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Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef
RecJ was originally identified in Escherichia coli and plays an important role in the DNA repair and recombination pathways. Thermococcus kodakarensis, a hyperthermophilic archaeon, has two RecJ-like nucleases. These proteins are designated as GAN (GINS-associated nuclease) and HAN (Hef-associated n...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717133/ https://www.ncbi.nlm.nih.gov/pubmed/29209094 http://dx.doi.org/10.1038/s41598-017-17306-0 |
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author | Nagata, Mariko Ishino, Sonoko Yamagami, Takeshi Simons, Jan-Robert Kanai, Tamotsu Atomi, Haruyuki Ishino, Yoshizumi |
author_facet | Nagata, Mariko Ishino, Sonoko Yamagami, Takeshi Simons, Jan-Robert Kanai, Tamotsu Atomi, Haruyuki Ishino, Yoshizumi |
author_sort | Nagata, Mariko |
collection | PubMed |
description | RecJ was originally identified in Escherichia coli and plays an important role in the DNA repair and recombination pathways. Thermococcus kodakarensis, a hyperthermophilic archaeon, has two RecJ-like nucleases. These proteins are designated as GAN (GINS-associated nuclease) and HAN (Hef-associated nuclease), based on the protein they interact with. GAN is probably a counterpart of Cdc45 in the eukaryotic CMG replicative helicase complex. HAN is considered mainly to function with Hef for restoration of the stalled replication fork. In this study, we characterized HAN to clarify its functions in Thermococcus cells. HAN showed single-strand specific 3′ to 5′ exonuclease activity, which was stimulated in the presence of Hef. A gene disruption analysis revealed that HAN was non-essential for viability, but the ΔganΔhan double mutant did not grow under optimal conditions at 85 °C. This deficiency was not fully recovered by introducing the mutant han gene, encoding the nuclease-deficient HAN protein, back into the genome. These results suggest that the unstable replicative helicase complex without GAN performs ineffective fork progression, and thus the stalled fork repair system including HAN becomes more important. The nuclease activity of HAN is required for the function of this protein in T. kodakarensis. |
format | Online Article Text |
id | pubmed-5717133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57171332017-12-08 Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef Nagata, Mariko Ishino, Sonoko Yamagami, Takeshi Simons, Jan-Robert Kanai, Tamotsu Atomi, Haruyuki Ishino, Yoshizumi Sci Rep Article RecJ was originally identified in Escherichia coli and plays an important role in the DNA repair and recombination pathways. Thermococcus kodakarensis, a hyperthermophilic archaeon, has two RecJ-like nucleases. These proteins are designated as GAN (GINS-associated nuclease) and HAN (Hef-associated nuclease), based on the protein they interact with. GAN is probably a counterpart of Cdc45 in the eukaryotic CMG replicative helicase complex. HAN is considered mainly to function with Hef for restoration of the stalled replication fork. In this study, we characterized HAN to clarify its functions in Thermococcus cells. HAN showed single-strand specific 3′ to 5′ exonuclease activity, which was stimulated in the presence of Hef. A gene disruption analysis revealed that HAN was non-essential for viability, but the ΔganΔhan double mutant did not grow under optimal conditions at 85 °C. This deficiency was not fully recovered by introducing the mutant han gene, encoding the nuclease-deficient HAN protein, back into the genome. These results suggest that the unstable replicative helicase complex without GAN performs ineffective fork progression, and thus the stalled fork repair system including HAN becomes more important. The nuclease activity of HAN is required for the function of this protein in T. kodakarensis. Nature Publishing Group UK 2017-12-05 /pmc/articles/PMC5717133/ /pubmed/29209094 http://dx.doi.org/10.1038/s41598-017-17306-0 Text en © The Author(s) 2017 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 Nagata, Mariko Ishino, Sonoko Yamagami, Takeshi Simons, Jan-Robert Kanai, Tamotsu Atomi, Haruyuki Ishino, Yoshizumi Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef |
title | Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef |
title_full | Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef |
title_fullStr | Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef |
title_full_unstemmed | Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef |
title_short | Possible function of the second RecJ-like protein in stalled replication fork repair by interacting with Hef |
title_sort | possible function of the second recj-like protein in stalled replication fork repair by interacting with hef |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717133/ https://www.ncbi.nlm.nih.gov/pubmed/29209094 http://dx.doi.org/10.1038/s41598-017-17306-0 |
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