A distant upstream promoter of the HNF-4α gene connects the transcription factors involved in maturity-onset diabetes of the young
Maturity-onset diabetes of the young (MODY) is a monogenic, autosomal dominant subtype of early-onset diabetes mellitus due to defective insulin secretion by the pancreatic beta -cell in humans. Five different genes have been identified including those encoding the tissue-specific transcription fact...
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Published in | Human molecular genetics Vol. 10; no. 19; pp. 2089 - 2097 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Oxford University Press
15.09.2001
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Subjects | |
Online Access | Get full text |
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Summary: | Maturity-onset diabetes of the young (MODY) is a monogenic, autosomal dominant subtype of early-onset diabetes mellitus due to defective insulin secretion by the pancreatic beta -cell in humans. Five different genes have been identified including those encoding the tissue-specific transcription factors expressed in pancreatic beta -cells, i.e. HNF-4 alpha (MODY1), HNF-1 alpha (MODY3), IPF-1 (also known as PDX-1, MODY4) and HNF-1 beta (MODY5). Analyzing the transcription of the HNF-4 alpha gene, we now identify an alternative promoter, P2, which is 46 kb 5' to the previously identified P1 promoter of the human gene. Based on RT-PCR this distant upstream P2 promoter represents the major transcription site in pancreatic beta -cells, but is also used in hepatic cells. Transfection assays with various deletions and mutants of the P2 promoter reveal functional binding sites for HNF-1 alpha , HNF-1 beta and IPF-1, the other transcription factors known to encode MODY genes. We demonstrate the significance of this alternative promoter in a large MODY family where a mutated IPF-1 binding site in the P2 promoter of the HNF-4 alpha gene co-segregates with diabetes (LOD score 3.25). These data suggest a regulatory network of the four MODY transcription factors interconnected at the distant upstream P2 promoter of the HNF-4 alpha gene. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0964-6906 1460-2083 |
DOI: | 10.1093/hmg/10.19.2089 |