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Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the Silkworm, Bombyx mori
Dosage compensation—equalizing gene expression levels in response to differences in gene dose or copy number—is classically considered to play a critical role in the evolution of heteromorphic sex chromosomes. As the X and Y diverge through degradation and gene loss on the Y (or the W in female-hete...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296447/ https://www.ncbi.nlm.nih.gov/pubmed/21508430 http://dx.doi.org/10.1093/gbe/evr036 |
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author | Walters, James R. Hardcastle, Thomas J. |
author_facet | Walters, James R. Hardcastle, Thomas J. |
author_sort | Walters, James R. |
collection | PubMed |
description | Dosage compensation—equalizing gene expression levels in response to differences in gene dose or copy number—is classically considered to play a critical role in the evolution of heteromorphic sex chromosomes. As the X and Y diverge through degradation and gene loss on the Y (or the W in female-heterogametic ZW taxa), it is expected that dosage compensation will evolve to correct for sex-specific differences in gene dose. Although this is observed in some organisms, recent genome-wide expression studies in other taxa have revealed striking exceptions. In particular, reports that both birds and the silkworm moth (Bombyx mori) lack dosage compensation have spurred speculation that this is the rule for all female-heterogametic taxa. Here, we revisit the issue of dosage compensation in silkworm by replicating and extending the previous analysis. Contrary to previous reports, our efforts reveal a pattern typically associated with dosage compensated taxa: the global male:female expression ratio does not differ between the Z and autosomes. We believe the previous report of unequal male:female ratios on the Z reflects artifacts of microarray normalization in conjunction with not testing a major assumption that the male:female global expression ratio was unbiased for autosomal loci. However, we also find that the global Z chromosome expression is significantly reduced relative to autosomes, a pattern not expected in dosage compensated taxa. This combination of male:female parity with an overall reduction in expression for sex-linked loci is not consistent with the prevailing evolutionary theory of sex chromosome evolution and dosage compensation. |
format | Online Article Text |
id | pubmed-3296447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32964472012-03-07 Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the Silkworm, Bombyx mori Walters, James R. Hardcastle, Thomas J. Genome Biol Evol Research Article Dosage compensation—equalizing gene expression levels in response to differences in gene dose or copy number—is classically considered to play a critical role in the evolution of heteromorphic sex chromosomes. As the X and Y diverge through degradation and gene loss on the Y (or the W in female-heterogametic ZW taxa), it is expected that dosage compensation will evolve to correct for sex-specific differences in gene dose. Although this is observed in some organisms, recent genome-wide expression studies in other taxa have revealed striking exceptions. In particular, reports that both birds and the silkworm moth (Bombyx mori) lack dosage compensation have spurred speculation that this is the rule for all female-heterogametic taxa. Here, we revisit the issue of dosage compensation in silkworm by replicating and extending the previous analysis. Contrary to previous reports, our efforts reveal a pattern typically associated with dosage compensated taxa: the global male:female expression ratio does not differ between the Z and autosomes. We believe the previous report of unequal male:female ratios on the Z reflects artifacts of microarray normalization in conjunction with not testing a major assumption that the male:female global expression ratio was unbiased for autosomal loci. However, we also find that the global Z chromosome expression is significantly reduced relative to autosomes, a pattern not expected in dosage compensated taxa. This combination of male:female parity with an overall reduction in expression for sex-linked loci is not consistent with the prevailing evolutionary theory of sex chromosome evolution and dosage compensation. Oxford University Press 2011-04-20 /pmc/articles/PMC3296447/ /pubmed/21508430 http://dx.doi.org/10.1093/gbe/evr036 Text en © The Author(s) 2011. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Walters, James R. Hardcastle, Thomas J. Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the Silkworm, Bombyx mori |
title | Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the
Silkworm, Bombyx mori |
title_full | Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the
Silkworm, Bombyx mori |
title_fullStr | Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the
Silkworm, Bombyx mori |
title_full_unstemmed | Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the
Silkworm, Bombyx mori |
title_short | Getting a Full Dose? Reconsidering Sex Chromosome Dosage Compensation in the
Silkworm, Bombyx mori |
title_sort | getting a full dose? reconsidering sex chromosome dosage compensation in the
silkworm, bombyx mori |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296447/ https://www.ncbi.nlm.nih.gov/pubmed/21508430 http://dx.doi.org/10.1093/gbe/evr036 |
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