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Pregled bibliografske jedinice broj: 786437

Different genome stability proteins underpin primed and naıve adaptation in E. coli CRISPR-Cas immunity


Ivančić-Baće, Ivana; Cass, Simon D.; Wearne, Stephen J.; Bolt, Edward L.
Different genome stability proteins underpin primed and naıve adaptation in E. coli CRISPR-Cas immunity // Nucleic acids research, 43 (2015), 22; 10821-10830 doi:10.1093/nar/gkv1213 (međunarodna recenzija, članak, znanstveni)


Naslov
Different genome stability proteins underpin primed and naıve adaptation in E. coli CRISPR-Cas immunity

Autori
Ivančić-Baće, Ivana ; Cass, Simon D. ; Wearne, Stephen J. ; Bolt, Edward L.

Izvornik
Nucleic acids research (0305-1048) 43 (2015), 22; 10821-10830

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
CRISPR-Cas; Cas1; RecG; PriA; PolA; E. coli

Sažetak
CRISPR-Cas is a prokaryotic immune system built from capture and integration of invader DNA into CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) loci, termed ‘Adaptation’, which is dependent on Cas1 and Cas2 proteins. In Escherichia coli, Cascade-Cas3 degrades invader DNA to effect immunity, termed ‘Interference’. Adaptation can interact with interference (‘primed’), or is independent of it (‘naıve’). We demonstrate that primed adaptation requires the RecG helicase and PriA protein to be present. Genetic analysis of mutant phenotypes suggests that RecG is needed to dissipate R-loops at blocked replication forks. Additionally, we identify that DNA polymerase I is important for both primed and naive adaptation, and that RecB is needed for na¨ıve adaptation. Purified Cas1-Cas2 protein shows specificity for binding to and nicking forked DNA within single strand gaps, and collapsing forks into DNA duplexes. The data suggest that different genome stability systems interact with primed or naıve adaptation when responding to blocked or collapsed invader DNA replication. In this model, RecG and Cas3 proteins respond to invader DNA replication forks that are blocked by Cascade interference, enabling DNA capture. RecBCD targets DNA ends at collapsed forks, enabling DNA capture without interference. DNA polymerase I is proposed to fill DNA gaps during spacer integration.

Izvorni jezik
Engleski

Znanstvena područja
Biologija



POVEZANOST RADA


Ustanove
Prirodoslovno-matematički fakultet, Zagreb

Autor s matičnim brojem:
Ivana Ivančić Baće, (217264)

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Uključenost u ostale bibliografske baze podataka:


  • CAB Abstracts


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