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Structure and operation of the DNA-translocating type I DNA restriction enzymes

Authors :
Laurie P. Cooper
Philip Callow
John H. White
David T. F. Dryden
Christopher K. Kennaway
Gareth A. Roberts
Jean-Baptiste Artero
Chun Feng Song
John Trinick
William V. Nicholson
Wojciech Potrzebowski
Anna Swiderska
James E. Taylor
Angnieszka Obarska-Kosinska
Janusz M. Bujnicki
Geoff Kneale
Source :
Kennaway, C K, Taylor, J E, Song, C F, Potrzebowski, W, Nicholson, W, White, J H, Swiderska, A, Obarska-Kosinska, A, Callow, P, Cooper, L P, Roberts, G A, Artero, J-B, Bujnicki, J M, Trinick, J, Kneale, G G & Dryden, D T F 2012, ' Structure and operation of the DNA-translocating type I DNA restriction enzymes ', Genes & Development, vol. 26, no. 1, pp. 92-104 . https://doi.org/10.1101/gad.179085.111
Publication Year :
2012

Abstract

Type I DNA restriction/modification (RM) enzymes are molecular machines found in the majority of bacterial species. Their early discovery paved the way for the development of genetic engineering. They control (restrict) the influx of foreign DNA via horizontal gene transfer into the bacterium while maintaining sequence-specific methylation (modification) of host DNA. The endonuclease reaction of these enzymes on unmethylated DNA is preceded by bidirectional translocation of thousands of base pairs of DNA toward the enzyme. We present the structures of two type I RM enzymes, EcoKI and EcoR124I, derived using electron microscopy (EM), small-angle scattering (neutron and X-ray), and detailed molecular modeling. DNA binding triggers a large contraction of the open form of the enzyme to a compact form. The path followed by DNA through the complexes is revealed by using a DNA mimic anti-restriction protein. The structures reveal an evolutionary link between type I RM enzymes and type II RM enzymes.

Details

ISSN :
15495477
Volume :
26
Issue :
1
Database :
OpenAIRE
Journal :
Genesdevelopment
Accession number :
edsair.doi.dedup.....4b23d465c8c869dc39aa92bac0997968
Full Text :
https://doi.org/10.1101/gad.179085.111