Ethylene is a gaseous #phytohormone with a wide range of roles from plant development to immunity. Ernest Starling in 1905 defined a hormone as mobile chemical messenger synthesized by a multicellular organism, that has physiological activity distant from the site of synthesis.
The effect of ethylene on plants was first noted in the 1900s, when it leaked from illumination gas used in lamps and affected plants nearby. But it was Dimitry Neljubow, who in a series of experiments identified ethlyene as the active substance in the illumination gas in 1905.
Neljubow already used the #TripleResponse. He noted pea seedlings growing shorter, thicker epicotyls which bend horizontally, when grown with light from illumination gas, but not outdoors or in the dark. He then tested all components distilled from the gas & identified ethylene.
This work by Neljubow showed that the gaseous ethylene could induce physiological effects. Part 1 of Starlings definition of a hormone. Now part 2 was missing: That ethylene is actually produced by the organisms in which it functions.
Scientists have long noticed that some fruit affect other plants around them in the same way as ethylene. For example, apples could affect the sprouting of potato tubers – just like ethylene treatment. It was therefore speculated that some plants may be able to produce ethylene.
And in 1934, Richard Gane was indeed able to distill ~0.6 g of ethylene from the gas given off by 60 pounds of apples over 4 weeks. So part 2 of the definition of a hormone, "produced by the organism itself", also seemed to apply in the case of ethylene.
In 1935 William Crocker, Alfred Hitchcock,& Percy Zimmerman published more data on ethylene effects on plant growth & senescence, and first explicitly put it in one group with the #phytohormone#Auxin in their report “Similarities in the effects of ethlyene and the plant auxins”.
The next major leaps came after the adoption of Arabidopsis as model plant for genetics:
Chris Somerville had already demonstrated how Arabidopsis mutants could readily be used to identify new components of signaling pathways.
Somerville teamed up with Anthony Bleecker, @mestelle & Hans Kende to screen for Arabidopsis mutants with an altered triple response: Seedlings grown in darkness with ethylene have (1) shorter and (2) thicker hypocotyls & (3) exaggerated apical hooks - Clearly visible phenotypes.
By screening for mutants without this response, the team identified the ETR gene, coding for one plant ETHYLENE RECEPTOR. And using the same approach, Plinio Guzman & @JosephKieber from @JoeEcker's lab quickly added the receptor CTR1 and the signaling regulator EIN2 (1990/93).
So by the 1990s, it was clear that ethylene was indeed a gaseous hormone,& several parts of its signaling pathway were known. And on top of its general meaning for plant development, ethylene also quickly became commercially important to control fruit ripening in transport.
As this was the first discovery that a gas can act as a signal molecule in an organism, and with the finding that one cell produces the gas, which then penetrates through membranes & regulates the function of another cell representing an entirely new principle for signalling...
...the @NobelPrize committee awarded the 1998 Prize in Physiology/Medicine to... 🥁... Robert Furchgott, Louis Ignarro & Ferid Murad, who just 20 years prior identified “nitric oxide as gaseous signalling molecule in human cells” - over 40(!) years after ethylene was described!
In the committee's reasoning, they used the exact words I used 2 tweets before this one to describe ethylene, including the obviously wrong claim that "this (nitric oxide) was the first discovery that a gas can act as a signal molecule in the organism"! 😳🙄😖 #PlantBlindness
Hans Kende commented on this decision in @ScienceMagazine, the journal that published their 1988 ETR paper, but as we all know, still nothing has changed, and pioneering plant work is still regularly overlooked. science.org/doi/10.1126/sc…
Since then, we have learned a lot more about ethylene signaling in plants, and you can find a nice overview article by Brad Binder here: jbc.org/article/S0021-… , and a history of ethylene research here: link.springer.com/article/10.100…
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#PlantScienceClassics #17: The Mildew Resistance Locus O (MLO). 80 years ago Rudolf Freisleben & Alfred Lein created the first powdery mildew resistant barley plant. 30yrs ago the gene was mapped, 25yrs ago cloned-yet it's mode of action remains a mystery. doi.org/10.1007/BF0148…
Powdery mildew is a fungal disease of many crop plants, most prominently maybe barley and wheat, where outbreaks can reduce grain quality & yield, and ruin complete harvests. Visible are the fluffy patches formed by the fungus (Blumeria graminis f. sp. hordei).
Freisleben used radiation-induced mutagenesis to create the barley 𝘮𝘭𝘰 mutant, which showed full resistant to this pathogen. A massive agricultural breakthrough!
See also Classic #2, to read about how Emmy Stein has developed this technique in 1921:
#PlantScienceClassics #16: A linkage map of Arabidopsis thaliana. In 1983 the legendary Maarten Koornneef published a genetic map of A. thaliana, the basis for genetic work & an important contribution towards the acceptance of Arabidopsis as plant model. doi.org/10.1093/oxford…
In the early 1980s scientists finally adopted A. thaliana as model plant. At this point, several mutants were available, but their positions in the genome were mostly unknown. This was years before genome sequences became available,&genetic maps were still based on recombination.
Arabidopsis pioneer György Rédei did linkage analyses with 14 loci in the 1960s, but his genetic map from 1965 suggested 6 linkage groups – 1 more than chromosomes. Curiously, A. D. McKelvie created another map in parallel - & found 4 groups, 1 less than chromosomes.
#PlantScienceClassics #15 #PlantScienceFails #1: The auxin-independent (axi) Nicotiana tabacum lines. In 1992 Richard Walden et al. (specifically co-worker Inge Czaja) published activation-tagged axi protoplasts @ScienceMagazine that could divide&grow in the absence of any auxin!
The development of plant transformation in the early 1980s (classics #6&13) was inspirational for many scientists. Among them was Richard Walden, who teamed up with plant transformation pioneers Barbara & Thomas Hohn to leverage this advance to develop the “Agroinfection" method.
He then joined the next transformation pioneer, Jeff Schell, to develop more such tools. Their first was Activation-Tagging: 4 CaMV 35S enhancers (classic#9) were placed at the RB of the T-DNA. That way, they would overexpress the plant gene next to which the T-DNA was inserted.
#PlantScienceClassics #14: Mendelian inheritance. In 1866 Gregor Mendel published his work on dominant/recessive trait inheritance in peas, establishing the hereditary rules on which modern genetics is based. But nobody cared,& his scientific career ended. biodiversitylibrary.org/page/48299076
Mendel had always been interested in nature, and grew/kept and observed plants and bees in his parent’s garden. He later decided to become a monk and teacher. However, he failed teacher’s exam in 1850 & 1856, & eventually settled on being a monk and substitute teacher.
He satisfied his curiosity as a naturalist by keeping and observing plants and bees in the monastery garden, and eventually became interested in how traits are determined through generations. So he started to conduct crossing experiments with mice with grey or white fur.
Do you know Daisy Roulland-Dussoix? She is one of the discoverers of restriction enzymes, who’s findings paved the way for the development of recombinant DNA and cloning technologies. Accordingly, the finding was rewarded with a #NobelPrize. But the prize didn’t go to her... 🧵👇
Daisy Roulland-Dussoix worked with Werner Arber to study the mechanism for the observed host-specificity of λ Phages. It was known from an important 1953 paper (Bertani & Weigle) that phages, that had replicated in a certain E. coli strain, could only re-infect the same strain.
Roulland-Dussoix & Arber showed that host-specificity is linked with the phage’s DNA. Using phages carrying radiolabeled DNA, they showed that progeny with 2 parental DNA strands retained specificity, while progeny with newly synthesized daughter strands could adapt to new hosts.
#PlantScienceClassics #13: Floral Dip. Almost 25 years ago, in 1998, Steven Clough & Andrew Bent published their geniously simple Arabidopsis transformation protocol @ThePlantJournal: Dipping a plant upside down into Agrobacterium solution - et voilà! doi.org/10.1046/j.1365…
I have covered the plant transformation backstory in Classic#6, the T-DNA, so here I will focus on the events after 1983, the year plant transformation was established. These first transformants all were plants regenerated from cultured cells as calli.
Simply transforming an adult plant was not yet possible. One of the prerequisite toward this aim was the acceptance of Arabidopsis thaliana as a model plant (see also Classic#4), and the demonstration that A. thaliana was transformable via Agrobacterium.