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dc.contributor.authorMeisel, Richard P.
dc.contributor.authorAsgari, Danial
dc.contributor.authorSchlamp, Florencia
dc.contributor.authorUnckless, Robert L.
dc.date.accessioned2023-02-28T16:13:18Z
dc.date.available2023-02-28T16:13:18Z
dc.date.issued2022-07-06
dc.identifier.citationRichard P Meisel, Danial Asgari, Florencia Schlamp, Robert L Unckless, Induction and inhibition of Drosophila X chromosome gene expression are both impeded by the dosage compensation complex, G3 Genes|Genomes|Genetics, Volume 12, Issue 9, September 2022, jkac165, https://doi.org/10.1093/g3journal/jkac165en_US
dc.identifier.urihttp://hdl.handle.net/1808/33966
dc.description.abstractSex chromosomes frequently differ from the autosomes in the frequencies of genes with sexually dimorphic or tissue-specific expression. Multiple hypotheses have been put forth to explain the unique gene content of the X chromosome, including selection against male-beneficial X-linked alleles, expression limits imposed by the haploid dosage of the X in males, and interference by the dosage compensation complex on expression in males. Here, we investigate these hypotheses by examining differential gene expression in Drosophila melanogaster following several treatments that have widespread transcriptomic effects: bacterial infection, viral infection, and abiotic stress. We found that genes that are induced (upregulated) by these biotic and abiotic treatments are frequently under-represented on the X chromosome, but so are those that are repressed (downregulated) following treatment. We further show that whether a gene is bound by the dosage compensation complex in males can largely explain the paucity of both up- and downregulated genes on the X chromosome. Specifically, genes that are bound by the dosage compensation complex, or close to a dosage compensation complex high-affinity site, are unlikely to be up- or downregulated after treatment. This relationship, however, could partially be explained by a correlation between differential expression and breadth of expression across tissues. Nonetheless, our results suggest that dosage compensation complex binding, or the associated chromatin modifications, inhibit both up- and downregulation of X chromosome gene expression within specific contexts, including tissue-specific expression. We propose multiple possible mechanisms of action for the effect, including a role of Males absent on the first, a component of the dosage compensation complex, as a dampener of gene expression variance in both males and females. This effect could explain why the Drosophila X chromosome is depauperate in genes with tissue-specific or induced expression, while the mammalian X has an excess of genes with tissue-specific expression.en_US
dc.publisherOxford University Pressen_US
dc.rightsCopyright The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectTranscriptionen_US
dc.subjectChromatinen_US
dc.subjectSex chromosomesen_US
dc.subjectExpression varianceen_US
dc.subjectMales absent on the firsten_US
dc.titleInduction and inhibition of Drosophila X chromosome gene expression are both impeded by the dosage compensation complexen_US
dc.typeArticleen_US
kusw.kuauthorUnckless, Robert L.
kusw.kudepartmentMolecular Biosciencesen_US
dc.identifier.doi10.1093/g3journal/jkac165en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC9434221en_US
dc.rights.accessrightsopenAccessen_US


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Copyright The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.
Except where otherwise noted, this item's license is described as: Copyright The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.