Evidence map›Paper›PMID 23104114›Full record

ArticlePlant signaling & behavior2013

Identification of an EMS-induced causal mutation in a gene required for boron-mediated root development by low-coverage genome re-sequencing in Arabidopsis.

Ryo Tabata, Takehiro Kamiya, Shuji Shigenobu, Katsushi Yamaguchi, Masashi Yamada, Mitsuyasu Hasebe, Toru Fujiwara, Shinichiro Sawa

Open access · hybridAbstract read
In one paragraph

Article in Plant signaling & behavior, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.9field-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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Breeding science · 2018
    Article
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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

8 authors at 5 institutions in 4 countries.

Ryo TabataGraduate School of Science and Technology; Kumamoto University; Kumamoto, Japan.
Takehiro KamiyaDepartment of Applied Biological Chemistry; Graduate School of Agricultural and Life Sciences; University of Tokyo; Tokyo, Japan.
Shuji ShigenobuFunctional Genomics Facility; National Institute for Basic Biology; Okazaki, Japan.
Katsushi YamaguchiFunctional Genomics Facility; National Institute for Basic Biology; Okazaki, Japan.
Masashi YamadaDepartment of Biology and IGSP Center for Systems Biology; Duke University; Durham, NC USA.
Mitsuyasu HasebeDivision of Evolutionary Biology; National Institute for Basic Biology; Okazaki, Japan; School of Life Science; The Graduate University for Advanced Studies; Okazaki, Japan; ERATO; Japan Science and Technology Agency; Okazaki, Japan.
Toru FujiwaraDepartment of Applied Biological Chemistry; Graduate School of Agricultural and Life Sciences; University of Tokyo; Tokyo, Japan.
Shinichiro SawaGraduate School of Science and Technology; Kumamoto University; Kumamoto, Japan.
Genomics (United Kingdom) · GBKumamoto University · JPTokyo University of Pharmacy and Life Sciences · JPDuke University · USInstitut de Biologia Evolutiva · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next-generation sequencing (NGS) technologies enable the rapid production of an enormous quantity of sequence data. These powerful new technologies allow the identification of mutations by whole-genome sequencing. However, most reported NGS-based mapping methods, which are based on bulked segregant analysis, are costly and laborious. To address these limitations, we designed a versatile NGS-based mapping method that consists of a combination of low- to medium-coverage multiplex SOLiD (Sequencing by Oligonucleotide Ligation and Detection) and classical genetic rough mapping. Using only low to medium coverage reduces the SOLiD sequencing costs and, since just 10 to 20 mutant F 2 plants are required for rough mapping, the operation is simple enough to handle in a laboratory with limited space and funding. As a proof of principle, we successfully applied this method to identify the CTR1, which is involved in boron-mediated root development, from among a population of high boron requiring Arabidopsis thaliana mutants. Our work demonstrates that this NGS-based mapping method is a moderately priced and versatile method that can readily be applied to other model organisms.

Indexed as

Genes, PlantMutationArabidopsisBoronChromosome MappingEthyl MethanesulfonateHigh-Throughput Nucleotide SequencingPlant RootsProtein KinasesSequence Analysis, DNABoronCTR1 protein, ArabidopsisEthyl MethanesulfonateProtein KinasesArabidopsis thalianaboronlow- to medium-coverage sequencingmutant mappingnext-generation sequencing

Identifiers

PMID23104114
PMCPMC3745560
OpenAlexW1988447220

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.