Direct CRISPR spacer acquisition from RNA by a natural reverse transcriptase–Cas1 fusion protein

Author:

Silas Sukrit12,Mohr Georg3,Sidote David J.3,Markham Laura M.3,Sanchez-Amat Antonio4,Bhaya Devaki5,Lambowitz Alan M.3,Fire Andrew Z.1

Affiliation:

1. Department of Pathology, Stanford University, Stanford, CA 94305, USA.

2. Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.

3. Institute for Cellular and Molecular Biology, Department of Molecular Biosciences, University of Texas–Austin, Austin, TX 78712, USA.

4. Department of Genetics and Microbiology, Universidad de Murcia, Murcia 30100, Spain.

5. Department of Plant Biology, Carnegie Institution for Science, Stanford, CA 94305, USA.

Abstract

CRISPR-Cas captures invading RNA The CRISPR (clustered regularly interspaced short palindromic repeat) system provides bacteria with an adaptive immune response. DNA captured from viruses and plasmids by CRISPR-associated protein 1 (Cas1) is used by bacteria to target the invaders' for destruction. Silas et al. discover that certain classes of the Cas1 gene are fused to a reverse transcriptase gene ( RT-Cas1 ) (see the Perspective by Sontheimer and Marraffini). These RT-Cas1 proteins are able to capture and directly incorporate both DNA and RNA into CRISPR loci. RT-Cas1 systems could be effective against parasitic RNA species, or even to modulate bacterial gene expression. Science , this issue p. 10.1126/science.aad4234 ; see also p. 920

Funder

Howard Hughes Medical Institute

NIH

Welch Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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