TY - JOUR
T1 - Arm sequences contribute to the architecture and catalytic function of a λ integrase-Holliday junction complex
AU - Radman-Livaja, Marta
AU - Shaw, Christine
AU - Azaro, Marco
AU - Biswas, Tapan
AU - Ellenberger, Tom
AU - Landy, Arthur
N1 - Funding Information:
We thank Christine Lank for technical assistance, Joan Boyles for manuscript preparation, and members of the Landy and Ellenberger laboratories for comments and suggestions. We are grateful to Jeffrey Gardner for communication of results prior to publication. This work was supported by NIH grants GM33928 and GM62723 to A.L. and NIH grant GM59902 to T.E.
PY - 2003/3/1
Y1 - 2003/3/1
N2 - λ integrase (Int) mediates recombination between attachment sites on λ phage and E. coli DNAs. With the assistance of accessory proteins that induce DNA loops, Int bridges pairs of distinct arm- and core-type DNA binding sites to form synapsed recombination complexes, which then recombine via a Holliday junction (HJ) intermediate. We show that, in addition to promoting the proper positioning of Int protomers, the arm sequences facilitate the catalytic activities of the Int tetramer, independent of accessory proteins or physical continuity between the arm and core sites. We have determined the architecture of ternary complexes containing a HJ, Int, and P′1,2 arm-type DNA. These structures accommodate simultaneous binding of Int to direct-repeat arm sites and indirect-repeat core sites and afford a new view of the higher-order recombinogenic complexes.
AB - λ integrase (Int) mediates recombination between attachment sites on λ phage and E. coli DNAs. With the assistance of accessory proteins that induce DNA loops, Int bridges pairs of distinct arm- and core-type DNA binding sites to form synapsed recombination complexes, which then recombine via a Holliday junction (HJ) intermediate. We show that, in addition to promoting the proper positioning of Int protomers, the arm sequences facilitate the catalytic activities of the Int tetramer, independent of accessory proteins or physical continuity between the arm and core sites. We have determined the architecture of ternary complexes containing a HJ, Int, and P′1,2 arm-type DNA. These structures accommodate simultaneous binding of Int to direct-repeat arm sites and indirect-repeat core sites and afford a new view of the higher-order recombinogenic complexes.
UR - http://www.scopus.com/inward/record.url?scp=0344806949&partnerID=8YFLogxK
U2 - 10.1016/S1097-2765(03)00111-4
DO - 10.1016/S1097-2765(03)00111-4
M3 - Article
C2 - 12667459
AN - SCOPUS:0344806949
SN - 1097-2765
VL - 11
SP - 783
EP - 794
JO - Molecular cell
JF - Molecular cell
IS - 3
ER -