Evidence map›Paper›PMID 27040840›Full record

ReviewPlanta2016

The importance of strigolactone transport regulation for symbiotic signaling and shoot branching.

Lorenzo Borghi, Guo-Wei Liu, Aurélia Emonet, Tobias Kretzschmar, Enrico Martinoia

Open access · hybridAbstract readReview
In one paragraph

Review in Planta, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
18.5field-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

28 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Lessons from a century of apical dominance research.Journal of experimental botany · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. How Strigolactone Shapes Shoot Architecture.Frontiers in plant science · 2022
    Review
  13. Transport mechanisms of plant hormones.Current opinion in plant biology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

5 authors at 3 institutions in 2 countries.

Lorenzo BorghiInstitute of Plant and Microbial Biology, University of Zurich, 8008, Zurich, Switzerland. lorenzo.borghi@uzh.ch.ORCID http://orcid.org/0000-0002-9631-9694
Guo-Wei LiuInstitute of Plant and Microbial Biology, University of Zurich, 8008, Zurich, Switzerland.
Aurélia EmonetFaculté de biologie et médecine, Département de biologie moléculaire végétale, Université de Lausanne, 1015, Lausanne, Switzerland.
Tobias KretzschmarInternational Rice Research Institute (IRRI), Plant Breeding Genetics and Biotechnology, 4031, Laguna, Philippines.
Enrico MartinoiaInstitute of Plant and Microbial Biology, University of Zurich, 8008, Zurich, Switzerland.
University of Zurich · CHInternational Rice Research Institute · PHUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MAIN

conclusionThis review presents the role of strigolactone transport in regulating plant root and shoot architecture, plant-fungal symbiosis and the crosstalk with several phytohormone pathways. The authors, based on their data and recently published results, suggest that long-distance, as well local strigolactone transport might occur in a cell-to-cell manner rather than via the xylem stream. Strigolactones (SLs) are recently characterized carotenoid-derived phytohormones. They play multiple roles in plant architecture and, once exuded from roots to soil, in plant-rhizosphere interactions. Above ground SLs regulate plant developmental processes, such as lateral bud outgrowth, internode elongation and stem secondary growth. Below ground, SLs are involved in lateral root initiation, main root elongation and the establishment of the plant-fungal symbiosis known as mycorrhiza. Much has been discovered on players and patterns of SL biosynthesis and signaling and shown to be largely conserved among different plant species, however little is known about SL distribution in plants and its transport from the root to the soil. At present, the only characterized SL transporters are the ABCG protein PLEIOTROPIC DRUG RESISTANCE 1 from Petunia axillaris (PDR1) and, in less detail, its close homologue from Nicotiana tabacum PLEIOTROPIC DRUG RESISTANCE 6 (PDR6). PDR1 is a plasma membrane-localized SL cellular exporter, expressed in root cortex and shoot axils. Its expression level is regulated by its own substrate, but also by the phytohormone auxin, soil nutrient conditions (mainly phosphate availability) and mycorrhization levels. Hence, PDR1 integrates information from nutrient availability and hormonal signaling, thus synchronizing plant growth with nutrient uptake. In this review we discuss the effects of PDR1 de-regulation on plant development and mycorrhization, the possible cross-talk between SLs and other phytohormone transporters and finally the need for SL transporters in different plant species.

Indexed as

Plant DevelopmentBiological TransportCell CommunicationConserved SequenceLactonesPhylogenyPlant Growth RegulatorsPlant RootsPlant ShootsSequence Analysis, ProteinSymbiosisLactonesPlant Growth RegulatorsAuxinCell-to-cell transportLong-distance transportPDR1PhytohormonePlant architecturePolar localizationTransporter

Identifiers

PMID27040840
PMCPMC4875938
OpenAlexW2341870952

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.