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Microbial Arsenal of Antiviral Defenses – Part I

Biochemistry (Moscow), 2021-03, Vol.86 (3), p.319-337

2021

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Microbial Arsenal of Antiviral Defenses. Part II

Biochemistry (Moscow), 2021-04, Vol.86 (4), p.449-470

2021

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Interaction between transcribing RNA polymerase and topoisomerase I prevents R-loop formation in E. coli

Nature communications, 2022-08, Vol.13 (1), p.1-19, Article 4524

2022

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Avoidance of Trinucleotide Corresponding to Consensus Protospacer Adjacent Motif Controls the Efficiency of Prespacer Selection during Primed Adaptation

mBio, 2018-12, Vol.9 (6)

2018

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RecA-dependent or independent recombination of plasmid DNA generates a conflict with the host EcoKI immunity by launching restriction alleviation

Nucleic acids research, 2024-05, Vol.52 (9), p.5195-5208

2024

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Primed CRISPR adaptation in Escherichia coli cells does not depend on conformational changes in the Cascade effector complex detected in Vitro

Nucleic acids research, 2018-05, Vol.46 (8), p.4087-4098

2018

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Highly efficient primed spacer acquisition from targets destroyed by the Escherichia coli type I-E CRISPR-Cas interfering complex

Proceedings of the National Academy of Sciences - PNAS, 2016-07, Vol.113 (27), p.7626-7631

2016

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PpCas9 from Pasteurella pneumotropica - a compact Type II-C Cas9 ortholog active in human cells

Nucleic acids research, 2020-12, Vol.48 (21), p.12297-12309

2020

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CRISPR interference and priming varies with individual spacer sequences

Nucleic acids research, 2015-12, Vol.43 (22), p.10831-10847

2015

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DNA targeting by Clostridium cellulolyticum CRISPR-Cas9 Type II-C system

Nucleic acids research, 2020-02, Vol.48 (4), p.2026-2034

2020

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Spacer-length DNA intermediates are associated with Cas1 in cells undergoing primed CRISPR adaptation

Nucleic acids research, 2017-04, Vol.45 (6), p.3297-3307

2017

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

Molecular microbiology, 2019-06, Vol.111 (6), p.1558-1570

2019

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Position of Deltaproteobacteria Cas12e nuclease cleavage sites depends on spacer length of guide RNA

RNA biology, 2020-10, Vol.17 (10), p.1472-1479

2020

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Host nucleases generate prespacers for primed adaptation in the E. coli type I-E CRISPR-Cas system

Science advances, 2022-11, Vol.8 (47), p.eabn8650-eabn8650

2022

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Microbial Arsenal of Antiviral Defenses – Part I

Microbial Arsenal of Antiviral Defenses. Part II

Interaction between transcribing RNA polymerase and topoisomerase I prevents R-loop formation in E. coli

Avoidance of Trinucleotide Corresponding to Consensus Protospacer Adjacent Motif Controls the Efficiency of Prespacer Selection during Primed Adaptation

RecA-dependent or independent recombination of plasmid DNA generates a conflict with the host EcoKI immunity by launching restriction alleviation

Primed CRISPR adaptation in Escherichia coli cells does not depend on conformational changes in the Cascade effector complex detected in Vitro

Highly efficient primed spacer acquisition from targets destroyed by the Escherichia coli type I-E CRISPR-Cas interfering complex

PpCas9 from Pasteurella pneumotropica - a compact Type II-C Cas9 ortholog active in human cells

CRISPR interference and priming varies with individual spacer sequences

DNA targeting by Clostridium cellulolyticum CRISPR-Cas9 Type II-C system

Spacer-length DNA intermediates are associated with Cas1 in cells undergoing primed CRISPR adaptation

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

Position of Deltaproteobacteria Cas12e nuclease cleavage sites depends on spacer length of guide RNA

Host nucleases generate prespacers for primed adaptation in the E. coli type I-E CRISPR-Cas system

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