Evidence map›Paper›PMID 27558889›Full record

ArticleAnnals of botany2016

Poplar woody taproot under bending stress: the asymmetric response of the convex and concave sides.

Elena De Zio, Dalila Trupiano, Antonio Montagnoli, Mattia Terzaghi, Donato Chiatante, Alessandro Grosso, Mauro Marra, Andrea Scaloni, Gabriella S Scippa

Open access · bronzeAbstract read
In one paragraph

Article in Annals of botany, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
7.5field-weighted citation impact, top 4% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Elena De ZioDipartimento di Bioscienze e Territorio, University of Molise, 86090 Pesche (IS), Italy.
Dalila TrupianoDipartimento di Bioscienze e Territorio, University of Molise, 86090 Pesche (IS), Italy.
Antonio MontagnoliDipartimento di Biotecnologie e Scienze della Vita, University of Insubria, 21100 Varese, Italy.
Mattia TerzaghiDipartimento di Biotecnologie e Scienze della Vita, University of Insubria, 21100 Varese, Italy.
Donato ChiatanteDipartimento di Biotecnologie e Scienze della Vita, University of Insubria, 21100 Varese, Italy.
Alessandro GrossoDipartimento di Biologia, University of Rome 'Tor Vergata', 00133 Rome, Italy.
Mauro MarraDipartimento di Biologia, University of Rome 'Tor Vergata', 00133 Rome, Italy.
Andrea ScaloniProteomics and Mass Spectrometry Laboratory, ISPAAM, National Research Council, 80147 Napoli, Italy.
Gabriella S ScippaDipartimento di Bioscienze e Territorio, University of Molise, 86090 Pesche (IS), Italy.
University of Insubria · ITUniversity of Molise · ITUniversity of Rome Tor Vergata · ITIstituto per il Sistema Produzione Animale in Ambiente Mediterraneo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims Progress has been made in understanding the physiological and molecular basis of root response to mechanical stress, especially in the model plant Arabidopsis thaliana, in which bending causes the initiation of lateral root primordia toward the convex side of the bent root. In the case of woody roots, it has been reported that mechanical stress induces an asymmetric distribution of lateral roots and reaction wood formation, but the mechanisms underlying these responses are largely unknown. In the present work, the hypothesis was tested that bending could determine an asymmetric response in the two sides of the main root axis as cells are stretched on the convex side and compressed on the concave side. Methods Woody taproots of 20 seedlings were bent to an angle of 90° using a steel net. Changes in the anatomy, lignin and phytohormone content and proteome expression in the two sides of the bent root were analysed; anatomical changes, including dissimilarities and similarities to those found in poplar bent woody stem, were also considered. Key Results Compression forces at the concave side of poplar root induced the formation of reaction wood which presented a high lignin content and was associated with the induction of cambium cell activity. Auxin seemed to be the main hormone triggering lignin deposition and cell wall strengthening in the concave sides. Abscisic acid appeared to function in the water stress response induced by xylem structures and/or osmotic alterations in the compression sides, whereas gibberellins may control cell elongation and gravitropisms. Conclusions Poplar root reaction wood showed characteristics different from those produced in bent stem. Besides providing biomechanical functions, a bent root ensures water uptake and transport in the deforming condition induced by tension and compression forces by two different strategies: an increase in xylem thickness in the compressed side, and lateral root formation in the tension side.

Indexed as

Mechanical stressphytohormonesproteomicsreaction woodroot anatomy

Identifiers

PMID27558889
PMCPMC5055640
OpenAlexW2513584058

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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.