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Clamp loader ATPases and the evolution of DNA replication machinery

Clamp loaders are pentameric ATPases of the AAA+ family that operate to ensure processive DNA replication. They do so by loading onto DNA the ring-shaped sliding clamps that tether the polymerase to the DNA. Structural and biochemical analysis of clamp loaders has shown how, despite differences in c...

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Detalles Bibliográficos
Autores principales: Kelch, Brian A, Makino, Debora L, O'Donnell, Mike, Kuriyan, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331839/
https://www.ncbi.nlm.nih.gov/pubmed/22520345
http://dx.doi.org/10.1186/1741-7007-10-34
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author Kelch, Brian A
Makino, Debora L
O'Donnell, Mike
Kuriyan, John
author_facet Kelch, Brian A
Makino, Debora L
O'Donnell, Mike
Kuriyan, John
author_sort Kelch, Brian A
collection PubMed
description Clamp loaders are pentameric ATPases of the AAA+ family that operate to ensure processive DNA replication. They do so by loading onto DNA the ring-shaped sliding clamps that tether the polymerase to the DNA. Structural and biochemical analysis of clamp loaders has shown how, despite differences in composition across different branches of life, all clamp loaders undergo the same concerted conformational transformations, which generate a binding surface for the open clamp and an internal spiral chamber into which the DNA at the replication fork can slide, triggering ATP hydrolysis, release of the clamp loader, and closure of the clamp round the DNA. We review here the current understanding of the clamp loader mechanism and discuss the implications of the differences between clamp loaders from the different branches of life.
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spelling pubmed-33318392012-04-21 Clamp loader ATPases and the evolution of DNA replication machinery Kelch, Brian A Makino, Debora L O'Donnell, Mike Kuriyan, John BMC Biol Review Clamp loaders are pentameric ATPases of the AAA+ family that operate to ensure processive DNA replication. They do so by loading onto DNA the ring-shaped sliding clamps that tether the polymerase to the DNA. Structural and biochemical analysis of clamp loaders has shown how, despite differences in composition across different branches of life, all clamp loaders undergo the same concerted conformational transformations, which generate a binding surface for the open clamp and an internal spiral chamber into which the DNA at the replication fork can slide, triggering ATP hydrolysis, release of the clamp loader, and closure of the clamp round the DNA. We review here the current understanding of the clamp loader mechanism and discuss the implications of the differences between clamp loaders from the different branches of life. BioMed Central 2012-04-20 /pmc/articles/PMC3331839/ /pubmed/22520345 http://dx.doi.org/10.1186/1741-7007-10-34 Text en Copyright ©2012 Kelch et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Kelch, Brian A
Makino, Debora L
O'Donnell, Mike
Kuriyan, John
Clamp loader ATPases and the evolution of DNA replication machinery
title Clamp loader ATPases and the evolution of DNA replication machinery
title_full Clamp loader ATPases and the evolution of DNA replication machinery
title_fullStr Clamp loader ATPases and the evolution of DNA replication machinery
title_full_unstemmed Clamp loader ATPases and the evolution of DNA replication machinery
title_short Clamp loader ATPases and the evolution of DNA replication machinery
title_sort clamp loader atpases and the evolution of dna replication machinery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331839/
https://www.ncbi.nlm.nih.gov/pubmed/22520345
http://dx.doi.org/10.1186/1741-7007-10-34
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