Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure. Academic Article uri icon

Overview

MeSH

  • Adolescent
  • Adult
  • African Continental Ancestry Group
  • Aged
  • Aged, 80 and over
  • European Continental Ancestry Group
  • Female
  • Genetic Variation
  • Heart Rate
  • Humans
  • Male
  • Middle Aged
  • Nigeria
  • United States
  • Young Adult

MeSH Major

  • Autonomic Nervous System
  • Blood Pressure
  • Dopamine beta-Hydroxylase
  • Genetic Predisposition to Disease
  • Hypertension
  • Polymorphism, Single Nucleotide

abstract

  • Dopamine beta-hydroxylase (DBH) plays an essential role in catecholamine synthesis by converting dopamine into norepinephrine. Here we systematically investigated DBH polymorphisms associated with enzymatic activity as well as autonomic and blood pressure (BP)/disease phenotypes in vivo. Seventy genetic variants were discovered at the locus; across ethnicities, much of the promoter was spanned by a 5' haplotype block, with a larger block spanning the promoter in whites than blacks. DBH secretion was predicted by genetic variants in the DBH promoter, rather than the amino acid coding region. The C allele of common promoter variant C-970T increased plasma DBH activity, epinephrine excretion, the heritable change in BP during environmental stress in twin pairs, and also predicted higher basal BP in three independent populations. Mutagenesis and expression studies with isolated/transfected DBH promoter/luciferase reporters in chromaffin cells indicated that variant C-970T was functional. C-970T partially disrupted consensus transcriptional motifs for n-MYC and MEF-2, and this variant affected not only basal expression, but also the response to exogenous/co-transfected n-MYC or MEF-2; during chromatin immunoprecipitation, these two endogenous factors interacted with the motif. These results suggest that common DBH promoter variant C-970T plays a role in the pathogenesis of human essential hypertension: common genetic variation in the DBH promoter region seems to initiate a cascade of biochemical and physiological changes eventuating in alterations of basal BP. These observations suggest new molecular strategies for probing the pathophysiology, risk, and rational treatment of systemic hypertension.

publication date

  • January 2010

has subject area

  • Adolescent
  • Adult
  • African Continental Ancestry Group
  • Aged
  • Aged, 80 and over
  • Autonomic Nervous System
  • Blood Pressure
  • Dopamine beta-Hydroxylase
  • European Continental Ancestry Group
  • Female
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Heart Rate
  • Humans
  • Hypertension
  • Male
  • Middle Aged
  • Nigeria
  • Polymorphism, Single Nucleotide
  • United States
  • Young Adult

Research

keywords

  • Journal Article
  • Twin Study

Identity

Language

  • eng

PubMed Central ID

  • PMC2860271

Digital Object Identifier (DOI)

  • 10.1097/HJH.0b013e328332bc87

PubMed ID

  • 20009769

Additional Document Info

start page

  • 76

end page

  • 86

volume

  • 28

number

  • 1