Journal
MOLECULAR CELL
Volume 64, Issue 3, Pages 616-623Publisher
CELL PRESS
DOI: 10.1016/j.molcel.2016.08.038
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Funding
- U.S. National Science Foundation
- Rita Allen Scholars Program
- Sinsheimer Foundation Award
- NIH Director's New Innovator Award [1DP2AI104556-01]
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CRISPR-Cas systems defend prokaryotes against viruses and plasmids. Short DNA segments of the invader, known as spacers, are stored in the CRISPR array as immunological memories. New spacers are added invariably to the 50 end of the array; therefore, the first spacer matches the latest foreign threat. Whether this highly polarized order of spacer insertion influences CRISPR-Cas immunity has not been explored. Here we show that a conserved sequence located immediately upstream of the CRISPR array specifies the site of new spacer integration. Mutation of this sequence results in erroneous incorporation of new spacers into the middle of the array. We show that spacers added through polarized acquisition give rise to more robust CRISPR-Cas immunity than spacers added to the middle of the array. This study demonstrates that the CRISPR-Cas system specifies the site of spacer integration to optimize the immune response against the most immediate threat to the host.
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