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The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise
Nucleosomal organization at gene promoters is critical for transcription, with a nucleosome-depleted region (NDR) at transcription start sites (TSSs) being required for transcription initiation. How NDRs and the precise positioning of the +1 nucleosomes are maintained on active genes remains unclear...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446542/ https://www.ncbi.nlm.nih.gov/pubmed/30819819 http://dx.doi.org/10.1101/gad.321489.118 |
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author | Lam, Kin Chung Chung, Ho-Ryun Semplicio, Giuseppe Iyer, Shantanu S. Gaub, Aline Bhardwaj, Vivek Holz, Herbert Georgiev, Plamen Akhtar, Asifa |
author_facet | Lam, Kin Chung Chung, Ho-Ryun Semplicio, Giuseppe Iyer, Shantanu S. Gaub, Aline Bhardwaj, Vivek Holz, Herbert Georgiev, Plamen Akhtar, Asifa |
author_sort | Lam, Kin Chung |
collection | PubMed |
description | Nucleosomal organization at gene promoters is critical for transcription, with a nucleosome-depleted region (NDR) at transcription start sites (TSSs) being required for transcription initiation. How NDRs and the precise positioning of the +1 nucleosomes are maintained on active genes remains unclear. Here, we report that the Drosophila nonspecific lethal (NSL) complex is necessary to maintain this stereotypical nucleosomal organization at promoters. Upon NSL1 depletion, nucleosomes invade the NDRs at TSSs of NSL-bound genes. NSL complex member NSL3 binds to TATA-less promoters in a sequence-dependent manner. The NSL complex interacts with the NURF chromatin remodeling complex and is necessary and sufficient to recruit NURF to target promoters. Not only is the NSL complex essential for transcription, but it is required for accurate TSS selection for genes with multiple TSSs. Furthermore, loss of the NSL complex leads to an increase in transcriptional noise. Thus, the NSL complex establishes a canonical nucleosomal organization that enables transcription and determines TSS fidelity. |
format | Online Article Text |
id | pubmed-6446542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64465422019-05-07 The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise Lam, Kin Chung Chung, Ho-Ryun Semplicio, Giuseppe Iyer, Shantanu S. Gaub, Aline Bhardwaj, Vivek Holz, Herbert Georgiev, Plamen Akhtar, Asifa Genes Dev Research Paper Nucleosomal organization at gene promoters is critical for transcription, with a nucleosome-depleted region (NDR) at transcription start sites (TSSs) being required for transcription initiation. How NDRs and the precise positioning of the +1 nucleosomes are maintained on active genes remains unclear. Here, we report that the Drosophila nonspecific lethal (NSL) complex is necessary to maintain this stereotypical nucleosomal organization at promoters. Upon NSL1 depletion, nucleosomes invade the NDRs at TSSs of NSL-bound genes. NSL complex member NSL3 binds to TATA-less promoters in a sequence-dependent manner. The NSL complex interacts with the NURF chromatin remodeling complex and is necessary and sufficient to recruit NURF to target promoters. Not only is the NSL complex essential for transcription, but it is required for accurate TSS selection for genes with multiple TSSs. Furthermore, loss of the NSL complex leads to an increase in transcriptional noise. Thus, the NSL complex establishes a canonical nucleosomal organization that enables transcription and determines TSS fidelity. Cold Spring Harbor Laboratory Press 2019-04-01 /pmc/articles/PMC6446542/ /pubmed/30819819 http://dx.doi.org/10.1101/gad.321489.118 Text en © 2019 Lam et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Paper Lam, Kin Chung Chung, Ho-Ryun Semplicio, Giuseppe Iyer, Shantanu S. Gaub, Aline Bhardwaj, Vivek Holz, Herbert Georgiev, Plamen Akhtar, Asifa The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
title | The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
title_full | The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
title_fullStr | The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
title_full_unstemmed | The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
title_short | The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
title_sort | nsl complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446542/ https://www.ncbi.nlm.nih.gov/pubmed/30819819 http://dx.doi.org/10.1101/gad.321489.118 |
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