The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats

<p>Abstract</p> <p>Background</p> <p>Elevated plant sterol accumulation has been reported in the spontaneously hypertensive rat (SHR), the stroke-prone spontaneously hypertensive rat (SHRSP) and the Wistar-Kyoto (WKY) rat. Additionally, a blood pressure quantitative tra...

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Main Authors: Klein Richard, Sato Masao, Egashira Nami, Ikeda Ikuo, Helou Khalil, Lu Kangmo, Lee Mi-Hye, Klett Eric, Pandit Bhaswati, Yu Hongwei, Batta Ashok, Salen Gerald, Patel Shailendra B
Format: Article
Language:English
Published: BMC 2003-06-01
Series:BMC Cardiovascular Disorders
Online Access:http://www.biomedcentral.com/1471-2261/3/4
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spelling doaj-805a96ed78a8484faeec2a681b8587a32020-11-25T03:07:17ZengBMCBMC Cardiovascular Disorders1471-22612003-06-0131410.1186/1471-2261-3-4The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive ratsKlein RichardSato MasaoEgashira NamiIkeda IkuoHelou KhalilLu KangmoLee Mi-HyeKlett EricPandit BhaswatiYu HongweiBatta AshokSalen GeraldPatel Shailendra B<p>Abstract</p> <p>Background</p> <p>Elevated plant sterol accumulation has been reported in the spontaneously hypertensive rat (SHR), the stroke-prone spontaneously hypertensive rat (SHRSP) and the Wistar-Kyoto (WKY) rat. Additionally, a blood pressure quantitative trait locus (QTL) has been mapped to rat chromosome 6 in a New Zealand genetically hypertensive rat strain (GH rat). ABCG5 and ABCG8 (encoding sterolin-1 and sterolin-2 respectively) have been shown to be responsible for causing sitosterolemia in humans. These genes are organized in a head-to-head configuration at the <it>STSL </it>locus on human chromosome 2p21.</p> <p>Methods</p> <p>To investigate whether mutations in <it>Abcg5</it> or <it>Abcg8</it> exist in SHR, SHRSP, WKY and GH rats, we initiated a systematic search for the genetic variation in coding and non-coding region of <it>Abcg5</it> and <it>Abcg8</it> genes in these strains. We isolated the rat cDNAs for these genes and characterized the genomic structure and tissue expression patterns, using standard molecular biology techniques and FISH for chromosomal assignments.</p> <p>Results</p> <p>Both rat <it>Abcg5</it> and <it>Abcg8</it> genes map to chromosome band 6q12. These genes span ~40 kb and contain 13 exons and 12 introns each, in a pattern identical to that of the <it>STSL </it>loci in mouse and man. Both <it>Abcg5</it> and <it>Abcg8</it> were expressed only in liver and intestine. Analyses of DNA from SHR, SHRSP, GH, WKY, Wistar, Wistar King A (WKA) and Brown Norway (BN) rat strains revealed a homozygous G to T substitution at nucleotide 1754, resulting in the coding change Gly583Cys in sterolin-1 only in rats that are both sitosterolemic and hypertensive (SHR, SHRSP and WKY).</p> <p>Conclusions</p> <p>The rat <it>STSL </it>locus maps to chromosome 6q12. A non-synonymous mutation in <it>Abcg5</it>, Gly583Cys, results in sitosterolemia in rat strains that are also hypertensive (WKY, SHR and SHRSP). Those rat strains that are hypertensive, but not sitosterolemic (e.g. GH rat) do not have mutations in <it>Abcg5 </it>or <it>Abcg8</it>. This mutation allows for expression and apparent apical targeting of <it>Abcg5</it> protein in the intestine. These rat strains may therefore allow us to study the pathophysiological mechanisms involved in the human disease of sitosterolemia.</p> http://www.biomedcentral.com/1471-2261/3/4
collection DOAJ
language English
format Article
sources DOAJ
author Klein Richard
Sato Masao
Egashira Nami
Ikeda Ikuo
Helou Khalil
Lu Kangmo
Lee Mi-Hye
Klett Eric
Pandit Bhaswati
Yu Hongwei
Batta Ashok
Salen Gerald
Patel Shailendra B
spellingShingle Klein Richard
Sato Masao
Egashira Nami
Ikeda Ikuo
Helou Khalil
Lu Kangmo
Lee Mi-Hye
Klett Eric
Pandit Bhaswati
Yu Hongwei
Batta Ashok
Salen Gerald
Patel Shailendra B
The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
BMC Cardiovascular Disorders
author_facet Klein Richard
Sato Masao
Egashira Nami
Ikeda Ikuo
Helou Khalil
Lu Kangmo
Lee Mi-Hye
Klett Eric
Pandit Bhaswati
Yu Hongwei
Batta Ashok
Salen Gerald
Patel Shailendra B
author_sort Klein Richard
title The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
title_short The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
title_full The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
title_fullStr The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
title_full_unstemmed The rat <it>STSL </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
title_sort rat <it>stsl </it>locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats
publisher BMC
series BMC Cardiovascular Disorders
issn 1471-2261
publishDate 2003-06-01
description <p>Abstract</p> <p>Background</p> <p>Elevated plant sterol accumulation has been reported in the spontaneously hypertensive rat (SHR), the stroke-prone spontaneously hypertensive rat (SHRSP) and the Wistar-Kyoto (WKY) rat. Additionally, a blood pressure quantitative trait locus (QTL) has been mapped to rat chromosome 6 in a New Zealand genetically hypertensive rat strain (GH rat). ABCG5 and ABCG8 (encoding sterolin-1 and sterolin-2 respectively) have been shown to be responsible for causing sitosterolemia in humans. These genes are organized in a head-to-head configuration at the <it>STSL </it>locus on human chromosome 2p21.</p> <p>Methods</p> <p>To investigate whether mutations in <it>Abcg5</it> or <it>Abcg8</it> exist in SHR, SHRSP, WKY and GH rats, we initiated a systematic search for the genetic variation in coding and non-coding region of <it>Abcg5</it> and <it>Abcg8</it> genes in these strains. We isolated the rat cDNAs for these genes and characterized the genomic structure and tissue expression patterns, using standard molecular biology techniques and FISH for chromosomal assignments.</p> <p>Results</p> <p>Both rat <it>Abcg5</it> and <it>Abcg8</it> genes map to chromosome band 6q12. These genes span ~40 kb and contain 13 exons and 12 introns each, in a pattern identical to that of the <it>STSL </it>loci in mouse and man. Both <it>Abcg5</it> and <it>Abcg8</it> were expressed only in liver and intestine. Analyses of DNA from SHR, SHRSP, GH, WKY, Wistar, Wistar King A (WKA) and Brown Norway (BN) rat strains revealed a homozygous G to T substitution at nucleotide 1754, resulting in the coding change Gly583Cys in sterolin-1 only in rats that are both sitosterolemic and hypertensive (SHR, SHRSP and WKY).</p> <p>Conclusions</p> <p>The rat <it>STSL </it>locus maps to chromosome 6q12. A non-synonymous mutation in <it>Abcg5</it>, Gly583Cys, results in sitosterolemia in rat strains that are also hypertensive (WKY, SHR and SHRSP). Those rat strains that are hypertensive, but not sitosterolemic (e.g. GH rat) do not have mutations in <it>Abcg5 </it>or <it>Abcg8</it>. This mutation allows for expression and apparent apical targeting of <it>Abcg5</it> protein in the intestine. These rat strains may therefore allow us to study the pathophysiological mechanisms involved in the human disease of sitosterolemia.</p>
url http://www.biomedcentral.com/1471-2261/3/4
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