IMR Press / FBL / Volume 18 / Issue 1 / DOI: 10.2741/4102

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Review
A proposal: Source of single strand DNA that elicits the SOS response
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1 Chiara Indiani Manhattan College 4513 Manhattan College Pkwy, Riverdale, NY 10471, USA
2 Mike O’Donnell The Rockefeller University Howard Hughes Medical Institute, 1230 York Avenue New York, NY 10065, USA
Front. Biosci. (Landmark Ed) 2013, 18(1), 312–323; https://doi.org/10.2741/4102
Published: 1 January 2013
Abstract

Chromosome replication is performed by numerous proteins that function together as a “replisome”. The replisome machinery duplicates both strands of the parental DNA simultaneously. Upon DNA damage to the cell, replisome action produces single-strand DNA to which RecA binds, enabling its activity in cleaving the LexA repressor and thus inducing the SOS response. How singlestrand DNA is produced by a replisome acting on damaged DNA is not clear. For many years it has been assumed the single-strand DNA is generated by the replicative helicase, which continues unwinding DNA even after DNA polymerase stalls at a template lesion. Recent studies indicate another source of the single-strand DNA, resulting from an inherently dynamic replisome that may hop over template lesions on both leading and lagging strands, thereby leaving single-strand gaps in the wake of the replication fork. These single-strand gaps are proposed to be the origin of the single-strand DNA that triggers the SOS response after DNA damage.

Keywords
SOS response
Translesion Synthesis
DNA repair
lesion bypass
DNA polymerase
Sliding Clamp
Review
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