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Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster

Copy-number variants (CNVs) reshape gene structure, modulate gene expression, and contribute to significant phenotypic variation. Previous studies have revealed CNV patterns in natural populations of Drosophila melanogaster and suggested that selection and mutational bias shape genomic patterns of C...

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Autores principales: Zhou, Jun, Lemos, Bernardo, Dopman, Erik B., Hartl, Daniel L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227403/
https://www.ncbi.nlm.nih.gov/pubmed/21979154
http://dx.doi.org/10.1093/gbe/evr023
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author Zhou, Jun
Lemos, Bernardo
Dopman, Erik B.
Hartl, Daniel L.
author_facet Zhou, Jun
Lemos, Bernardo
Dopman, Erik B.
Hartl, Daniel L.
author_sort Zhou, Jun
collection PubMed
description Copy-number variants (CNVs) reshape gene structure, modulate gene expression, and contribute to significant phenotypic variation. Previous studies have revealed CNV patterns in natural populations of Drosophila melanogaster and suggested that selection and mutational bias shape genomic patterns of CNV. Although previous CNV studies focused on heterogeneous strains, here, we established a number of second-chromosome substitution lines to uncover CNV characteristics when homozygous. The percentage of genes harboring CNVs is higher than found in previous studies. More CNVs are detected in homozygous than heterozygous substitution strains, suggesting the comparative genomic hybridization arrays underestimate CNV owing to heterozygous masking. We incorporated previous gene expression data collected from some of the same substitution lines to investigate relationships between CNV gene dosage and expression. Most genes present in CNVs show no evidence of increased or diminished transcription, and the fraction of such dosage-insensitive CNVs is greater in heterozygotes. More than 70% of the dosage-sensitive CNVs are recessive with undetectable effects on transcription in heterozygotes. A deficiency of singletons in recessive dosage-sensitive CNVs supports the hypothesis that most CNVs are subject to negative selection. On the other hand, relaxed purifying selection might account for the higher number of protein–protein interactions in dosage-insensitive CNVs than in dosage-sensitive CNVs. Dosage-sensitive CNVs that are upregulated and downregulated coincide with copy-number increases and decreases. Our results help clarify the relation between CNV dosage and gene expression in the D. melanogaster genome.
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spelling pubmed-32274032011-11-30 Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster Zhou, Jun Lemos, Bernardo Dopman, Erik B. Hartl, Daniel L. Genome Biol Evol Special Collection Copy-number variants (CNVs) reshape gene structure, modulate gene expression, and contribute to significant phenotypic variation. Previous studies have revealed CNV patterns in natural populations of Drosophila melanogaster and suggested that selection and mutational bias shape genomic patterns of CNV. Although previous CNV studies focused on heterogeneous strains, here, we established a number of second-chromosome substitution lines to uncover CNV characteristics when homozygous. The percentage of genes harboring CNVs is higher than found in previous studies. More CNVs are detected in homozygous than heterozygous substitution strains, suggesting the comparative genomic hybridization arrays underestimate CNV owing to heterozygous masking. We incorporated previous gene expression data collected from some of the same substitution lines to investigate relationships between CNV gene dosage and expression. Most genes present in CNVs show no evidence of increased or diminished transcription, and the fraction of such dosage-insensitive CNVs is greater in heterozygotes. More than 70% of the dosage-sensitive CNVs are recessive with undetectable effects on transcription in heterozygotes. A deficiency of singletons in recessive dosage-sensitive CNVs supports the hypothesis that most CNVs are subject to negative selection. On the other hand, relaxed purifying selection might account for the higher number of protein–protein interactions in dosage-insensitive CNVs than in dosage-sensitive CNVs. Dosage-sensitive CNVs that are upregulated and downregulated coincide with copy-number increases and decreases. Our results help clarify the relation between CNV dosage and gene expression in the D. melanogaster genome. Oxford University Press 2011-10-06 /pmc/articles/PMC3227403/ /pubmed/21979154 http://dx.doi.org/10.1093/gbe/evr023 Text en The Author(s) 2011. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Collection
Zhou, Jun
Lemos, Bernardo
Dopman, Erik B.
Hartl, Daniel L.
Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster
title Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster
title_full Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster
title_fullStr Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster
title_full_unstemmed Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster
title_short Copy-Number Variation: The Balance between Gene Dosage and Expression in Drosophila melanogaster
title_sort copy-number variation: the balance between gene dosage and expression in drosophila melanogaster
topic Special Collection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227403/
https://www.ncbi.nlm.nih.gov/pubmed/21979154
http://dx.doi.org/10.1093/gbe/evr023
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