270-7306/99/$04.00+0
Mutator Phenotypes Conferred by MLH1
Overexpression and by Heterozygosity for mlh1
Mutations
Polina V.
Shcherbakova and
Thomas A.
Kunkel*
Laboratory of Molecular Genetics, National
Institute of Environmental Health Sciences, Research Triangle Park,
North Carolina 27709
Received 16 October 1998/Returned for modification 23 November
1998/Accepted 14 December 1998
Loss of DNA mismatch repair due to mutation or diminished
expression of the MLH1 gene is associated with genome
instability and cancer. In this study, we used a yeast model system to
examine three circumstances relevant to modulation of MLH1
function. First, overexpression of wild-type MLH1 was found
to cause a strong elevation of mutation rates at three different loci,
similar to the mutator effect of MLH1 gene inactivation.
Second, haploid yeast strains with any of six mlh1 missense
mutations that mimic germ line mutations found in human cancer patients
displayed a strong mutator phenotype consistent with loss of mismatch
repair function. Five of these mutations affect amino acids that are
homologous to residues suggested by recent crystal structure and
biochemical analysis of Escherichia coli MutL to
participate in ATP binding and hydrolysis. Finally, using a highly
sensitive reporter gene, we detected a mutator phenotype of diploid
yeast strains that are heterozygous for mlh1 mutations.
Evidence suggesting that this mutator effect results not from reduced
mismatch repair in the MLH1/mlh1 cells but rather from loss
of the wild-type MLH1 allele in a fraction of cells is
presented. Exposure to bleomycin or to UV irradiation strongly enhanced
mutagenesis in the heterozygous strain but had little effect on the
mutation rate in the wild-type strain. This damage-induced hypermutability may be relevant to cancer in humans with germ line
mutations in only one MLH1 allele.
*
Corresponding author. Mailing address: Laboratory of
Molecular Genetics, National Institute of Environmental Health
Sciences, Research Triangle Park, NC 27709. Phone: (919) 541-2644. Fax: (919) 541-7613. E-mail: kunkel{at}niehs.nih.gov.
Molecular and Cellular Biology, April 1999, p. 3177-3183, Vol. 19, No. 4
0270-7306/99/$04.00+0
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