Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation

Journal Article (2019)
Author(s)

Olga Musharova (Skolkovo Institute of Science and Technology, Russian Academy of Sciences)

Vasily Sitnik (Skolkovo Institute of Science and Technology)

Marnix Vlot (Wageningen University & Research)

Ekaterina Savitskaya (Skolkovo Institute of Science and Technology, Russian Academy of Sciences)

Kirill A. Datsenko (Purdue University)

Andrey Krivoy (Skolkovo Institute of Science and Technology)

Ivan Fedorov (Skolkovo Institute of Science and Technology)

Ekaterina Semenova (Rutgers University)

Stan J.J. Brouns (Kavli institute of nanoscience Delft, Wageningen University & Research, TU Delft - Applied Sciences)

Konstantin Severinov (Russian Academy of Sciences, Rutgers University, Skolkovo Institute of Science and Technology)

Research Group
BN/Stan Brouns Lab
DOI related publication
https://doi.org/10.1111/mmi.14237 Final published version
More Info
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Publication Year
2019
Language
English
Research Group
BN/Stan Brouns Lab
Issue number
6
Volume number
111
Pages (from-to)
1558-1570
Downloads counter
246
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Institutional Repository
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Abstract

CRISPR interference occurs when a protospacer recognized by the CRISPR RNA is destroyed by Cas effectors. In Type I CRISPR-Cas systems, protospacer recognition can lead to «primed adaptation» – acquisition of new spacers from in cis located sequences. Type I CRISPR-Cas systems require the presence of a trinucleotide protospacer adjacent motif (PAM) for efficient interference. Here, we investigated the ability of each of 64 possible trinucleotides located at the PAM position to induce CRISPR interference and primed adaptation by the Escherichia coli Type I-E CRISPR-Cas system. We observed clear separation of PAM variants into three groups: those unable to cause interference, those that support rapid interference and those that lead to reduced interference that occurs over extended periods of time. PAM variants unable to support interference also did not support primed adaptation; those that supported rapid interference led to no or low levels of adaptation, while those that caused attenuated levels of interference consistently led to highest levels of adaptation. The results suggest that primed adaptation is fueled by the products of CRISPR interference. Extended over time interference with targets containing «attenuated» PAM variants provides a continuous source of new spacers leading to high overall level of spacer acquisition.