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Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process

Proliferating cell nuclear antigen (PCNA) is a DNA clamp that functions in key roles for DNA replication and repair. After the completion of DNA synthesis, PCNA should be unloaded from DNA in a timely way. The ATAD5-RFC-Like Complex (ATAD5-RLC) unloads PCNA from DNA. However, the mechanism of the PC...

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Autores principales: Ryu, Eunjin, Ha, Na Young, Jung, Woojae, Yoo, Juyeong, Myung, Kyungjae, Kang, Sukhyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180478/
https://www.ncbi.nlm.nih.gov/pubmed/35681528
http://dx.doi.org/10.3390/cells11111832
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author Ryu, Eunjin
Ha, Na Young
Jung, Woojae
Yoo, Juyeong
Myung, Kyungjae
Kang, Sukhyun
author_facet Ryu, Eunjin
Ha, Na Young
Jung, Woojae
Yoo, Juyeong
Myung, Kyungjae
Kang, Sukhyun
author_sort Ryu, Eunjin
collection PubMed
description Proliferating cell nuclear antigen (PCNA) is a DNA clamp that functions in key roles for DNA replication and repair. After the completion of DNA synthesis, PCNA should be unloaded from DNA in a timely way. The ATAD5-RFC-Like Complex (ATAD5-RLC) unloads PCNA from DNA. However, the mechanism of the PCNA-unloading process remains unclear. In this study, we determined the minimal PCNA-unloading domain (ULD) of ATAD5. We identified several motifs in the ATAD5 ULD that are essential in the PCNA-unloading process. The C-terminus of ULD is required for the stable association of RFC2-5 for active RLC formation. The N-terminus of ULD participates in the opening of the PCNA ring. ATAD5-RLC was more robustly bound to open-liable PCNA compared to the wild type. These results suggest that distinct motifs of the ATAD5 ULD participate in each step of the PCNA-unloading process.
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spelling pubmed-91804782022-06-10 Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process Ryu, Eunjin Ha, Na Young Jung, Woojae Yoo, Juyeong Myung, Kyungjae Kang, Sukhyun Cells Article Proliferating cell nuclear antigen (PCNA) is a DNA clamp that functions in key roles for DNA replication and repair. After the completion of DNA synthesis, PCNA should be unloaded from DNA in a timely way. The ATAD5-RFC-Like Complex (ATAD5-RLC) unloads PCNA from DNA. However, the mechanism of the PCNA-unloading process remains unclear. In this study, we determined the minimal PCNA-unloading domain (ULD) of ATAD5. We identified several motifs in the ATAD5 ULD that are essential in the PCNA-unloading process. The C-terminus of ULD is required for the stable association of RFC2-5 for active RLC formation. The N-terminus of ULD participates in the opening of the PCNA ring. ATAD5-RLC was more robustly bound to open-liable PCNA compared to the wild type. These results suggest that distinct motifs of the ATAD5 ULD participate in each step of the PCNA-unloading process. MDPI 2022-06-03 /pmc/articles/PMC9180478/ /pubmed/35681528 http://dx.doi.org/10.3390/cells11111832 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ryu, Eunjin
Ha, Na Young
Jung, Woojae
Yoo, Juyeong
Myung, Kyungjae
Kang, Sukhyun
Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process
title Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process
title_full Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process
title_fullStr Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process
title_full_unstemmed Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process
title_short Distinct Motifs in ATAD5 C-Terminal Domain Modulate PCNA Unloading Process
title_sort distinct motifs in atad5 c-terminal domain modulate pcna unloading process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180478/
https://www.ncbi.nlm.nih.gov/pubmed/35681528
http://dx.doi.org/10.3390/cells11111832
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