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The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex

Dosage compensation has evolved in concert with Y-chromosome degeneration in many taxa that exhibit heterogametic sex chromosomes. Dosage compensation overcomes the biological challenge of a “half dose” of X chromosome gene transcripts in the heterogametic sex. The need to equalize gene expression o...

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Autores principales: Deitz, Kevin C, Takken, Willem, Slotman, Michel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037052/
https://www.ncbi.nlm.nih.gov/pubmed/29860336
http://dx.doi.org/10.1093/gbe/evy108
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author Deitz, Kevin C
Takken, Willem
Slotman, Michel A
author_facet Deitz, Kevin C
Takken, Willem
Slotman, Michel A
author_sort Deitz, Kevin C
collection PubMed
description Dosage compensation has evolved in concert with Y-chromosome degeneration in many taxa that exhibit heterogametic sex chromosomes. Dosage compensation overcomes the biological challenge of a “half dose” of X chromosome gene transcripts in the heterogametic sex. The need to equalize gene expression of a hemizygous X with that of autosomes arises from the fact that the X chromosomes retain hundreds of functional genes that are actively transcribed in both sexes and interact with genes expressed on the autosomes. Sex determination and heterogametic sex chromosomes have evolved multiple times in Diptera, and in each case the genetic control of dosage compensation is tightly linked to sex determination. In the Anopheles gambiae species complex (Culicidae), maleness is conferred by the Y-chromosome gene Yob, which despite its conserved role between species is polymorphic in its copy number between them. Previous work demonstrated that male An. gambiae s.s. males exhibit complete dosage compensation in pupal and adult stages. In the present study, we have extended this analysis to three sister species in the An. gambiae complex: An. coluzzii, An. arabiensis, and An. quadriannulatus. In addition, we analyzed dosage compensation in bi-directional F1 hybrids between these species to determine if hybridization results in the mis-regulation and disruption of dosage compensation. Our results confirm that dosage compensation operates in the An. gambiae species complex through the hypertranscription of the male X chromosome. Additionally, dosage compensation in hybrid males does not differ from parental males, indicating that hybridization does not result in the mis-regulation of dosage compensation.
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spelling pubmed-60370522018-07-12 The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex Deitz, Kevin C Takken, Willem Slotman, Michel A Genome Biol Evol Research Article Dosage compensation has evolved in concert with Y-chromosome degeneration in many taxa that exhibit heterogametic sex chromosomes. Dosage compensation overcomes the biological challenge of a “half dose” of X chromosome gene transcripts in the heterogametic sex. The need to equalize gene expression of a hemizygous X with that of autosomes arises from the fact that the X chromosomes retain hundreds of functional genes that are actively transcribed in both sexes and interact with genes expressed on the autosomes. Sex determination and heterogametic sex chromosomes have evolved multiple times in Diptera, and in each case the genetic control of dosage compensation is tightly linked to sex determination. In the Anopheles gambiae species complex (Culicidae), maleness is conferred by the Y-chromosome gene Yob, which despite its conserved role between species is polymorphic in its copy number between them. Previous work demonstrated that male An. gambiae s.s. males exhibit complete dosage compensation in pupal and adult stages. In the present study, we have extended this analysis to three sister species in the An. gambiae complex: An. coluzzii, An. arabiensis, and An. quadriannulatus. In addition, we analyzed dosage compensation in bi-directional F1 hybrids between these species to determine if hybridization results in the mis-regulation and disruption of dosage compensation. Our results confirm that dosage compensation operates in the An. gambiae species complex through the hypertranscription of the male X chromosome. Additionally, dosage compensation in hybrid males does not differ from parental males, indicating that hybridization does not result in the mis-regulation of dosage compensation. Oxford University Press 2018-06-01 /pmc/articles/PMC6037052/ /pubmed/29860336 http://dx.doi.org/10.1093/gbe/evy108 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Deitz, Kevin C
Takken, Willem
Slotman, Michel A
The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex
title The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex
title_full The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex
title_fullStr The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex
title_full_unstemmed The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex
title_short The Effect of Hybridization on Dosage Compensation in Member Species of the Anopheles gambiae Species Complex
title_sort effect of hybridization on dosage compensation in member species of the anopheles gambiae species complex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037052/
https://www.ncbi.nlm.nih.gov/pubmed/29860336
http://dx.doi.org/10.1093/gbe/evy108
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