Evidence map›Paper›PMID 28800607›Full record

ArticlePloS one2017

RNA-sequencing-based transcriptome and biochemical analyses of steroidal saponin pathway in a complete set of Allium fistulosum-A. cepa monosomic addition lines.

Mostafa Abdelrahman, Magdi El-Sayed, Shusei Sato, Hideki Hirakawa, Shin-Ichi Ito, Keisuke Tanaka, Yoko Mine, Nobuo Sugiyama, Yutaka Suzuki, Naoki Yamauchi and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
17.7field-weighted citation impact, top 1% 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

20 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
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  3. Plants (Basel, Switzerland) · 2022
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  12. Omics approaches inPeerJ · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Mostafa AbdelrahmanLaboratory of Vegetable Crop Science, College of Agriculture, Graduate School of Sciences and Technology for Innovation, Japan.
Magdi El-SayedBotany Department, Faculty of Science, Aswan University, Aswan, Egypt.
Shusei SatoGraduate School of Life Sciences, Tohoku University, Aoba-ku, Sendai, Japan.
Hideki HirakawaKazusa DNA Research Institute, Kisarazu, Chiba, Japan.
Shin-Ichi ItoLaboratory of Molecular Plant Pathology, College of Agriculture, Graduate School of Sciences and Technology for Innovation, Japan.
Keisuke TanakaThe NODAI Genome Research Center, Tokyo University of Agriculture, Tokyo, Japan.
Yoko MineDepartment of Agriculture, Faculty of Agriculture, Tokyo University of Agriculture, Tokyo, Japan.
Nobuo SugiyamaDepartment of Agriculture, Faculty of Agriculture, Tokyo University of Agriculture, Tokyo, Japan.
Yutaka SuzukiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, Japan.
Naoki YamauchiLaboratory of Vegetable Crop Science, College of Agriculture, Graduate School of Sciences and Technology for Innovation, Japan.
Masayoshi ShigyoLaboratory of Vegetable Crop Science, College of Agriculture, Graduate School of Sciences and Technology for Innovation, Japan.ORCID 0000-0003-4014-6613
Tokyo University of Agriculture · JPTohoku University · JPAswan University · EGKazusa DNA Research Institute · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genus Allium is a rich source of steroidal saponins, and its medicinal properties have been attributed to these bioactive compounds. The saponin compounds with diverse structures play a pivotal role in Allium's defense mechanism. Despite numerous studies on the occurrence and chemical structure of steroidal saponins, their biosynthetic pathway in Allium species is poorly understood. The monosomic addition lines (MALs) of the Japanese bunching onion (A. fistulosum, FF) with an extra chromosome from the shallot (A. cepa Aggregatum group, AA) are powerful genetic resources that enable us to understand many physiological traits of Allium. In the present study, we were able to isolate and identify Alliospiroside A saponin compound in A. fistulosum with extra chromosome 2A from shallot (FF2A) and its role in the defense mechanism against Fusarium pathogens. Furthermore, to gain molecular insight into the Allium saponin biosynthesis pathway, high-throughput RNA-Seq of the root, bulb, and leaf of AA, MALs, and FF was carried out using Illumina's HiSeq 2500 platform. An open access Allium Transcript Database (Allium TDB, http://alliumtdb.kazusa.or.jp) was generated based on RNA-Seq data. The resulting assembled transcripts were functionally annotated, revealing 50 unigenes involved in saponin biosynthesis. Differential gene expression (DGE) analyses of AA and MALs as compared with FF (as a control) revealed a strong up-regulation of the saponin downstream pathway, including cytochrome P450, glycosyltransferase, and beta-glucosidase in chromosome 2A. An understanding of the saponin compounds and biosynthesis-related genes would facilitate the development of plants with unique saponin content and, subsequently, improved disease resistance.

Indexed as

AlliumBiological AssayBiosynthetic PathwaysGene Expression ProfilingGene Expression Regulation, PlantGenes, PlantModels, BiologicalSaponinsSequence Analysis, RNASteroidsTranscriptomeSaponinsSteroids

Identifiers

PMID28800607
PMCPMC5553718
OpenAlexW2744370150

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.