Evidence map›Paper›PMID 33147260›Full record

ArticlePloS one2020

Bacterial genome editing by coupling Cre-lox and CRISPR-Cas9 systems.

Hualan Liu, David S Robinson, Zong-Yen Wu, Rita Kuo, Yasuo Yoshikuni, Ian K Blaby, Jan-Fang Cheng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Hualan LiuUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.ORCID 0000-0002-9636-3855
David S RobinsonUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Zong-Yen WuUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Rita KuoUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Yasuo YoshikuniUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Ian K BlabyUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Jan-Fang ChengUS Department of Energy Joint Genome Institute, Berkeley, California, United States of America.
Lawrence Berkeley National Laboratory · USJoint Genome Institute · USNational Chung Hsing University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The past decade has been a golden age for microbiology, marked by the discovery of an unprecedented increase in the number of novel bacterial species. Yet gaining biological knowledge of those organisms has not kept pace with sequencing efforts. To unlock this genetic potential there is an urgent need for generic (i.e. non-species specific) genetic toolboxes. Recently, we developed a method, termed chassis-independent recombinase-assisted genome engineering (CRAGE), enabling the integration and expression of large complex gene clusters directly into the chromosomes of diverse bacteria. Here we expand upon this technology by incorporating CRISPR-Cas9 allowing precise genome editing across multiple bacterial species. To do that we have developed a landing pad that carries one wild-type and two mutant lox sites to allow integration of foreign DNA at two locations through Cre-lox recombinase-mediated cassette exchange (RMCE). The first RMCE event is to integrate the Cas9 and the DNA repair protein genes RecET, and the second RMCE event enables the integration of customized sgRNA and a repair template. Following this workflow, we achieved precise genome editing in four different gammaproteobacterial species. We also show that the inserted landing pad and the entire editing machinery can be removed scarlessly after editing. We report here the construction of a single landing pad transposon and demonstrate its functionality across multiple species. The modular design of the landing pad and accessory vectors allows design and assembly of genome editing platforms for other organisms in a similar way. We believe this approach will greatly expand the list of bacteria amenable to genetic manipulation and provides the means to advance our understanding of the microbial world.

Indexed as

CRISPR-Cas SystemsGene EditingGenome, BacterialIntegrasesPhotorhabdusCre recombinaseIntegrases

Identifiers

PMID33147260
PMCPMC7641437
OpenAlexW3095320258

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.