Evidence map›Paper›PMID 30865619›Full record

ArticlePLoS genetics2019

Connective auxin transport contributes to strigolactone-mediated shoot branching control independent of the transcription factor BRC1.

Martin van Rongen, Tom Bennett, Fabrizio Ticchiarelli, Ottoline Leyser

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
11.9field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Lessons from a century of apical dominance research.Journal of experimental botany · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

4 authors at 1 institution in 1 country.

Martin van RongenSainsbury Laboratory, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-1441-367X
Tom BennettSainsbury Laboratory, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0003-1612-4019
Fabrizio TicchiarelliSainsbury Laboratory, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0001-5744-2393
Ottoline LeyserSainsbury Laboratory, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0003-2161-3829
University of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The shoot systems of plants are built by the action of the primary shoot apical meristem, established during embryogenesis. In the axil of each leaf produced by the primary meristem, secondary axillary shoot apical meristems are established. The dynamic regulation of the activity of these axillary meristems gives shoot systems their extraordinary plasticity of form. The ability of plants to activate or repress these axillary meristems appropriately requires communication between meristems that is environmentally sensitive. The transport network of the plant hormone auxin has long been implicated as a central player in this tuneable communication system, with other systemically mobile hormones, such as strigolactone and cytokinin, acting in part by modulating auxin transport. Until recently, the polar auxin transport stream, which provides a high conductance auxin transport route down stems dominated by the auxin export protein PIN-FORMED1 (PIN1), has been the focus for understanding long range auxin transport in the shoot. However, recently additional auxin exporters with important roles in the shoot have been identified, including PIN3, PIN4 and PIN7. These proteins contribute to a wider less polar stem auxin transport regime, which we have termed connective auxin transport (CAT), because of its role in communication across the shoot system. Here we present a genetic analysis of the role of CAT in shoot branching. We demonstrate that in Arabidopsis, CAT plays an important role in strigolactone-mediated shoot branching control, with the triple pin3pin4pin7 mutant able to suppress partially the highly branched phenotype of strigolactone deficient mutants. In contrast, the branchy phenotype of mutants lacking the axillary meristem-expressed transcription factor, BRANCHED1 (BRC1) is unaffected by pin3pin4pin7. We further demonstrate that mutation in the ABCB19 auxin export protein, which like PIN3 PIN4 and PIN7 is widely expressed in stems, has very different effects, implicating ABCB19 in auxin loading at axillary bud apices.

Indexed as

ArabidopsisArabidopsis ProteinsATP-Binding Cassette TransportersBiological Transport, ActiveGene Expression Regulation, DevelopmentalGene Expression Regulation, PlantGenes, PlantIndoleacetic AcidsKineticsLactonesMembrane Transport ProteinsMeristemModels, BiologicalMutationPhenotypePlant Growth RegulatorsABCB19 protein, ArabidopsisArabidopsis ProteinsATP-Binding Cassette TransportersBRC1 protein, ArabidopsisIndoleacetic AcidsLactonesMembrane Transport ProteinsPIN3 protein, ArabidopsisPIN4 protein, ArabidopsisPIN7 protein, ArabidopsisPlant Growth RegulatorsTranscription Factors

Identifiers

PMID30865619
PMCPMC6433298
OpenAlexW2921737581

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.