Author

L. Randau

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:bacteria (other)· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Assay:DNA methylation· 1

Frequent Co-Authors

J. Russel· 2 shared R. Pinilla-Redondo· 2 shared S. J. Soerensen· 2 shared A. Cuenod· 1 shared A. Egli· 1 shared A. R. Davidson· 1 shared A. R. Hall· 1 shared C. L. Beisel· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersMicrobiology

J. Russel

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Type IV-A3 CRISPR-Cas systems drive inter-plasmid conflicts by acquiring spacers in trans

F. Benz, S. Camara-Wilpert, J. Russel, K. G. Wandera, R. Cepaite, M. Ares-Arroyo, J. V. Gomes-Filho, F. Englert, J. Kuehn, S. Gloor, A. Cuenod, M. Aguila-Sans, L. Maccario, A. Egli, L. Randau, , R. Pinilla-Redondo

This study shows type IV-A3 CRISPR-Cas systems use host adaptation machinery to update their CRISPR arrays and interfere with plasmid and phage transfer, supporting their role in plasmid competition.

bioRxiv · Jun 23, 2023 · PreprintMicrobiology

An anti-CRISPR protein induces strong non-specific DNA binding activity in a CRISPR-Cas complex

W.-T. Lu, C. N. Trost, H. Muller-Esparza, L. Randau, A. R. Davidson

This study shows that AcrIF9 enhances non-specific DNA binding in a CRISPR-Cas complex, which is conserved across homologues and suggests a new mechanism for Acr function.

bioRxiv · May 28, 2020 · PreprintMicrobiology

Type IV CRISPR-Cas systems are highly diverse and involved in competition between plasmids

R. Pinilla-Redondo, D. Mayo-Munoz, J. Russel, R. A. Garrett, L. Randau, S. J. Soerensen, S. A. Shah

This study identifies a diverse range of type IV CRISPR-Cas systems primarily found on plasmids, revealing their role in plasmid competition and cross-talk with type I systems.

bioRxiv · Sep 24, 2019Microbiology