Arm sequences contribute to the architecture and catalytic function of a λ integrase-holliday junction complex

被引:26
作者
Radman-Livaja, M
Shaw, C
Azaro, M
Biswas, T
Ellenberger, T
Landy, A
机构
[1] Brown Univ, Dept Biochem Mol Biol & Cell Biol, Providence, RI 02912 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
[4] Univ Med & Dent New Jersey, Dept Microbiol Mol Genet & Immunol, New Brunswick, NJ 08903 USA
[5] Canc Inst New Jersey, New Brunswick, NJ 08903 USA
关键词
D O I
10.1016/S1097-2765(03)00111-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
lambda integrase (Int) mediates recombination between attachment sites on lambda 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.
引用
收藏
页码:783 / 794
页数:12
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