Variable Transcriptional Regulation of the Human Aldosterone Synthase Gene Causes Salt-Dependent High Blood Pressure in Transgenic Mice. (February 2015)
- Record Type:
- Journal Article
- Title:
- Variable Transcriptional Regulation of the Human Aldosterone Synthase Gene Causes Salt-Dependent High Blood Pressure in Transgenic Mice. (February 2015)
- Main Title:
- Variable Transcriptional Regulation of the Human Aldosterone Synthase Gene Causes Salt-Dependent High Blood Pressure in Transgenic Mice
- Authors:
- Mopidevi, Brahmaraju
Kaw, Meenakshi K.
Puri, Nitin
Ponnala, Madhusudan
Jain, Sudhir
Rana, Anita
Keetha, Narsimha R.
Khuder, Sadik A.
Fiering, Steven N.
Kumar, Ashok - Abstract:
- Abstract : Background—: Aldosterone, synthesized in the adrenal cortex by the enzyme CYP11B2, induces positive sodium balance and predisposes to hypertension. Various investigators, using genomic DNA analyses, have linked -344T polymorphism in the human CYP11B2 (h CYP11B2 ) gene to human hypertension. h CYP11B2 gene promoter has 3 single-nucleotide polymorphisms in linkage disequilibrium: T/A at -663, T/C at -470, and C/T at -344. Variants ACT occur together and form the haplotype-I (Hap-I), whereas variants TTC constitute Hap-II. We hypothesize that these single-nucleotide polymorphisms, when present together, will lead to haplotype-dependent differences in the transcriptional regulation of the h CYP11B2 gene and affect blood pressure regulation. Methods and Results—: We evaluated differences in tissue expression in vivo and consequential effects on blood pressure stemming from the 2 haplotypes. Novel transgenic mice with the h CYP11B2 gene, targeted to the mouse HPRT locus, with either Hap-II or Hap-I variant are used in this study. Our results show increased adrenal and renal expression of h CYP11B2 in transgenic mice with Hap-I when compared with mice with Hap-II. Importantly, we observed increased baseline blood pressure in Hap-I transgenic mice, an effect accentuated by a high-salt diet. Pathophysiological effects of elevated aldosterone were corroborated by our results showing upregulation of proinflammatory markers in renal tissues from the transgenic mice withAbstract : Background—: Aldosterone, synthesized in the adrenal cortex by the enzyme CYP11B2, induces positive sodium balance and predisposes to hypertension. Various investigators, using genomic DNA analyses, have linked -344T polymorphism in the human CYP11B2 (h CYP11B2 ) gene to human hypertension. h CYP11B2 gene promoter has 3 single-nucleotide polymorphisms in linkage disequilibrium: T/A at -663, T/C at -470, and C/T at -344. Variants ACT occur together and form the haplotype-I (Hap-I), whereas variants TTC constitute Hap-II. We hypothesize that these single-nucleotide polymorphisms, when present together, will lead to haplotype-dependent differences in the transcriptional regulation of the h CYP11B2 gene and affect blood pressure regulation. Methods and Results—: We evaluated differences in tissue expression in vivo and consequential effects on blood pressure stemming from the 2 haplotypes. Novel transgenic mice with the h CYP11B2 gene, targeted to the mouse HPRT locus, with either Hap-II or Hap-I variant are used in this study. Our results show increased adrenal and renal expression of h CYP11B2 in transgenic mice with Hap-I when compared with mice with Hap-II. Importantly, we observed increased baseline blood pressure in Hap-I transgenic mice, an effect accentuated by a high-salt diet. Pathophysiological effects of elevated aldosterone were corroborated by our results showing upregulation of proinflammatory markers in renal tissues from the transgenic mice with Hap-I. Conclusions—: These findings characterize the haplotype-dependent regulation of the h CYP11B2 gene where -344T serves as a reporter polymorphism and show that Hap-I leads to increased expression of h CYP11B2, with permissive effects on blood pressure and inflammatory milieu. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Circulation. Volume 8:Number 1(2015)
- Journal:
- Circulation
- Issue:
- Volume 8:Number 1(2015)
- Issue Display:
- Volume 8, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 8
- Issue:
- 1
- Issue Sort Value:
- 2015-0008-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-02
- Subjects:
- aldosterone -- gene expression regulation -- genetics -- renin–angiotensin system
Arrhythmia -- Periodicals
Heart -- Electric properties -- Periodicals
616.1042 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=01337497-000000000-00000 ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCGENETICS.114.000694 ↗
- Languages:
- English
- ISSNs:
- 1942-325X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.262520
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5279.xml