» Articles » PMID: 17143582

Distinct Quantitative Trait Loci for Kidney, Cardiac, and Aortic Mass Dissociated from and Associated with Blood Pressure in Dahl Congenic Rats

Overview
Journal Mamm Genome
Specialty Genetics
Date 2006 Dec 5
PMID 17143582
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Blood pressure (BP) is largely determined by quantitative trait loci (QTLs) in Dahl salt-sensitive (DSS) rats. Little is known about QTLs controlling kidney (K), cardiac (C), and aortic (A) mass (i.e. Km, Cm, and Am, respectively) of DSS rats independent of BP. Their identification can facilitate our understanding of end organ damage. In this work, 36 congenic strains were employed to define QTLs for Km, Cm, and Am either independent of or associated with BP. Five new QTLs, i.e., KmQTLs, that influence Km independent of Cm, Am, and BP were defined. Four new CakmQTLs were defined for Cm, Am, and Km independent of BP. Among them, the CakmC10QTL1 interval contained 13 genes and undefined loci, and none was known to influence the phenotypes in question, paving the way for a novel gene discovery. Among 17 individual QTLs for BP, 14 also affected Cm, Km, and Am, i.e., they are BpcakmQTLs. In contrast, one BpQTL had no effect on Cm, Am, and Kam. Therefore, BP and Cm, Am, and Km have distinct and shared genetic determinants. The discovery of individual Km and Cakm QTLs will likely facilitate the identification of mechanisms underlying renal, cardiac, and/or aortic hypertrophy independent of hypertension.

Citing Articles

Deep transcriptomic profiling of Dahl salt-sensitive rat kidneys with mutant form of Resp18.

Ashraf U, Mell B, Jose P, Kumarasamy S Biochem Biophys Res Commun. 2021; 572:35-40.

PMID: 34340197 PMC: 8528512. DOI: 10.1016/j.bbrc.2021.07.071.


Hypothalamic Norepinephrine Concentration and Heart Mass in Hypertensive ISIAH Rats Are Associated with a Genetic Locus on Chromosome 18.

Redina O, Smolenskaya S, Polityko Y, Ershov N, Gilinsky M, Markel A J Pers Med. 2021; 11(2).

PMID: 33498741 PMC: 7911892. DOI: 10.3390/jpm11020067.


Candidate genes in quantitative trait loci associated with absolute and relative kidney weight in rats with Inherited Stress Induced Arterial Hypertension.

Redina O, Smolenskaya S, Klimov L, Markel A BMC Genet. 2015; 16 Suppl 1:S1.

PMID: 25707311 PMC: 4331803. DOI: 10.1186/1471-2156-16-S1-S1.


Impact of salt exposure on N-acetylgalactosamine-4-sulfatase (arylsulfatase B) activity, glycosaminoglycans, kininogen, and bradykinin.

Kotlo K, Bhattacharyya S, Yang B, Feferman L, Tejaskumar S, Linhardt R Glycoconj J. 2013; 30(7):667-76.

PMID: 23385884 PMC: 3866634. DOI: 10.1007/s10719-013-9468-8.


Molecular mechanisms of experimental salt-sensitive hypertension.

Joe B, Shapiro J J Am Heart Assoc. 2012; 1(3):e002121.

PMID: 23130148 PMC: 3487327. DOI: 10.1161/JAHA.112.002121.


References
1.
Dutil J, Deng A . Further chromosomal mapping of a blood pressure QTL in Dahl rats on chromosome 2 using congenic strains. Physiol Genomics. 2001; 6(1):3-9. DOI: 10.1152/physiolgenomics.2001.6.1.3. View

2.
Charron S, Lambert R, Eliopoulos V, Duong C, Menard A, Roy J . A loss of genome buffering capacity of Dahl salt-sensitive model to modulate blood pressure as a cause of hypertension. Hum Mol Genet. 2005; 14(24):3877-84. DOI: 10.1093/hmg/ddi412. View

3.
Garrett M, Rapp J . Two closely linked interactive blood pressure QTL on rat chromosome 5 defined using congenic Dahl rats. Physiol Genomics. 2002; 8(2):81-6. DOI: 10.1152/physiolgenomics.00080.2001. View

4.
Moujahidine M, Dutil J, Hamet P, Deng A . Congenic mapping of a blood pressure QTL on chromosome 16 of Dahl rats. Mamm Genome. 2002; 13(3):153-6. DOI: 10.1007/BF02684020. View

5.
Innes B, McLaughlin M, Kapuscinski M, Jacob H, Harrap S . Independent genetic susceptibility to cardiac hypertrophy in inherited hypertension. Hypertension. 1998; 31(3):741-6. DOI: 10.1161/01.hyp.31.3.741. View