Evidence map›Paper›PMID 29996713›Full record

ArticleRNA biology2019

Marker-free genome editing in Ustilago trichophora with the CRISPR-Cas9 technology.

Simon Huck, Josephine Bock, Jörg Girardello, Marc Gauert, Ümit Pul

Abstract read
In one paragraph

Article in RNA biology, 2019. 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
–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

6 citing papers in PubMed.

  1. Review
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  6. 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

5 authors.

Simon Hucka B.R.A.I.N AG , Zwingenberg , Germany.
Josephine Bocka B.R.A.I.N AG , Zwingenberg , Germany.
Jörg Girardelloa B.R.A.I.N AG , Zwingenberg , Germany.
Marc Gauerta B.R.A.I.N AG , Zwingenberg , Germany.
Ümit Pula B.R.A.I.N AG , Zwingenberg , Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this communication, we report the adaptation of the CRISPR-Cas9 technology in Ustilago trichophora prototrophic wild-type isolate obtained from its natural host Echinochloa crus-galli. The established CRISPR vector and method enable a rapid and marker-free introduction of Cas9-induced non-homologous end-joining (NHEJ) dependent mutation at the targeted gene. Moreover, the method allows a specific modification of the chromosomal DNA sequence by Cas9-induced homologous recombination using short DNA repair templates. The results demonstrate the applicability of the CRISPR-Cas9 technology in U. trichophora for both gene knock-out by the NHEJ pathway and specific gene modification by templated genome editing, paving the way for rapid metabolic engineering of this Ustilago species for industrial applications.

Indexed as

Gene EditingBase SequenceChromosomes, FungalCRISPR-Associated Protein 9CRISPR-Cas SystemsGenetic MarkersGenome, FungalHomologous RecombinationUstilagoCRISPR-Associated Protein 9Genetic MarkersCas9CRISPRgenome editingUstilago trichophora

Identifiers

PMID29996713
PMCPMC6546355

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.