Evidence map›Paper›PMID 26044828›Full record

ArticleBMC plant biology2015

Heterologous expression and transcript analysis of gibberellin biosynthetic genes of grasses reveals novel functionality in the GA3ox family.

Stephen Pearce, Alison K Huttly, Ian M Prosser, Yi-dan Li, Simon P Vaughan, Barbora Gallova, Archana Patil, Jane A Coghill, Jorge Dubcovsky, Peter Hedden and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 3 pooled it
19.7field-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

68 citing papers in PubMed, 3 syntheses or guidelines pooled it, 141 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Meta-QTLs, ortho-meta-QTLs and candidate genes for grain yield and associated traits in wheat (Triticum aestivum L.).TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2022
    Pooled it
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  7. Learning fromInternational journal of molecular sciences · 2025
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  13. Molecular mechanisms underlying the signal perception and transduction during seed germination.Molecular breeding : new strategies in plant improvement · 2024
    Review
  14. Overexpression of 9-International journal of molecular sciences · 2023
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  15. Article
  16. WheatProceedings of the National Academy of Sciences of the United States of America · 2023
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  19. Article
  20. An autoactiveProceedings of the National Academy of Sciences of the United States of America · 2022
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8 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Stephen PearceDepartment of Plant Sciences, University of California, Davis, CA, 95616, USA. sppearce@ucdavis.edu.
Alison K HuttlyDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. alison.huttly@rothamsted.ac.uk.
Ian M ProsserDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. ian.prosser@gmx.com.
Yi-dan LiDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. liyidan@foxmail.com.
Simon P VaughanDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. simon.vaughan@rothamsted.ac.uk.
Barbora GallovaDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. bylynka14@hotmail.com.
Archana PatilDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. archana.patil@rothamsted.ac.uk.
Jane A CoghillUniversity of Bristol Transcriptomics Facility, School of Biological Sciences, Bristol, BS8 1UG, UK. jane.coghill@bristol.ac.uk.
Jorge DubcovskyDepartment of Plant Sciences, University of California, Davis, CA, 95616, USA. jdubcovsky@ucdavis.edu.
Peter HeddenDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. peter.hedden@rothamsted.ac.uk.
Andrew L PhillipsDepartment of Plant Biology and Crop Science, Rothamsted Research, Harpenden, AL5 2JQ, UK. andy.phillips@rothamsted.ac.uk.
Rothamsted Research · GBHoward Hughes Medical Institute · USUniversity of Bristol · GBUniversity of California, Davis · US

Funding

Biotechnology and Biological Sciences Research Council BB/D019001/1Biotechnology and Biological Sciences Research Council BB/E006922/1Biotechnology and Biological Sciences Research Council BBS/E/C/00004161Biotechnology and Biological Sciences Research Council BBS/E/C/00004951Howard Hughes Medical Institute
6 · The paper itself

Abstract

backgroundThe gibberellin (GA) pathway plays a central role in the regulation of plant development, with the 2-oxoglutarate-dependent dioxygenases (2-ODDs: GA20ox, GA3ox, GA2ox) that catalyse the later steps in the biosynthetic pathway of particularly importance in regulating bioactive GA levels. Although GA has important impacts on crop yield and quality, our understanding of the regulation of GA biosynthesis during wheat and barley development remains limited. In this study we identified or assembled genes encoding the GA 2-ODDs of wheat, barley and Brachypodium distachyon and characterised the wheat genes by heterologous expression and transcript analysis.

resultsThe wheat, barley and Brachypodium genomes each contain orthologous copies of the GA20ox, GA3ox and GA2ox genes identified in rice, with the exception of OsGA3ox1 and OsGA2ox5 which are absent in these species. Some additional paralogs of 2-ODD genes were identified: notably, a novel gene in the wheat B genome related to GA3ox2 was shown to encode a GA 1-oxidase, named as TaGA1ox-B1. This enzyme is likely to be responsible for the abundant 1β-hydroxylated GAs present in developing wheat grains. We also identified a related gene in barley, located in a syntenic position to TaGA1ox-B1, that encodes a GA 3,18-dihydroxylase which similarly accounts for the accumulation of unusual GAs in barley grains. Transcript analysis showed that some paralogs of the different classes of 2-ODD were expressed mainly in a single tissue or at specific developmental stages. In particular, TaGA20ox3, TaGA1ox1, TaGA3ox3 and TaGA2ox7 were predominantly expressed in developing grain. More detailed analysis of grain-specific gene expression showed that while the transcripts of biosynthetic genes were most abundant in the endosperm, genes encoding inactivation and signalling components were more highly expressed in the seed coat and pericarp.

conclusionsThe comprehensive expression and functional characterisation of the multigene families encoding the 2-ODD enzymes of the GA pathway in wheat and barley will provide the basis for a better understanding of GA-regulated development in these species. This analysis revealed the existence of a novel, endosperm-specific GA 1-oxidase in wheat and a related GA 3,18-dihydroxylase enzyme in barley that may play important roles during grain expansion and development.

Indexed as

Genes, PlantMultigene FamilyBiocatalysisBiosynthetic PathwaysBrachypodiumGene Expression Regulation, PlantGibberellinsHordeumMixed Function OxygenasesOryzaPhylogenyPoaceaeRNA, MessengerSequence Analysis, RNASignal TransductionTriticumGibberellinsMixed Function OxygenasesRNA, Messenger

Identifiers

PMID26044828
PMCPMC4455330
OpenAlexW1602062117

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.