Evidence map›Paper›PMID 26451892›Full record

ArticleACS synthetic biology2015

Targeted Large-Scale Deletion of Bacterial Genomes Using CRISPR-Nickases.

Kylie Standage-Beier, Qi Zhang, Xiao Wang

Open access · greenAbstract readLetter
In one paragraph

Article in ACS synthetic biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Recent advances in genome-scale engineering inEngineering microbiology · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Recent Advances in CRISPR-Cas Technologies for Synthetic Biology.Journal of microbiology (Seoul, Korea) · 2023
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Portable CRISPR-Cas9Applied and environmental microbiology · 2021
    Article
  16. Article
  17. CRISPR/Cas Technologies and Their Applications inFrontiers in bioengineering and biotechnology · 2021
    Review
  18. Article
  19. Review
  20. CRISPR-Cas9/CRISPRi tools for cell factory construction in E. coli.World journal of microbiology & biotechnology · 2020
    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

3 authors at 1 institution in 1 country.

Kylie Standage-BeierSchool of Life Sciences, ‡School of Biological and Health Systems Engineering, Arizona State University , Tempe, Arizona 85287, United States.
Qi ZhangSchool of Life Sciences, ‡School of Biological and Health Systems Engineering, Arizona State University , Tempe, Arizona 85287, United States.
Xiao WangSchool of Life Sciences, ‡School of Biological and Health Systems Engineering, Arizona State University , Tempe, Arizona 85287, United States.
Arizona State University · US

Funding

Forward engineering to understand gene regulatory network topologiesR01GM106081 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI WANG, XIAO · 2014 to 2018
$1.7M
NIGMS NIH HHS GM106081NIGMS NIH HHS R01 GM106081
6 · The paper itself

Abstract

Programmable CRISPR-Cas systems have augmented our ability to produce precise genome manipulations. Here we demonstrate and characterize the ability of CRISPR-Cas derived nickases to direct targeted recombination of both small and large genomic regions flanked by repetitive elements in Escherichia coli. While CRISPR directed double-stranded DNA breaks are highly lethal in many bacteria, we show that CRISPR-guided nickase systems can be programmed to make precise, nonlethal, single-stranded incisions in targeted genomic regions. This induces recombination events and leads to targeted deletion. We demonstrate that dual-targeted nicking enables deletion of 36 and 97 Kb of the genome. Furthermore, multiplex targeting enables deletion of 133 Kb, accounting for approximately 3% of the entire E. coli genome. This technology provides a framework for methods to manipulate bacterial genomes using CRISPR-nickase systems. We envision this system working synergistically with preexisting bacterial genome engineering methods.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsGene DeletionGenome, BacterialRecombination, GeneticSynthetic BiologyCas9 nickasechromosome deletionCRISPRdirect repeatsgenome engineeringrecombination

Identifiers

PMID26451892
PMCPMC4655420
OpenAlexW2204786127

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.