Cargando…

Unencumbered Pol β lyase activity in nucleosome core particles

Packaging of DNA into the nucleosome core particle (NCP) is considered to exert constraints to all DNA-templated processes, including base excision repair where Pol β catalyzes two key enzymatic steps: 5′-dRP lyase gap trimming and template-directed DNA synthesis. Despite its biological significance...

Descripción completa

Detalles Bibliográficos
Autores principales: Rodriguez, Yesenia, Howard, Michael J., Cuneo, Matthew J., Prasad, Rajendra, Wilson, Samuel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587807/
https://www.ncbi.nlm.nih.gov/pubmed/28911106
http://dx.doi.org/10.1093/nar/gkx593
_version_ 1783262064724148224
author Rodriguez, Yesenia
Howard, Michael J.
Cuneo, Matthew J.
Prasad, Rajendra
Wilson, Samuel H.
author_facet Rodriguez, Yesenia
Howard, Michael J.
Cuneo, Matthew J.
Prasad, Rajendra
Wilson, Samuel H.
author_sort Rodriguez, Yesenia
collection PubMed
description Packaging of DNA into the nucleosome core particle (NCP) is considered to exert constraints to all DNA-templated processes, including base excision repair where Pol β catalyzes two key enzymatic steps: 5′-dRP lyase gap trimming and template-directed DNA synthesis. Despite its biological significance, knowledge of Pol β activities on NCPs is still limited. Here, we show that removal of the 5′-dRP block by Pol β is unaffected by NCP constraints at all sites tested and is even enhanced near the DNA ends. In contrast, strong inhibition of DNA synthesis is observed. These results indicate 5′-dRP gap trimming proceeds unperturbed within the NCP; whereas, gap filling is strongly limited. In the absence of additional factors, base excision repair in NCPs will stall at the gap-filling step.
format Online
Article
Text
id pubmed-5587807
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-55878072017-09-11 Unencumbered Pol β lyase activity in nucleosome core particles Rodriguez, Yesenia Howard, Michael J. Cuneo, Matthew J. Prasad, Rajendra Wilson, Samuel H. Nucleic Acids Res Genome Integrity, Repair and Replication Packaging of DNA into the nucleosome core particle (NCP) is considered to exert constraints to all DNA-templated processes, including base excision repair where Pol β catalyzes two key enzymatic steps: 5′-dRP lyase gap trimming and template-directed DNA synthesis. Despite its biological significance, knowledge of Pol β activities on NCPs is still limited. Here, we show that removal of the 5′-dRP block by Pol β is unaffected by NCP constraints at all sites tested and is even enhanced near the DNA ends. In contrast, strong inhibition of DNA synthesis is observed. These results indicate 5′-dRP gap trimming proceeds unperturbed within the NCP; whereas, gap filling is strongly limited. In the absence of additional factors, base excision repair in NCPs will stall at the gap-filling step. Oxford University Press 2017-09-06 2017-07-11 /pmc/articles/PMC5587807/ /pubmed/28911106 http://dx.doi.org/10.1093/nar/gkx593 Text en Published by Oxford University Press on behalf of Nucleic Acids Research 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US.
spellingShingle Genome Integrity, Repair and Replication
Rodriguez, Yesenia
Howard, Michael J.
Cuneo, Matthew J.
Prasad, Rajendra
Wilson, Samuel H.
Unencumbered Pol β lyase activity in nucleosome core particles
title Unencumbered Pol β lyase activity in nucleosome core particles
title_full Unencumbered Pol β lyase activity in nucleosome core particles
title_fullStr Unencumbered Pol β lyase activity in nucleosome core particles
title_full_unstemmed Unencumbered Pol β lyase activity in nucleosome core particles
title_short Unencumbered Pol β lyase activity in nucleosome core particles
title_sort unencumbered pol β lyase activity in nucleosome core particles
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587807/
https://www.ncbi.nlm.nih.gov/pubmed/28911106
http://dx.doi.org/10.1093/nar/gkx593
work_keys_str_mv AT rodriguezyesenia unencumberedpolblyaseactivityinnucleosomecoreparticles
AT howardmichaelj unencumberedpolblyaseactivityinnucleosomecoreparticles
AT cuneomatthewj unencumberedpolblyaseactivityinnucleosomecoreparticles
AT prasadrajendra unencumberedpolblyaseactivityinnucleosomecoreparticles
AT wilsonsamuelh unencumberedpolblyaseactivityinnucleosomecoreparticles