TY - JOUR
T1 - Determinants of directionality in lambda site-specific recombination
AU - Bushman, Wade
AU - Yin, Samuel
AU - Thio, Liu Lin
AU - Landy, Arthur
N1 - Funding Information:
We thank Ken Abremskt and Sue Wickner for advlce on Xis purlflcatlon, Klyoshl Mlzuuchl for plasmid pMM291; David Brautlgan, Sungman Cha, and Mike Fried for helpful dlscussions; Llna Vargas for assistance with DNA sequencing and nuclease-protectjon experiments and Shirley Rodrlgues for technlcai assistance. This work was supported by grant Al 13544 from the National lnstltutes of Health. S. Y. was a recipient of a Damon Runyon - Walter Winchell Cancer Fund postdoctoral fellowshlp.
PY - 1984/12
Y1 - 1984/12
N2 - The DNA structural features governing directionality in λ site-specific recombination are shown to reside in regions of the phage attachment site more than 70 bp to the left and more than 40 bp to the right of the cross-over region. Disposition of these sequences on the same attachment site in integration, and on different attachment sites in excision, determines the opposite effects of Xis protein upon the two reactions (stimulation of excision and inhibition of integration). The binding of Xis to two adjacent directly repeated sequences in the left phage arm is shown to occur in a highly cooperative manner, to alter the conformation of the DNA, and to produce a 32-fold stimulation of Int binding to an adjacent locus.
AB - The DNA structural features governing directionality in λ site-specific recombination are shown to reside in regions of the phage attachment site more than 70 bp to the left and more than 40 bp to the right of the cross-over region. Disposition of these sequences on the same attachment site in integration, and on different attachment sites in excision, determines the opposite effects of Xis protein upon the two reactions (stimulation of excision and inhibition of integration). The binding of Xis to two adjacent directly repeated sequences in the left phage arm is shown to occur in a highly cooperative manner, to alter the conformation of the DNA, and to produce a 32-fold stimulation of Int binding to an adjacent locus.
UR - http://www.scopus.com/inward/record.url?scp=0021676510&partnerID=8YFLogxK
U2 - 10.1016/0092-8674(84)90477-X
DO - 10.1016/0092-8674(84)90477-X
M3 - Article
C2 - 6239693
AN - SCOPUS:0021676510
SN - 0092-8674
VL - 39
SP - 699
EP - 706
JO - Cell
JF - Cell
IS - 3 PART 2
ER -