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Gene mapping and genome-wide discovery approaches in the spontaneously hypertensive rat have yielded limited progress in understanding the genetic basis of hypertension.
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This review highlights the limited progress and ongoing challenges in using the spontaneously hypertensive rat model to map the polygenic basis of hypertension.
The application of gene mapping methods to uncover the genetic basis of hypertension in the inbred spontaneously hypertensive rat (SHR) began over 25 yr ago. This animal provides a useful model of genetic high blood pressure, and some of its features are described. In particular, it appears to be a polygenic model of disease, and polygenes participate in human hypertension genetic risk. The SHR hypertension alleles were fixed rapidly by selective breeding in just a few generations and so are presumably common genetic variants present in the outbred Wistar strain from which SHR was created. This review provides a background to the origins and genesis of this rat line. It considers its usefulness as a model organism for a common cardiovascular disease. The progress and obstacles facing mapping are considered in depth, as are the emergence and application of other genome-wide genetic discovery approaches that have been applied to investigate this model. Candidate genes, their identification, and the evidence to support their potential role in blood pressure elevation are considered. The review assesses the progress that has arisen from this work has been limited. Consideration is given to some of the factors that have impeded progress, and prospects for advancing understanding of the genetic basis of hypertension in this model are discussed.
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Peter A. Doris (2017) conducted a review in Hypertension. Gene mapping and genome-wide genetic discovery approaches was evaluated. Gene mapping and genome-wide discovery approaches in the spontaneously hypertensive rat have yielded limited progress in understanding the genetic basis of hypertension.
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