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Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

Identifieur interne : 005A02 ( Main/Exploration ); précédent : 005A01; suivant : 005A03

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

Auteurs : Rachel Soemedi [Royaume-Uni] ; Ana Topf [Royaume-Uni] ; Ian J. Wilson [Royaume-Uni] ; Rebecca Darlay [Royaume-Uni] ; Thahira Rahman [Royaume-Uni] ; Elise Glen [Royaume-Uni] ; Darroch Hall [Royaume-Uni] ; NI HUANG [Royaume-Uni] ; Jamie Bentham [Royaume-Uni] ; Shoumo Bhattacharya [Royaume-Uni] ; Catherine Cosgrove [Royaume-Uni] ; J. David Brook [Royaume-Uni] ; Javier Granados-Riveron [Royaume-Uni] ; Kerry Setchfield [Royaume-Uni] ; Frances Bu'Lock [Royaume-Uni] ; Chris Thornborough [Royaume-Uni] ; Koenraad Devriendt [Belgique] ; Jeroen Breckpot [Belgique] ; Michael Hofbeck [Allemagne] ; Mark Lathrop [France] ; Anita Rauch [Suisse] ; Gillian M. Blue [Australie] ; David S. Winlaw [Australie] ; Matthew Hurles [Royaume-Uni] ; Mauro Santibanez-Koref [Royaume-Uni] ; Heather J. Cordell [Royaume-Uni] ; Judith A. Goodship [Royaume-Uni] ; Bernard D. Keavney [Royaume-Uni]

Source :

RBID : Pascal:12-0146760

Descripteurs français

English descriptors

Abstract

Recurrent rearrangements of chromosome 1q21.1 that occur via non-allelic homologous recombination have been associated with variable phenotypes exhibiting incomplete penetrance, including congenital heart disease (CHD). However, the gene or genes within the ˜1 Mb critical region responsible for each of the associated phenotypes remains unknown. We examined the 1 q21.1 locus in 948 patients with tetralogy of Fallot (TOF), 1488 patients with other forms of CHD and 6760 ethnically matched controls using single nucleotide polymorphism genotyping arrays (Illumina 660W and Affymetrix 6.0) and multiplex ligation-dependent probe amplification. We found that duplication of 1q21.1 was more common in cases of TOF than in controls [odds ratio (OR) 30.9, 95% confidence interval (CI) 8.9-107.6); P = 2.2 x 10-7], but deletion was not. In contrast, deletion of 1q21.1 was more common in cases of non-TOF CHD than in controls [OR 5.5 (95% CI 1.4-22.0); P = 0.04] while duplication was not. We also detected rare (n = 3) 100-200 kb duplications within the critical region of 1q21.1 in cases of TOF. These small duplications encompassed a single gene in common, GJA5, and were enriched in cases of TOF in comparison to controls [OR = 10.7 (95% CI 1.8-64.3), P = 0.01]. These findings show that duplication and deletion at chromosome 1q21.1 exhibit a degree of phenotypic specificity in CHD, and implicate GJA5 as the gene responsible for the CHD phenotypes observed with copy number imbalances at this locus.


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<title xml:lang="en" level="a">Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls</title>
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<name sortKey="Soemedi, Rachel" sort="Soemedi, Rachel" uniqKey="Soemedi R" first="Rachel" last="Soemedi">Rachel Soemedi</name>
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<country>Belgique</country>
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<country>Belgique</country>
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<country>Allemagne</country>
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<s1>Commissariat a I'Energie Atomique</s1>
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<country>Suisse</country>
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<country>Australie</country>
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<sZ>25 aut.</sZ>
<sZ>26 aut.</sZ>
<sZ>27 aut.</sZ>
<sZ>28 aut.</sZ>
</inist:fA14>
<country>Royaume-Uni</country>
<wicri:noRegion>Newcastle</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Human molecular genetics : (Print)</title>
<title level="j" type="abbreviated">Hum. mol. genet. : (Print)</title>
<idno type="ISSN">0964-6906</idno>
<imprint>
<date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Human molecular genetics : (Print)</title>
<title level="j" type="abbreviated">Hum. mol. genet. : (Print)</title>
<idno type="ISSN">0964-6906</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Chromosome</term>
<term>Congenital cardiopathy</term>
<term>Duplication</term>
<term>Gene rearrangement</term>
<term>Genetics</term>
<term>Human</term>
<term>Phenotype</term>
<term>Regulation(control)</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Phénotype</term>
<term>Chromosome</term>
<term>Génétique</term>
<term>Réarrangement génique</term>
<term>Duplication</term>
<term>Homme</term>
<term>Régulation</term>
<term>Cardiopathie congénitale</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Génétique</term>
<term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Recurrent rearrangements of chromosome 1q21.1 that occur via non-allelic homologous recombination have been associated with variable phenotypes exhibiting incomplete penetrance, including congenital heart disease (CHD). However, the gene or genes within the ˜1 Mb critical region responsible for each of the associated phenotypes remains unknown. We examined the 1 q21.1 locus in 948 patients with tetralogy of Fallot (TOF), 1488 patients with other forms of CHD and 6760 ethnically matched controls using single nucleotide polymorphism genotyping arrays (Illumina 660W and Affymetrix 6.0) and multiplex ligation-dependent probe amplification. We found that duplication of 1q21.1 was more common in cases of TOF than in controls [odds ratio (OR) 30.9, 95% confidence interval (CI) 8.9-107.6); P = 2.2 x 10
<sup>-7</sup>
], but deletion was not. In contrast, deletion of 1q21.1 was more common in cases of non-TOF CHD than in controls [OR 5.5 (95% CI 1.4-22.0); P = 0.04] while duplication was not. We also detected rare (n = 3) 100-200 kb duplications within the critical region of 1q21.1 in cases of TOF. These small duplications encompassed a single gene in common, GJA5, and were enriched in cases of TOF in comparison to controls [OR = 10.7 (95% CI 1.8-64.3), P = 0.01]. These findings show that duplication and deletion at chromosome 1q21.1 exhibit a degree of phenotypic specificity in CHD, and implicate GJA5 as the gene responsible for the CHD phenotypes observed with copy number imbalances at this locus.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Allemagne</li>
<li>Australie</li>
<li>Belgique</li>
<li>France</li>
<li>Royaume-Uni</li>
<li>Suisse</li>
</country>
<region>
<li>Angleterre</li>
<li>Canton de Zurich</li>
<li>Nottinghamshire</li>
<li>Nouvelle-Galles du Sud</li>
<li>Oxfordshire</li>
<li>Île-de-France</li>
</region>
<settlement>
<li>Nottingham</li>
<li>Oxford</li>
<li>Sydney</li>
<li>Zurich</li>
<li>Évry (Essonne)</li>
</settlement>
<orgName>
<li>Université d'Oxford</li>
<li>Université de Nottingham</li>
<li>Université de Zurich</li>
</orgName>
</list>
<tree>
<country name="Royaume-Uni">
<noRegion>
<name sortKey="Soemedi, Rachel" sort="Soemedi, Rachel" uniqKey="Soemedi R" first="Rachel" last="Soemedi">Rachel Soemedi</name>
</noRegion>
<name sortKey="Bentham, Jamie" sort="Bentham, Jamie" uniqKey="Bentham J" first="Jamie" last="Bentham">Jamie Bentham</name>
<name sortKey="Bhattacharya, Shoumo" sort="Bhattacharya, Shoumo" uniqKey="Bhattacharya S" first="Shoumo" last="Bhattacharya">Shoumo Bhattacharya</name>
<name sortKey="Brook, J David" sort="Brook, J David" uniqKey="Brook J" first="J. David" last="Brook">J. David Brook</name>
<name sortKey="Bu Lock, Frances" sort="Bu Lock, Frances" uniqKey="Bu Lock F" first="Frances" last="Bu'Lock">Frances Bu'Lock</name>
<name sortKey="Cordell, Heather J" sort="Cordell, Heather J" uniqKey="Cordell H" first="Heather J." last="Cordell">Heather J. Cordell</name>
<name sortKey="Cosgrove, Catherine" sort="Cosgrove, Catherine" uniqKey="Cosgrove C" first="Catherine" last="Cosgrove">Catherine Cosgrove</name>
<name sortKey="Darlay, Rebecca" sort="Darlay, Rebecca" uniqKey="Darlay R" first="Rebecca" last="Darlay">Rebecca Darlay</name>
<name sortKey="Glen, Elise" sort="Glen, Elise" uniqKey="Glen E" first="Elise" last="Glen">Elise Glen</name>
<name sortKey="Goodship, Judith A" sort="Goodship, Judith A" uniqKey="Goodship J" first="Judith A." last="Goodship">Judith A. Goodship</name>
<name sortKey="Granados Riveron, Javier" sort="Granados Riveron, Javier" uniqKey="Granados Riveron J" first="Javier" last="Granados-Riveron">Javier Granados-Riveron</name>
<name sortKey="Hall, Darroch" sort="Hall, Darroch" uniqKey="Hall D" first="Darroch" last="Hall">Darroch Hall</name>
<name sortKey="Hurles, Matthew" sort="Hurles, Matthew" uniqKey="Hurles M" first="Matthew" last="Hurles">Matthew Hurles</name>
<name sortKey="Keavney, Bernard D" sort="Keavney, Bernard D" uniqKey="Keavney B" first="Bernard D." last="Keavney">Bernard D. Keavney</name>
<name sortKey="Ni Huang" sort="Ni Huang" uniqKey="Ni Huang" last="Ni Huang">NI HUANG</name>
<name sortKey="Rahman, Thahira" sort="Rahman, Thahira" uniqKey="Rahman T" first="Thahira" last="Rahman">Thahira Rahman</name>
<name sortKey="Santibanez Koref, Mauro" sort="Santibanez Koref, Mauro" uniqKey="Santibanez Koref M" first="Mauro" last="Santibanez-Koref">Mauro Santibanez-Koref</name>
<name sortKey="Setchfield, Kerry" sort="Setchfield, Kerry" uniqKey="Setchfield K" first="Kerry" last="Setchfield">Kerry Setchfield</name>
<name sortKey="Thornborough, Chris" sort="Thornborough, Chris" uniqKey="Thornborough C" first="Chris" last="Thornborough">Chris Thornborough</name>
<name sortKey="Topf, Ana" sort="Topf, Ana" uniqKey="Topf A" first="Ana" last="Topf">Ana Topf</name>
<name sortKey="Wilson, Ian J" sort="Wilson, Ian J" uniqKey="Wilson I" first="Ian J." last="Wilson">Ian J. Wilson</name>
</country>
<country name="Belgique">
<noRegion>
<name sortKey="Devriendt, Koenraad" sort="Devriendt, Koenraad" uniqKey="Devriendt K" first="Koenraad" last="Devriendt">Koenraad Devriendt</name>
</noRegion>
<name sortKey="Breckpot, Jeroen" sort="Breckpot, Jeroen" uniqKey="Breckpot J" first="Jeroen" last="Breckpot">Jeroen Breckpot</name>
</country>
<country name="Allemagne">
<noRegion>
<name sortKey="Hofbeck, Michael" sort="Hofbeck, Michael" uniqKey="Hofbeck M" first="Michael" last="Hofbeck">Michael Hofbeck</name>
</noRegion>
</country>
<country name="France">
<region name="Île-de-France">
<name sortKey="Lathrop, Mark" sort="Lathrop, Mark" uniqKey="Lathrop M" first="Mark" last="Lathrop">Mark Lathrop</name>
</region>
</country>
<country name="Suisse">
<region name="Canton de Zurich">
<name sortKey="Rauch, Anita" sort="Rauch, Anita" uniqKey="Rauch A" first="Anita" last="Rauch">Anita Rauch</name>
</region>
</country>
<country name="Australie">
<region name="Nouvelle-Galles du Sud">
<name sortKey="Blue, Gillian M" sort="Blue, Gillian M" uniqKey="Blue G" first="Gillian M." last="Blue">Gillian M. Blue</name>
</region>
<name sortKey="Winlaw, David S" sort="Winlaw, David S" uniqKey="Winlaw D" first="David S." last="Winlaw">David S. Winlaw</name>
</country>
</tree>
</affiliations>
</record>

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