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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...

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Autores principales: Lam, Kin Chung, Chung, Ho-Ryun, Semplicio, Giuseppe, Iyer, Shantanu S., Gaub, Aline, Bhardwaj, Vivek, Holz, Herbert, Georgiev, Plamen, Akhtar, Asifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2019
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.
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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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