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.
Back-to-back with this first paper, Roulland-Dussoix & Arber then add that the phage DNA is degraded immediately after injection into the E. coli cell,& that the DNA can be ‘rescued’ by the infection of additional DNA, suggesting competition between the DNA for recognition sites.
It therefore seemed that enzymes, that competitively bind the DNA are involved in this process. These host enzymes are degrading the invasive phage DNA, and are thus ‘restricting’ the phage’s ability to infect the host cell: restriction enzymes.
In 1968 Meselson & Yuan identified the first restriction enzyme, the type I endonuclease EcoK from E. coli, followed by Smith & Wilcox, who identified the type II enzyme HindII in 1970, & Mertz & Davis who found EcoRI in 1972,& also showed that this enzyme produces ‘sticky-ends’.
The lab of Daniel Nathans then proceeded to use these restriction enzymes to cut up the simian virus 40 genome into 11 defined pieces, followed by gel-separation, demonstrating that endonuclease analysis could be used for DNA mapping of genomes.
Then, in 1972/1973, restriction enzymes were used to splice gene fragments into plasmids and shuttled into bacterial cells, where they were replicated and expressed. Molecular cloning was developed,& with it started the Molecular Biology Revolution, changing the world forever.
Accordingly, Nobel Prizes were in order! And the 1978 Prize in Physiology and Medicine "for the discovery of restriction enzymes and their application to problems of molecular genetics" went to Werner Arber, Daniel Nathans & Hamilton O. Smith. Daisy Roulland-Dussoix was ignored.
Thankfully, Daisy Roulland-Dussoix went on to have a long and successful career in science despite this, initially continuing work on restriction enzymes & cloning with Herbert Boyer & eventually becoming a leading expert on mycobacterium/mycoplasmas.
Daisy Roulland-Dussoix died January 5, 2014. I would have liked to end this with a nice obituary for her, but unfortunately I could not find one...
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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.
#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.
#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.