Prof. Edward (Ted) Farmer

Defending captured carbon / protecting carbon capture | Our past activities
 

Defending captured carbon / protecting carbon capture


The approximately 500 gigatons of carbon in living terrestrial vegetation is potentially valuable food for animals, however, most living plant mass remains uneaten in nature. Our research aims to understand why this is and, specifically, how plants defend themselves. We discovered that a lipid-derived signal, jasmonate, controls antiherbivore defence responses and limits the activity of detritivores. The jasmonate pathway operates at a major nexus in the carbon cycle, limiting carbon flow from both living and dead plants to higher trophic levels. The laboratory uses genetic and electrophysiological techniques to study jasmonate pathway activation.

 

Current research

We focus on how plant defense responses are activated in the seconds following wounding. This process involves long-distance electrical signals known as slow wave potentials (SWPs) that powerfully activate jasmonate synthesis in xylem cell niches. The goal is to understand how these signals are generated, propagated and decoded. To do this, we combine electrophysiology, genetics and whole-plant physiology approaches in Arabidopsis. A genetic understanding of leaf-to-leaf electrical signals in plants has long eluded researchers. This is now changing with the identification of several key genes through research ongoing in our laboratory.

NEW: A review highlighting progress in uncovering the genetic basis of electrical signalling in plants :  Here.

 

 

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When leaf 8 of a wild-type adult-phase plant is wounded, electrical signals travel to a sector of distal leaves to trigger increased cytosolic calcium levels and to activate the jasmonate pathway. The glr3.3 and glr3.6 single mutants show overall weaker responses in leaves distal to wounds. However, the glr3.1 mutation makes the wound responses in leaves 13 and 16 asymmetrical. Clade 3 GLRs control axial and radial damage signalling in plants.

 

 

 

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Our past activities

Main contributions in italic

LONG DISTANCE WOUND SIGNALS

In response to wounding, jasmonates can be made within and proximal to wounds and also in distal tissues. Jasmonate synthesis can be activated by long distance wound signals other than mobile jasmonates. The nature of these signals has long been a mystery.

Showed that leaf-to-leaf wound signals that activate jasmonate synthesis move at speeds in the cm/min range (J. Biol. Chem. 283, 16400) and made the first constrained (minimum and maximum) velocity estimates for the speed of long distance wound signals that travel from leaf to leaf after wounding (J. Biol. Chem. 284, 34506). We showed that these long distance wound signals move through well-defined parastichies (J. Biol. Chem. 284, 34506 ; New Phytol. 197, 566).

Showed that clade 3 GLUTAMATE RECEPTOR-LIKE (GLR) proteins mediate electrical signalling in plants (Nature 500, 422).

Showed that the AHA1 proton pump functions to re-build membrane potentials after wounding (PNAS 116, 20226-20321).

We found that the first burst of jasmonate made in leaves distal to wounds in Arabidopsis originates from the activity of LOX6, an enzyme localized to xylem contact cells (New Phytol. 197, 566).

Developed aphids as living electrodes and used them to characterize GLR-dependent electrical signals in phloem sieve tubes (New Phytol. 203, 674).

In 2018 we discovered that two non-adjacent vascular cell types (xylem contact cells and phloem sieve elements) are necessary for the transmission of electrical signals from leaf to leaf (PNAS 115, 10178). Interestingly, endomembranes within these cells are implicated in controlling the ion fluxes underlying the electrical signals and this is consistent with other results from genetics studies (New Phytol. 216, 1161).

Rapidly propagated (ms) pressure signals in the xylem were thought to underlie slow wave potential propagation. However, we failed to find these signals in wounded Arabidopsis and instead found that leaves deform as insect-induced SWPs propagate from leaf to leaf (PNAS 116, 26066). These data were used in the development of a model that implies an important role of phloem turgor pressure linked to electrical signalling (New Phytol. accepted).

 

 

JASMONATES

Proposed with C.A. Ryan a central role of jasmonate in the plant immune system (PNAS 1990, 87, 7713) and published the first model integrating wound signaling and damage-associated molecular pattern (DAMP) signalling leading to jasmonate synthesis and defense (Plant Cell 1992, 4, 129). The year 2020 marks 30 years of research on jasmonates and plant defense!

Performed the first experiments to investigate the effects of a signal transduction pathway on the feeding behavior of a vertebrate herbivore (Mol. Ecol. 21, 2534-2541).

We showed that wound-response leaf growth restriction is mediated by the jasmonate pathway (Plant Cell 19, 2470).

When leaves are wounded the aerial growth of plants is reduced. We showed how root growth in these plants is controlled genetically so that reduced growth of stems is balanced by reduced root growth (PNAS 110, 15473).

Developed the first assays to assess the contribution of jasmonate signalling to root (PLoS Gen. 11(6) :e1005300) growth restriction after wounding and developed novel shoot to root wounding assays for Arabidopsis seedlings (PNAS 110, 15473 ; PLoS Gen. 11(6) : e1005300).

We showed that the genetic architecture of the jasmonate pathway is different in roots and aerial tissues (PNAS 110, 15473) and identified cell-specific regulatory layers that prevent activation of the jasmonate pathway in healthy roots (PLoS Gen. 11(6) :e1005300).

Co-discovered (in parallel with the goups of J. Browse and R. Solano) members of the 'JAZ' family of repressor proteins and shown that a natural transcript from JAS1/JAZ10 plays a role in wound-induced growth inhbition. Also descibed the 'Jas' motif as a functional element in this protein (Plant Cell 19, 2470).

Discovered a new jasmonate (dnOPDA) and revealed a novel 'hexadecanoid' branch of the jasmonate biosynthetic pathway (PNAS 94, 10473).

Showed that monogalactosyldiacylglyerol (MGDG) is a likely in vivo substrate for jasmonate synthesis (PNAS 94, 10473).

Showed that cyclopentenone jasmonates (OPDA & dnOPDA) can act as signals (PNAS 98, 12837).

Described the principal roles of all four Arabidopsis 13-lipoxygenases in vegetative tissues : LOX2 makes the precusorsors of arabidopsides, LOX3 and 4 control wound-response growth restriction, LOX6 makes JA precursors in xylem contact cells (New Phytol. 197, 566 ; J. Biol. Chem. 284, 34506 ; Plant Physiol. 2020).

Quantitated (using microarrays and statistical analysis) the number of chewing insect-inducible genes that are regulated throught the jasmonate signal pathway (an estimated 67-84%) (Plant Cell 16, 3132) and shown that a specialist and a generalist insect activate this pathway almost equally.

Showed that jasmonate signalling promotes the establishment of an oxidising environment near a wound (Plant Physiol. 156, 1797).

We showed that endogenous jasmonate can move axially and radially from cell to cell in plants (Plant Physiol. 169, 2244).

Identified fou2, a wound-mimic mutant containing a single missense mutation in the vacuolar voltage-gated cation channel TPC1 (Plant J. 49, 889 ; Plant Cell Physiol. 48, 1775).
 

 

MEMBRANES AS STRUCTURAL ANTIOXIDANTS

Tissues in which there is a high production of ROS (e.g. retina, neurons, thylakoids etc.) are particularly rich in oxidation-sensitive polyunsaturated fatty acids (PUFAs). At the subcellular level the membranes with the highest PUFA levels are often found where ROS are produced (e.g. mitochondria and chloroplasts).Why is this? Using genetic approaches we found that polyunsaturated fatty acids have roles as sinks for ROS. That is, membranes rich in these fatty acids can now be regarded as supramolecular antioxidants (J. Biol. Chem. 284, 1702; Ann. Rev. Plant Biol. 64, 429).

Showed that malondialdehyde (MDA) is an intermediate in a lipid repair cycle (J. Biol. Chem. 291, 13005).

 

Reactive Electrophile Species (RES)

Proposed that 'reactive electrophile species' (RES) could play roles in abiotic stress responses and in the 'abiotic component' of biotic attack in plants (Plant J. 24, 467; Nature 411, 854). 

Demonstrated powerful biological activity in the ubiquitous and highly studied lipid peroxidation marker malondialdehyde (MDA) (Plant J. 37, 877) and showed that linolenic acid is the major source of damaging reactive molecules produced by non-enzymatic oxidation in leaves (J. Biol. Chem. 202, 35749).

Developed a whole-body malondialdehyde mapping technique for the in situ visualization of MDA in complex organisms (J. Biol. Chem. 202, 35749) and discovered inducible pools of MDA in stem cell-rich tissues including the pericycle (J. Biol. Chem. 287, 8954-8962).

Proposed the ‘lipid stress hypothesis’ with M.J. Mueller (Ann. Rev. Plant Biol. 64, 429). Stress triggers fatty acid de-esterification from membranes. Oxidized fatty acids induce chaperones that might act as binding surfaces for the displaced fatty acids that could otherwise disrupt hydrophobic protein-protein interaction surfaces.

 

Biologically active cell wall fragments

Showed that biologically active pectic fragments (oligogalacturonides) are egg-box conformers where oligogalacturonides are bound to calcium ions (J. Biol. Chem. 266, 3140).

 

Remorin: a new family of proteins

Discovered the remorin group of plasma membrane proteins (PNAS 86, 1539; Plant Cell 8, 2265). 'Remorins may be associated with the cytoskeleton or membrane skeleton i.e., in superstructures that help determine cell integrity and/or act as scaffolds for signaling in defense or development' (Plant Mol. Biol. 55, 579).

 

Oxylipins control a major biological transition: from detritivory to herbivory

Evolution from detritivory (feeding on dead tissues) to herbivory (feeding on living plants) is one of the major transitions in biology. We starved isopod crustaceans (detritivores) and let them loose on Arabidopsis and rice mutants in jasmonate synthesis. The isopods started to feed on the living mutant plants but rarely damaged the WT. This shows that the absence of a signal pathway (the jasmonate pathway) in one organism causes a profound (transitional) effect on feeding in another (PNAS 106, 935).

 

Why do herbivores often cut round holes in leaves?

Now and again some of the things one finds changes the way one looks at nature. Herbivores often cut highly regular circles and semi-circles of leaf tissue. Birds often use the light coming through these holes to help them find caterpillars. In part the fact that insects often cut clean circles in leaves can be explained because it is simple and 'mechanically economic' (the insect doesn't have to move much) to do this. But there is more to the story : In carefully analysing microarray data we saw that some herbivores probably try to extract the maximum area of leaf tissue while leaving the minimal length of cut edge, so as to minimise stimulating plant defenses Plant Cell 12, 707). Perhaps insects understand calculus.

 

Missing phytoalexins from potato

Good candidates for low molecular mass antibiotics (phytoalexins) from the leaves of the historically and commercially important plant potato were unknown. They turned out to be relatively unstable molecules that had been described in vitro but that had previously escaped detection in living organisms. We identified divinyl ether fatty acids for the first time in nature in these leaves and proposed a role as antimicrobial compounds (Plant Cell 11, 485). They are the best candidates for the long-lost phytoalexins in potato leaves, the primary infection site for potato blight.

 

Community resources

Our laboratory has strongly supported the development of central, shared community resources in molecular biology and played a role in the establishment of the Lausanne DNA Array Facility.

 

 

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Contact:

Prof. Edward Farmer
University of Lausanne
Département de Biologie Moléculaire Végétale
UNIL-Sorge
Biophore Building
CH-1015 Lausanne
Switzerland

Tel: +41-21-692-4228
Fax: +41-21-692-4195
Edward.Farmer@unil.ch

 

Biophore - CH-1015 Lausanne
Switzerland
Tel. +41 21 692 41 90
Fax +41 21 692 41 95