JOINTS MADE BY RECA PROTEIN IN THE INTERIOR OF LINEAR DUPLEX DNA - EFFECTS OF SINGLE-STRANDED ENDS, LENGTH OF HOMOLOGY, AND DYNAMIC STATE

Citation
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
Citations number
42
Categorie Soggetti
Biology
Journal title
ISSN journal
00062960
Volume
33
Issue
38
Year of publication
1994
Pages
11486 - 11492
Database
ISI
SICI code
0006-2960(1994)33:38<11486:JMBRPI>2.0.ZU;2-S
Abstract
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.