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          Document History for Document ID 236906

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Document Version Version Comment Date Status
236906.0 [No comment] 30.01.2007 15:45 Released

ID: 236906.0, MPI für biophysikalische Chemie / Molekulare Biologie (Dr. Thomas M. Jovin)
The Cfr10I restriction enzyme is functional as a tetramer
Authors:Siksnys, V.; Skirgaila, R.; Sasnaukas, G.; Urbanke, C.; Cherny, D. I.; Grazulis, S.; Huber, R.
Language:English
Date of Publication (YYYY-MM-DD):1999
Title of Journal:Journal of Molecular Biology
Volume:291
Start Page:1105
End Page:1118
Copyright:Jahrbuch 2000, Copyright MPG 2000
Review Status:not specified
Audience:Not Specified
Intended Educational Use:No
Abstract / Description:It is thought that most of TypeII restriction endonucleases interact with DNA as homodimers. The Cfr10I is a typical TypeII restriction enzyme that recognises 5’-PuØCCGGPy sequence and cleaves it as indicated by the arrow. Gel-filtration and analytical ultracentrifugation data presented here indicate that Cfr10I is a homotetramer in solution. The only SfiI restriction enzyme that recognises long interrupted recognition sequence 5’-GGCCNNNNNGGCC has been previously reported to operate as a tetramer, however its structure is unknown. Analysis of Cfr10I crystals revealed that a single molecule in the asymmetric unit is repeated by D2 symmetry to form a tetramer. To determine whether the packing of the Cfr10I in the crystal reflects the quaternary structure of the protein in solution, the tryptophan W220 residue located at the putative dimer-dimer interface was mutated to alanine and the structural and functional consequences of the substitution were analysed. Equilibrium sedimentation experiments revealed that in contrast to the wild type Cfr10I, the W220A mutant exists in solution predominantly as a dimer. In addition, the tetramer seems to be a catalytically important form of Cfr10I since the DNA cleavage activity of the W220A mutant is <0.1% of that of the wild type enzyme. Further, analysis of plasmid DNA cleavage suggests that the Cfr10I tetramer is able to interact with two copies of the recognition sequence, located on the same DNA molecule. Indeed, electron microscopy studies demonstrated that two distant recognition sites are brought together through the DNA looping induced by the simultaneous binding of the Cfr10I tetramer to both sites. These data are consistent with the tetramer being a functionally important form of Cfr10I.
Free Keywords:Cfr10I; quaternary structure; restriction enzyme; site-directed mutagenesis
Last Change of the Resource (YYYY-MM-DD):2005-08-05
External Publication Status:published
Document Type:Article
Communicated by:N. N.
Affiliations:MPI für biophysikalische Chemie/Abt. Thomas Jovin / 060
MPI für Biochemie
Identifiers:LOCALID:11480