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INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module

The Integrator complex processes 3′-ends of spliceosomal small nuclear RNAs (snRNAs). Furthermore, it regulates transcription of protein coding genes by terminating transcription after unstable pausing. The molecular basis for Integrator’s functions remains obscure. Here, we show that INTS10, Asunde...

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Autores principales: Sabath, Kevin, Stäubli, Melanie L., Marti, Sabrina, Leitner, Alexander, Moes, Murielle, Jonas, Stefanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347597/
https://www.ncbi.nlm.nih.gov/pubmed/32647223
http://dx.doi.org/10.1038/s41467-020-17232-2
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author Sabath, Kevin
Stäubli, Melanie L.
Marti, Sabrina
Leitner, Alexander
Moes, Murielle
Jonas, Stefanie
author_facet Sabath, Kevin
Stäubli, Melanie L.
Marti, Sabrina
Leitner, Alexander
Moes, Murielle
Jonas, Stefanie
author_sort Sabath, Kevin
collection PubMed
description The Integrator complex processes 3′-ends of spliceosomal small nuclear RNAs (snRNAs). Furthermore, it regulates transcription of protein coding genes by terminating transcription after unstable pausing. The molecular basis for Integrator’s functions remains obscure. Here, we show that INTS10, Asunder/INTS13 and INTS14 form a separable, functional Integrator module. The structure of INTS13-INTS14 reveals a strongly entwined complex with a unique chain interlink. Unexpected structural homology to the Ku70-Ku80 DNA repair complex suggests nucleic acid affinity. Indeed, the module displays affinity for DNA and RNA but prefers RNA hairpins. While the module plays an accessory role in snRNA maturation, it has a stronger influence on transcription termination after pausing. Asunder/INTS13 directly binds Integrator’s cleavage module via a conserved C-terminal motif that is involved in snRNA processing and required for spermatogenesis. Collectively, our data establish INTS10-INTS13-INTS14 as a nucleic acid-binding module and suggest that it brings cleavage module and target transcripts into proximity.
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spelling pubmed-73475972020-07-13 INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module Sabath, Kevin Stäubli, Melanie L. Marti, Sabrina Leitner, Alexander Moes, Murielle Jonas, Stefanie Nat Commun Article The Integrator complex processes 3′-ends of spliceosomal small nuclear RNAs (snRNAs). Furthermore, it regulates transcription of protein coding genes by terminating transcription after unstable pausing. The molecular basis for Integrator’s functions remains obscure. Here, we show that INTS10, Asunder/INTS13 and INTS14 form a separable, functional Integrator module. The structure of INTS13-INTS14 reveals a strongly entwined complex with a unique chain interlink. Unexpected structural homology to the Ku70-Ku80 DNA repair complex suggests nucleic acid affinity. Indeed, the module displays affinity for DNA and RNA but prefers RNA hairpins. While the module plays an accessory role in snRNA maturation, it has a stronger influence on transcription termination after pausing. Asunder/INTS13 directly binds Integrator’s cleavage module via a conserved C-terminal motif that is involved in snRNA processing and required for spermatogenesis. Collectively, our data establish INTS10-INTS13-INTS14 as a nucleic acid-binding module and suggest that it brings cleavage module and target transcripts into proximity. Nature Publishing Group UK 2020-07-09 /pmc/articles/PMC7347597/ /pubmed/32647223 http://dx.doi.org/10.1038/s41467-020-17232-2 Text en © The Author(s) 2020 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
Sabath, Kevin
Stäubli, Melanie L.
Marti, Sabrina
Leitner, Alexander
Moes, Murielle
Jonas, Stefanie
INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module
title INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module
title_full INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module
title_fullStr INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module
title_full_unstemmed INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module
title_short INTS10–INTS13–INTS14 form a functional module of Integrator that binds nucleic acids and the cleavage module
title_sort ints10–ints13–ints14 form a functional module of integrator that binds nucleic acids and the cleavage module
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347597/
https://www.ncbi.nlm.nih.gov/pubmed/32647223
http://dx.doi.org/10.1038/s41467-020-17232-2
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