Literature DB >> 11414700

Quantitative trait loci for body weight, blood pressure, blood glucose, and serum lipids: linkage analysis with wild rats (Rattus norvegicus).

I Klöting1, P Kovács, J van den Brandt.   

Abstract

To study polygenetically inherited human diseases like hypertension, inbred rat strains are usually the preferred models. Because many inbred generations under optimized environmental conditions may have led to the survival of "silent" disease genes, we used a cross between one wild rat and genetically hypertensive SHR rats to analyze quantitative trait loci (QTLs) of blood pressure and related traits. The (Wild x SHR)F1 hybrids were transferred into a pathogen-free environment by wet-hysterectomy and were backcrossed onto SHR to generate first backcross hybrids (BC1). Progeny from one F1 female (n = 72) were phenotypically and genetically characterized to map QTLs. Significant, subsignificant, and suggestive evidence was found for more sex-specific than common linkage of blood pressure and most blood-pressure-related traits. Male- and female-specific regions were determined on different chromosomes for blood pressures (Chrs. 2 and 7 vs 5 and 11), body weight (Chrs. 10 vs 18), and blood glucose (Chr. 17 vs 20). A linkage in both males and females was shown for serum triglycerides on chromosomes 6 and 17, respectively, and blood glucose on chromosome 15. For serum total cholesterol, a significant linkage was found on chromosome 14 only in males. Our findings not only indicate the complex character of quantitative traits per se but also show impressively their dependence on sex, age, and strains in cosegregation analysis. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11414700     DOI: 10.1006/bbrc.2001.5091

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  5 in total

1.  Systematic polymorphism discovery after genome-wide identification of potential susceptibility loci in a hereditary rodent model of human hypertension.

Authors:  Ryan S Friese; Geert W Schmid-Schönbein; Daniel T O'Connor
Journal:  Blood Press       Date:  2011-03-23       Impact factor: 2.835

2.  Novel genes on rat chromosome 10 are linked to body fat mass, preadipocyte number and adipocyte size.

Authors:  A Weingarten; L Turchetti; K Krohn; I Klöting; M Kern; P Kovacs; M Stumvoll; M Blüher; N Klöting
Journal:  Int J Obes (Lond)       Date:  2016-07-27       Impact factor: 5.095

Review 3.  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

4.  Single-Nucleotide Polymorphisms (SNPs) Both Associated with Hypertension and Contributing to Accelerated-Senescence Traits in OXYS Rats.

Authors:  Vasiliy A Devyatkin; Olga E Redina; Natalia A Muraleva; Nataliya G Kolosova
Journal:  Int J Mol Sci       Date:  2020-05-17       Impact factor: 5.923

5.  Dahl (S x R) congenic strain analysis confirms and defines a chromosome 5 female-specific blood pressure quantitative trait locus to <7 Mbp.

Authors:  Victoria L M Herrera; Khristine A Pasion; Ann Marie Moran; Nelson Ruiz-Opazo
Journal:  PLoS One       Date:  2012-07-30       Impact factor: 3.240

  5 in total

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