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PMID: 6220808 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Studies on the properties of P1 site-specific recombination: evidence for topologically unlinked products following recombination.

Cell ·Vol. 32 ·No. 4 ·1983-04-00 ·Pages 1301-11

Abremski K, Hoess R, Sternberg N

Abstract

Bacteriophage P1 encodes its own site-specific recombination system consisting of a site at which recombination takes place called loxP and a recombinase called Cre. A number of lambda and plasmid substrates containing two loxP sites have been constructed. Using these substrates we have shown both in vivo and in vitro that a fully functional loxP site is composed of no more than 60 bp. In vitro, when an extract containing Cre is used, recombination between loxP sites on supercoiled, nicked-circle or linear DNA occurs efficiently. The most surprising result from the in vitro studies is that 50% of the products of recombination between loxP sites on a supercoiled DNA substrate are present as free supercoiled circles. The ability to produce free products starting with a supercoiled substrate suggests a rather unique property of Cre-mediated lox recombination, the implications of which are discussed in terms of possible effects of the protein on the topology of the DNA molecule.

MeSH Terms
Bacteriophage lambda/genetics Coliphages/genetics DNA, Superhelical/genetics DNA, Viral/genetics Escherichia coli/genetics Genes, Viral Magnesium/pharmacology Models, Genetic Plasmids Recombination, Genetic Spermidine/pharmacology
Chemicals
DNA, Superhelical DNA, Viral Magnesium Spermidine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Abremski K
Hoess R
Sternberg N
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1983-04-00
Pages
1301-11
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · N01-CO-23909 · United States
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