Literature DB >> 23757391

Theoretical model for gene-gene, gene-environment, and gene-sex interactions based on congenic-strain analysis of blood pressure in Dahl salt-sensitive rats.

John P Rapp1.   

Abstract

There is a significant literature describing quantitative trait loci (QTL) controlling blood pressure (BP) in the Dahl salt-sensitive (S) rat. In studies to identify the genes underlying BP QTL it has been common practice to place chromosomal segments from low BP strains on the genetic background of the S rat and then reduce the congenic segments by substitution mapping. The present work suggests a model to simulate genetic interactions found using such congenic strains. The QTL are considered to be switches that can be either in series or in parallel represented by the logic operators AND or OR, respectively. The QTL switches can be on/off switches but are also allowed specific leak properties. The QTL switches are represented by a "universal" switch consisting of two molecules binding to form a complex. Genetic inputs enter the model as allelic products of one of the binding molecules and environmental variation (including dietary salt- and sex-related differences) enters as an influence on the concentration of the other binding molecule. The pairwise interactions of QTL are very well simulated and fall into recognizable patterns. There is, however, often more than one assumed model to predict a given pattern so that all patterns do not necessarily have a unique solution. Nevertheless, the models obtained provide a framework for placing the QTL in pathways relative to one another. Moreover, based on their leak properties pairs of QTL could be identified in which one QTL may alter the properties of the other QTL.

Entities:  

Keywords:  QTL; epistasis; genetic hypertension; quantitative trait loci; salt-sensitive hypertension

Mesh:

Year:  2013        PMID: 23757391     DOI: 10.1152/physiolgenomics.00046.2013

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  7 in total

1.  Do epistatic modules exist in the genetic control of blood pressure in Dahl rats? A critical perspective.

Authors:  John P Rapp; Bina Joe
Journal:  Physiol Genomics       Date:  2013-11-05       Impact factor: 3.107

2.  Dr Lewis Kitchener Dahl, the Dahl rats, and the "inconvenient truth" about the genetics of hypertension.

Authors:  Bina Joe
Journal:  Hypertension       Date:  2015-02-02       Impact factor: 10.190

3.  Elevation of fumarase attenuates hypertension and can result from a nonsynonymous sequence variation or increased expression depending on rat strain.

Authors:  Kristie Usa; Yong Liu; Aron M Geurts; Yuan Cheng; Jozef Lazar; Maria Angeles Baker; Michael Grzybowski; Yongcheng He; Zhongmin Tian; Mingyu Liang
Journal:  Physiol Genomics       Date:  2017-07-28       Impact factor: 3.107

4.  Will the real Dahl S rat please stand up?

Authors:  John P Rapp; Michael R Garrett
Journal:  Am J Physiol Renal Physiol       Date:  2019-09-23

5.  High-resolution mapping of a novel rat blood pressure locus on chromosome 9 to a region containing the Spp2 gene and colocalization of a QTL for bone mass.

Authors:  Ying Nie; Sivarajan Kumarasamy; Harshal Waghulde; Xi Cheng; Blair Mell; Piotr J Czernik; Beata Lecka-Czernik; Bina Joe
Journal:  Physiol Genomics       Date:  2016-04-25       Impact factor: 3.107

Review 6.  Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans.

Authors:  Sandosh Padmanabhan; Bina Joe
Journal:  Physiol Rev       Date:  2017-10-01       Impact factor: 37.312

7.  Integrative genomic analysis of blood pressure and related phenotypes in rats.

Authors:  Fumihiko Takeuchi; Yi-Qiang Liang; Masato Isono; Michiko Tajima; Zong Hu Cui; Yoko Iizuka; Takanari Gotoda; Toru Nabika; Norihiro Kato
Journal:  Dis Model Mech       Date:  2021-05-19       Impact factor: 5.758

  7 in total

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