Trees acclimation to strains induced by wind: from genes expression to stem structure

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Trees acclimation to strains induced by wind: from genes expression to stem structure

Ludovic Martin, Eric Badel, Nathalie Fournier-Leblanc, Mélanie Decourteix, Catherine Lenne, Catherine Coutand, Bruno Moulia, Jean-Louis Julien

To cite this version:

Ludovic Martin, Eric Badel, Nathalie Fournier-Leblanc, Mélanie Decourteix, Catherine Lenne, et al.. Trees acclimation to strains induced by wind: from genes expression to stem structure. Journées scientifiques du GDR 3544 ” Sciences du Bois ”, Centre National de la Recherche Scientifique (CNRS). Montpellier, FRA., Nov 2012, Montpellier, France. 1 p. �hal-00964723�

Trees acclimation to strains induced by wind:

from genes expression to stem structure

Mechanical signals are important factors that control plants growth and development. External mechanical loadings, such as wind, lead to a decrease of primary growth, an increase of secondary growth, modifications of stems mechanical properties and biomass reallocation to roots.

Biomechanical studies on tomato and poplar demonstrated that tissue strains are sensed by plants (1), (2). A biomechanical model was proposed, assuming that each cell produces a signal (dSi) whose intensity depends on strain level (ε), volume and sensitivity of the cell. At organ or tissue level, the integrative thigmomorphogenetical signal Si can be predicted by integrating the longitudinal strains (Sstrains), applied to the tissue (3).

1

_{L. Martin,}

_{E. Badel,}

_{N. Leblanc-Fournier,}

_{M. Decourteix,}

_{C. Lenne,}

_{C. Coutand,}

_{B. Moulia and}

_{J.L. Julien}

1 Université BLAISE PASCAL, UMR547 PIAF, F-63177 AUBIERE 2 INRA, UMR547 PIAF, F-63100 CLERMONT-FERRAND

References :

(1) Coutand C. and Moulia B. (2000). Biomechanical study of the effect of a controlled bending on tomato stem elongation: local strain sensing and spatial integration of the signal. Journal of Experimental Botany 51(352): 1825-1842. (2) Coutand C.*, Martin L.*, Leblanc-Fournier N., Decourteix M., Julien J.L. and Moulia B. (2009). Strain mechanosensing quantitatively controls diameter growth and PtaZFP2 gene expression in poplar. Plant Physiology 151: 1-10.

(3) Moulia B., Der Loughian C., Bastien R., Martin L., Rodriguez M., Gourcilleau D., Barbacci A., Badel E., Franchel J., Lenne C., Roeckel-Drevet P., Allain J.M., Frachisse J.M., de Langre E., Coutand C., Leblanc-Fournier N., and Julien J.L. (2011). Integrative

mechanobiology of growth and architectural development in changing mechanical environments. In P. Wojtaszek [ed.], Mechanical integration of Plant Cells and Plants, Signaling and Communication in Plants 9, 269-302. Springler-Verlag Berlin Heidelberg.

(4) Martin L., Leblanc-Fournier N., Julien J.L., Moulia B. and Coutand C. (2010). Acclimation kinetics of physiological and molecular responses of plants to multiple mechanical loadings. Journal of Experimental Botany 31: 2403-2412.

Plants accommodation to repeated mechanical stimuli

dSi Si ε dSi dSi dSi  

dx

dy

dz

k

S

k

Si



.





.

.

.



.

Controlled stem bending

Experimental bending device which allowed to quantify the level of longitudinal strains during the stem bending.

An integrative model of mechanosensing: S

m

0 0.1 0.2 0.3 0.4 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Time (days) D a il y d ia m e te r g ro w th ( m m /d a y ) Single bending (1B) Repeated bendings (9B-1d) Model 9x1B Model 3x1B *** *** 0 100 200 300 400 C 1B 2B-1d 3B-1d 4B-1d 5B-1d Bending treatment P ta Z F P 2 r e la ti v e t ra n s c ri p ts a b u n d a n c e 0 100 200 300 400 C 1B 2B-1d 2B-3d 2B-5d 2B-7d 2B-10d Bending treatment P ta Z F P 2 r e la ti v e t ra n s c ri p ts a b u n d a n c e 0 200 400 600 800 1000 C 1B 2B-1d 3B-1d 4B-1d 5B-1d Bending treatment P ta T C H 4 r e la ti v e t ra n s c rp it s a b u n d a n c e 0 200 400 600 800 1000 C 1B 2B-1d 2B-3d 2B-5d 2B-7d 2B-10d Bending treatment P ta T C H 4 r e la ti v e t ra n s c ri p ts a b u n d a n c e

Response of secondary growth to repeated daily bending. Open circles represent growth response to

one single bending (1B). Closed circles represent growth response to 9 successive bendings at 1-day intervals (9B-1d). Dash squares, model of additive effects (linear time integration, 9x1B). Open squares, model with a sensitivity shift after 3 daily bendings (3x1B; accomodation).

Mechanoresponsive genes expression after repeated daily bending.

C : control (no load). 1B : one single bending. xB-yd : x bendings each separated by y days. PtaZFP2 : Populus tremula*alba Zinc Finger Protein2 gene, PtaTCH4 : Populus tremula*alba Touch4 xyloglucan endotransglucosylase/hydrolyse gene. Significant differences (P < 0.05) of responses are indicated by different letters.

Stem anatomical modifications induced by multiple bendings.

(a) to (d) Control plants. (e) to (h) Plants subjected to 6 bendings, 2 successive bendings separated by 1 day, 3 days without sollicitations between each set of bendings. (a, b, e, f) Toluidine blue staining. (c, d, g, f) Blue astra-safratine staining.

c: cambium, cp: cortical parenchyma, fw: flexure wood, gl: G layer, ph: phloem, pi: pith, scl: sclerenchyma, x: xyelm, xf: xylem fiber, xr: xylem ray, xv: xylem vessel.

Multiple mechanical stimuli affect anatomical pattern and secondary growth rate

In nature, mechanical stimuli do not occur as a single bending. In this experiment, successive bendings were separated at day scale, mimicking the alternance between windy or quiet weather.

p cp (a) x c ph 500 µm c xv xf xr scl ph (b) 50 µm Gl (h) xf 20 µm scl (f) 50 µm xv xr xf c ph p fw cp (e) x c ph 500 µm (d) xf xv xr 20 µm fw x cp c ph p 500 µm (g) x cp c ph p 500 µm (c) Q-PCR

As soon as a second bending was applied, a diminution of growth and molecular responses to subsequent bending were observed. Our results show that plants acclimate rapidly to mechanical loadings and a desensitization period of a few days occurs after a single transitory bending. This acclimation process provides a basis for a mechanistic analysis of response sensitivity to mechanical loadings such as wind (4).

(a) (b) -1 -0.5 0 0.5 1 -1 -0.8 -0.6 -0.4 -0.2 0 0.2 0.4 0.6 0.8 1 0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1 (c) ε_LL )) ( 1 )( , ( ) , (i t C i t i R    _LL 

Cambial activity induced by local strains applied to the stem: experimentations and modelling.

Plants were subjected to 3 successive daily bendings per week during 4 months. (a) Transversal section of a stimulated plant. (b) Relative ovalisation induced by bending. (c) Strain field for living tissues. (d) Weekly growth rate measurements (blue lines) and growth rate modeling (red lines).

Strain field

Strain

direction

In response to bendings, cambium activity is impacted by the strain. Growth rate is identically stimulated according to the strain level both in the stretched part and in the compressed part of the stem. Wood differentiation is modulated according to the type of mechanical loading (tension and compression).

c a b b b b d a b a a a a c ab abc ab bc c d a b b _b b c 15 15 10 10 5 5 0 5 0 5 10 10 (d)