Evidence map›Paper›PMID 36995618›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

CRISPR/LbCas12a-Mediated Genome Editing in Soybean.

Dawei Liang, Yubo Liu, Chao Li, Qin Wen, Jianping Xu, Lizhao Geng, Chunxia Liu, Huaibing Jin, Yang Gao, Heng Zhong and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. 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. Article
  2. Establishment of the CRISPR-Cpf1 gene editing system inSynthetic and systems biotechnology · 2025
    Article
  3. Article
  4. Article
  5. Advances in Soybean Genetic Improvement.Plants (Basel, Switzerland) · 2024
    Review
  6. Article
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

20 authors.

Dawei LiangSyngenta Biotechnology China Co., Ltd., Beijing, China. dawei.liang@syngenta.com.
Yubo LiuSyngenta Biotechnology China Co., Ltd., Beijing, China.
Chao LiSyngenta Biotechnology China Co., Ltd., Beijing, China.
Qin WenSyngenta Biotechnology China Co., Ltd., Beijing, China.
Jianping XuSyngenta Biotechnology China Co., Ltd., Beijing, China.
Lizhao GengSyngenta Biotechnology China Co., Ltd., Beijing, China.
Chunxia LiuSyngenta Biotechnology China Co., Ltd., Beijing, China.
Huaibing JinSyngenta Biotechnology China Co., Ltd., Beijing, China.
Yang GaoSyngenta Biotechnology China Co., Ltd., Beijing, China.
Heng ZhongSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
John DawsonSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Bin TianSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Brenden BarcoSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Xiujuan SuSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Shujie DongSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Changbao LiSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Sivamani ElumalaiSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Qiudeng QueSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA. qiudeng.que@syngenta.com.
Ian JepsonSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.
Liang ShiSeeds Research, Syngenta Crop Protection, LLC, Research Triangle Park, NC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently methods for generating soybean edited lines are time-consuming, inefficient, and limited to certain genotypes. Here we describe a fast and highly efficient genome editing method based on CRISPR-Cas12a nuclease system in soybean. The method uses Agrobacterium-mediated transformation to deliver editing constructs and uses aadA or ALS genes as selectable marker. It only takes about 45 days to obtain greenhouse-ready edited plants at higher than 30% transformation efficiency and 50% editing rate. The method is applicable to other selectable markers including EPSPS and has low transgene chimera rate. The method is also genotype-flexible and has been applied to genome editing of several elite soybean varieties.

Indexed as

CRISPR-Cas SystemsGene EditingEndonucleasesGenome, PlantGlycine maxPlants, Genetically ModifiedEndonucleasesCRISPR-LbCas12aFast transformationGenotype-independent transformationPlant selectable marker geneSoybean genome editingSoybean transformation

Identifiers

PMID36995618

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.