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Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire
KAT6 histone acetyltransferases (HATs) are highly conserved in eukaryotes and have been shown to play important roles in transcriptional regulation. Here, we demonstrate that the Drosophila KAT6 Enok acetylates histone H3 Lys 23 (H3K23) in vitro and in vivo. Mutants lacking functional Enok exhibited...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265678/ https://www.ncbi.nlm.nih.gov/pubmed/25512562 http://dx.doi.org/10.1101/gad.249730.114 |
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author | Huang, Fu Paulson, Ariel Dutta, Arnob Venkatesh, Swaminathan Smolle, Michaela Abmayr, Susan M. Workman, Jerry L. |
author_facet | Huang, Fu Paulson, Ariel Dutta, Arnob Venkatesh, Swaminathan Smolle, Michaela Abmayr, Susan M. Workman, Jerry L. |
author_sort | Huang, Fu |
collection | PubMed |
description | KAT6 histone acetyltransferases (HATs) are highly conserved in eukaryotes and have been shown to play important roles in transcriptional regulation. Here, we demonstrate that the Drosophila KAT6 Enok acetylates histone H3 Lys 23 (H3K23) in vitro and in vivo. Mutants lacking functional Enok exhibited defects in the localization of Oskar (Osk) to the posterior end of the oocyte, resulting in loss of germline formation and abdominal segments in the embryo. RNA sequencing (RNA-seq) analysis revealed that spire (spir) and maelstrom (mael), both required for the posterior localization of Osk in the oocyte, were down-regulated in enok mutants. Chromatin immunoprecipitation showed that Enok is localized to and acetylates H3K23 at the spir and mael genes. Furthermore, Gal4-driven expression of spir in the germline can largely rescue the defective Osk localization in enok mutant ovaries. Our results suggest that the Enok-mediated H3K23 acetylation (H3K23Ac) promotes the expression of spir, providing a specific mechanism linking oocyte polarization to histone modification. |
format | Online Article Text |
id | pubmed-4265678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42656782015-06-15 Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire Huang, Fu Paulson, Ariel Dutta, Arnob Venkatesh, Swaminathan Smolle, Michaela Abmayr, Susan M. Workman, Jerry L. Genes Dev Research Paper KAT6 histone acetyltransferases (HATs) are highly conserved in eukaryotes and have been shown to play important roles in transcriptional regulation. Here, we demonstrate that the Drosophila KAT6 Enok acetylates histone H3 Lys 23 (H3K23) in vitro and in vivo. Mutants lacking functional Enok exhibited defects in the localization of Oskar (Osk) to the posterior end of the oocyte, resulting in loss of germline formation and abdominal segments in the embryo. RNA sequencing (RNA-seq) analysis revealed that spire (spir) and maelstrom (mael), both required for the posterior localization of Osk in the oocyte, were down-regulated in enok mutants. Chromatin immunoprecipitation showed that Enok is localized to and acetylates H3K23 at the spir and mael genes. Furthermore, Gal4-driven expression of spir in the germline can largely rescue the defective Osk localization in enok mutant ovaries. Our results suggest that the Enok-mediated H3K23 acetylation (H3K23Ac) promotes the expression of spir, providing a specific mechanism linking oocyte polarization to histone modification. Cold Spring Harbor Laboratory Press 2014-12-15 /pmc/articles/PMC4265678/ /pubmed/25512562 http://dx.doi.org/10.1101/gad.249730.114 Text en © 2014 Huang et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Paper Huang, Fu Paulson, Ariel Dutta, Arnob Venkatesh, Swaminathan Smolle, Michaela Abmayr, Susan M. Workman, Jerry L. Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
title | Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
title_full | Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
title_fullStr | Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
title_full_unstemmed | Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
title_short | Histone acetyltransferase Enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
title_sort | histone acetyltransferase enok regulates oocyte polarization by promoting expression of the actin nucleation factor spire |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265678/ https://www.ncbi.nlm.nih.gov/pubmed/25512562 http://dx.doi.org/10.1101/gad.249730.114 |
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