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pubmed-article:19563912pubmed:abstractTextOur aim was to identify an insulin response element (IRE) in the lipoprotein lipase (LPL) gene. We identified a 19 bp sequence as a putative IRE in LPL non-coding exon 10 using bioinformatics. Upon sequencing the IRE region, a novel 5 bp deletion was identified in Hispanics (N=406) with a carrier frequency of 4.2% but not in non-Hispanic whites (N=604) or Africans. Electrophoretic mobility shift assay revealed binding sites for regulatory factor(s) in muscle cell nuclear extracts with putative IRE sequence. Antibody supershift assay using human aorta smooth muscle cell nuclear extract revealed that Elk-1 specifically binds to putative IRE. TaqMan real-time RT-PCR of the 5 bp deletion, the mutant and wild type cDNA expressed in COS-1 and human muscle cells revealed that the 5 bp deletion was associated with modest reduction in LPL expression. There was also a slight reduction in LPL translation in the deletion mutant. Our data suggest the presence of an IRE in the 3'UTR of the LPL gene.lld:pubmed
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pubmed-article:19563912pubmed:articleTitleIdentification and characterization of a novel 5 bp deletion in a putative insulin response element in the lipoprotein lipase gene.lld:pubmed
pubmed-article:19563912pubmed:affiliationDepartment of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15261, USA.lld:pubmed
pubmed-article:19563912pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19563912pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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