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The Response of the Replication Apparatus to Leading Template Strand Blocks

Duplication of the genome requires the replication apparatus to overcome a variety of impediments, including covalent DNA adducts, the most challenging of which is on the leading template strand. Replisomes consist of two functional units, a helicase to unwind DNA and polymerases to synthesize it. T...

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Autores principales: Bellani, Marina A., Shaik, Althaf, Majumdar, Ishani, Ling, Chen, Seidman, Michael M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10670059/
https://www.ncbi.nlm.nih.gov/pubmed/37998342
http://dx.doi.org/10.3390/cells12222607
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author Bellani, Marina A.
Shaik, Althaf
Majumdar, Ishani
Ling, Chen
Seidman, Michael M.
author_facet Bellani, Marina A.
Shaik, Althaf
Majumdar, Ishani
Ling, Chen
Seidman, Michael M.
author_sort Bellani, Marina A.
collection PubMed
description Duplication of the genome requires the replication apparatus to overcome a variety of impediments, including covalent DNA adducts, the most challenging of which is on the leading template strand. Replisomes consist of two functional units, a helicase to unwind DNA and polymerases to synthesize it. The helicase is a multi-protein complex that encircles the leading template strand and makes the first contact with a leading strand adduct. The size of the channel in the helicase would appear to preclude transit by large adducts such as DNA: protein complexes (DPC). Here we discuss some of the extensively studied pathways that support replication restart after replisome encounters with leading template strand adducts. We also call attention to recent work that highlights the tolerance of the helicase for adducts ostensibly too large to pass through the central channel.
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spelling pubmed-106700592023-11-11 The Response of the Replication Apparatus to Leading Template Strand Blocks Bellani, Marina A. Shaik, Althaf Majumdar, Ishani Ling, Chen Seidman, Michael M. Cells Review Duplication of the genome requires the replication apparatus to overcome a variety of impediments, including covalent DNA adducts, the most challenging of which is on the leading template strand. Replisomes consist of two functional units, a helicase to unwind DNA and polymerases to synthesize it. The helicase is a multi-protein complex that encircles the leading template strand and makes the first contact with a leading strand adduct. The size of the channel in the helicase would appear to preclude transit by large adducts such as DNA: protein complexes (DPC). Here we discuss some of the extensively studied pathways that support replication restart after replisome encounters with leading template strand adducts. We also call attention to recent work that highlights the tolerance of the helicase for adducts ostensibly too large to pass through the central channel. MDPI 2023-11-11 /pmc/articles/PMC10670059/ /pubmed/37998342 http://dx.doi.org/10.3390/cells12222607 Text en © 2023 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 Review
Bellani, Marina A.
Shaik, Althaf
Majumdar, Ishani
Ling, Chen
Seidman, Michael M.
The Response of the Replication Apparatus to Leading Template Strand Blocks
title The Response of the Replication Apparatus to Leading Template Strand Blocks
title_full The Response of the Replication Apparatus to Leading Template Strand Blocks
title_fullStr The Response of the Replication Apparatus to Leading Template Strand Blocks
title_full_unstemmed The Response of the Replication Apparatus to Leading Template Strand Blocks
title_short The Response of the Replication Apparatus to Leading Template Strand Blocks
title_sort response of the replication apparatus to leading template strand blocks
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10670059/
https://www.ncbi.nlm.nih.gov/pubmed/37998342
http://dx.doi.org/10.3390/cells12222607
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