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A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex
The Mre11/Rad50 complex is a central player in various genome maintenance pathways. Here, we report a novel mode of nuclease action found for the Escherichia coli Mre11/Rad50 complex, SbcC(2)/D(2) complex (SbcCD). SbcCD cuts off the top of a cruciform DNA by making incisions on both strands and cont...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787754/ https://www.ncbi.nlm.nih.gov/pubmed/26319016 http://dx.doi.org/10.1093/nar/gkv855 |
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author | Lim, Chew Theng Lai, Pey Jiun Leach, David R. F. Maki, Hisaji Furukohri, Asako |
author_facet | Lim, Chew Theng Lai, Pey Jiun Leach, David R. F. Maki, Hisaji Furukohri, Asako |
author_sort | Lim, Chew Theng |
collection | PubMed |
description | The Mre11/Rad50 complex is a central player in various genome maintenance pathways. Here, we report a novel mode of nuclease action found for the Escherichia coli Mre11/Rad50 complex, SbcC(2)/D(2) complex (SbcCD). SbcCD cuts off the top of a cruciform DNA by making incisions on both strands and continues cleaving the dsDNA stem at ∼10-bp intervals. Using linear-shaped DNA substrates, we observed that SbcCD cleaved dsDNA using this activity when the substrate was 110 bp long, but that on shorter substrates the cutting pattern was changed to that predicted for the activity of a 3′-5′ exonuclease. Our results suggest that SbcCD processes hairpin and linear dsDNA ends with this novel DNA end-dependent binary endonuclease activity in response to substrate length rather than using previously reported activities. We propose a model for this mode of nuclease action, which provides new insight into SbcCD activity at a dsDNA end. |
format | Online Article Text |
id | pubmed-4787754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47877542016-03-14 A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex Lim, Chew Theng Lai, Pey Jiun Leach, David R. F. Maki, Hisaji Furukohri, Asako Nucleic Acids Res Genome Integrity, Repair and Replication The Mre11/Rad50 complex is a central player in various genome maintenance pathways. Here, we report a novel mode of nuclease action found for the Escherichia coli Mre11/Rad50 complex, SbcC(2)/D(2) complex (SbcCD). SbcCD cuts off the top of a cruciform DNA by making incisions on both strands and continues cleaving the dsDNA stem at ∼10-bp intervals. Using linear-shaped DNA substrates, we observed that SbcCD cleaved dsDNA using this activity when the substrate was 110 bp long, but that on shorter substrates the cutting pattern was changed to that predicted for the activity of a 3′-5′ exonuclease. Our results suggest that SbcCD processes hairpin and linear dsDNA ends with this novel DNA end-dependent binary endonuclease activity in response to substrate length rather than using previously reported activities. We propose a model for this mode of nuclease action, which provides new insight into SbcCD activity at a dsDNA end. Oxford University Press 2015-11-16 2015-08-28 /pmc/articles/PMC4787754/ /pubmed/26319016 http://dx.doi.org/10.1093/nar/gkv855 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 Lim, Chew Theng Lai, Pey Jiun Leach, David R. F. Maki, Hisaji Furukohri, Asako A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex |
title | A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex |
title_full | A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex |
title_fullStr | A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex |
title_full_unstemmed | A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex |
title_short | A novel mode of nuclease action is revealed by the bacterial Mre11/Rad50 complex |
title_sort | novel mode of nuclease action is revealed by the bacterial mre11/rad50 complex |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787754/ https://www.ncbi.nlm.nih.gov/pubmed/26319016 http://dx.doi.org/10.1093/nar/gkv855 |
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