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DNA polymerase ι is acetylated in response to S(N)2 alkylating agents
DNA polymerase iota (Polι) belongs to the Y-family of DNA polymerases that are involved in DNA damage tolerance through their role in translesion DNA synthesis. Like all other Y-family polymerases, Polι interacts with proliferating cell nuclear antigen (PCNA), Rev1, ubiquitin and ubiquitinated-PCNA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423139/ https://www.ncbi.nlm.nih.gov/pubmed/30886224 http://dx.doi.org/10.1038/s41598-019-41249-3 |
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author | McIntyre, Justyna Sobolewska, Aleksandra Fedorowicz, Mikolaj McLenigan, Mary P. Macias, Matylda Woodgate, Roger Sledziewska-Gojska, Ewa |
author_facet | McIntyre, Justyna Sobolewska, Aleksandra Fedorowicz, Mikolaj McLenigan, Mary P. Macias, Matylda Woodgate, Roger Sledziewska-Gojska, Ewa |
author_sort | McIntyre, Justyna |
collection | PubMed |
description | DNA polymerase iota (Polι) belongs to the Y-family of DNA polymerases that are involved in DNA damage tolerance through their role in translesion DNA synthesis. Like all other Y-family polymerases, Polι interacts with proliferating cell nuclear antigen (PCNA), Rev1, ubiquitin and ubiquitinated-PCNA and is also ubiquitinated itself. Here, we report that Polι also interacts with the p300 acetyltransferase and is acetylated. The primary acetylation site is K550, located in the Rev1-interacting region. However, K550 amino acid substitutions have no effect on Polι’s ability to interact with Rev1. Interestingly, we find that acetylation of Polι significantly and specifically increases in response to S(N)2 alkylating agents and to a lower extent to S(N)1 alkylating and oxidative agents. As we have not observed acetylation of Polι’s closest paralogue, DNA polymerase eta (Polη), with which Polι shares many functional similarities, we believe that this modification might exclusively regulate yet to be determined, and separate function(s) of Polι. |
format | Online Article Text |
id | pubmed-6423139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64231392019-03-26 DNA polymerase ι is acetylated in response to S(N)2 alkylating agents McIntyre, Justyna Sobolewska, Aleksandra Fedorowicz, Mikolaj McLenigan, Mary P. Macias, Matylda Woodgate, Roger Sledziewska-Gojska, Ewa Sci Rep Article DNA polymerase iota (Polι) belongs to the Y-family of DNA polymerases that are involved in DNA damage tolerance through their role in translesion DNA synthesis. Like all other Y-family polymerases, Polι interacts with proliferating cell nuclear antigen (PCNA), Rev1, ubiquitin and ubiquitinated-PCNA and is also ubiquitinated itself. Here, we report that Polι also interacts with the p300 acetyltransferase and is acetylated. The primary acetylation site is K550, located in the Rev1-interacting region. However, K550 amino acid substitutions have no effect on Polι’s ability to interact with Rev1. Interestingly, we find that acetylation of Polι significantly and specifically increases in response to S(N)2 alkylating agents and to a lower extent to S(N)1 alkylating and oxidative agents. As we have not observed acetylation of Polι’s closest paralogue, DNA polymerase eta (Polη), with which Polι shares many functional similarities, we believe that this modification might exclusively regulate yet to be determined, and separate function(s) of Polι. Nature Publishing Group UK 2019-03-18 /pmc/articles/PMC6423139/ /pubmed/30886224 http://dx.doi.org/10.1038/s41598-019-41249-3 Text en © The Author(s) 2019 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 McIntyre, Justyna Sobolewska, Aleksandra Fedorowicz, Mikolaj McLenigan, Mary P. Macias, Matylda Woodgate, Roger Sledziewska-Gojska, Ewa DNA polymerase ι is acetylated in response to S(N)2 alkylating agents |
title | DNA polymerase ι is acetylated in response to S(N)2 alkylating agents |
title_full | DNA polymerase ι is acetylated in response to S(N)2 alkylating agents |
title_fullStr | DNA polymerase ι is acetylated in response to S(N)2 alkylating agents |
title_full_unstemmed | DNA polymerase ι is acetylated in response to S(N)2 alkylating agents |
title_short | DNA polymerase ι is acetylated in response to S(N)2 alkylating agents |
title_sort | dna polymerase ι is acetylated in response to s(n)2 alkylating agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423139/ https://www.ncbi.nlm.nih.gov/pubmed/30886224 http://dx.doi.org/10.1038/s41598-019-41249-3 |
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