Affiliation:
1. Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts
Abstract
ABSTRACT
We found that the nucleotide excision repair protein UvrA, which is involved in DNA damage recognition, localizes to the entire chromosome both before and after damage in living
Bacillus subtilis
cells. We suggest that the UvrA
2
B damage recognition complex is constantly scanning the genome, searching for lesions in the DNA. We also found that DNA damage induces a dramatic reconfiguration of the chromosome such that it no longer fills the entire cell as it does during normal growth. This reconfiguration is reversible after low doses of damage and is dependent on the damage-induced SOS response. We suggest that this reconfiguration of the chromosome after damage may be either a reflection of ongoing DNA repair or an active mechanism to protect the cell’s genome. Similar observations have been made in
Escherichia coli
, indicating that the alteration of chromosome structure after DNA damage may be a widespread phenomenon.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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