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Direct visualization of DNA baton pass between replication factors bound to PCNA
In Eukarya and Archaea, the lagging strand synthesis is accomplished mainly by three key factors, DNA polymerase (Pol), flap endonuclease (FEN), and DNA ligase (Lig), in the DNA replication process. These three factors form important complexes with proliferating cell nuclear antigen (PCNA), thereby...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6212441/ https://www.ncbi.nlm.nih.gov/pubmed/30385773 http://dx.doi.org/10.1038/s41598-018-34176-2 |
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author | Mayanagi, Kouta Ishino, Sonoko Shirai, Tsuyoshi Oyama, Takuji Kiyonari, Shinichi Kohda, Daisuke Morikawa, Kosuke Ishino, Yoshizumi |
author_facet | Mayanagi, Kouta Ishino, Sonoko Shirai, Tsuyoshi Oyama, Takuji Kiyonari, Shinichi Kohda, Daisuke Morikawa, Kosuke Ishino, Yoshizumi |
author_sort | Mayanagi, Kouta |
collection | PubMed |
description | In Eukarya and Archaea, the lagging strand synthesis is accomplished mainly by three key factors, DNA polymerase (Pol), flap endonuclease (FEN), and DNA ligase (Lig), in the DNA replication process. These three factors form important complexes with proliferating cell nuclear antigen (PCNA), thereby constructing a platform that enable each protein factor to act successively and smoothly on DNA. The structures of the Pol-PCNA-DNA and Lig-PCNA-DNA complexes alone have been visualized by single particle analysis. However, the FEN-PCNA-DNA complex structure remains unknown. In this report, we for the first time present this tertiary structure determined by single particle analysis. We also successfully visualized the structure of the FEN-Lig-PCNA-DNA complex, corresponding to a putative intermediate state between the removal of the DNA flap by FEN and the sealing of the nicked DNA by Lig. This structural study presents the direct visualization of the handing-over action, which proceeds between different replication factors on a single PCNA clamp bound to DNA. We detected a drastic conversion of the DNA from a bent form to a straight form, in addition to the dynamic motions of replication factors in the switching process. |
format | Online Article Text |
id | pubmed-6212441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62124412018-11-06 Direct visualization of DNA baton pass between replication factors bound to PCNA Mayanagi, Kouta Ishino, Sonoko Shirai, Tsuyoshi Oyama, Takuji Kiyonari, Shinichi Kohda, Daisuke Morikawa, Kosuke Ishino, Yoshizumi Sci Rep Article In Eukarya and Archaea, the lagging strand synthesis is accomplished mainly by three key factors, DNA polymerase (Pol), flap endonuclease (FEN), and DNA ligase (Lig), in the DNA replication process. These three factors form important complexes with proliferating cell nuclear antigen (PCNA), thereby constructing a platform that enable each protein factor to act successively and smoothly on DNA. The structures of the Pol-PCNA-DNA and Lig-PCNA-DNA complexes alone have been visualized by single particle analysis. However, the FEN-PCNA-DNA complex structure remains unknown. In this report, we for the first time present this tertiary structure determined by single particle analysis. We also successfully visualized the structure of the FEN-Lig-PCNA-DNA complex, corresponding to a putative intermediate state between the removal of the DNA flap by FEN and the sealing of the nicked DNA by Lig. This structural study presents the direct visualization of the handing-over action, which proceeds between different replication factors on a single PCNA clamp bound to DNA. We detected a drastic conversion of the DNA from a bent form to a straight form, in addition to the dynamic motions of replication factors in the switching process. Nature Publishing Group UK 2018-11-01 /pmc/articles/PMC6212441/ /pubmed/30385773 http://dx.doi.org/10.1038/s41598-018-34176-2 Text en © The Author(s) 2018 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 Mayanagi, Kouta Ishino, Sonoko Shirai, Tsuyoshi Oyama, Takuji Kiyonari, Shinichi Kohda, Daisuke Morikawa, Kosuke Ishino, Yoshizumi Direct visualization of DNA baton pass between replication factors bound to PCNA |
title | Direct visualization of DNA baton pass between replication factors bound to PCNA |
title_full | Direct visualization of DNA baton pass between replication factors bound to PCNA |
title_fullStr | Direct visualization of DNA baton pass between replication factors bound to PCNA |
title_full_unstemmed | Direct visualization of DNA baton pass between replication factors bound to PCNA |
title_short | Direct visualization of DNA baton pass between replication factors bound to PCNA |
title_sort | direct visualization of dna baton pass between replication factors bound to pcna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6212441/ https://www.ncbi.nlm.nih.gov/pubmed/30385773 http://dx.doi.org/10.1038/s41598-018-34176-2 |
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