Hale, C.R., Sonali, M., Elmore, J., Pfister, N., Compton, M., Olson S., Resch, A.M., Glover III, C.V.C., Graveley B.R., Terns, R.M., and M.P. Terns. 2012. Molecular Cell 45:292-302.
Small RNAs target invaders for silencing in the CRISPR-Cas pathways that protect bacteria and archaea from viruses and plasmids. The CRISPR RNAs (crRNAs) contain sequence elements acquired from invaders that guide CRISPR-associated (Cas) proteins back to the complementary invading DNA or RNA. Here, we have analyzed essential features of the crRNAs associated with the Cas RAMP module (Cmr) effector complex, which cleaves targeted RNAs. We show that Cmr crRNAs contain an 8 nucleotide 5′ sequence tag (also found on crRNAs associated with other CRISPR-Cas pathways) that is critical for crRNA function and can be used to engineer crRNAs that direct cleavage of novel targets. We also present data that indicate that the Cmr complex cleaves an endogenous complementary RNA in Pyrococcus furiosus, providing direct in vivo evidence of RNA targeting by the CRISPR-Cas system. Our findings indicate that the CRISPR RNA-Cmr protein pathway may be exploited to cleave RNAs of interest.
*The Donkey anti-Chicken IgY agarose and HRP-Donkey anti-Chicken IgY used in this publication were manufactured by Gallus Immunotech Inc.
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