Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome
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Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome. / Ou, Jianghua; Rasmussen, Merete; Westers, Helga; Andersen, Sofie D; Jager, Paul O; Kooi, Krista A; Niessen, Renée C; Eggen, Bart J L; Nielsen, Finn C; Kleibeuker, Jan H; Sijmons, Rolf H; Rasmussen, Lene J; Hofstra, Robert M W.
In: Genes, Chromosomes & Cancer, Vol. 48, No. 4, 2009, p. 340-50.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome
AU - Ou, Jianghua
AU - Rasmussen, Merete
AU - Westers, Helga
AU - Andersen, Sofie D
AU - Jager, Paul O
AU - Kooi, Krista A
AU - Niessen, Renée C
AU - Eggen, Bart J L
AU - Nielsen, Finn C
AU - Kleibeuker, Jan H
AU - Sijmons, Rolf H
AU - Rasmussen, Lene J
AU - Hofstra, Robert M W
N1 - Keywords: Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Carrier Proteins; Cell Line; Colorectal Neoplasms, Hereditary Nonpolyposis; Computer Simulation; DNA Mutational Analysis; Humans; Molecular Sequence Data; Mutation, Missense; Nuclear Proteins; Protein Transport; Sequence Alignment; Two-Hybrid System Techniques
PY - 2009
Y1 - 2009
N2 - So far 18 MLH3 germline mutations/variants have been identified in familial colorectal cancer cases. Sixteen of these variants are amino acid substitutions of which the pathogenic nature is still unclear. These substitutions are known as unclassified variants or UVs. To clarify a possible role for eight of these MLH3 UVs identified in suspected Lynch syndrome patients, we performed several biochemical tests. We determined the protein expression and stability, protein localization and interaction of the mutant MLH3 proteins with wildtype MLH1. All eight MLH3 UVs gave protein expression levels comparable with wildtype MLH3. Furthermore, the UV-containing proteins, in contrast to previous studies, were all localized normally in the nucleus and they interacted normally with wildtype MLH1. Our different biochemical assays yielded no evidence that the eight MLH3 UVs tested are the cause of hereditary colorectal cancer, including Lynch syndrome.
AB - So far 18 MLH3 germline mutations/variants have been identified in familial colorectal cancer cases. Sixteen of these variants are amino acid substitutions of which the pathogenic nature is still unclear. These substitutions are known as unclassified variants or UVs. To clarify a possible role for eight of these MLH3 UVs identified in suspected Lynch syndrome patients, we performed several biochemical tests. We determined the protein expression and stability, protein localization and interaction of the mutant MLH3 proteins with wildtype MLH1. All eight MLH3 UVs gave protein expression levels comparable with wildtype MLH3. Furthermore, the UV-containing proteins, in contrast to previous studies, were all localized normally in the nucleus and they interacted normally with wildtype MLH1. Our different biochemical assays yielded no evidence that the eight MLH3 UVs tested are the cause of hereditary colorectal cancer, including Lynch syndrome.
U2 - 10.1002/gcc.20644
DO - 10.1002/gcc.20644
M3 - Journal article
C2 - 19156873
VL - 48
SP - 340
EP - 350
JO - Genes, Chromosomes & Cancer
JF - Genes, Chromosomes & Cancer
SN - 1045-2257
IS - 4
ER -
ID: 20010678