Evidence map›Paper›PMID 34174821›Full record

ArticleBMC genomics2021

Construction of a high-density linkage map and graphical representation of the arrangement of transcriptome-based unigene markers on the chromosomes of onion, Allium cepa L.

Satoshi Fujito, Turgut Yigit Akyol, Takuya Mukae, Tadayuki Wako, Ken-Ichiro Yamashita, Hikaru Tsukazaki, Hideki Hirakawa, Keisuke Tanaka, Yoko Mine, Shusei Sato and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Integrating Genetic and Chromosome Maps ofInternational journal of molecular sciences · 2022
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  5. Development of a genome-wide marker design workflow for onions and its application in target amplicon sequencing-based genotyping.DNA research : an international journal for rapid publication of reports on genes and genomes · 2022
    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

11 authors at 7 institutions in 2 countries.

Satoshi FujitoInstitute of Vegetable and Floriculture Science, National Agriculture and Food Research Organization (NARO), 360 Kusawa, Ano, 514-2392, Tsu, Mie, Japan.
Turgut Yigit AkyolGraduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, 980-8577, Sendai, Miyagi, Japan.
Takuya MukaeGraduate School of Sciences and Technology for Innovation, Yamaguchi University, 1677-1 Yoshida, 753-8515, Yamaguchi, Yamaguchi, Japan.
Tadayuki WakoInstitute of Vegetable and Floriculture Science, National Agriculture and Food Research Organization (NARO), 360 Kusawa, Ano, 514-2392, Tsu, Mie, Japan.
Ken-Ichiro YamashitaInstitute of Vegetable and Floriculture Science, National Agriculture and Food Research Organization (NARO), 360 Kusawa, Ano, 514-2392, Tsu, Mie, Japan.
Hikaru TsukazakiInstitute of Vegetable and Floriculture Science, National Agriculture and Food Research Organization (NARO), 360 Kusawa, Ano, 514-2392, Tsu, Mie, Japan.
Hideki HirakawaKazusa DNA Research Institute, 2-6-7 Kazusa-Kamatari, Kisarazu, 292-0818, Chiba, Japan.
Keisuke TanakaThe NODAI Genome Research Center, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, 156-8502, Tokyo, Japan.
Yoko MineDepartment of Agriculture, Tokyo University of Agriculture, 1737 Funako, 243-0034, Atsugi-shi, Kanagawa, Japan.
Shusei SatoGraduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, 980-8577, Sendai, Miyagi, Japan. shuseis@ige.tohoku.ac.jp.
Masayoshi ShigyoGraduate School of Sciences and Technology for Innovation, Yamaguchi University, 1677-1 Yoshida, 753-8515, Yamaguchi, Yamaguchi, Japan. shigyo@yamaguchi-u.ac.jp.
National Agriculture and Food Research Organization · JPTohoku University · JPTokyo University of Agriculture · JPYamaguchi University · JPInstitute of Vegetable and Floriculture Science · JPKazusa DNA Research Institute · JPMinistry of Agriculture, Forestry and Fisheries · JP

Funding

Agriculture, Forestry and Fisheries Research Council 17935637Agriculture, Forestry and Fisheries Research Council 20320561Japan Society for the Promotion of Science 26292020
6 · The paper itself

Abstract

backgroundGenomic information for Allium cepa L. is limited as it is heterozygous and its genome is very large. To elucidate potential SNP markers obtained by NGS, we used a complete set of A. fistulosum L.-A. cepa monosomic addition lines (MALs) and doubled haploids (DHs). These were the parental lines of an A. cepa mapping population for transcriptome-based SNP genotyping.

resultsWe mapped the transcriptome sequence reads from a series of A. fistulosum-A. cepa MALs onto the unigene sequence of the doubled haploid shallot A. cepa Aggregatum group (DHA) and compared the MAL genotype call for parental bunching onion and shallot transcriptome mapping data. We identified SNP sites with at least four reads on 25,462 unigenes. They were anchored on eight A. cepa chromosomes. A single SNP site was identified on 3,278 unigenes and multiple SNPs were identified on 22,184 unigenes. The chromosome marker information was made public via the web database Allium TDB ( http://alliumtdb.kazusa.or.jp/ ). To apply transcriptome based genotyping approach for genetic mapping, we gathered RNA sequence data from 96 lines of a DHA × doubled haploid bulb onion A. cepa common onion group (DHC) mapping population. After selecting co-dominant SNP sites, 16,872 SNPs were identified in 5,339 unigenes. Of these, at least two SNPs with identical genotypes were found in 1,435 unigenes. We developed a linkage map using genotype information from these unigenes. All unigene markers mapped onto the eight chromosomes and graphical genotyping was conducted based on the unigene order information. Another 2,963 unigenes were allocated onto the eight chromosomes. To confirm the accuracy of this transcriptome-based genetic linkage map, conventional PCR-based markers were used for linkage analysis. All SNP - and PCR-based markers were mapped onto the expected linkage groups and no inconsistency was found among these chromosomal locations.

conclusionsEffective transcriptome analysis with unique Allium resources successfully associated numerous chromosome markers with unigene information and a high-density A. cepa linkage map. The information on these unigene markers is valuable in genome sequencing and useful trait detection in Allium.

Indexed as

AlliumOnionsChromosome MappingChromosomes, PlantPolymorphism, Single NucleotideTranscriptomeAllium cepa L.Bulb onionLinkage mapShallotTranscriptome-based SNP genotyping

Identifiers

PMID34174821
PMCPMC8236188
OpenAlexW3110978163

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.