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Molecular Insights into Poly(ADP-ribose) Recognition and Processing
Poly(ADP-ribosyl)ation is a post-translational protein modification involved in the regulation of important cellular functions including DNA repair, transcription, mitosis and apoptosis. The amount of poly(ADP-ribosyl)ation (PAR) in cells reflects the balance of synthesis, mediated by the PARP prote...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030884/ https://www.ncbi.nlm.nih.gov/pubmed/24970154 http://dx.doi.org/10.3390/biom3010001 |
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author | Žaja, Roko Mikoč, Andreja Barkauskaite, Eva Ahel, Ivan |
author_facet | Žaja, Roko Mikoč, Andreja Barkauskaite, Eva Ahel, Ivan |
author_sort | Žaja, Roko |
collection | PubMed |
description | Poly(ADP-ribosyl)ation is a post-translational protein modification involved in the regulation of important cellular functions including DNA repair, transcription, mitosis and apoptosis. The amount of poly(ADP-ribosyl)ation (PAR) in cells reflects the balance of synthesis, mediated by the PARP protein family, and degradation, which is catalyzed by a glycohydrolase, PARG. Many of the proteins mediating PAR metabolism possess specialised high affinity PAR-binding modules that allow the efficient sensing or processing of the PAR signal. The identification of four such PAR-binding modules and the characterization of a number of proteins utilising these elements during the last decade has provided important insights into how PAR regulates different cellular activities. The macrodomain represents a unique PAR-binding module which is, in some instances, known to possess enzymatic activity on ADP-ribose derivatives (in addition to PAR-binding). The most recently discovered example for this is the PARG protein, and several available PARG structures have provided an understanding into how the PARG macrodomain evolved into a major enzyme that maintains PAR homeostasis in living cells. |
format | Online Article Text |
id | pubmed-4030884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40308842014-06-24 Molecular Insights into Poly(ADP-ribose) Recognition and Processing Žaja, Roko Mikoč, Andreja Barkauskaite, Eva Ahel, Ivan Biomolecules Review Poly(ADP-ribosyl)ation is a post-translational protein modification involved in the regulation of important cellular functions including DNA repair, transcription, mitosis and apoptosis. The amount of poly(ADP-ribosyl)ation (PAR) in cells reflects the balance of synthesis, mediated by the PARP protein family, and degradation, which is catalyzed by a glycohydrolase, PARG. Many of the proteins mediating PAR metabolism possess specialised high affinity PAR-binding modules that allow the efficient sensing or processing of the PAR signal. The identification of four such PAR-binding modules and the characterization of a number of proteins utilising these elements during the last decade has provided important insights into how PAR regulates different cellular activities. The macrodomain represents a unique PAR-binding module which is, in some instances, known to possess enzymatic activity on ADP-ribose derivatives (in addition to PAR-binding). The most recently discovered example for this is the PARG protein, and several available PARG structures have provided an understanding into how the PARG macrodomain evolved into a major enzyme that maintains PAR homeostasis in living cells. MDPI 2012-12-21 /pmc/articles/PMC4030884/ /pubmed/24970154 http://dx.doi.org/10.3390/biom3010001 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Žaja, Roko Mikoč, Andreja Barkauskaite, Eva Ahel, Ivan Molecular Insights into Poly(ADP-ribose) Recognition and Processing |
title | Molecular Insights into Poly(ADP-ribose) Recognition and Processing |
title_full | Molecular Insights into Poly(ADP-ribose) Recognition and Processing |
title_fullStr | Molecular Insights into Poly(ADP-ribose) Recognition and Processing |
title_full_unstemmed | Molecular Insights into Poly(ADP-ribose) Recognition and Processing |
title_short | Molecular Insights into Poly(ADP-ribose) Recognition and Processing |
title_sort | molecular insights into poly(adp-ribose) recognition and processing |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030884/ https://www.ncbi.nlm.nih.gov/pubmed/24970154 http://dx.doi.org/10.3390/biom3010001 |
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