Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy

<p>Abstract</p> <p>Background</p> <p>The Down syndrome phenotype has been attributed to overexpression of chromosome 21 (Hsa21) genes. However, the expression profile of Hsa21 genes in trisomic human subjects as well as their effects on genes located on different chromo...

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Main Authors: Olla Carlo, D'Armiento Maria, Genesio Rita, Greco Dario, Negri Rosa, D'Agostino Paola, Fabbrini Floriana, Conti Anna, Paladini Dario, Zannini Mariastella, Nitsch Lucio
Format: Article
Language:English
Published: BMC 2007-08-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/8/268
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spelling doaj-c2c883b2523a444e948ab266b41587392020-11-24T20:55:01ZengBMCBMC Genomics1471-21642007-08-018126810.1186/1471-2164-8-268Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomyOlla CarloD'Armiento MariaGenesio RitaGreco DarioNegri RosaD'Agostino PaolaFabbrini FlorianaConti AnnaPaladini DarioZannini MariastellaNitsch Lucio<p>Abstract</p> <p>Background</p> <p>The Down syndrome phenotype has been attributed to overexpression of chromosome 21 (Hsa21) genes. However, the expression profile of Hsa21 genes in trisomic human subjects as well as their effects on genes located on different chromosomes are largely unknown. Using oligonucleotide microarrays we compared the gene expression profiles of hearts of human fetuses with and without Hsa21 trisomy.</p> <p>Results</p> <p>Approximately half of the 15,000 genes examined (87 of the 168 genes on Hsa21) were expressed in the heart at 18–22 weeks of gestation. Hsa21 gene expression was globally upregulated 1.5 fold in trisomic samples. However, not all genes were equally dysregulated and 25 genes were not upregulated at all. Genes located on other chromosomes were also significantly dysregulated. Functional class scoring and gene set enrichment analyses of 473 genes, differentially expressed between trisomic and non-trisomic hearts, revealed downregulation of genes encoding mitochondrial enzymes and upregulation of genes encoding extracellular matrix proteins. There were no significant differences between trisomic fetuses with and without heart defects.</p> <p>Conclusion</p> <p>We conclude that dosage-dependent upregulation of Hsa21 genes causes dysregulation of the genes responsible for mitochondrial function and for the extracellular matrix organization in the fetal heart of trisomic subjects. These alterations might be harbingers of the heart defects associated with Hsa21 trisomy, which could be based on elusive mechanisms involving genetic variability, environmental factors and/or stochastic events.</p> http://www.biomedcentral.com/1471-2164/8/268
collection DOAJ
language English
format Article
sources DOAJ
author Olla Carlo
D'Armiento Maria
Genesio Rita
Greco Dario
Negri Rosa
D'Agostino Paola
Fabbrini Floriana
Conti Anna
Paladini Dario
Zannini Mariastella
Nitsch Lucio
spellingShingle Olla Carlo
D'Armiento Maria
Genesio Rita
Greco Dario
Negri Rosa
D'Agostino Paola
Fabbrini Floriana
Conti Anna
Paladini Dario
Zannini Mariastella
Nitsch Lucio
Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
BMC Genomics
author_facet Olla Carlo
D'Armiento Maria
Genesio Rita
Greco Dario
Negri Rosa
D'Agostino Paola
Fabbrini Floriana
Conti Anna
Paladini Dario
Zannini Mariastella
Nitsch Lucio
author_sort Olla Carlo
title Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
title_short Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
title_full Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
title_fullStr Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
title_full_unstemmed Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
title_sort altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2007-08-01
description <p>Abstract</p> <p>Background</p> <p>The Down syndrome phenotype has been attributed to overexpression of chromosome 21 (Hsa21) genes. However, the expression profile of Hsa21 genes in trisomic human subjects as well as their effects on genes located on different chromosomes are largely unknown. Using oligonucleotide microarrays we compared the gene expression profiles of hearts of human fetuses with and without Hsa21 trisomy.</p> <p>Results</p> <p>Approximately half of the 15,000 genes examined (87 of the 168 genes on Hsa21) were expressed in the heart at 18–22 weeks of gestation. Hsa21 gene expression was globally upregulated 1.5 fold in trisomic samples. However, not all genes were equally dysregulated and 25 genes were not upregulated at all. Genes located on other chromosomes were also significantly dysregulated. Functional class scoring and gene set enrichment analyses of 473 genes, differentially expressed between trisomic and non-trisomic hearts, revealed downregulation of genes encoding mitochondrial enzymes and upregulation of genes encoding extracellular matrix proteins. There were no significant differences between trisomic fetuses with and without heart defects.</p> <p>Conclusion</p> <p>We conclude that dosage-dependent upregulation of Hsa21 genes causes dysregulation of the genes responsible for mitochondrial function and for the extracellular matrix organization in the fetal heart of trisomic subjects. These alterations might be harbingers of the heart defects associated with Hsa21 trisomy, which could be based on elusive mechanisms involving genetic variability, environmental factors and/or stochastic events.</p>
url http://www.biomedcentral.com/1471-2164/8/268
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