What is it about?
As all organisms bacteria cope with DNA damages with repair mechanisms. Nucleotide excision repair is a mechanism to remove UV-induced damages. In this work, we applied recently developed technology eXcision Repair sequencing (XR-seq) to map repair events in Escherichia coli. We compared wild-type strain with knock-out strains to understand the effects of Mfd, UvrD and Phr proteins on genome-wide excision repair profiles.
Featured Image
Why is it important?
In transcription-coupled repair (TCR), nucleotide excision repair occurs most rapidly in the template strand of actively transcribed genes. TCR has been observed in a limited set of genes directly assayed in Escherichia coli cells. In vitro, Mfd translocase performs reactions necessary to mediate TCR: It removes RNA polymerase blocked by a template strand lesion and rapidly delivers repair enzymes to the lesion. Here we map the location of repair sites in different E. coli strains. Results showed that Mfd-dependent TCR is widespread in the E. coli genome. Results with UvrD helicase demonstrated its role in basal repair, but no overall role in TCR.
Read the Original
This page is a summary of: Genome-wide transcription-coupled repair in
Escherichia coli
is mediated by the Mfd translocase, Proceedings of the National Academy of Sciences, February 2017, Proceedings of the National Academy of Sciences,
DOI: 10.1073/pnas.1700230114.
You can read the full text:
Contributors
The following have contributed to this page







