Literature DB >> 12559909

Sequence of the loxP site determines the order of strand exchange by the Cre recombinase.

Linda Lee1, Paul D Sadowski.   

Abstract

Conservative site-specific recombinases of the integrase family carry out recombination via a Holliday intermediate. The Cre recombinase, a member of the integrase family, was previously shown to initiate recombination by cleaving and exchanging preferentially on the bottom strand of its loxP target sequence. We have confirmed this strand bias for an intermolecular recombination reaction that used wild-type loxP sites and Cre protein. We have examined the sequence determinants for this strand preference by selectively mutating the two asymmetric scissile base-pairs in the lox site (those immediately adjacent to the sites of cleavage by Cre). We found that the initial strand exchange occurs preferentially next to the scissile G residue. Resolution of the Holliday intermediate thus formed takes place preferentially next to the scissile A residue. Lys86, which contacts the scissile nucleotides in the Cre-lox crystal structures, was important for establishing the strand preference in the resolution of the loxP-Holliday intermediate, but not for the initiation of recombination between loxP sites.

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Year:  2003        PMID: 12559909     DOI: 10.1016/s0022-2836(02)01429-8

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  15 in total

1.  Crystal structure of a wild-type Cre recombinase-loxP synapse reveals a novel spacer conformation suggesting an alternative mechanism for DNA cleavage activation.

Authors:  Eric Ennifar; Joachim E W Meyer; Frank Buchholz; A Francis Stewart; Dietrich Suck
Journal:  Nucleic Acids Res       Date:  2003-09-15       Impact factor: 16.971

2.  DNA recombination with a heterospecific Cre homolog identified from comparison of the pac-c1 regions of P1-related phages.

Authors:  Brian Sauer; Jeffrey McDermott
Journal:  Nucleic Acids Res       Date:  2004-11-18       Impact factor: 16.971

3.  Protein-induced local DNA bends regulate global topology of recombination products.

Authors:  Quan Du; Alexei Livshits; Agnieszka Kwiatek; Makkuni Jayaram; Alexander Vologodskii
Journal:  J Mol Biol       Date:  2007-02-11       Impact factor: 5.469

Review 4.  Challenging a paradigm: the role of DNA homology in tyrosine recombinase reactions.

Authors:  Lara Rajeev; Karolina Malanowska; Jeffrey F Gardner
Journal:  Microbiol Mol Biol Rev       Date:  2009-06       Impact factor: 11.056

5.  Spatially directed assembly of a heterotetrameric Cre-Lox synapse restricts recombination specificity.

Authors:  Kathy A Gelato; Shelley S Martin; Patty H Liu; April A Saunders; Enoch P Baldwin
Journal:  J Mol Biol       Date:  2008-03-04       Impact factor: 5.469

6.  Insights into the preferential order of strand exchange in the Cre/loxP recombinase system: impact of the DNA spacer flanking sequence and flexibility.

Authors:  Josephine Abi-Ghanem; Sergey A Samsonov; M Teresa Pisabarro
Journal:  J Comput Aided Mol Des       Date:  2015-01-03       Impact factor: 3.686

7.  Multiple levels of affinity-dependent DNA discrimination in Cre-LoxP recombination.

Authors:  Kathy A Gelato; Shelley S Martin; Scott Wong; Enoch P Baldwin
Journal:  Biochemistry       Date:  2006-10-10       Impact factor: 3.162

8.  Reversed DNA strand cleavage specificity in initiation of Cre-LoxP recombination induced by the His289Ala active-site substitution.

Authors:  Kathy A Gelato; Shelley S Martin; Enoch P Baldwin
Journal:  J Mol Biol       Date:  2005-10-05       Impact factor: 5.469

9.  Control of directionality in the DNA strand-exchange reaction catalysed by the tyrosine recombinase TnpI.

Authors:  Virginie Vanhooff; Christophe Normand; Christine Galloy; Anca M Segall; Bernard Hallet
Journal:  Nucleic Acids Res       Date:  2009-12-30       Impact factor: 16.971

10.  Homology-dependent interactions determine the order of strand exchange by IntDOT recombinase.

Authors:  Jennifer Laprise; Sumiko Yoneji; Jeffrey F Gardner
Journal:  Nucleic Acids Res       Date:  2009-12-01       Impact factor: 16.971

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