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Identification of genes that are associated with DNA repeats in prokaryotes
Article first published online: 25 APR 2002
Volume 43, Issue 6, pages 1565–1575, March 2002
How to Cite
Jansen, Ruud., Embden, Jan. D. A. v., Gaastra, Wim. and Schouls, Leo. M. (2002), Identification of genes that are associated with DNA repeats in prokaryotes. Molecular Microbiology, 43: 1565–1575. doi: 10.1046/j.1365-2958.2002.02839.x
- Issue published online: 25 APR 2002
- Article first published online: 25 APR 2002
Using in silico analysis we studied a novel family of repetitive DNA sequences that is present among both domains of the prokaryotes (Archaea and Bacteria), but absent from eukaryotes or viruses. This family is characterized by direct repeats, varying in size from 21 to 37 bp, interspaced by similarly sized non-repetitive sequences. To appreciate their characteri-stic structure, we will refer to this family as the clustered regularly interspaced short palindromic repeats (CRISPR). In most species with two or more CRISPR loci, these loci were flanked on one side by a common leader sequence of 300–500 b. The direct repeats and the leader sequences were conserved within a species, but dissimilar between species. The presence of multiple chromosomal CRISPR loci suggests that CRISPRs are mobile elements. Four CRISPR-associated (cas) genes were identified in CRISPR-containing prokaryotes that were absent from CRISPR-negative prokaryotes. The cas genes were invariably located adjacent to a CRISPR locus, indicating that the cas genes and CRISPR loci have a functional relationship. The cas3 gene showed motifs characteristic for helicases of the superfamily 2, and the cas4 gene showed motifs of the RecB family of exonucleases, suggesting that these genes are involved in DNA metabolism or gene expression. The spatial coherence of CRISPR and cas genes may stimulate new research on the genesis and biological role of these repeats and genes.