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Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism

To counteract the breakdown of genome integrity, eukaryotic cells have developed a network of surveillance pathways to prevent and resolve DNA damage. Recent data has recognized the importance of RNA binding proteins (RBPs) in DNA damage repair (DDR) pathways. Here, we describe Nol12 as a multifunct...

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Autores principales: Scott, Daniel D., Trahan, Christian, Zindy, Pierre J., Aguilar, Lisbeth C., Delubac, Marc Y., Van Nostrand, Eric L., Adivarahan, Srivathsan, Wei, Karen E., Yeo, Gene W., Zenklusen, Daniel, Oeffinger, Marlene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716212/
https://www.ncbi.nlm.nih.gov/pubmed/29069457
http://dx.doi.org/10.1093/nar/gkx963
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author Scott, Daniel D.
Trahan, Christian
Zindy, Pierre J.
Aguilar, Lisbeth C.
Delubac, Marc Y.
Van Nostrand, Eric L.
Adivarahan, Srivathsan
Wei, Karen E.
Yeo, Gene W.
Zenklusen, Daniel
Oeffinger, Marlene
author_facet Scott, Daniel D.
Trahan, Christian
Zindy, Pierre J.
Aguilar, Lisbeth C.
Delubac, Marc Y.
Van Nostrand, Eric L.
Adivarahan, Srivathsan
Wei, Karen E.
Yeo, Gene W.
Zenklusen, Daniel
Oeffinger, Marlene
author_sort Scott, Daniel D.
collection PubMed
description To counteract the breakdown of genome integrity, eukaryotic cells have developed a network of surveillance pathways to prevent and resolve DNA damage. Recent data has recognized the importance of RNA binding proteins (RBPs) in DNA damage repair (DDR) pathways. Here, we describe Nol12 as a multifunctional RBP with roles in RNA metabolism and genome maintenance. Nol12 is found in different subcellular compartments—nucleoli, where it associates with ribosomal RNA and is required for efficient separation of large and small subunit precursors at site 2; the nucleoplasm, where it co-localizes with the RNA/DNA helicase Dhx9 and paraspeckles; as well as GW/P-bodies in the cytoplasm. Loss of Nol12 results in the inability of cells to recover from DNA stress and a rapid p53-independent ATR-Chk1-mediated apoptotic response. Nol12 co-localizes with DNA repair proteins in vivo including Dhx9, as well as with TOPBP1 at sites of replication stalls, suggesting a role for Nol12 in the resolution of DNA stress and maintenance of genome integrity. Identification of a complex Nol12 interactome, which includes NONO, Dhx9, DNA-PK and Stau1, further supports the protein's diverse functions in RNA metabolism and DNA maintenance, establishing Nol12 as a multifunctional RBP essential for genome integrity.
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spelling pubmed-57162122020-08-18 Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism Scott, Daniel D. Trahan, Christian Zindy, Pierre J. Aguilar, Lisbeth C. Delubac, Marc Y. Van Nostrand, Eric L. Adivarahan, Srivathsan Wei, Karen E. Yeo, Gene W. Zenklusen, Daniel Oeffinger, Marlene Nucleic Acids Res RNA and RNA-protein complexes To counteract the breakdown of genome integrity, eukaryotic cells have developed a network of surveillance pathways to prevent and resolve DNA damage. Recent data has recognized the importance of RNA binding proteins (RBPs) in DNA damage repair (DDR) pathways. Here, we describe Nol12 as a multifunctional RBP with roles in RNA metabolism and genome maintenance. Nol12 is found in different subcellular compartments—nucleoli, where it associates with ribosomal RNA and is required for efficient separation of large and small subunit precursors at site 2; the nucleoplasm, where it co-localizes with the RNA/DNA helicase Dhx9 and paraspeckles; as well as GW/P-bodies in the cytoplasm. Loss of Nol12 results in the inability of cells to recover from DNA stress and a rapid p53-independent ATR-Chk1-mediated apoptotic response. Nol12 co-localizes with DNA repair proteins in vivo including Dhx9, as well as with TOPBP1 at sites of replication stalls, suggesting a role for Nol12 in the resolution of DNA stress and maintenance of genome integrity. Identification of a complex Nol12 interactome, which includes NONO, Dhx9, DNA-PK and Stau1, further supports the protein's diverse functions in RNA metabolism and DNA maintenance, establishing Nol12 as a multifunctional RBP essential for genome integrity. Oxford University Press 2017-12-01 2017-10-23 /pmc/articles/PMC5716212/ /pubmed/29069457 http://dx.doi.org/10.1093/nar/gkx963 Text en © The Author(s) 2017. 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 RNA and RNA-protein complexes
Scott, Daniel D.
Trahan, Christian
Zindy, Pierre J.
Aguilar, Lisbeth C.
Delubac, Marc Y.
Van Nostrand, Eric L.
Adivarahan, Srivathsan
Wei, Karen E.
Yeo, Gene W.
Zenklusen, Daniel
Oeffinger, Marlene
Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism
title Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism
title_full Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism
title_fullStr Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism
title_full_unstemmed Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism
title_short Nol12 is a multifunctional RNA binding protein at the nexus of RNA and DNA metabolism
title_sort nol12 is a multifunctional rna binding protein at the nexus of rna and dna metabolism
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716212/
https://www.ncbi.nlm.nih.gov/pubmed/29069457
http://dx.doi.org/10.1093/nar/gkx963
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