Nucleic Acids Research, 2001, Vol. 29, No. 23 4892-4900
© 2001 Oxford University Press
The P1 phage replication protein RepA contacts an otherwise inaccessible thymine N3 proton by DNA distortion or base flipping
Intramural Research Support Program, SAIC, National Cancer Institute at Frederick, Frederick, MD 21702-1201, USA and 1National Cancer Institute at Frederick, Laboratory of Experimental and Computational Biology, Building 469, PO Box B, Frederick, MD 21702-1201, USA
The RepA protein from bacteriophage P1 binds DNA to initiate replication. RepA covers one face of the DNA and the binding site has a completely conserved T that directly faces RepA from the minor groove at position +7. Although all four bases can be distinguished through contacts in the major groove of B-form DNA, contacts in the minor groove cannot easily distinguish between A and T bases. Therefore the 100% conservation at this position cannot be accounted for by direct contacts approaching into the minor groove of B-form DNA. RepA binding sites with modified base pairs at position +7 were used to investigate contacts with RepA. The data show that RepA contacts the N3 proton of T at position +7 and that the T=A hydrogen bonds are already broken in the DNA before RepA binds. To accommodate the N3 proton contact the T+7 /A+7' base pair must be distorted. One possibility is that T+7 is flipped out of the helix. The energetics of the contact allows RepA to distinguish between all four bases, accounting for the observed high sequence conservation. After protein binding, base pair distortion or base flipping could initiate DNA melting as the second step in DNA replication.
* To whom correspondence should be addressed. Tel: +1 301 846 5581; Fax: +1 301 846 5598; Email: toms{at}ncifcrf.gov Present address: Paul N. Hengen, Applied Biosystems, 3833 North First Street, San Jose, CA 95134-1701, USA
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