Cargando…

Drosophila Brahma complex remodels nucleosome organizations in multiple aspects

ATP-dependent chromatin remodeling complexes regulate nucleosome organizations. In Drosophila, gene Brm encodes the core Brahma complex, the ATPase subunit of SWI/SNF class of chromatin remodelers. Its role in modulating the nucleosome landscape in vivo is unclear. In this study, we knocked down Brm...

Descripción completa

Detalles Bibliográficos
Autores principales: Shi, Jiejun, Zheng, Meizhu, Ye, Youqiong, Li, Min, Chen, Xiaolong, Hu, Xinjie, Sun, Jin, Zhang, Xiaobai, Jiang, Cizhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150808/
https://www.ncbi.nlm.nih.gov/pubmed/25081211
http://dx.doi.org/10.1093/nar/gku717
_version_ 1782332960468369408
author Shi, Jiejun
Zheng, Meizhu
Ye, Youqiong
Li, Min
Chen, Xiaolong
Hu, Xinjie
Sun, Jin
Zhang, Xiaobai
Jiang, Cizhong
author_facet Shi, Jiejun
Zheng, Meizhu
Ye, Youqiong
Li, Min
Chen, Xiaolong
Hu, Xinjie
Sun, Jin
Zhang, Xiaobai
Jiang, Cizhong
author_sort Shi, Jiejun
collection PubMed
description ATP-dependent chromatin remodeling complexes regulate nucleosome organizations. In Drosophila, gene Brm encodes the core Brahma complex, the ATPase subunit of SWI/SNF class of chromatin remodelers. Its role in modulating the nucleosome landscape in vivo is unclear. In this study, we knocked down Brm in Drosophila third instar larvae to explore the changes in nucleosome profiles and global gene transcription. The results show that Brm knockdown leads to nucleosome occupancy changes throughout the entire genome with a bias in occupancy decrease. In contrast, the knockdown has limited impacts on nucleosome position shift. The knockdown also alters another important physical property of nucleosome positioning, fuzziness. Nucleosome position shift, gain or loss and fuzziness changes are all enriched in promoter regions. Nucleosome arrays around the 5′ ends of genes are reorganized in five patterns as a result of Brm knockdown. Intriguingly, the concomitant changes in the genes adjacent to the Brahma-dependent remodeling regions have important roles in development and morphogenesis. Further analyses reveal abundance of AT-rich motifs for transcription factors in the remodeling regions.
format Online
Article
Text
id pubmed-4150808
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-41508082014-12-01 Drosophila Brahma complex remodels nucleosome organizations in multiple aspects Shi, Jiejun Zheng, Meizhu Ye, Youqiong Li, Min Chen, Xiaolong Hu, Xinjie Sun, Jin Zhang, Xiaobai Jiang, Cizhong Nucleic Acids Res Gene regulation, Chromatin and Epigenetics ATP-dependent chromatin remodeling complexes regulate nucleosome organizations. In Drosophila, gene Brm encodes the core Brahma complex, the ATPase subunit of SWI/SNF class of chromatin remodelers. Its role in modulating the nucleosome landscape in vivo is unclear. In this study, we knocked down Brm in Drosophila third instar larvae to explore the changes in nucleosome profiles and global gene transcription. The results show that Brm knockdown leads to nucleosome occupancy changes throughout the entire genome with a bias in occupancy decrease. In contrast, the knockdown has limited impacts on nucleosome position shift. The knockdown also alters another important physical property of nucleosome positioning, fuzziness. Nucleosome position shift, gain or loss and fuzziness changes are all enriched in promoter regions. Nucleosome arrays around the 5′ ends of genes are reorganized in five patterns as a result of Brm knockdown. Intriguingly, the concomitant changes in the genes adjacent to the Brahma-dependent remodeling regions have important roles in development and morphogenesis. Further analyses reveal abundance of AT-rich motifs for transcription factors in the remodeling regions. Oxford University Press 2014-09-02 2014-07-31 /pmc/articles/PMC4150808/ /pubmed/25081211 http://dx.doi.org/10.1093/nar/gku717 Text en © The Author(s) 2014. 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 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
Shi, Jiejun
Zheng, Meizhu
Ye, Youqiong
Li, Min
Chen, Xiaolong
Hu, Xinjie
Sun, Jin
Zhang, Xiaobai
Jiang, Cizhong
Drosophila Brahma complex remodels nucleosome organizations in multiple aspects
title Drosophila Brahma complex remodels nucleosome organizations in multiple aspects
title_full Drosophila Brahma complex remodels nucleosome organizations in multiple aspects
title_fullStr Drosophila Brahma complex remodels nucleosome organizations in multiple aspects
title_full_unstemmed Drosophila Brahma complex remodels nucleosome organizations in multiple aspects
title_short Drosophila Brahma complex remodels nucleosome organizations in multiple aspects
title_sort drosophila brahma complex remodels nucleosome organizations in multiple aspects
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150808/
https://www.ncbi.nlm.nih.gov/pubmed/25081211
http://dx.doi.org/10.1093/nar/gku717
work_keys_str_mv AT shijiejun drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT zhengmeizhu drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT yeyouqiong drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT limin drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT chenxiaolong drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT huxinjie drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT sunjin drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT zhangxiaobai drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects
AT jiangcizhong drosophilabrahmacomplexremodelsnucleosomeorganizationsinmultipleaspects