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NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability

NUCKS1 (nuclear casein kinase and cyclin-dependent kinase substrate 1) is a 27 kD chromosomal, vertebrate-specific protein, for which limited functional data exist. Here, we demonstrate that NUCKS1 shares extensive sequence homology with RAD51AP1 (RAD51 associated protein 1), suggesting that these t...

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Autores principales: Parplys, Ann C., Zhao, Weixing, Sharma, Neelam, Groesser, Torsten, Liang, Fengshan, Maranon, David G., Leung, Stanley G., Grundt, Kirsten, Dray, Eloïse, Idate, Rupa, Østvold, Anne Carine, Schild, David, Sung, Patrick, Wiese, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787752/
https://www.ncbi.nlm.nih.gov/pubmed/26323318
http://dx.doi.org/10.1093/nar/gkv859
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author Parplys, Ann C.
Zhao, Weixing
Sharma, Neelam
Groesser, Torsten
Liang, Fengshan
Maranon, David G.
Leung, Stanley G.
Grundt, Kirsten
Dray, Eloïse
Idate, Rupa
Østvold, Anne Carine
Schild, David
Sung, Patrick
Wiese, Claudia
author_facet Parplys, Ann C.
Zhao, Weixing
Sharma, Neelam
Groesser, Torsten
Liang, Fengshan
Maranon, David G.
Leung, Stanley G.
Grundt, Kirsten
Dray, Eloïse
Idate, Rupa
Østvold, Anne Carine
Schild, David
Sung, Patrick
Wiese, Claudia
author_sort Parplys, Ann C.
collection PubMed
description NUCKS1 (nuclear casein kinase and cyclin-dependent kinase substrate 1) is a 27 kD chromosomal, vertebrate-specific protein, for which limited functional data exist. Here, we demonstrate that NUCKS1 shares extensive sequence homology with RAD51AP1 (RAD51 associated protein 1), suggesting that these two proteins are paralogs. Similar to the phenotypic effects of RAD51AP1 knockdown, we find that depletion of NUCKS1 in human cells impairs DNA repair by homologous recombination (HR) and chromosome stability. Depletion of NUCKS1 also results in greatly increased cellular sensitivity to mitomycin C (MMC), and in increased levels of spontaneous and MMC-induced chromatid breaks. NUCKS1 is critical to maintaining wild type HR capacity, and, as observed for a number of proteins involved in the HR pathway, functional loss of NUCKS1 leads to a slow down in DNA replication fork progression with a concomitant increase in the utilization of new replication origins. Interestingly, recombinant NUCKS1 shares the same DNA binding preference as RAD51AP1, but binds to DNA with reduced affinity when compared to RAD51AP1. Our results show that NUCKS1 is a chromatin-associated protein with a role in the DNA damage response and in HR, a DNA repair pathway critical for tumor suppression.
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spelling pubmed-47877522016-03-14 NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability Parplys, Ann C. Zhao, Weixing Sharma, Neelam Groesser, Torsten Liang, Fengshan Maranon, David G. Leung, Stanley G. Grundt, Kirsten Dray, Eloïse Idate, Rupa Østvold, Anne Carine Schild, David Sung, Patrick Wiese, Claudia Nucleic Acids Res Genome Integrity, Repair and Replication NUCKS1 (nuclear casein kinase and cyclin-dependent kinase substrate 1) is a 27 kD chromosomal, vertebrate-specific protein, for which limited functional data exist. Here, we demonstrate that NUCKS1 shares extensive sequence homology with RAD51AP1 (RAD51 associated protein 1), suggesting that these two proteins are paralogs. Similar to the phenotypic effects of RAD51AP1 knockdown, we find that depletion of NUCKS1 in human cells impairs DNA repair by homologous recombination (HR) and chromosome stability. Depletion of NUCKS1 also results in greatly increased cellular sensitivity to mitomycin C (MMC), and in increased levels of spontaneous and MMC-induced chromatid breaks. NUCKS1 is critical to maintaining wild type HR capacity, and, as observed for a number of proteins involved in the HR pathway, functional loss of NUCKS1 leads to a slow down in DNA replication fork progression with a concomitant increase in the utilization of new replication origins. Interestingly, recombinant NUCKS1 shares the same DNA binding preference as RAD51AP1, but binds to DNA with reduced affinity when compared to RAD51AP1. Our results show that NUCKS1 is a chromatin-associated protein with a role in the DNA damage response and in HR, a DNA repair pathway critical for tumor suppression. Oxford University Press 2015-11-16 2015-08-31 /pmc/articles/PMC4787752/ /pubmed/26323318 http://dx.doi.org/10.1093/nar/gkv859 Text en © The Author(s) 2015. 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 Genome Integrity, Repair and Replication
Parplys, Ann C.
Zhao, Weixing
Sharma, Neelam
Groesser, Torsten
Liang, Fengshan
Maranon, David G.
Leung, Stanley G.
Grundt, Kirsten
Dray, Eloïse
Idate, Rupa
Østvold, Anne Carine
Schild, David
Sung, Patrick
Wiese, Claudia
NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability
title NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability
title_full NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability
title_fullStr NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability
title_full_unstemmed NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability
title_short NUCKS1 is a novel RAD51AP1 paralog important for homologous recombination and genome stability
title_sort nucks1 is a novel rad51ap1 paralog important for homologous recombination and genome stability
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787752/
https://www.ncbi.nlm.nih.gov/pubmed/26323318
http://dx.doi.org/10.1093/nar/gkv859
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