| Literature DB >> 20193754 |
Alison J Shield1, Tracy P Murray, Jean Y Cappello, Marjorie Coggan, Philip G Board.
Abstract
The level of glutathione transferase Kappa (GSTK1-1) has been correlated with obesity (Liu et.al. 2008 PNAS 105: 18302-7) and a polymorphism in the hGSTK1 promoter has been associated with insulin secretion and fat deposition (Gao et al 2009 Endocr J 56: 487-94). We searched for additional polymorphisms that may influence GSTK1-1 function or expression. Two SNPs were identified in the 5' non-coding region. A SNP at -1308 that occurs in Chinese subjects is predicted to eliminate a FXR/RXR transcription factor-binding site and causes a 55% increase in transcription rate in HepG2 cells and a 59% decrease in HEK293 cells. These data suggest that the impact of this polymorphism is complex and tissue specific. A SNP at -1032 alters a methylation site and represses transcription by 38%. These observations provide the first functional insight into genetic factors that regulate hGSTK1 expression and may directly influence insulin secretion and fat deposition. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20193754 DOI: 10.1016/j.ygeno.2010.02.007
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736