Evidence map›Paper›PMID 32991234›Full record

ReviewRNA biology2021

Type II anti-CRISPR proteins as a new tool for synthetic biology.

Yadan Zhang, Mario Andrea Marchisio

Open access · bronzeAbstract readReview
In one paragraph

Review in RNA biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. AnMicroorganisms · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Tips, Tricks, and Potential Pitfalls of CRISPR Genome Editing inFrontiers in bioengineering and biotechnology · 2022
    Review
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.

Yadan ZhangSchool of Pharmaceutical Science and Technology, Tianjin University, Tianjin, China.ORCID 0000-0003-0993-0709
Mario Andrea MarchisioSchool of Pharmaceutical Science and Technology, Tianjin University, Tianjin, China.ORCID 0000-0002-5102-1069

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clustered regularly interspaced short palindromic repeats (CRISPR)-Cas (CRISPR-associated proteins) system represents, in prokaryotes, an adaptive and inheritable immune response against invading DNA. The discovery of anti-CRISPR proteins (Acrs), which are inhibitors of CRISPR-Cas, mainly encoded by phages and prophages, showed a co-evolution history between prokaryotes and phages. In the past decade, the CRISPR-Cas systems together with the corresponding Acrs have been turned into a genetic-engineering tool. Among the six types of CRISPR-Cas characterized so far, type II CRISPR-Cas system is the most popular in biotechnology. Here, we discuss about the discovery, the reported inhibitory mechanisms, and the applications in both gene editing and gene transcriptional regulation of type II Acrs. Moreover, we provide insights into future potential research and feasible applications.

Indexed as

CRISPR-Cas SystemsArchaeaBacteriaBacteriophagesBiological CoevolutionBiotechnologyClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Associated Protein 9Gene EditingHumansProphagesRNA, Guide, CRISPR-Cas SystemsSynthetic BiologyCRISPR-Associated Protein 9RNA, Guide, CRISPR-Cas SystemsCas9CRISPR-Cas systemgene editingsynthetic biologytranscriptional regulationtype II anti-CRISPRs

Identifiers

PMID32991234
PMCPMC8244766
OpenAlexW3090492997

What OpenQuestion holds

Textmetadata
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.