hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6.

The genetic and biochemical properties of three human MutS homologues, hMSH2, hMSH3, and hMSH6, have been examined. The full-length hMSH6 cDNA and genomic locus were isolated and characterized, and it was demonstrated that the hMSH6 gene consisted of 10 exons and mapped to chromosome 2p15-16. The hMSH3 cDNA was in ...
some cases found to contain a 27-bp deletion resulting in a loss of nine amino acids, depending on the individual from which the cDNA was isolated. hMSH2, hMSH3, and hMSH6 all showed similar tissue-specific expression patterns. hMSH2 protein formed a complex with both hMSH3 and hMSH6 proteins, similar to protein complexes demonstrated by studies of the Saccharomyces cerevisiae MSH2, MSH3, and MSH6. hMSH2 was also found to form a homomultimer complex, but neither hMSH3 nor hMSH6 appear to interact with themselves or each other. Analysis of the mismatched nucleotide-binding specificity of the hMSH2-hMSH3 and hMSH2-hMSH6 protein complexes showed that they have overlapping but not identical binding specificity. These results help to explain the distribution of mutations in different mismatch-repair genes seen in hereditary nonpolyposis colon cancer.
Mesh Terms:
Base Sequence, Binding Sites, Chromosome Mapping, Chromosomes, Human, Pair 2, Cloning, Molecular, Colorectal Neoplasms, Hereditary Nonpolyposis, DNA Primers, DNA Repair, DNA, Complementary, DNA-Binding Proteins, Exons, Fungal Proteins, Gene Library, Hela Cells, Humans, Molecular Sequence Data, MutS Homolog 2 Protein, Oligodeoxyribonucleotides, Protein Binding, Protein Biosynthesis, RNA, Messenger, Recombinant Proteins, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Sequence Deletion, Substrate Specificity, Transcription, Genetic
Proc. Natl. Acad. Sci. U.S.A.
Date: Nov. 26, 1996
Download Curated Data For This Publication
2202
Switch View:
  • Interactions 3