» Articles » PMID: 21979154

Copy-number Variation: the Balance Between Gene Dosage and Expression in Drosophila Melanogaster

Overview
Date 2011 Oct 8
PMID 21979154
Citations 59
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Identify Candidate Genes Associated with the Weight and Egg Quality Traits in Wenshui Green Shell-Laying Chickens by the Copy Number Variation-Based Genome-Wide Association Study.

Yang S, Ning C, Yang C, Li W, Zhang Q, Wang D Vet Sci. 2024; 11(2).

PMID: 38393094 PMC: 10892766. DOI: 10.3390/vetsci11020076.


From genomic spectrum of NTRK genes to adverse effects of its inhibitors, a comprehensive genome-based and real-world pharmacovigilance analysis.

Cui Z, Zhai Z, Xie D, Wang L, Cheng F, Lou S Front Pharmacol. 2024; 15:1329409.

PMID: 38357305 PMC: 10864613. DOI: 10.3389/fphar.2024.1329409.


Paralog transcriptional differentiation in the D. melanogaster-specific gene family Sdic across populations and spermatogenesis stages.

Clifton B, Hariyani I, Kimura A, Luo F, Nguyen A, Ranz J Commun Biol. 2023; 6(1):1069.

PMID: 37864070 PMC: 10589255. DOI: 10.1038/s42003-023-05427-4.


Genome-wide identification of candidate copy number polymorphism genes associated with complex traits of Tibetan-sheep.

Tian D, Sun D, Ren Q, Zhang P, Zhang Z, Zhang W Sci Rep. 2023; 13(1):17283.

PMID: 37828092 PMC: 10570297. DOI: 10.1038/s41598-023-44402-1.


Rapid molecular diversification and homogenization of clustered major ampullate silk genes in Argiope garden spiders.

Baker R, Corvelo A, Hayashi C PLoS Genet. 2022; 18(12):e1010537.

PMID: 36508456 PMC: 9779670. DOI: 10.1371/journal.pgen.1010537.


References
1.
Veitia R . Exploring the etiology of haploinsufficiency. Bioessays. 2002; 24(2):175-84. DOI: 10.1002/bies.10023. View

2.
Barker D, Schafer M, White R . Restriction sites containing CpG show a higher frequency of polymorphism in human DNA. Cell. 1984; 36(1):131-8. DOI: 10.1016/0092-8674(84)90081-3. View

3.
Feuk L, Carson A, Scherer S . Structural variation in the human genome. Nat Rev Genet. 2006; 7(2):85-97. DOI: 10.1038/nrg1767. View

4.
DeBolt S . Copy number variation shapes genome diversity in Arabidopsis over immediate family generational scales. Genome Biol Evol. 2010; 2:441-53. PMC: 2997553. DOI: 10.1093/gbe/evq033. View

5.
Beckmann J, Estivill X, Antonarakis S . Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability. Nat Rev Genet. 2007; 8(8):639-46. DOI: 10.1038/nrg2149. View