Human Molecular Genetics, 2001, Vol. 10, No. 24 2737-2743
© 2001 Oxford University Press
A functional assay for mutations in tumor suppressor genes caused by mismatch repair deficiency
Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA 98195-7720, USA
The coding sequences of multiple human tumor suppressor genes include microsatellite sequences that are prone to mutations. Saccharomyces cerevisiae strains deficient in DNA mismatch repair (MMR) can be used to determine de novo mutation rates of these human tumor suppressor genes as well as any other gene sequence. Microsatellites in human TGFBR2, PTEN and APC genes were placed in yeast vectors and analyzed in isogenic yeast strains that were wild-type or deletion mutants for MSH2 or MLH1. In MMR-deficient strains, the vector containing the (A)10 microsatellite sequence of TGFBR2 had a mutation rate (mutations/cell division) of 1.4 x 10–4, compared to a mutation rate of 1.7 x 10–6 in the wild-type strain. In MMR-deficient strains, mutation rates in PTEN and APC were also elevated above background levels. PTEN mutation rates were higher in both msh2 (4.4 x 10–5) and mlh1 strains (2.3 x 10–5). APC mutation rates in the msh2 strain (2.4 x 10–6) and the mlh1 strain (1.7 x 10–6) were also significantly, but less dramatically, elevated over background. Mutations selected for in the yeast screen were identical to those previously observed in human tumor samples with microsatellite instability (MSI). This functional assay has applicability in providing quantitative data about microsatellite mutation rates caused by MMR deficiency in any human tumor suppressor gene sequence. It can also be applied as a genetic screen to identify new genes that are vulnerable to such microsatellite mutations and thus may be involved in the neoplastic development of tumors with MSI.
+ To whom correspondence should be addressed. Tel: +1 206 616 4294; Fax: +1 206 616 4295; Email: mcking@u.washington.edu
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