4.4 Article

Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter region

期刊

JOURNAL OF HUMAN GENETICS
卷 55, 期 5, 页码 278-284

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/jhg.2010.22

关键词

dual luciferase reporter gene assay; electrophoretic mobility shift assay; delta-opioid receptor gene; PCR; promoter polymorphism

资金

  1. National Institute of Drug Abuse (NIDA) [K99/R00DA022891, R01 DA12690, R01 DA12849, K12 DA000167]
  2. Alcoholic Beverage Medical Research Foundation (ABMRF)
  3. National Institute of Neurological Disorders and Stroke (NINDS) [R01NS043530]
  4. National Institute of Aging (NIA) [AG030970]
  5. Claude D Pepper Older Americans Independence Center at Yale University School of Medicine
  6. VA CT MIRECC Center
  7. Ortho-McNeil Pharmaceuticals (Raritan, NJ, USA)
  8. H. Lundbeck A/S (Copenhagen, Denmark)
  9. Forest Pharmaceuticals (St Louis, MO, USA)
  10. elbion NV (Leuven, Belgium)
  11. Sanofi-Aventis (Bridgewater, NJ, USA)
  12. Solvay Pharmaceuticals (Brussels, Belgium)
  13. Alkermes (Cambridge, MA, USA)
  14. Ortho-McNeil Pharmaceuticals
  15. Bristol-Myers Squibb Company (New York, NY, USA)
  16. Merck (Whitehouse Station, NJ, USA)

向作者/读者索取更多资源

The delta-opioid receptor mediates rewarding effects of many substances of abuse. We reported an increased frequency of the minor G-allele of single-nucleotide polymorphism (SNP) rs569356 (the only variant identified so far in the promoter region of the delta-opioid receptor gene (OPRD1)) in subjects with opioid dependence. In this study, we examined the functional significance of this variant. OPRD1 promoter region harboring SNP rs569356 was amplified by PCR and inserted into a firefly luciferase reporter vector. HEK293 cells were co-transfected with these constructs and a renilla luciferase vector to control for transfection efficiency. Expression of firefly luciferase (driven by the OPRD1 promoter) was measured by a dual luciferase reporter assay and normalized by renilla luciferase expression. Moreover, alleles altering expression were further assessed for binding of human brain nuclear proteins by electrophoretic mobility shift assay (EMSA). The minor G-allele was associated with significantly greater expression levels of firefly luciferase than the major A-allele of SNP rs569356 (P=0.003). EMSA also showed specific gel shift bands, suggesting that SNP rs569356 is situated in the binding site of potential transcription factors. These results suggest that the minor G-allele of SNP rs569356 may enhance transcription factor binding and increase OPRD1 expression. Journal of Human Genetics (2010) 55, 278-284; doi:10.1038/jhg.2010.22; published online 19 March 2010

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