Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene

• Published in: Diabetes (New York, N.Y.) Vol. 46; no. 10; pp. 1648 - 1651
• Main Authors: Gragnoli, C., Lindner, T., Cockburn, B. N., Kaisaki, P. J., Gragnoli, F., Marozzi, G., Bell, G. I.
• Format: Journal Article
• Language: English
• Published: Alexandria, VA American Diabetes Association 01.10.1997
• Subjects: Animals; Base Sequence; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Binding Sites; Biological and medical sciences; Diabetes Mellitus, Type 2 - genetics; Diabetes. Impaired glucose tolerance; DNA - chemistry; DNA - metabolism; DNA Mutational Analysis; DNA-Binding Proteins; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Female; Genetic Linkage; Hepatocyte Nuclear Factor 1; Hepatocyte Nuclear Factor 1-alpha; Hepatocyte Nuclear Factor 1-beta; Hepatocyte Nuclear Factor 4; Humans; Italy; Male; Medical sciences; Molecular Sequence Data; Mutation; Nuclear Proteins; Pedigree; Phosphoproteins - metabolism; Polymerase Chain Reaction; Promoter Regions, Genetic; Sequence Alignment; Transcription Factors - genetics; Transcription Factors - metabolism; Italy; Europe; Endocrinopathy; Human; Maturity onset diabetes young; Messenger RNA; Family study; Transcription promoter; Genetics; Binding site; Mutation
• ISSN: 0012-1797; 1939-327X; 0012-1797
• DOI: 10.2337/diabetes.46.10.1648

Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene. C Gragnoli , T Lindner , B N Cockburn , P J Kaisaki , F Gragnoli , G Marozzi and G I Bell Howard Hughes Medical Institute, University of Chicago, Illinois, USA. Abstract Recent studies have shown that mutations in the transcription factor hepatocyte nuclear factor (HNF)-1 alpha are the cause of one form of maturity-onset diabetes of the young (MODY3). These studies have identified mutations in the mRNA and protein coding regions of this gene that result in the synthesis of an abnormal mRNA or protein. Here, we report an Italian family in which an A-->C substitution at nucleotide-58 of the promoter region of the HNF-1 alpha gene cosegregates with MODY. This mutation is located in a highly conserved region of the promoter and disrupts the binding site for the transcription factor HNF-4 alpha, mutations in the gene encoding HNF-4 alpha being another cause of MODY (MODY1). This result demonstrates that decreased levels of HNF-1 alpha per se can cause MODY. Moreover, it indicates that both the promoter and coding regions of the HNF-1 alpha gene should be screened for mutations in subjects thought to have MODY because of mutations in this gene.