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Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing

In Drosophila, female development is governed by a single RNA-binding protein, Sex-lethal (Sxl), that controls the expression of key factors involved in dosage compensation, germline homeostasis and the establishment of female morphology and behaviour. Sxl expression in female flies is maintained by...

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Autores principales: Moschall, Rebecca, Rass, Mathias, Rossbach, Oliver, Lehmann, Gerhard, Kullmann, Lars, Eichner, Norbert, Strauss, Daniela, Meister, Gunter, Schneuwly, Stephan, Krahn, Michael P, Medenbach, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411925/
https://www.ncbi.nlm.nih.gov/pubmed/30590805
http://dx.doi.org/10.1093/nar/gky1284
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author Moschall, Rebecca
Rass, Mathias
Rossbach, Oliver
Lehmann, Gerhard
Kullmann, Lars
Eichner, Norbert
Strauss, Daniela
Meister, Gunter
Schneuwly, Stephan
Krahn, Michael P
Medenbach, Jan
author_facet Moschall, Rebecca
Rass, Mathias
Rossbach, Oliver
Lehmann, Gerhard
Kullmann, Lars
Eichner, Norbert
Strauss, Daniela
Meister, Gunter
Schneuwly, Stephan
Krahn, Michael P
Medenbach, Jan
author_sort Moschall, Rebecca
collection PubMed
description In Drosophila, female development is governed by a single RNA-binding protein, Sex-lethal (Sxl), that controls the expression of key factors involved in dosage compensation, germline homeostasis and the establishment of female morphology and behaviour. Sxl expression in female flies is maintained by an auto-regulatory, positive feedback loop with Sxl controlling splicing of its own mRNA. Until now, it remained unclear how males prevent accidental triggering of the Sxl expression cascade and protect themselves against runaway protein production. Here, we identify the protein Sister-of-Sex-lethal (Ssx) as an inhibitor of Sxl auto-regulatory splicing. Sxl and Ssx have a comparable RNA-binding specificity and compete for binding to RNA regulatory elements present in the Sxl transcript. In cultured Drosophila cells, Sxl-induced changes to alternative splicing can be reverted by the expression of Ssx. Moreover, in adult male flies ablation of the ssx gene results in a low level of productive Sxl mRNA splicing and Sxl protein production in isolated, clonal cell populations. In sum, this demonstrates that Ssx safeguards male animals against Sxl protein production to reinforce a stable, male-specific gene expression pattern.
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spelling pubmed-64119252019-03-18 Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing Moschall, Rebecca Rass, Mathias Rossbach, Oliver Lehmann, Gerhard Kullmann, Lars Eichner, Norbert Strauss, Daniela Meister, Gunter Schneuwly, Stephan Krahn, Michael P Medenbach, Jan Nucleic Acids Res Gene regulation, Chromatin and Epigenetics In Drosophila, female development is governed by a single RNA-binding protein, Sex-lethal (Sxl), that controls the expression of key factors involved in dosage compensation, germline homeostasis and the establishment of female morphology and behaviour. Sxl expression in female flies is maintained by an auto-regulatory, positive feedback loop with Sxl controlling splicing of its own mRNA. Until now, it remained unclear how males prevent accidental triggering of the Sxl expression cascade and protect themselves against runaway protein production. Here, we identify the protein Sister-of-Sex-lethal (Ssx) as an inhibitor of Sxl auto-regulatory splicing. Sxl and Ssx have a comparable RNA-binding specificity and compete for binding to RNA regulatory elements present in the Sxl transcript. In cultured Drosophila cells, Sxl-induced changes to alternative splicing can be reverted by the expression of Ssx. Moreover, in adult male flies ablation of the ssx gene results in a low level of productive Sxl mRNA splicing and Sxl protein production in isolated, clonal cell populations. In sum, this demonstrates that Ssx safeguards male animals against Sxl protein production to reinforce a stable, male-specific gene expression pattern. Oxford University Press 2019-03-18 2018-12-27 /pmc/articles/PMC6411925/ /pubmed/30590805 http://dx.doi.org/10.1093/nar/gky1284 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 Gene regulation, Chromatin and Epigenetics
Moschall, Rebecca
Rass, Mathias
Rossbach, Oliver
Lehmann, Gerhard
Kullmann, Lars
Eichner, Norbert
Strauss, Daniela
Meister, Gunter
Schneuwly, Stephan
Krahn, Michael P
Medenbach, Jan
Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing
title Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing
title_full Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing
title_fullStr Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing
title_full_unstemmed Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing
title_short Drosophila Sister-of-Sex-lethal reinforces a male-specific gene expression pattern by controlling Sex-lethal alternative splicing
title_sort drosophila sister-of-sex-lethal reinforces a male-specific gene expression pattern by controlling sex-lethal alternative splicing
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411925/
https://www.ncbi.nlm.nih.gov/pubmed/30590805
http://dx.doi.org/10.1093/nar/gky1284
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