The Interwoven Architecture of the Mu Transposase Couples DNA Synapsis to Catalysis
Identifieur interne : 001659 ( Istex/Checkpoint ); précédent : 001658; suivant : 001660The Interwoven Architecture of the Mu Transposase Couples DNA Synapsis to Catalysis
Auteurs : Hector Aldaz [États-Unis] ; Eugene Schuster [États-Unis] ; Tania A. Baker [États-Unis]Source :
- Cell [ 0092-8674 ] ; 1996.
English descriptors
- Teeft :
- Acidic, Active monomer, Active protein, Active site, Active sites, Active subunit, Active subunits, Active tetramer, Active transposase, Agarose, Binding activity, Binding domain, Binding sites, Biol, Catalysis, Catalytic, Catalytic residues, Catalyze, Catalyze strand transfer, Chaconas, Chem, Cleavage, Cleavage sites, Cleavage step, Covalently, Craigie, Domain, Domain iiia, Domain iiib, Embo, Fragment, Genome, Harshey, Iiia, Inactive subunits, Inactive transposase, Integrase, Jayaram, Joinable, Joinable substrate, Mizuuchi, Monomer, Oligonucleotides, Partner substratea, Personal communication, Phage, Phage genome, Possible arrangements, Recombinase, Recombination, Recombination sites, Recombining dnas, Savilahti, Stcs, Strand, Strand transfer, Subunit, Subunit arrangement, Surette, Synapsis, Tetramer, Tetramer assembly, Tetramers, Total reaction, Total reaction mixture, Trans, Transposase, Transposase acts, Transposase subunits, Transposase tetramer, Transposition, Transposition reactions, Unjoinable, Unjoinable substrate, Unjoinable substrates, Unjoined, Unpublished data.
Abstract
Abstract: Mu transposition occurs exclusively using a pair of recombination sites found at the ends of the phage genome. To address the mechanistic basis of this specificity, we have determined both where the individual subunits of the tetrameric transposase bind on the DNA and where they catalyze DNA joining. We demonstrate that subunits do not catalyze recombination at the site adjacent to where they are bound, but rather on the opposite end of the phage genome. Furthermore, subunits bound to two different sites contribute to catalysis of one reaction step. This interwoven subunit arrangement suggests a molecular explanation for the precision with which recombination occurs using a pair of DNA signals and provides an example of the way in which the architecture of a protein–DNA complex can define the reaction products.
Url:
DOI: 10.1016/S0092-8674(00)81102-2
Affiliations:
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ISTEX:365354F68B0CD54059610042AED543B886AEC623Le document en format XML
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<term>Joinable substrate</term>
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<front><div type="abstract" xml:lang="en">Abstract: Mu transposition occurs exclusively using a pair of recombination sites found at the ends of the phage genome. To address the mechanistic basis of this specificity, we have determined both where the individual subunits of the tetrameric transposase bind on the DNA and where they catalyze DNA joining. We demonstrate that subunits do not catalyze recombination at the site adjacent to where they are bound, but rather on the opposite end of the phage genome. Furthermore, subunits bound to two different sites contribute to catalysis of one reaction step. This interwoven subunit arrangement suggests a molecular explanation for the precision with which recombination occurs using a pair of DNA signals and provides an example of the way in which the architecture of a protein–DNA complex can define the reaction products.</div>
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