Abstract
Mismatch repair genes MSH2 and MLH1 are the two major genes implicated in hereditary nonpolyposis colorectal cancer. For the past years, we have successfully searched for mutations in both genes in affected Portuguese families, by SSCP and DNA sequencing analysis but because of the advantages that DHPLC offers, we have established conditions in our laboratory to use this new method. While screening for mutations by both methods, in 35 individuals belonging to HNPCC Portuguese families, 4 novel MLH1 mutations (c.307-1G>C; c.1023delG [p.R341fsX366]; c.2154_2155delCA [p.H718fsX721], c.2154_2155dupCA [p.I719fsX782]), an unclassified variant (c.-28A>T) and one silent MSH2 polymorphism (c.2766T>C) have been identified.
Copyright 2003 Wiley-Liss, Inc.
MeSH terms
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Adaptor Proteins, Signal Transducing
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Adult
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Carrier Proteins
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Chromatography, High Pressure Liquid
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Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis
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Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
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DNA Mutational Analysis / methods*
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DNA-Binding Proteins / genetics*
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Humans
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Middle Aged
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MutL Protein Homolog 1
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MutS Homolog 2 Protein
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Mutation*
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Neoplasm Proteins / genetics*
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Nuclear Proteins
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Polymorphism, Genetic*
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Polymorphism, Single-Stranded Conformational
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Portugal
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Proto-Oncogene Proteins / genetics*
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Sequence Analysis, DNA / methods
Substances
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Adaptor Proteins, Signal Transducing
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Carrier Proteins
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DNA-Binding Proteins
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MLH1 protein, human
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Neoplasm Proteins
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Nuclear Proteins
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Proto-Oncogene Proteins
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MSH2 protein, human
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MutL Protein Homolog 1
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MutS Homolog 2 Protein