Literature DB >> 3528147

Specific contacts between the FLP protein of the yeast 2-micron plasmid and its recombination site.

R C Bruckner, M M Cox.   

Abstract

Contact points between the FLP protein of the yeast 2-micron plasmid and its recombination site have been defined. Important features of the region previously defined as the minimal recombination site in vitro include a pair of 13-base pair inverted repeats separated by an 8-base pair spacer. The two FLP protein-binding sites within this region are 12 base pairs in length. In each case they include the internal 11 base pairs of one of the 13-base pair repeats, as well as the adjacent base pair within the spacer. The internal 6 base pairs within the spacer are not involved in binding or recognition by FLP protein. When the size of the spacer is increased or decreased by one base pair, the distance between the cleavage points is also increased or decreased correspondingly by one base pair. Points of cleavage are unaffected by changes in the spacer sequence. Specific contact points involving purine residues, identified by methylation protection and recombination interference experiments, are located in both the major and minor grooves of the DNA. Additional contact points between FLP protein and phosphate groups in the phosphate-deoxyribose backbone are clustered near the cleavage sites.

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Year:  1986        PMID: 3528147

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

1.  Integration of human immunodeficiency virus DNA: adduct interference analysis of required DNA sites.

Authors:  F D Bushman; R Craigie
Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-15       Impact factor: 11.205

2.  Synthesis of an enzymatically active FLP recombinase in vitro: search for a DNA-binding domain.

Authors:  A A Amin; P D Sadowski
Journal:  Mol Cell Biol       Date:  1989-05       Impact factor: 4.272

3.  Synapsis, strand scission, and strand exchange induced by the FLP recombinase: analysis with half-FRT sites.

Authors:  A Amin; H Roca; K Luetke; P D Sadowski
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

4.  Characterization of Holliday structures in FLP protein-promoted site-specific recombination.

Authors:  L Meyer-Leon; R B Inman; M M Cox
Journal:  Mol Cell Biol       Date:  1990-01       Impact factor: 4.272

5.  Asymmetry in Flp-mediated cleavage.

Authors:  K H Luetke; B P Zhao; P D Sadowski
Journal:  Nucleic Acids Res       Date:  1997-11-01       Impact factor: 16.971

6.  Mutations in the 2-microns circle site-specific recombinase that abolish recombination without affecting substrate recognition.

Authors:  P V Prasad; L J Young; M Jayaram
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

7.  Holliday intermediates and reaction by-products in FLP protein-promoted site-specific recombination.

Authors:  L Meyer-Leon; L C Huang; S W Umlauf; M M Cox; R B Inman
Journal:  Mol Cell Biol       Date:  1988-09       Impact factor: 4.272

8.  Selection of novel, specific single-stranded DNA sequences by Flp, a duplex-specific DNA binding protein.

Authors:  X D Zhu; P D Sadowski
Journal:  Nucleic Acids Res       Date:  1998-03-01       Impact factor: 16.971

9.  FLP recombinase is an enzyme.

Authors:  C A Gates; M M Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1988-07       Impact factor: 11.205

10.  Purification of the FLP site-specific recombinase by affinity chromatography and re-examination of basic properties of the system.

Authors:  L Meyer-Leon; C A Gates; J M Attwood; E A Wood; M M Cox
Journal:  Nucleic Acids Res       Date:  1987-08-25       Impact factor: 16.971

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