G. Reddy et al., JOINTS MADE BY RECA PROTEIN IN THE INTERIOR OF LINEAR DUPLEX DNA - EFFECTS OF SINGLE-STRANDED ENDS, LENGTH OF HOMOLOGY, AND DYNAMIC STATE, Biochemistry, 33(38), 1994, pp. 11486-11492
The importance of 3' single-stranded ends in homologous recombination
led us to reevaluate reactions of single strands at homologous sites i
n the interior of linear duplex DNA. As the length of homology increas
ed, the yield of joints increased up to about 2 kb of homology, at whi
ch the apparent yields were the same at either 3' or 5'single-stranded
ends, or away from ends, although such joints were qualitatively diff
erent. In the presence of RecA protein and ATP, joints that formed bet
ween any of these single strands and interior sequences in duplex DNA
were in a dynamic state in which they constantly recycled. Consequentl
y, their apparent yields at steady state were sensitive to conditions
of reaction, such as the concentrations of DNA, salt, and ATP us ADP,
observations which rationalize conflicting reports in the literature.
The dynamic state of joints in the interior of duplex DNA strengthens
the conclusion [see Burnett et al. (1994)] that RecA protein dissociat
es joints when it cannot displace the 5' end of a strand from the reci
pient duplex.