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Published on: July 29, 2010
Mutation in the mismatch repair gene Msh6 causes cancer susceptibility
1Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Abstract:
Mice carrying a null mutation in the mismatch repair gene Msh6 were generated by gene targeting. Cells that were homozygous for the mutation did not produce any detectable MSH6 protein, and extracts prepared from these cells were defective for repair of single nucleotide mismatches. Repair of 1, 2, and 4 nucleotide insertion/deletion mismatches was unaffected. Mice that were homozygous for the mutation had a reduced life span. The mice developed a spectrum of tumors, the most predominant of which were gastrointestinal tumors and B- as well as T-cell lymphomas. The tumors did not show any microsatellite instability. We conclude that MSH6 mutations, like those in some other members of the family of mismatch repair genes, lead to cancer susceptibility, and germline mutations in this gene may be associated with a cancer predisposition syndrome that does not show microsatellite instability.
Insights
Mice lacking the MSH6 mismatch repair gene developed tumors and had shorter lifespans. This suggests MSH6 mutations contribute to cancer susceptibility, even without microsatellite instability.
Area of Science:
- Genetics
- Molecular Biology
- Cancer Research
Background:
- DNA mismatch repair (MMR) is crucial for genomic stability.
- The MSH6 gene is a key component of the MMR system.
- Defects in MMR genes are linked to various cancers.
Purpose of the Study:
- To investigate the role of MSH6 in DNA repair and cancer development.
- To characterize the phenotype of Msh6-deficient mice.
Main Methods:
- Gene targeting was used to create Msh6-null mice.
- Cellular extracts were assessed for mismatch repair activity.
- Tumor development and microsatellite instability were analyzed in mutant mice.
Main Results:
- Msh6-homozygous cells showed defective repair of single nucleotide mismatches.
- Msh6-deficient mice had reduced lifespans and developed various tumors, including gastrointestinal tumors and lymphomas.
- Tumors in these mice did not exhibit microsatellite instability.
Conclusions:
- MSH6 is essential for repairing single nucleotide mismatches.
- MSH6 mutations confer cancer susceptibility.
- Germline MSH6 mutations may be associated with a cancer predisposition syndrome independent of microsatellite instability.
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