Endogenous mechanical stresses regulate plant growth and development. Tensile stress in epidermal cells affects microtubule reorientation and anisotropic cell wall deposition, and mechanical stimulus at the meristem regulates trafficking and polar localization of auxin transporters. However, the mechanical regulation of other plant growth regulators has not been demonstrated. Here we propose that during seed growth, mechanical stress exerted by the expanding embryo and endosperm is perceived by a specific mechanosensitive cell layer in the seed coat. We show that the adaxial epidermis of the outer integument thickens its cell wall in a mechanosensitive fashion, demonstrates microtubule dynamics consistent with mechanical stress perception and shows mechanosensitive expression of ELA1, a regulator of seed size and gibberellic acid (GA) metabolism. By exploiting physical and genetic compartmentalization, and combining genetic and surgical techniques, we propose a mechanistic link between mechanical stress and GA accumulation that regulates seed development.
Studies of mechanical signalling in plant tissues at the cellular level are hampered by the difficulty of distinguishing responses to mechanical signals from those related to wounding and/or changes in intercellular communication. The Arabidopsis seed is comprised of the embryo, endosperm and seed coat, each of which is genetically distinct. Its small size and relative accessibility, and the availability of high quality in silico transcriptome resources1, make it an attractive model system. Histological and genetic studies suggest that no symplastic connections exist between the seed coat and the endosperm2,3. The possibility that mechanical signalling could be involved in coordinating seed development has been evoked previously by studies showing that final seed size is determined by the interplay of expansion of the syncytial endosperm soon after fertilization (controlled by a pathway involving the receptor kinase HAIKU2 (IKU2)) with the regulated growth of the surrounding seed coat4.
In plants, growth is thought to be restricted by the epidermal cell layer and driven by the combined turgor pressure of cells underlying this cell layer. This generates tissue tension in the epidermis, which is counteracted by thickening of the outer epidermal cell wall5,6,7. At fertilization, the Arabidopsis seed coat is composed of four to five living cell layers derived from two organs, the outer integument (two cell layers; abaxial (outer) epidermis (oi-ab) and adaxial (inner) epidermis (oi-ad)) and the inner integument (abaxial epidermis (ii-ab) and adaxial epidermis (endothelium), separated by one internal cell layer in more chalazal zones of the seed coat) (Fig. 1a). The outer cell layer of the developing Arabidopsis seed (oi-ab) differentiates into a highly specialized cell type designed for rupture and release of mucilage on seed imbibition8,9. In contrast, the cell wall separating oi-ad from ii-ab (‘wall 3’) has been described as being thickened, based upon histological observations8,9, suggesting that it could restrict seed growth.
Here we show not only that wall 3 is thickened in a mechanosensitive manner specifically by oi-ad, but that this cell layer also shows microtubule dynamics consistent with mechanical stress perception and the mechanosensitive expression of a regulator of seed size and gibberellic acid (GA) metabolism.
To determine from which cell layer the material in wall 3 originates, we observed developing seeds by transmission electron microscopy. In seeds containing expanding and fully expanded embryos, wall 3 is the thickest periclinal cell wall in the seed coat (Supplementary Fig. 1 and Fig. 1). Consistent with it representing a zone of fusion between two epidermal surfaces, an electron-dense layer of cutin-like material is observed within wall 3 at early stages of seed development (Fig. 1b), and remains visible throughout much of the seed development, ‘marking’ the original boundary between the two integuments. Observation of the asymmetric positioning of this zone at later developmental stages shows that the vast majority of cell wall material laid down in wall 3 originates from oi-ad (Fig. 1c,d). Because epidermal cells are known to thicken their cell walls in response to mechanical stress5,6,7, we hypothesized that oi-ad might be the site of response to physical stretching imposed by early endosperm expansion. We, therefore, compared the histological and immunohistological observations of wall 3 in wild-type seeds 15 DAP, with haiku2 (iku2-2 (ref. 10)) mutant seeds in which early endosperm expansion is dramatically reduced. In the latter, wall 3 stains less strongly with calcofluor (staining cellulose), and with the monoclonal antibody LM19 (which detects de-esterified homogalacturonan11), suggesting that it is thinner in iku2 mutants (Fig. 1e–j). Since IKU2 is expressed in the endosperm10, we propose that thickening is controlled non-autonomously by endosperm expansion.
Microtubule orientation and bundling change in the presence of mechanical stresses in growing tissues and can therefore be used as a marker of stress patterns12,13,14,15,16. We documented microtubule behaviour in the cells of oi-ab and oi-ad before and after fertilization using lines expressing a GFP (green fluorescent protein) fusion to Tubulin Alpha 6 (ref. 17) or an red fluorescent protein fusion to MAP65 (ref. 18), which mark microtubules and bundled microtubules, respectively. Microtubules within the oi-ab of unfertilized ovules are arranged in arrays along the short axis of the cell (Supplementary Fig. 2 and Fig. 2a,b). Post fertilization, microtubules reorganize and become randomly orientated within each cell, with no evident bundling or supracellular organization observed (Fig. 2e,f). After 72–96 h, microtubules start to coalesce at a point in the centre of each cell corresponding to the position of the future columella (Supplementary Fig. 3). In contrast, microtubules in oi-ad become increasingly highly bundled post fertilization (Fig. 2g,h) in comparison with non-fertilized controls (Fig. 2c,d), with supracellular organization visible. Differences in bundling between the outer and inner cell layer are particularly dramatic when MAP65 is observed (Fig. 2f compared to Fig. 2h). The images shown in Fig. 2 are typical of the situation observed in three independent time courses and in at least 10 individual seeds for every time point. To confirm that the microtubules of oi-ab are capable of reorienting in response to mechanical stress, we developed a technique for compressing developing seeds within siliques, whilst still attached to the mother plant (Supplementary Fig. 4). Dissecting and imaging seeds expressing the Lti6b marker19 after long (24 h) compressions in this apparatus confirms that seed coats are distorted, but not damaged (Supplementary Fig. 5). After 24 h of compression in this apparatus, we found that microtubules in oi-ab had undergone a dramatic reorientation, suggesting that they are capable of responding to mechanical stresses, but are not subject to such stresses during normal development (Fig. 2i–k). Although we are unable to visualize microtubules in deeper cell layers for technical reasons, these observations, together with the presence of cell wall thickening, support the hypothesis that oi-ad is the major site for the perception of, and response to, mechanical stresses during normal seed development.
To test this hypothesis further, we surgically altered the turgor pressure applied by the expanding syncytial endosperm on the seed coat. We imaged developing seeds expressing the membrane marker Lti6b-GFP, 6 days after fertilization (early heart stage, endosperm uncellularized (Supplementary Fig. 6 for staging)). We then gently ‘blew out’ the endosperm by microinjecting a small bubble of air into the endosperm cavity and reimaged the seeds within 15–20 min. Pre-surgery imaging allows clear visualization of the membranes of oi-ab, oi-ad and the underlying ii-ad (composed of characteristic elongated cells; Fig. 2l,m and Supplementary Fig. 7). Membranes lose their integrity in oi-ad post surgery, despite the fact that those in over- and underlying cell layers can still be clearly observed (100% n=30 seeds). When post-surgery seeds are imaged in the presence of propidium iodide (which does not enter intact seeds at this stage), we observe strong uniform nuclear staining specifically in oi-ad, suggesting that these cells lose their integrity in response to the changes in mechanical stress imposed on them (Fig. 2l,m and Supplementary Fig. 7). Oi-ad thus appears to be particularly sensitive to mechanical perturbation.
After endosperm cellularization initiates at the early heart stage in wild-type seeds, seed size does not increase significantly. However, in plants heterozygous for a recessive loss of function mutation in the ZHOUPI (ZOU) gene, which encodes an endosperm-specific bHLH transcription factor necessary for endosperm breakdown as the embryo starts to expand at the early torpedo stage20,21,22, we find that seeds containing a mutant endosperm and embryo become significantly larger than their siblings before desiccation (Supplementary Fig. 8). We hypothesized that this could be due to competition for space within the seed coat, between the persistent endosperm and the expanding embryo. We interrogated available transcriptional data generated in zou-4 mutant versus wild-type seeds at the mid torpedo stage of embryo development22 to identify genes expressed in the seed coat (based on in silico data1) and upregulated in the zou-4 mutant background. One such gene is At5g24910, which encodes the cytochrome p450 mono-oxygenase CYP714A1, also named EUI-LIKE P450 A1 (ELA1)23,24. Upregulation of ELA1 in zou mutants is confirmed using quantitative reverse transcription PCR (Fig. 3a). ELA1 is also significantly upregulated in iku2 mutants at the torpedo stage, and more strongly upregulated in zou-4 iku2-2 double mutants than in either single mutant. In zou-4 iku2-2 double mutants we note a significantly decreased seed viability, due to testa rupture in 30–50% of developing seeds (Supplementary Fig. 9). We propose that the lack of wall 3 strengthening in iku2 mutants leads to increased oi-ad stretching during embryo growth, and that this is compounded by endosperm persistance in zou-4 iku2-2 double mutants, leading to testa rupture (Fig. 4e).
The seed expression pattern of ELA1 was investigated by both in situ hybridization (Supplementary Fig. 10) and by the generation of a promoter fusion to a sequence encoding the nuclear VENUS-N7 protein fusion (Fig. 3b). ELA1 is expressed most strongly in oi-ad, with weaker expression also observed in the internal cell layer of the inner integument at early stages. Using the apparatus described previously (Supplementary Fig. 4), we observe that the transcript levels of ELA1 respond positively to the application of exogenous mechanical stress after 24 h of compression (Fig. 4a). When identical experiments are carried out on lines expressing pELA1:VENUS-N7, no ectopic expression of this marker is observed (Supplementary Fig. 11a), suggesting that increased transcript levels are restricted to the native expression domain. Quantification of nuclear fluorescence in these lines supports an upregulation in the activity of the ELA1 promoter both following seed compression (Fig. 4b and Supplementary Fig. 11b) and in seeds containing zou-4 mutant endosperm and embryo (Fig. 3c,d). In contrast, the expression of RGP4 (ref. 25) and At1g63300, two other seed coat-specific genes showing similar global expression profiles to ELA1, ELA2, a close homologue and direct physical neighbour of ELA1 (ref. 23) and RGP3, an endosperm-specific gene25, is not affected by mechanical stress application (Supplementary Fig. 12). Although the loss of ELA1 function alone does not affect the seed size, ELA1, together with ELA2, has previously been shown to restrict seed expansion23. However, ELA2 is expressed both in the seed coat and in the endosperm (Supplementary Fig. 13). We therefore generated amiRNA lines targeting both ELA1 and ELA2 under the ELA1 promoter (Supplementary Fig. 14a,b). Although the plants are otherwise phenotypically normal, we detect statistically significant increases in seed length and area in two independent lines showing reduction in ELA1 expression (Fig. 4c,d and Supplementary Fig. 14c), confirming that ELA1 and ELA2 act together in the seed coat to limit seed size.
The control of final seed size in angiosperms is known to involve a fine balance between endosperm expansion and controlled seed coat extension. We interpret our observations of cytoskeletal behaviour, micromanipulations and structural studies in wild-type and iku2 mutants as suggesting that the control of seed coat extension involves mechanoresponsive cell wall thickening by the adaxial epidermis of the outer integument. On the basis of our results, we propose that early in seed development this layer senses mechanical stresses exerted on the seed coat by the expanding syncytial endosperm and reacts by reinforcing its ‘outer’ cell wall (wall 3) to form a ‘corset’ around the developing seed. Our analysis of zou and iku2 mutants suggests that the final seed size may then be fine-tuned by the mechanosensitive regulation of genes such as ELA1 within this cell layer in response to pressure exerted by the zygotic compartment (our interpretation is presented schematically in Fig. 4e). ELA1 and ELA2 are involved in the deactivation of bioactive GAs, potent stimulators of expansion which act, in part, by regulating the transcription of cell wall-modifying enzymes23,24,26. Until now, no direct link has been demonstrated between the regulation of GA levels and responses to mechanical stress. We propose that ELA1 may provide such a link.
Plant growth conditions and transformation
For staged materials, plants were grown under continuous light at 16 °C to slow down development, and flowers were emasculated and hand pollinated to ensure maximum synchronicity. Otherwise plants were grown under standard long-day conditions (21 °C, 16 h light/8 h dark). Comparisons were carried out on plants grown side by side under identical conditions. Agrobacterium-mediated plant transformation was carried out using the floral dip method27. In brief, the plants were allowed to bolt. Agrobacterium strains containing desired binary vectors were grown plated at high density onto YEB plates with the suitable antibiotics and incubated at 28 °C for 2–3 days. Bacteria were scraped off plates into 30 ml of LB to give an OD600 of around 2.0. This solution was diluted in four volumes of a solution containing 5% sucrose and 0.03% Silwet L-77 (surfactant; Lehle Seeds). Plants were dipped in the solution for 10 s, with gentle agitation, covered with plastic bags for 24 h and then allowed to set seed.
TEM analysis of cell wall structure
Seeds for transmission electron microscopy analysis was removed from siliques by removal of the replum tissue with attached seeds, fixed in paraformaldehyde 3.2%+glutaraldehyde 2.5% in 0.1 M phosphate buffer (pH7.2) overnight at 4 °C, rinsed, postfixed in 1% OsO4 in phosphate buffer overnight at 4 °C, rinsed, stained with tannic acid (1% in water) for 30 min, rinsed, dehydrated through an ethanol series and impregnated in increasing concentrations of SPURR28 resin over a period of 4 days before being polymerized at 70 °C for 19 h, sectioned (65 nm sections) and imaged at 80 kV using an FEI TEM tecnai Spirit with 4 k × 4 k eagle ccd.
Immunolocalization and calcofluor staining of seeds
Seeds were fixed in ice-cold PEM buffer (50 mm PIPES, 5 mm EGTA and 5 mm MgSO4, pH 6.9) containing 4% (w/v) paraformaldehyde. Samples were placed under vacuum (3 × 30 min on ice), rinsed in PBS, dehydrated through an ethanol series and infiltrated with increasing concentrations of LR White resin in absolute ethanol (London Resin Company) over 8 days before being polymerized at 60 °C. Sections (1.0 μm) were cut using a glass knife on a Leica RM6626 microtome. Sections were incubated in PBS containing 3% (w/v) milk protein and a 10-fold dilution of antibody hybridoma supernatant (LM19, Plant Probes)11 for 1 h, washed and incubated with a 100-fold dilution of fluorescently labelled (ab96963, Abcam) for 1 h in the dark. Samples were washed and counterstained with filtered Calcofluor White M2R (fluorescent brightener 28; Sigma-Aldrich) at 0.25 μg ml−1 and mounted in VECTASHIELD (Eurobio).
Living seeds were imaged by opening siliques on adhesive tape on the base of a small Petri dish, submerging in water and imaging using a dipping lens with a long working distance. When stated, seeds were stained by incubating for 10 min in 5 mg ml−1 propidium iodide, and rinsing twice before mounting in water. Confocal imaging was carried out on a Zeiss LSM700. Fluorescence and light microscopy imaging was carried out using a Zeiss axioimager 2.
Total RNA was extracted using the Spectrum Plant Total RNA Kit (Sigma). Total RNAs were digested with Turbo DNA-free DNase I (Ambion) according to the manufacturer’s instructions. RNA was reverse transcribed using the SuperScript VILO cDNA Synthesis Kit (Invitrogen) according to the manufacturer’s protocol. PCR reactions were performed in an optical 96-well plate in the StepOne Plus Real Time PCR System (Applied Biosystems), using FastStart Universal SYBR Green Master (Rox) (Roche), in a final volume of 20 μl, according to the manufacturer’s instructions. The following standard thermal profile was used for all PCR reactions: 95 °C for 10 min, 40 cycles of 95 °C for 10 s, and 60 °C for 30 s. Data were analysed using the StepOne Software v2.2 (Applied Biosystems). As a reference, primers for the EIF4A cDNA were used. PCR efficiency (E) was estimated from the data obtained from standard curve amplification using the equation E=10−1/slope. Expression levels are presented as E−ΔCt, where ΔCt=CtGOI−CtEIF4A. Primers are listed in Supplementary Table 1.
The ELA1 promoter was amplified using primers listed in Supplementary Table 1 and cloned using restriction enzymes (BamH1 and Not1) into a modified version of pDONR P4-P1R (Life Technologies), before being incorporated into final constructions using Gateway technology. The ELA1/ELA2 amiRNA construct was designed using a web-based microRNA designer (http://wmd3.weigelworld.org/cgi-bin/webapp.cgi) and cloned into pDONR 221 (Life Technologies). Triple recombinations of appropriate entry vector combinations were performed into either pART27 (ref. 29; kanamycin resistance) or pH7m34GW30 (hygromycin resistance).
DNA templates for the probes used in in situ hybridizations were amplified using the primers listed in Supplementary Table 1. Digoxigenin-labelled RNA probes were produced and hybridized to tissue sections following standard procedures. In brief, siliques were opened, fixed overnight in ice-cold PBS containing 4% paraformaldehyde, dehydrated through an ethanol series, embedded in Paraplast Plus (Mc Cormick Scientific) and sectioned (8 μm). Immobilized sections were dewaxed and hydrated, treated with 2 × saline sodium citrate (15 min), digested for 30 min at 37 °C with proteinase K (20 μg ml−1 in 50 mM Tris-HCl, pH 7.5, 5 mM EDTA), treated for 2 min with 0.2% glycine in PBS, rinsed, postfixed with 4% paraformaldehyde in PBS (10 min, 4 °C), rinsed, treated with 0.25% w/v acetic anhydride in 100 mM triethanolamine (pH 8.0 with HCl) for 10 min, rinsed and dehydrated. Sections were then hybridized under coverslips overnight at 50 °C with RNA probes (produced using DIG RNA labelling kit (Roche)) diluted in DIG easy Hyb solution (Roche) following the manufacturer’s instructions. Following hybridization, the slides were extensively washed in 0.1 × saline sodium citrate and 0.5% SDS at 50 °C (3 h), blocked for 45 min in 1% blocking solution (Roche) in TBS and for 45 minutes in BSA solution (1% BSA, 0.3% Triton-X-100, 100 mM Tris-HCl, 100 mM NaCl, 50 mM MgCl2), and then incubated in a 1/1,000 dilution of in alkaline phosphatase-conjugated anti-digoxigenin antibody (Roche) in BSA solution for 2 h at RT. Sections were extensively washed in BSA solution, rinsed and treated overnight in the dark with a buffered NBT/BCIP solution. Samples were rinsed in water before air drying and mounting in Entellan (Sigma).
Tissue compressions and microinjection experiments
Microinjection experiments were carried out using an Eppendorf Femtojet microinjection and micromanipulation apparatus equipped with Femtotips II injecting needles (inner diameter 0.5 μm, outer diameter 0.7 μm). Seed compression experiments were performed using a custom tissue vice described in Supplementary Fig. 4. Quantification of nuclear fluorescence was carried out using standard software in the ImageJ image analysis package31. Analysis of microtubule anisotropy was carried out using the ImageJ plug in FibrilTool32.
How to cite this article: Creff, A. et al. A mechanically sensitive cell layer regulates the physical properties of the Arabidopsis seed coat. Nat. Commun. 6:6382 doi: 10.1038/ncomms7382 (2015).
Le, B. H. et al. Global analysis of gene activity during Arabidopsis seed development and identification of seed-specific transcription factors. Proc. Natl Acad. Sci. USA 107, 8063–8070 (2010).
Stadler, R., Lauterbach, C. & Sauer, N. Cell-to-cell movement of green fluorescent protein reveals post-phloem transport in the outer integument and identifies symplastic domains in Arabidopsis seeds and embryos. Plant Physiol. 139, 701–712 (2005).
Ingram, G. C. Family life at close quarters: communication and constraint in angiosperm seed development. Protoplasma 247, 195–214 (2010).
Garcia, D., Fitz Gerald, J. N. & Berger, F. Maternal control of integument cell elongation and zygotic control of endosperm growth are coordinated to determine seed size in Arabidopsis. Plant Cell 17, 52–60 (2005).
Kutschera, U. The role of the epidermis in the control of elongation growth in stems and coleoptiles. Bot. Acta 105, 246–252 (1992).
Kutschera, U. The growing outer epidermal wall: design and physiological role of a composite structure. Ann. Bot. 101, 615–621 (2008).
Kutschera, U. & Niklas, K. J. The epidermal-growth-control theory of stem elongation: an old and a new perspective. J. Plant Physiol. 164, 1395–1409 (2007).
Western, T. L. et al. Isolation and characterization of mutants defective in seed coat mucilage secretory cell development in Arabidopsis. Plant Physiol. 127, 998–1011 (2001).
Beeckman, T., De Rycke, R., Viane, R. & Inze, D. Histological study of seed coat development in Arabidopsis thaliana. J. Plant Res. 113, 139–148 (2000).
Luo, M., Dennis, E. S., Berger, F., Peacock, W. J. & Chaudhury, A. MINISEED3 (MINI3), a WRKY family gene, and HAIKU2 (IKU2), a leucine-rich repeat (LRR) KINASE gene, are regulators of seed size in Arabidopsis. Proc. Natl Acad. Sci. USA 102, 17531–17536 (2005).
Verhertbruggen, Y., Marcus, S. E., Haeger, A., Ordaz-Ortiz, J. J. & Knox, J. P. An extended set of monoclonal antibodies to pectic homogalacturonan. Carbohydr. Res. 344, 1858–1862 (2009).
Jacques, E., Verbelen, J. P. & Vissenberg, K. Mechanical stress in Arabidopsis leaves orients microtubules in a ‘continuous’ supracellular pattern. BMC Plant Biol. 13, 163 (2013).
Hamant, O. et al. Developmental patterning by mechanical signals in Arabidopsis. Science 322, 1650–1655 (2008).
Sampathkumar, A. et al. Subcellular and supracellular mechanical stress prescribes cytoskeleton behavior in Arabidopsis cotyledon pavement cells. Elife 3, e01967 (2014).
Li, S., Lei, L., Somerville, C. R. & Gu, Y. Cellulose synthase interactive protein 1 (CSI1) links microtubules and cellulose synthase complexes. Proc. Natl Acad. Sci. USA 109, 185–190 (2012).
Paradez, A., Wright, A. & Ehrhardt, D. W. Microtubule cortical array organization and plant cell morphogenesis. Curr. Opin. Plant Biol. 9, 571–578 (2006).
Hasezawa, S., Ueda, K. & Kumagai, F. Time-sequence observations of microtubule dynamics throughout mitosis in living cell suspensions of stable transgenic Arabidopsis—direct evidence for the origin of cortical microtubules at M/G1 interface. Plant Cell Physiol. 41, 244–250 (2000).
Fache, V. et al. Arabidopsis kinetochore fiber-associated MAP65-4 cross-links microtubules and promotes microtubule bundle elongation. Plant Cell 22, 3804–3815 (2010).
Cutler, S. R., Ehrhardt, D. W., Griffitts, J. S. & Somerville, C. R. Random GFP::cDNA fusions enable visualization of subcellular structures in cells of Arabidopsis at a high frequency. Proc. Natl Acad. Sci. USA 97, 3718–3723 (2000).
Denay, G. et al. Endosperm breakdown in Arabidopsis requires heterodimers of the basic helix-loop-helix proteins ZHOUPI and INDUCER OF CBP EXPRESSION 1. Development 141, 1222–1227 (2014).
Yang, S. et al. The endosperm-specific ZHOUPI gene of Arabidopsis thaliana regulates endosperm breakdown and embryonic epidermal development. Development 135, 3501–3509 (2008).
Xing, Q. et al. ZHOUPI controls embryonic cuticle formation via a signalling pathway involving the subtilisin protease ABNORMAL LEAF-SHAPE1 and the receptor kinases GASSHO1 and GASSHO2. Development 140, 770–779 (2013).
Zhang, Y. et al. Two Arabidopsis cytochrome P450 monooxygenases, CYP714A1 and CYP714A2, function redundantly in plant development through gibberellin deactivation. Plant J. 67, 342–353 (2011).
Yamaguchi, N. et al. Gibberellin acts positively then negatively to control onset of flower formation in Arabidopsis. Science 344, 638–641 (2014).
Rautengarten, C. et al. The interconversion of UDP-arabinopyranose and UDP-arabinofuranose is indispensable for plant development in Arabidopsis. Plant Cell 23, 1373–1390 (2011).
Bai, M. Y. et al. Brassinosteroid, gibberellin and phytochrome impinge on a common transcription module in Arabidopsis. Nat. Cell Biol. 14, 810–817 (2012).
Logemann, E., Birkenbihl, R. P., Ulker, B. & Somssich, I. E. An improved method for preparing Agrobacterium cells that simplifies the Arabidopsis transformation protocol. Plant Methods 2, 16 (2006).
Spurr, A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26, 31–43 (1969).
Gleave, A. P. A versatile binary vector system with a T-DNA organisational structure conducive to efficient integration of cloned DNA into the plant genome. Plant Mol. Biol. 20, 1203––1207 (1992).
Karimi, M., Inze, D. & Depicker, A. GATEWAY vectors for Agrobacterium-mediated plant transformation. Trends Plant Sci. 7, 193––195 (2002).
Schneider, C. A., Rasband, W. S. & Eliceiri, K. W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671–675 (2012).
Boudaoud, A. et al. FibrilTool, an ImageJ plug-in to quantify fibrillar structures in raw microscopy images. Nat. Protoc. 9, 457–463 (2014).
We thank Peter Rogowsky, Arezki Boudaoud, Olivier Hamant, Chloé Fourquin and Marie Delattre (ENS de Lyon) and Naomi Nakayama (University of Edinburgh) for their critical comments, advice and encouragement; Marc Moulin (ENS de Lyon workshops) for the fabrication of the tissue vice; Marilyn Vantard (CEA Grenoble) for the MAP65 line; the European Arabidopsis Stock Centre (NASC) for providing seed and the plant culture and the logistics and secretarial teams at the RDP for their support. This work was financed by a ‘Chaire d’excellence’ (ANR-10-CHEX-0011: mécanograine) from l’Agence National de la Recherche, France.
The authors declare no competing financial interests.
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Creff, A., Brocard, L. & Ingram, G. A mechanically sensitive cell layer regulates the physical properties of the Arabidopsis seed coat. Nat Commun 6, 6382 (2015). https://doi.org/10.1038/ncomms7382
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