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The mechanism of DNA replication termination in vertebrates

Eukaryotic DNA replication terminates when replisomes from adjacent replication origins converge. Termination involves local completion of DNA synthesis, decatenation of daughter molecules, and replisome disassembly. Termination has been difficult to study because termination events are generally as...

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Autores principales: Dewar, James M., Budzowska, Magda, Walter, Johannes C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575634/
https://www.ncbi.nlm.nih.gov/pubmed/26322582
http://dx.doi.org/10.1038/nature14887
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author Dewar, James M.
Budzowska, Magda
Walter, Johannes C.
author_facet Dewar, James M.
Budzowska, Magda
Walter, Johannes C.
author_sort Dewar, James M.
collection PubMed
description Eukaryotic DNA replication terminates when replisomes from adjacent replication origins converge. Termination involves local completion of DNA synthesis, decatenation of daughter molecules, and replisome disassembly. Termination has been difficult to study because termination events are generally asynchronous and sequence non-specific. To overcome these challenges, we paused converging replisomes with a site-specific barrier in Xenopus egg extracts. Upon removal of the barrier, forks underwent synchronous and site-specific termination, allowing mechanistic dissection of this process. We show that DNA synthesis does not slow detectably as forks approach each other and that leading strands pass each other unhindered before undergoing ligation to downstream lagging strands. Dissociation of CMG helicases occurs only after the final ligation step, and is not required for completion of DNA synthesis, strongly suggesting that converging CMGs pass one another and dissociate from double-stranded DNA. This termination mechanism allows rapid completion of DNA synthesis while avoiding premature replisome disassembly
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spelling pubmed-45756342016-03-17 The mechanism of DNA replication termination in vertebrates Dewar, James M. Budzowska, Magda Walter, Johannes C. Nature Article Eukaryotic DNA replication terminates when replisomes from adjacent replication origins converge. Termination involves local completion of DNA synthesis, decatenation of daughter molecules, and replisome disassembly. Termination has been difficult to study because termination events are generally asynchronous and sequence non-specific. To overcome these challenges, we paused converging replisomes with a site-specific barrier in Xenopus egg extracts. Upon removal of the barrier, forks underwent synchronous and site-specific termination, allowing mechanistic dissection of this process. We show that DNA synthesis does not slow detectably as forks approach each other and that leading strands pass each other unhindered before undergoing ligation to downstream lagging strands. Dissociation of CMG helicases occurs only after the final ligation step, and is not required for completion of DNA synthesis, strongly suggesting that converging CMGs pass one another and dissociate from double-stranded DNA. This termination mechanism allows rapid completion of DNA synthesis while avoiding premature replisome disassembly 2015-08-31 2015-09-17 /pmc/articles/PMC4575634/ /pubmed/26322582 http://dx.doi.org/10.1038/nature14887 Text en Reprints and permissions information is available at www.nature.com/reprints (http://www.nature.com/reprints)
spellingShingle Article
Dewar, James M.
Budzowska, Magda
Walter, Johannes C.
The mechanism of DNA replication termination in vertebrates
title The mechanism of DNA replication termination in vertebrates
title_full The mechanism of DNA replication termination in vertebrates
title_fullStr The mechanism of DNA replication termination in vertebrates
title_full_unstemmed The mechanism of DNA replication termination in vertebrates
title_short The mechanism of DNA replication termination in vertebrates
title_sort mechanism of dna replication termination in vertebrates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575634/
https://www.ncbi.nlm.nih.gov/pubmed/26322582
http://dx.doi.org/10.1038/nature14887
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