Nucleic Acids Research Advance Access first published online on May 30, 2007
This version published online on May 31, 2007
Nucleic Acids Research, doi:10.1093/nar/gkm360
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Web Server Issue |
CRISPRFinder: a web tool to identify clustered regularly interspaced short palindromic repeats
1Univ Paris-Sud, Institut de Génétique et Microbiologie, UMR 8621, Orsay, F-91405 and 2Centre dEtude du Bouchet, 5 rue Lavoisier, 91710 Vert le Petit, France
*To whom correspondence should be addressed. Tel: 33 1 69 15 30 01; Fax: 33 1 69 15 66 78; Email: Ibtissem.Grissa{at}igmors.u-psud.fr
Received January 25, 2007. Revised April 6, 2007. Accepted April 25, 2007.
Clustered regularly interspaced short palindromic repeats (CRISPRs) constitute a particular family of tandem repeats found in a wide range of prokaryotic genomes (half of eubacteria and almost all archaea). They consist of a succession of highly conserved regions (DR) varying in size from 23 to 47 bp, separated by similarly sized unique sequences (spacer) of usually viral origin. A CRISPR cluster is flanked on one side by an AT-rich sequence called the leader and assumed to be a transcriptional promoter. Recent studies suggest that this structure represents a putative RNA-interference-based immune system. Here we describe CRISPRFinder, a web service offering tools to (i) detect CRISPRs including the shortest ones (one or two motifs); (ii) define DRs and extract spacers; (iii) get the flanking sequences to determine the leader; (iv) blast spacers against Genbank database and (v) check if the DR is found elsewhere in prokaryotic sequenced genomes. CRISPRFinder is freely accessible at http://crispr.u-psud.fr/Server/CRISPRfinder.php.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
I. Grissa, G. Vergnaud, and C. Pourcel CRISPRcompar: a website to compare clustered regularly interspaced short palindromic repeats Nucleic Acids Res., April 28, 2008; (2008) gkn228v1. [Abstract] [Full Text] [PDF] |
||||
