Evidence map›Paper›PMID 27561783›Full record

ArticlePlant molecular biology2016

Cloning and characterization of soybean gene Fg1 encoding flavonol 3-O-glucoside/galactoside (1→6) glucosyltransferase.

Felipe Rojas Rodas, Shaokang Di, Yoshinori Murai, Tsukasa Iwashina, Satoko Sugawara, Tetsuya Mori, Ryo Nakabayashi, Keiko Yonekura-Sakakibara, Kazuki Saito, Ryoji Takahashi

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Article in Plant molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  3. Development of phytochemical genomics: From decoding metabolome to functional genomics and biotechnology of plant metabolism.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2025
    Review
  4. A Novel 3-International journal of molecular sciences · 2022
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4 · The record

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5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Felipe Rojas RodasGraduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8518, Japan.
Shaokang DiGraduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8518, Japan.
Yoshinori MuraiDepartment of Botany, National Museum of Nature and Science, Tsukuba, Ibaraki, 305-0005, Japan.
Tsukasa IwashinaDepartment of Botany, National Museum of Nature and Science, Tsukuba, Ibaraki, 305-0005, Japan.
Satoko SugawaraThe RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, 230-0045, Japan.
Tetsuya MoriThe RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, 230-0045, Japan.
Ryo NakabayashiThe RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, 230-0045, Japan.
Keiko Yonekura-SakakibaraThe RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, 230-0045, Japan.
Kazuki SaitoThe RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, 230-0045, Japan.
Ryoji TakahashiGraduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8518, Japan. masako@affrc.go.jp.ORCID http://orcid.org/0000-0003-0619-1066
RIKEN Center for Sustainable Resource Science · JPUniversity of Tsukuba · JPNational Museum of Nature and Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

key messageFlavonoids are important secondary metabolites in plants. Sugar-sugar glycosyltransferases are involved in the final step of flavonoid biosynthesis and contribute to the structural diversity of flavonoids. This manuscript describes the first cloning of a sugar-sugar glucosyltransferase gene in the UGT family that attaches glucose to the 6″-position of sugar bound to a flavonol. The results provide a glimpse on the possible evolution of sugar-sugar glycosyltransferase genes and identify putative amino acids responsible for the recognition of the hydroxyl group of the sugar moiety and specification of sugar. A scheme for the genetic control of flavonol glycoside biosynthesis is proposed. Flavonol glycosides (FGs) are predominant in soybean leaves and they show substantial differences among genotypes. In previous studies, we identified two flavonoid glycoside glycosyltransferase genes that segregated in recombinant inbred lines developed from a cross between cultivars Nezumisaya and Harosoy; one was responsible for the attachment of glucose to the 2″-position of glucose or galactose that is bound to the 3-position of kaempferol and the other was involved in the attachment of glucose to the 6″-position. This study was conducted to clone and characterize the 6″-glucosyltransferase gene. Linkage mapping indicated that the gene was located in the molecular linkage group I (chromosome 20). Based on the genome sequence, we cloned a candidate cDNA, GmF3G6"Gt from Harosoy but the corresponding cDNA could not be amplified by PCR from Nezumisaya. The coding region of GmF3G6″Gt in Harosoy is 1386 bp long encoding 462 amino acids. This gene was not expressed in leaves of Nezumisaya. The GmF3G6″Gt recombinant protein converted UDP-glucose and kaempferol 3-O-glucoside or kaempferol 3-O-galactoside to kaempferol 3-O-glucosyl-(1→6)-glucoside or kaempferol 3-O-glucosyl-(1→6)-galactoside, respectively. These results indicate that GmF3G6″Gt encodes a flavonol 3-O-glucoside/galactoside (1→6) glucosyltransferase and corresponds to the Fg1 gene. GmF3G6″Gt had an amino acid similarity of 82 % with GmF3G6″Rt encoding flavonol 3-O-glucoside/galactoside (1→6) rhamnosyltransferase, suggesting a recent evolutionary divergence of the two genes. This may be the first cloning of a sugar-sugar glucosyltransferase gene in the UGT family that attaches glucose to the 6″-position of sugar bound to a flavonol. A scheme for the control of FG biosynthesis is proposed.

Indexed as

Chromosome MappingCloning, MolecularGene Expression Regulation, PlantGlucosyltransferasesGlycine maxPlant Proteinsflavonol 3-O-glucosyltransferaseGlucosyltransferasesPlant ProteinsFg1 geneFlavonolFlavonol 3-O-glucoside/galactoside (1→6) glucosyltransferaseGlucosyltransferaseSoybean

Identifiers

PMID27561783
OpenAlexW2516106502

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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.