Consequences of Cas9 cleavage in the chromosome of Escherichia coli - Archive ouverte HAL Access content directly
Journal Articles Nucleic Acids Research Year : 2016

Consequences of Cas9 cleavage in the chromosome of Escherichia coli

(1) , (1)
1

Abstract

The RNA-guided Cas9 nuclease from CRISPR-Cas systems has emerged as a powerful biotechnological tool. The specificity of Cas9 can be reprogrammed to cleave desired sequences in a cell's chromosome simply by changing the sequence of a small guide RNA. Unlike in most eukaryotes, Cas9 cleavage in the chromosome of bacteria has been reported to kill the cell. However, the mechanism of cell death remains to be investigated. Bacteria mainly rely on homologous recombination (HR) with sister chromosomes to repair double strand breaks. Here, we show that the simultaneous cleavage of all copies of the Escherichia coli chromosome at the same position cannot be repaired, leading to cell death. However, inefficient cleavage can be tolerated through continuous repair by the HR pathway. In order to kill cells reliably, HR can be blocked using the Mu phage Gam protein. Finally, the introduction of the non-homologous end joining (NHEJ) pathway from Mycobacterium tuberculosis was not able to rescue the cells from Cas9-mediated killing, but did introduce small deletions at a low frequency. This work provides a better understanding of the consequences of Cas9 cleavage in bacterial chromosomes which will be instrumental in the development of future CRISPR tools.
Fichier principal
Vignette du fichier
gkw223.pdf (1.16 Mo) Télécharger le fichier
Origin : Publication funded by an institution
Loading...

Dates and versions

pasteur-01967442 , version 1 (03-01-2019)

Licence

Attribution - NonCommercial - CC BY 4.0

Identifiers

Cite

Lun Cui, David Bikard. Consequences of Cas9 cleavage in the chromosome of Escherichia coli. Nucleic Acids Research, 2016, 44 (9), pp.4243-4251. ⟨10.1093/nar/gkw223⟩. ⟨pasteur-01967442⟩

Collections

PASTEUR ANR
32 View
291 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More