Evidence map›Paper›PMID 35236570›Full record

ReviewTrends in biochemical sciences2022

Creating memories: molecular mechanisms of CRISPR adaptation.

Hayun Lee, Dipali G Sashital

Abstract readReview
In one paragraph

Review in Trends in biochemical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
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  18. CRISPR-Cas12a exhibits metal-dependent specificity switching.bioRxiv : the preprint server for biology · 2024
    Article
  19. Review
  20. Article
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

2 authors.

Hayun LeeDepartment of Biological and Chemical Engineering, Dongyang Mirae University, Seoul, South Korea. Electronic address: hayunlee@dongyang.ac.kr.
Dipali G SashitalRoy J. Carver Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames, IA, USA. Electronic address: sashital@iastate.edu.

Funding

Defining Mechanisms of Diverse CRISPR-Cas ComplexesR35GM140876 · NIGMS · IOWA STATE UNIVERSITY · PI Dipali Gurudutt Sashital · 2021 to 2026
$2.7M
Defining CRISPR adaptation and interference mechanisms in E. coliR01GM115874 · NIGMS · IOWA STATE UNIVERSITY · PI SASHITAL, DIPALI GURUDUTT · 2016 to 2021
$1.5M
NIGMS NIH HHS R01 GM115874NIGMS NIH HHS R35 GM140876
6 · The paper itself

Abstract

Prokaryotes use clustered regularly interspaced short palindromic repeat (CRISPR) and CRISPR-associated (Cas) proteins as an adaptive immune system. CRISPR-Cas systems preserve molecular memories of infections by integrating short fragments of foreign nucleic acids as spacers into the host CRISPR array in a process termed 'adaptation'. Functional spacers ensure a robust immune response by Cas effectors, which neutralizes subsequent infection through RNA-guided interference pathways. In this review, we summarize recent discoveries that have advanced our understanding of adaptation, with a focus on how functional spacers are generated and incorporated through many widespread, but type-specific, mechanisms. Finally, we highlight future directions and outstanding questions for a more thorough understanding of CRISPR adaptation.

Indexed as

CRISPR-Associated ProteinsCRISPR-Cas SystemsCRISPR-Associated ProteinsCas1-Cas2Cas4Cas9CRISPR-CasPAMspacers

Identifiers

PMID35236570
PMCPMC9106905

What OpenQuestion holds

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Registered trials

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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.