Evidence map›Paper›PMID 39007160›Full record

ArticleBio-protocol2024

Versatile Cloning Strategy for Efficient Multigene Editing in

Ziqiang P Li, Jennifer Huard, Emmanuelle M Bayer, Valérie Wattelet-Boyer

Abstract read
In one paragraph

Article in Bio-protocol, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Ziqiang P LiUMR 5200 Laboratoire de Biogenèse Membranaire, CNRS-University of Bordeaux, Villenave d'Ornon, France.
Jennifer HuardUMR 5200 Laboratoire de Biogenèse Membranaire, CNRS-University of Bordeaux, Villenave d'Ornon, France.
Emmanuelle M BayerUMR 5200 Laboratoire de Biogenèse Membranaire, CNRS-University of Bordeaux, Villenave d'Ornon, France.
Valérie Wattelet-BoyerUMR 5200 Laboratoire de Biogenèse Membranaire, CNRS-University of Bordeaux, Villenave d'Ornon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CRISPR-Cas9 technology has become an essential tool for plant genome editing. Recent advancements have significantly improved the ability to target multiple genes simultaneously within the same genetic background through various strategies. Additionally, there has been significant progress in developing methods for inducible or tissue-specific editing. These advancements offer numerous possibilities for tailored genome modifications. Building upon existing research, we have developed an optimized and modular strategy allowing the targeting of several genes simultaneously in combination with the synchronized expression of the Cas9 endonuclease in the egg cell. This system allows significant editing efficiency while avoiding mosaicism. In addition, the versatile system we propose allows adaptation to inducible and/or tissue-specific edition according to the promoter chosen to drive the expression of the Cas9 gene. Here, we describe a step-by-step protocol for generating the binary vector necessary for establishing

Indexed as

Arabidopsis thalianaCRISPR-Cas9Gateway® cloningGolden Gate cloningPlant genome editingsgRNA multiplexing

Identifiers

PMID39007160
PMCPMC11237983

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.