A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage
Copyright policy )A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage
Lynch syndrome is caused by germline mutations in 1 of the 4 DNA mismatch repair genes (MLH1, MSH2, MSH6, and PMS2). Mutations in MSH2 cause concomitant loss of hMSH6, whereas MLH1 mutations lead to concurrent loss of PMS2. Much less frequent mutations in MSH6 or PMS2 are associated with the isolated loss of the corresponding proteins. We here demonstrate the causative role of the first germline mutation of MSH2, c.1249-1251 dupGTT (p.417V-418I dupV), associated with normal hMSH2 expression and lack of hMSH6 protein despite a normal MSH6 gene sequence. hMSH6 protein was completely lost only in advanced cancer stages due to 2 different "second hits": a whole MSH2 gene deletion and a frame-shifting insertion in the MSH6 (C)8 repeat in the coding sequence.
- University of Bari Aldo Moro Italy
- American Board of Legal Medicine United States
- University of Modena and Reggio Emilia Italy
- National Cancer Institute Ukraine
Adult, Male, Base Sequence, Blotting, Western, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, Polymerase Chain Reaction, Pedigree, DNA-Binding Proteins, MutS Homolog 2 Protein, Humans, Immunoprecipitation, Multiplex Polymerase Chain Reaction, Germ-Line Mutation, Protein Binding
Adult, Male, Base Sequence, Blotting, Western, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, Polymerase Chain Reaction, Pedigree, DNA-Binding Proteins, MutS Homolog 2 Protein, Humans, Immunoprecipitation, Multiplex Polymerase Chain Reaction, Germ-Line Mutation, Protein Binding
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