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The replisome uses mRNA as a primer after colliding with RNA polymerase

Replication forks are impeded by DNA damage and protein-nucleic acid complexes such as transcribing RNA polymerase. For example, head-on collision of the replisome with RNA polymerase results in replication fork arrest. However, co-directional collision of the replisome with RNA polymerase has littl...

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Detalles Bibliográficos
Autores principales: Pomerantz, Richard T., O’Donnell, Mike
Formato: Texto
Lenguaje:English
Publicado: 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2605185/
https://www.ncbi.nlm.nih.gov/pubmed/19020502
http://dx.doi.org/10.1038/nature07527
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author Pomerantz, Richard T.
O’Donnell, Mike
author_facet Pomerantz, Richard T.
O’Donnell, Mike
author_sort Pomerantz, Richard T.
collection PubMed
description Replication forks are impeded by DNA damage and protein-nucleic acid complexes such as transcribing RNA polymerase. For example, head-on collision of the replisome with RNA polymerase results in replication fork arrest. However, co-directional collision of the replisome with RNA polymerase has little or no effect on fork progression. The current study examines co-directional collisions between a replisome and RNA polymerase in vitro. Surprisingly, we find that the E. coli replisome utilizes the RNA transcript as a primer to continue leading strand synthesis following the collision with RNA polymerase which is displaced from the DNA. This action results in a discontinuity in the leading strand, yet the replisome remains intact and bound to DNA during the entire process. These findings underscore the remarkable plasticity by which the replisome operates to circumvent obstacles in its path and may explain why the leading strand is synthesized discontinuously in vivo.
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spelling pubmed-26051852009-06-11 The replisome uses mRNA as a primer after colliding with RNA polymerase Pomerantz, Richard T. O’Donnell, Mike Nature Article Replication forks are impeded by DNA damage and protein-nucleic acid complexes such as transcribing RNA polymerase. For example, head-on collision of the replisome with RNA polymerase results in replication fork arrest. However, co-directional collision of the replisome with RNA polymerase has little or no effect on fork progression. The current study examines co-directional collisions between a replisome and RNA polymerase in vitro. Surprisingly, we find that the E. coli replisome utilizes the RNA transcript as a primer to continue leading strand synthesis following the collision with RNA polymerase which is displaced from the DNA. This action results in a discontinuity in the leading strand, yet the replisome remains intact and bound to DNA during the entire process. These findings underscore the remarkable plasticity by which the replisome operates to circumvent obstacles in its path and may explain why the leading strand is synthesized discontinuously in vivo. 2008-11-19 2008-12-11 /pmc/articles/PMC2605185/ /pubmed/19020502 http://dx.doi.org/10.1038/nature07527 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Pomerantz, Richard T.
O’Donnell, Mike
The replisome uses mRNA as a primer after colliding with RNA polymerase
title The replisome uses mRNA as a primer after colliding with RNA polymerase
title_full The replisome uses mRNA as a primer after colliding with RNA polymerase
title_fullStr The replisome uses mRNA as a primer after colliding with RNA polymerase
title_full_unstemmed The replisome uses mRNA as a primer after colliding with RNA polymerase
title_short The replisome uses mRNA as a primer after colliding with RNA polymerase
title_sort replisome uses mrna as a primer after colliding with rna polymerase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2605185/
https://www.ncbi.nlm.nih.gov/pubmed/19020502
http://dx.doi.org/10.1038/nature07527
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