Author
Listed:
- Q. Feng
(Vanderbilt University School of Medicine)
- K.C. Vickers
(Vanderbilt University School of Medicine
National Heart, Lung and Blood Institute, National Institutes of Health)
- M.P. Anderson
(National Heart, Lung and Blood Institute, National Institutes of Health)
- M.G. Levin
(National Heart, Lung and Blood Institute, National Institutes of Health)
- W. Chen
(Vanderbilt University School of Medicine)
- D.G. Harrison
(Vanderbilt University School of Medicine)
- R.A. Wilke
(Vanderbilt University School of Medicine)
Abstract
Type 1 cannabinoid receptor blockers increase high-density lipoprotein cholesterol levels. Although genetic variation in the type 1 cannabinoid receptor—encoded by the CNR1 gene—is known to influence high-density lipoprotein cholesterol level as well, human studies conducted to date have been limited to genetic markers such as haplotype-tagging single nucleotide polymorphisms. Here we identify rs806371 in the CNR1 promoter as the causal variant. We re-sequence the CNR1 gene and genotype all variants in a DNA biobank linked to comprehensive electronic medical records. By testing each variant for association with high-density lipoprotein cholesterol level in a clinical practice-based setting, we localize a putative functional allele to a 100-bp window in the 5′-flanking region. Assessment of variants in this window for functional impact on electrophoretic mobility shift assay identifies rs806371 as a novel regulatory binding element. Reporter gene assays confirm that rs806371 reduces gene expression, thereby linking CNR1 gene variation to high-density lipoprotein cholesterol level in humans.
Suggested Citation
Q. Feng & K.C. Vickers & M.P. Anderson & M.G. Levin & W. Chen & D.G. Harrison & R.A. Wilke, 2013.
"A common functional promoter variant links CNR1 gene expression to HDL cholesterol level,"
Nature Communications, Nature, vol. 4(1), pages 1-7, October.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2973
DOI: 10.1038/ncomms2973
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2973. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.