Evidence map›Paper›PMID 26284603›Full record

ArticleeLife2015

Intrinsic sequence specificity of the Cas1 integrase directs new spacer acquisition.

Clare Rollie, Stefanie Schneider, Anna Sophie Brinkmann, Edward L Bolt, Malcolm F White

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
7.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 111 citations in OpenAlex.

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  20. The CRISPR-associated Cas4 protein fromCurrent research in microbial sciences · 2021
    Article

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Clare RollieBiomedical Sciences Research Complex, University of St Andrews, St Andrews, United Kingdom.
Stefanie SchneiderFaculty of Medicine, Institute of Cell Biology, University of Duisburg-Essen, Essen, Germany.
Anna Sophie BrinkmannSchool of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, United Kingdom.
Edward L BoltSchool of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, United Kingdom.
Malcolm F WhiteBiomedical Sciences Research Complex, University of St Andrews, St Andrews, United Kingdom.ORCID http://orcid.org/0000-0003-1543-9342
University of Nottingham · GBUniversity of St Andrews · GBUniversity of Duisburg-Essen · DE

Funding

Biotechnology and Biological Sciences Research Council BB/M000400/1
6 · The paper itself

Abstract

The adaptive prokaryotic immune system CRISPR-Cas provides RNA-mediated protection from invading genetic elements. The fundamental basis of the system is the ability to capture small pieces of foreign DNA for incorporation into the genome at the CRISPR locus, a process known as Adaptation, which is dependent on the Cas1 and Cas2 proteins. We demonstrate that Cas1 catalyses an efficient trans-esterification reaction on branched DNA substrates, which represents the reverse- or disintegration reaction. Cas1 from both Escherichia coli and Sulfolobus solfataricus display sequence specific activity, with a clear preference for the nucleotides flanking the integration site at the leader-repeat 1 boundary of the CRISPR locus. Cas2 is not required for this activity and does not influence the specificity. This suggests that the inherent sequence specificity of Cas1 is a major determinant of the adaptation process.

Indexed as

Archaeal ProteinsCRISPR-Associated ProteinsEndodeoxyribonucleasesEscherichia coliEscherichia coli ProteinsRecombination, GeneticSubstrate SpecificitySulfolobus solfataricusArchaeal ProteinsCRISPR-Associated ProteinsEndodeoxyribonucleasesEscherichia coli ProteinsYgbT protein, E coliadaptationbiochemistryCRISPRE. coliintegraseSulfolobus solfataricus

Identifiers

PMID26284603
PMCPMC4574026
OpenAlexW1954044701

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.