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Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3
BACKGROUND: We have previously confirmed the importance of rat chromosome 3 (RNO3) genetic loci on blood pressure elevation, pulse pressure (PP) variability and renal pathology during salt challenge in the stroke-prone spontaneously hypertensive (SHRSP) rat. The aims of this study were to generate a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214373/ https://www.ncbi.nlm.nih.gov/pubmed/27755386 http://dx.doi.org/10.1097/HJH.0000000000001155 |
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author | Koh-Tan, H.H. Caline Dashti, Mohammed Wang, Ting Beattie, Wendy Mcclure, John Young, Barbara Dominiczak, Anna F. McBride, Martin W. Graham, Delyth |
author_facet | Koh-Tan, H.H. Caline Dashti, Mohammed Wang, Ting Beattie, Wendy Mcclure, John Young, Barbara Dominiczak, Anna F. McBride, Martin W. Graham, Delyth |
author_sort | Koh-Tan, H.H. Caline |
collection | PubMed |
description | BACKGROUND: We have previously confirmed the importance of rat chromosome 3 (RNO3) genetic loci on blood pressure elevation, pulse pressure (PP) variability and renal pathology during salt challenge in the stroke-prone spontaneously hypertensive (SHRSP) rat. The aims of this study were to generate a panel of RNO3 congenic sub-strains to genetically dissect the implicated loci and identify positional candidate genes by microarray expression profiling and analysis of next-generation sequencing data. METHOD AND RESULTS: A panel of congenic sub-strains were generated containing Wistar–Kyoto (WKY)-introgressed segments of varying size on the SHRSP genetic background, focused within the first 50 Mbp of RNO3. Haemodynamic profiling during salt challenge demonstrated significantly reduced systolic blood pressure, diastolic blood pressure and PP variability in SP.WKYGla3a, SP.WKYGla3c, SP.WKYGla3d and SP.WKYGla3e sub-strains. Only SBP and DBP were significantly reduced during salt challenge in SP.WKYGla3b and SP.WKYGla3f sub-strains, whereas SP.WKYGla3g rats did not differ in haemodynamic response to SHRSP. Those sub-strains demonstrating significantly reduced PP variability during salt challenge also demonstrated significantly reduced renal pathology and proteinuria. Microarray expression profiling prioritized two candidate genes for blood pressure regulation (Dnm1, Tor1b), localized within the common congenic interval shared by SP.WKYGla3d and SP.WKYGla3f strains, and one candidate gene for salt-induced PP variability and renal pathology (Rabgap1), located within the region unique to the SP.WKYGla3d strain. Comparison of next-generation sequencing data identified variants within additional positional genes that are likely to affect protein function. CONCLUSION: This study has identified distinct intervals on RNO3-containing genes that may be important for blood pressure regulation and renal pathology during salt challenge. |
format | Online Article Text |
id | pubmed-5214373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-52143732017-01-17 Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 Koh-Tan, H.H. Caline Dashti, Mohammed Wang, Ting Beattie, Wendy Mcclure, John Young, Barbara Dominiczak, Anna F. McBride, Martin W. Graham, Delyth J Hypertens ORIGINAL PAPERS: Genetic aspects BACKGROUND: We have previously confirmed the importance of rat chromosome 3 (RNO3) genetic loci on blood pressure elevation, pulse pressure (PP) variability and renal pathology during salt challenge in the stroke-prone spontaneously hypertensive (SHRSP) rat. The aims of this study were to generate a panel of RNO3 congenic sub-strains to genetically dissect the implicated loci and identify positional candidate genes by microarray expression profiling and analysis of next-generation sequencing data. METHOD AND RESULTS: A panel of congenic sub-strains were generated containing Wistar–Kyoto (WKY)-introgressed segments of varying size on the SHRSP genetic background, focused within the first 50 Mbp of RNO3. Haemodynamic profiling during salt challenge demonstrated significantly reduced systolic blood pressure, diastolic blood pressure and PP variability in SP.WKYGla3a, SP.WKYGla3c, SP.WKYGla3d and SP.WKYGla3e sub-strains. Only SBP and DBP were significantly reduced during salt challenge in SP.WKYGla3b and SP.WKYGla3f sub-strains, whereas SP.WKYGla3g rats did not differ in haemodynamic response to SHRSP. Those sub-strains demonstrating significantly reduced PP variability during salt challenge also demonstrated significantly reduced renal pathology and proteinuria. Microarray expression profiling prioritized two candidate genes for blood pressure regulation (Dnm1, Tor1b), localized within the common congenic interval shared by SP.WKYGla3d and SP.WKYGla3f strains, and one candidate gene for salt-induced PP variability and renal pathology (Rabgap1), located within the region unique to the SP.WKYGla3d strain. Comparison of next-generation sequencing data identified variants within additional positional genes that are likely to affect protein function. CONCLUSION: This study has identified distinct intervals on RNO3-containing genes that may be important for blood pressure regulation and renal pathology during salt challenge. Lippincott Williams & Wilkins 2017-02 2017-01-04 /pmc/articles/PMC5214373/ /pubmed/27755386 http://dx.doi.org/10.1097/HJH.0000000000001155 Text en Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | ORIGINAL PAPERS: Genetic aspects Koh-Tan, H.H. Caline Dashti, Mohammed Wang, Ting Beattie, Wendy Mcclure, John Young, Barbara Dominiczak, Anna F. McBride, Martin W. Graham, Delyth Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
title | Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
title_full | Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
title_fullStr | Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
title_full_unstemmed | Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
title_short | Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
title_sort | dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3 |
topic | ORIGINAL PAPERS: Genetic aspects |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214373/ https://www.ncbi.nlm.nih.gov/pubmed/27755386 http://dx.doi.org/10.1097/HJH.0000000000001155 |
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