MODY associated with two novel hepatocyte nuclear factor-1 alpha loss-of-function mutations (P112L and Q466X)

Maturity-onset diabetes of the young (MODY) is an autosomal dominant form o f diabetes characterized by early onset of pancreatic dysfunction. MODY typ e 3 is caused by mutations in the hepatocyte nuclear factor (HNF)-1 alpha. During a screening of Norwegian patients with suspected MODY we identified two novel HNF-1 alpha mutations, P112L and Q466X. The molecular mechanisms underlying the disease were studied by analyzing the DNA binding properties , transcriptional activation, and subcellular localization of HNF-1 alpha P 112L and Q466X compared to wild type HNF-1 alpha. P112L had reduced ability to bind an HNF1 consensus sequence and to activate transcription. Q486X di d not differ from wild type HNF-1 alpha in DNA binding activity. Transactiv ation, however, was markedly reduced. When both mutants were coexpressed wi th wild type HNF-1 alpha in HeLa cells, transcriptional activity appeared u naffected, suggesting that a dominant-negative mechanism was not present. I mmunolocalization experiments showed that P112L HNF-1 alpha was correctly t argeted to nuclei in HeLa cells. In contrast, some Q466X HNF-1 alpha protei n was retained in the cytoplasm, which indicated that the mechanism for nuc lear localization was disturbed. Thus, the HNF-1 alpha mutations P112L and Q466X both seem to impair pancreatic p cell function by loss of-function me chanisms; P112L by reduced DNA binding and reduced ability to transactivate , and Q466X by reduced transactivation and incomplete nuclear targeting. (C ) 2000 Academic Press.