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Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila
Jumonji (JmjC) domain proteins influence gene expression and chromatin organization by way of histone demethylation, which provides a means to regulate the activity of genes across the genome. JmjC proteins have been associated with many human diseases including various cancers, developmental and ne...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507883/ https://www.ncbi.nlm.nih.gov/pubmed/28701701 http://dx.doi.org/10.1038/s41598-017-05004-w |
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author | Shalaby, Nevine A. Sayed, Raheel Zhang, Qiao Scoggin, Shane Eliazer, Susan Rothenfluh, Adrian Buszczak, Michael |
author_facet | Shalaby, Nevine A. Sayed, Raheel Zhang, Qiao Scoggin, Shane Eliazer, Susan Rothenfluh, Adrian Buszczak, Michael |
author_sort | Shalaby, Nevine A. |
collection | PubMed |
description | Jumonji (JmjC) domain proteins influence gene expression and chromatin organization by way of histone demethylation, which provides a means to regulate the activity of genes across the genome. JmjC proteins have been associated with many human diseases including various cancers, developmental and neurological disorders, however, the shared biology and possible common contribution to organismal development and tissue homeostasis of all JmjC proteins remains unclear. Here, we systematically tested the function of all 13 Drosophila JmjC genes. Generation of molecularly defined null mutants revealed that loss of 8 out of 13 JmjC genes modify position effect variegation (PEV) phenotypes, consistent with their ascribed role in regulating chromatin organization. However, most JmjC genes do not critically regulate development, as 10 members are viable and fertile with no obvious developmental defects. Rather, we find that different JmjC mutants specifically alter the phenotypic outcomes in various sensitized genetic backgrounds. Our data demonstrate that, rather than controlling essential gene expression programs, Drosophila JmjC proteins generally act to “fine-tune” different biological processes. |
format | Online Article Text |
id | pubmed-5507883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55078832017-07-14 Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila Shalaby, Nevine A. Sayed, Raheel Zhang, Qiao Scoggin, Shane Eliazer, Susan Rothenfluh, Adrian Buszczak, Michael Sci Rep Article Jumonji (JmjC) domain proteins influence gene expression and chromatin organization by way of histone demethylation, which provides a means to regulate the activity of genes across the genome. JmjC proteins have been associated with many human diseases including various cancers, developmental and neurological disorders, however, the shared biology and possible common contribution to organismal development and tissue homeostasis of all JmjC proteins remains unclear. Here, we systematically tested the function of all 13 Drosophila JmjC genes. Generation of molecularly defined null mutants revealed that loss of 8 out of 13 JmjC genes modify position effect variegation (PEV) phenotypes, consistent with their ascribed role in regulating chromatin organization. However, most JmjC genes do not critically regulate development, as 10 members are viable and fertile with no obvious developmental defects. Rather, we find that different JmjC mutants specifically alter the phenotypic outcomes in various sensitized genetic backgrounds. Our data demonstrate that, rather than controlling essential gene expression programs, Drosophila JmjC proteins generally act to “fine-tune” different biological processes. Nature Publishing Group UK 2017-07-12 /pmc/articles/PMC5507883/ /pubmed/28701701 http://dx.doi.org/10.1038/s41598-017-05004-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shalaby, Nevine A. Sayed, Raheel Zhang, Qiao Scoggin, Shane Eliazer, Susan Rothenfluh, Adrian Buszczak, Michael Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila |
title | Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila |
title_full | Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila |
title_fullStr | Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila |
title_full_unstemmed | Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila |
title_short | Systematic discovery of genetic modulation by Jumonji histone demethylases in Drosophila |
title_sort | systematic discovery of genetic modulation by jumonji histone demethylases in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507883/ https://www.ncbi.nlm.nih.gov/pubmed/28701701 http://dx.doi.org/10.1038/s41598-017-05004-w |
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