Tomato Genetics: A Unexpected Journey Into a “Parallel Universe”

Tomato Genetics: A Unexpected Journey Into a “Parallel Universe”

Tomato Plant Genetics Art
Researchers at Michigan State University found that tomato plants utilize two separate metabolic pathways to produce acylsugars in roots and trichomes, offering new strategies for natural pest resistance in agriculture. Credit: SciTechDaily.com
In a new study recently published by Science Advances, Michigan State University researchers reveal an unexpected genetic revelation about the sugars found in “tomato tar,” shedding light on plant defense mechanisms and their potential applications in pest control.

Tomato tar, a familiar nuisance of avid gardeners, is the sticky, gold-black substance that clings to hands after touching the plant. It turns out that the characteristic stickiness of the substance serves an important purpose. It’s made of a type of sugar called acylsugar that acts as a natural flypaper for would-be pests. “Plants have evolved to make so many amazing poisons and other biologically active compounds,” said Michigan State researcher Robert Last, leader of the study. The Last lab specializes in acylsugars and the tiny, hair-like structures where they’re produced and stored, known as trichomes.

In a surprising discovery, researchers have found acylsugars, once thought to be found exclusively in trichomes, in tomato roots as well. This finding is a genetic enigma that raises as many questions as it does insights.

The objective of the MSU study was to learn about the origins and function of these root acylsugars. They found that not only do tomato plants synthesize chemically unique acylsugars in their roots and trichomes, but these acylsugars are produced through two parallel metabolic pathways. This is the equivalent of assembly lines in an auto factory making two different models of the same car, but never interacting.

MSU Tomato Seedlings
In Michigan State’s Department of Biochemistry and Molecular Biology, tomato seedlings are grown for the Last lab’s research into the Solanaceae plant family, also known as nightshades. The researchers analyzed unique chemical differences between roots and shoots, both of which contained acylsugars. Credit: Connor Yeck/MSU
These findings are helping scientists gain a better understanding of the resilience and evolutionary story of Solanaceae, or nightshades, a sprawling family of plants that includes tomatoes, eggplants, potatoes, peppers, tobacco, and petunias.

They could also provide valuable information for researchers looking to develop molecules made by plants into compounds to help humanity. “From pharmaceuticals, to pesticides, to sunscreens, many small molecules that humans have adapted for different uses come from the arms race between plants, microbes, and insects,” Last said.

Roots and Shoots

Beyond key chemicals essential for growth, plants also produce a treasure trove of compounds that play a crucial role in environmental interactions. These can attract useful pollinators and are the first line of defense against harmful organisms.

“What’s so remarkable about these specialized metabolites is that they’re typically synthesized in highly precise cells and tissues,” said Rachel Kerwin, a postdoctoral researcher at MSU and first author of the latest paper.

“Take for instance acylsugars. You won’t find them produced in the leaves or stems of a tomato plant. These physically sticky defense metabolites are made right in the tip of the trichomes.”

When it was reported that acylsugars could be found in tomato roots as well, Kerwin took it as a call for old-fashioned genetic detective work.

Jaynee Hart, Rachel Kerwin and Robert Last
From left to right: Jaynee Hart, Rachel Kerwin and Robert Last pose in front of analytical equipment at Michigan State University’s Mass Spectrometry and Metabolomics Core. The team of researchers unraveled an evolutionary and genetic mystery in tomato plants. Credit: Connor Yeck/MSU

“The presence of these acylsugars in roots was fascinating and led to so many questions. How did this happen, how are they being made and are they different from the trichome acylsugars we’ve been studying?”

To begin tackling the evolutionary enigma, lab members collaborated with specialists at MSU’s Mass Spectrometry and Metabolomics Core and staff at the Max T. Rogers Nuclear Magnetic Resonance facility.

In comparing metabolites from tomato seedlings’ roots and shoots, a variety of differences appeared. The basic chemical makeup of the aboveground and belowground acylsugars were noticeably different, so much so that they could be defined as different classes of acylsugars entirely.

Breaking the Car

Last, a University Distinguished Professor in MSU’s College of Natural Science’s Department of Biochemistry and Molecular Biology and Department of Plant Biology, offers a useful analogy to explain how a geneticist approaches biology. “Imagine trying to figure out how a car works by breaking one component at a time,” he said. “If you flatten a car’s tires and notice the engine still runs, you’ve discovered a critical fact even if you don’t know what the tires exactly do.”

Switch out car parts for genes, and you get a clearer picture of the work accomplished by the Last lab to further crack the code on root acylsugars.

Looking at public genetic sequence data, Kerwin noticed that many of the genes expressed in tomato trichome acylsugar production had close relatives in roots. After identifying an enzyme believed to be the first step in root acylsugar biosynthesis, the researchers began “breaking the car.”

When they knocked out the root acylsugar candidate gene, root acylsugar production vanished, leaving trichome acylsugar production untouched.

Meanwhile, when the well-studied trichome acylsugar gene was knocked out, root acylsugar production carried on as usual.

These findings offered striking proof of a suspected metabolic mirroring.

“Alongside the aboveground acylsugar pathway we’ve been studying for years, here we find this second parallel universe that exists underground,” Last said.

“This confirmed we have two pathways co-existing in the same plant,” Kerwin added.

To drive home this breakthrough, Jaynee Hart, a postdoctoral researcher and second author on the latest paper, looked closer at the functions of trichome and root enzymes.

Just as trichome enzymes and the acylsugars they produce are a well-studied chemical match, she found a promising link between root enzymes and the root acylsugars as well.

“Studying isolated enzymes is a powerful tool for ascertaining their activity and drawing conclusions about their functional role inside the plant cell,” Hart explained.

These findings were further proof of the parallel metabolic pathways that exist in a single tomato plant.

“Plants and cars are so different, yet similar in that when you open the proverbial hood you become aware of the multitude of parts and connections that make them function. This work gives us new knowledge about one of those parts in tomato plants and prompts further research into its evolution and function and whether we can make use of it in other ways,” said Pankaj Jaiswal, a program director at the U.S. National Science Foundation, which funded the work.

“The more we learn about living things — from tomatoes and other crops to animals and microbes — the broader the opportunities to employ that learning to benefit society,” he added.

Clusters Within Clusters

The paper also reports a fascinating and unexpected twist concerned with biosynthetic gene clusters, or BGCs.

BGCs are collections of genes that are physically grouped on the chromosome and contribute to a particular metabolic pathway. Previously, the Last lab identified a BGC containing genes linked to trichome acylsugars in tomato plants. Kerwin, Hart, and their collaborators have now discovered the root-expressed acylsugar enzyme resides in the same cluster.

“Usually in BGCs, the genes are co-expressed in the same tissues and under similar conditions,” said Kerwin.“But here, we have two separate yet interlinked groups of genes. Some expressed in trichomes, and some expressed in roots.”

This revelation led Kerwin to dive into the evolutionary trajectory of Solanaceae species, with hopes of identifying when and how these two unique acylsugar pathways developed. Specifically, the researchers drew attention to a moment some 19 million years ago when the enzyme responsible for trichome acylsugars was duplicated. This enzyme would one day be responsible for the newly discovered root-expressed acylsugar pathway.

The exact mechanism that “switched on” this enzyme in roots remains unknown, paving the way for the Last lab to continue to unpack the evolutionary and metabolic secrets of the nightshade family.

“Working with Solanaceae provides so many scientific resources, as well as a strong community of researchers,” said Kerwin.

“Through their importance as crops and in horticulture, these are plants humans have cared about for thousands of years.”

For Last, these breakthroughs are also a reminder of the importance of natural pesticides, which defense metabolites such as acylsugars ultimately represent.

“If we find that these root acylsugars are effective at repelling harmful organisms, could they be bred into other nightshades, thereby helping plants grow without the need for harmful synthetic fungicides and pesticides?” Last asked.

“These are questions at the core of humanity’s pursuit of purer water, safer food and a reduced reliance on harmful synthetic chemicals.”

Reference: “Tomato root specialized metabolites evolved through gene duplication and regulatory divergence within a biosynthetic gene cluster” by Rachel E. Kerwin, Jaynee E. Hart, Paul D. Fiesel, Yann-Ru Lou, Pengxiang Fan, A. Daniel Jones and Robert L. Last, 24 April 2024, Science Advances.
DOI: 10.1126/sciadv.adn3991

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Sunflower Secrets Unveiled: Multiple Origins of Flower Symmetry Discovered

Sunflower Secrets Unveiled: Multiple Origins of Flower Symmetry Discovered

Sunflower Family Tree
A new sunflower family tree reveals that flower symmetry evolved multiple times independently. Species of the sunflower family with or without bilateral flower symmetry. Chrysanthemum lavandulifolium (upper left) and Artemisia annua (upper right) are closely related species from the same tribe; the former has bilaterally symmetric flowers (the rays) and the latter does not. Rudbeckia hirta (lower left) from the sunflower tribe has bilaterally symmetric flowers, and Eupatorium chinense (lower right) from the Eupatorieae tribe does not; these two tribes are closely related groups. A sunflower (center) shows flowers with bilateral symmetry (the large petal-like flowers in the outer row) and without (the small flowers in the inner rows). Credit: Guojin Zhang, Ma laboratory, Penn State

The sunflower family tree revealed that flower symmetry evolved multiple times independently, a process called convergent evolution, among the members of this large plant family, according to a new analysis. The research team, led by a Penn State biologist, resolved more of the finer branches of the family tree, providing insight into how the sunflower family — which includes asters, daisies, and food crops like lettuce and artichoke — evolved.

A paper describing the analysis and findings, which researchers said may help identify useful traits to selectively breed plants with more desirable characteristics, appeared online in the journal Plant Communication.

“Convergent evolution describes the independent evolution of what appears to be the same trait in different species, like wings in birds and bats,” said Hong Ma, Huck Chair in Plant Reproductive Development and Evolution, professor of biology in the Eberly College of Science at Penn State and the leader of the research team. “This can make it difficult to determine how closely related two species are by comparing their traits, so having a detailed family tree based on DNA sequence is crucial to understanding how and when these traits evolved.”

Advances in Sunflower Family Genealogy

The sunflower head, for example, is actually a composite composed of multiple much smaller flowers. While the head is generally radially symmetric — it can be divided into two equal halves in multiple directions like a starfish or a pie — the individual flowers can have different forms of symmetry. According to the new study, bilateral symmetry — where there is only one line that divides the flower into two equal halves — has evolved and been lost multiple times independently in sunflowers over evolutionary history. The researchers found that this convergent evolution is likely related to changes in the number of copies and the expression patterns of the floral regulatory gene, CYC2.

In recent years, many family trees for a group of related species have been built by extensively using transcriptomes, which are the genetic sequences of essentially all of the genes expressed by a species, the researchers explained. Transcriptomes are easier to acquire than high-quality whole-genome sequences for a species but are still difficult and costly to prepare and require fresh plant samples. To increase the number of species available for comparison the team turned to low-coverage genome sequences, which are produced through a process called genome skimming and are relatively inexpensive and easy to prepare, even from dried plant samples.

“To get an accurate whole-genome sequence for a species, each letter of its DNA alphabet must be read — or covered — multiple times to minimize errors,” Ma said. “For the purposes of building a family tree, we show in this paper that we can get away with lower coverage genome sequences. This allowed us to increase the number of species in our analysis, which, in turn, allowed us to resolve more of the finer branches on the sunflower family tree.”

The team used a combination of publicly available and newly generated transcriptomes, along with a large number of newly obtained skimmed genomes, for a total of 706 species with representatives from 16 subfamilies, 41 tribes, and 144 subtribe-level groups in the sunflower family. The subfamilies are major subdivisions of the family, while the tribes and subtribe can contain one or more of genera, which is the classification level just above the species.

“Previous versions of the sunflower family tree had established the relationships among most of the subfamilies and many tribes, which are equivalent to the main branches of a tree,” Ma said. “With our increased sample size, we were able to resolve more of the smaller branches and twigs at the subtribe and genus level. This higher-resolution tree allowed us to reconstruct where and when traits like flower symmetry evolved, demonstrating that bilateral symmetry must have evolved many times independently.”

Molecular Insights and Future Directions

The team also studied the molecular evolution of genes involved in flower development among sunflowers. They found that one of these genes, CYC2, which is found in multiple copies in the genomes of each species, was activated in species with bilaterally symmetric flowers, suggesting that it might be part of the molecular basis for the convergent evolution of this trait. To further test this, the team performed experiments to quantify CYC2 gene expression in the flowers of species with different types of symmetry.

“Our analysis showed a clear relationship between CYC2 expression and flower symmetry, suggesting that changes in how these genes are used in various sunflower species is likely involved in the convergent evolution observed in the family,” Ma said. “The sunflower family is one of the two largest families of flowering plants containing over 28,000 species, including many economically important agricultural and horticultural species. Understanding how these species are related to one another allows us to determine how and when their traits evolved. This knowledge could also be used to identify useful traits that could be bred into domesticated species from closely related wild ones.”

Reference: “Nuclear phylogenomics of Asteraceae with increased sampling provides new insights into convergent morphological and molecular evolution” by Guojin Zhang, Junbo Yang, Caifei Zhang, Bohan Jiao, Jose L. Panero, Jie Cai, Zhi-Rong Zhang, Lian-Ming Gao, Tiangang Gao and Hong Ma, 25 February 2024, Plant Communications.
DOI: 10.1016/j.xplc.2024.100851

In addition to Ma, the research team includes Guojin Zhang at Penn State; Junbo Yang, Jie Cai, Zhi-Rong Zhang, and Lian-Ming Gao at the Kunming Institute of Botany in Kunming, China; Caifei Zhang at the Wuhan Botanical Garden and Sino-Africa Joint Research Centre in Wuhan, China; Bohan Jiao and Tiangang Gao at the State Key Laboratory of Plant Diversity and Specialty Crops in Beijing, China; and Jose L. Panero at the University of Texas, Austin.

Funding from the Eberly College of Science and the Huck Institutes of the Life Sciences at Penn State, the Strategic Priority Research Program of the Chinese Academy of Sciences, the Large-scale Scientific Facilities of the Chinese Academy of Sciences, and the National Natural Science Foundation of China supported this research.

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Newly Found Gene Enhances Photosynthesis, Boosts Plant Height

Newly Found Gene Enhances Photosynthesis, Boosts Plant Height

Chimera Photosynthesis Regulating Gene Origins
A team of scientists discovered a naturally occurring gene in the poplar tree that enhances photosynthetic activity and significantly boosts plant growth. The gene, Booster, contains DNA from two associated organisms found within the tree, and from a protein known as Rubisco that is essential to photosynthesis. Credit: Andy Sproles, ORNL/U.S. Dept. of Energy

The BOOSTER gene in poplar trees boosts photosynthesis and biomass, with potential applications for improving crop yields.

Researchers from the Center for Advanced Bioenergy and Bioproducts Innovation at the University of Illinois Urbana-Champaign, in collaboration with the Center for Bioenergy Innovation at Oak Ridge National Laboratory, have discovered a gene in poplar trees that improves photosynthesis and can boost tree height.

Chloroplasts are the principal cell structures that house the photosynthetic apparatus converting light energy into the chemical energy that fuels plant growth. Specifically, the Rubisco protein captures carbon dioxide from the atmosphere. Scientists have for years been working on ways to boost the amount of Rubisco in plants for greater crop yield and absorption of atmospheric CO2.

“Historically, a lot of studies have focused on steady-state photosynthesis where every condition is kept constant. However, this is not representative of the field environment in which light can vary all the time,” said Steven Burgess, an assistant professor of integrative biology at Illinois. “Over the last few years, these dynamic processes have been considered to be more important and are not well understood.”

Greenhouse Booster Plants
From left, ORNL’s Biruk Feyissa holds a five-month-old poplar tree expressing high levels of the BOOSTER gene, while colleague Wellington Muchero holds a tree of the same age with lower expression of the gene. Credit: Genevieve Martin/ORNL, U.S. Dept. of Energy

Unlocking Genetic Potential in Poplar Trees

In the new study, the researchers focused on poplar since it is a fast-growing crop and a leading candidate for making biofuels and bioproducts. They sampled ~1,000 trees in outdoor research plots and analyzed their physical characteristics and genetic makeup to perform a genome-wide association study. The team used the GWAS population to look for candidate genes that had been linked to photosynthetic quenching, a process that regulates how quickly plants adjust between sun and shade and dissipate excess energy from too much sun to avoid damage.

One of the genes, which the researchers named BOOSTER, was unusual because it is unique to poplar and although it is in the nuclear genome contains a sequence which originated from the chloroplast.

The team discovered that this gene was able to increase the Rubisco content and subsequent photosynthetic activity, resulting in taller polar plants when grown in greenhouse conditions. In field conditions, scientists found that genotypes with higher expression of BOOSTER were up to 37% taller, increasing biomass per plant. The team also inserted BOOSTER in a different plant, Arabidopsis, or thale cress, resulting in an increase in biomass and seed production. This finding indicates the wider applicability of BOOSTER to potentially trigger higher yields in other plants.

“It is an exciting first step, although these are small-scale experiments, and there is a lot of work to be done, if we can reproduce the results on a large scale, this gene has the potential to increase biomass production in crops,” Burgess said.

Next steps in the research could encompass testing in other bioenergy and food plants, with researchers recording plant productivity in varying growing conditions to analyze long-term success. They will also be investigating the other genes that were identified in the GWAS study that could contribute to crop improvement.

For more on this study, see Breakthrough Gene Supercharges Plant Growth and Boosts Photosynthesis.

Reference: “An orphan gene BOOSTER enhances photosynthetic efficiency and plant productivity” by Biruk A. Feyissa, Elsa M. de Becker, Coralie E. Salesse-Smith, Jin Zhang, Timothy B. Yates, Meng Xie, Kuntal De, Dhananjay Gotarkar, Margot S.S. Chen, Sara S. Jawdy, Dana L. Carper, Kerrie Barry, Jeremy Schmutz, David J. Weston, Paul E. Abraham, Chung-Jui Tsai, Jennifer L. Morrell-Falvey, Gail Taylor, Jin-Gui Chen, Gerald A. Tuskan and Wellington Muchero, 3 December 2024, Developmental Cell.
DOI: 10.1016/j.devcel.2024.11.002

The research was supported by CBI and CABBI, both sponsored by the DOE Office of Science Biological and Environmental Research Program.

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Boiling Alive? Scientific Proof That Crabs Feel Pain Sparks Calls for Humane Seafood Practices

Boiling Alive? Scientific Proof That Crabs Feel Pain Sparks Calls for Humane Seafood Practices

Shore Crab With Electrodes Attached
Electrodes measuring brain activity were attached to a shore crab, which was then subjected to mechanical and chemical stimuli. Credit: Eleftherios Kasiouras

University of Gothenburg researchers have provided scientific proof that shore crabs feel pain, urging a reevaluation of how shellfish are treated under EU animal welfare laws. This evidence supports the development of less painful methods for killing shellfish.

In our pursuit of improving the welfare of animals we consume, certain creatures are often overlooked. Researchers at the University of Gothenburg are now focusing on decapod crustaceans, which include shellfish delicacies such as prawns, lobsters, crabs, and crayfish. Currently, shellfish are not protected under animal welfare legislation in the EU, but this might be about to change—for a good reason, according to researchers.

Their study, recently published in the journal Biology, provides the first evidence that painful stimuli are sent to the brain of shore crabs, offering more proof that crustaceans feel pain.

Eleftherios Kasiouras
Eleftherios Kasiouras, PhD student at the Department of Biological and Environmental Sciences, University of Gothenburg. Credit: Eleftherios Kasiouras

“We need to find less painful ways to kill shellfish if we are to continue eating them. Because now we have scientific evidence that they both experience and react to pain,” said Lynne Sneddon, zoophysiologist at the University of Gothenburg.

Several research groups have previously conducted a number of observational studies on crustaceans, in which they were subjected to mechanical impact, electric shocks, or acids to soft tissues such as the antennae. These crustaceans reacted by touching the exposed area or trying to avoid the danger in repeated experiments, leading researchers to assume that they feel pain.

Pain Receptors in the Soft Tissues

The researchers at the University of Gothenburg are the first to carry out neurobiological studies by measuring the activity in the brain of a shore crab, through an EEG style measurement.

“We could see that the crab has some kind of pain receptors in its soft tissues, because we recorded an increase in brain activity when we applied a potentially painful chemical, a form of vinegar, to the crab’s soft tissues. The same happened when we applied external pressure to several of the crab’s body parts,” says Eleftherios Kasiouras, PhD student at the University of Gothenburg and lead author of the study.

Lynne Sneddon
Lynne Sneddon, Senior Lecturer in Zoophysiology at the Department of Biological and Environmental Sciences, University of Gothenburg. Credit: David Wolfenden

The activity of the central nervous system in the brain was measured in the crab when the soft tissues of claws, antennae, and legs were subjected to some form of stress. The responses show that shore crabs must have some form of pain signaling to the brain from these body parts. The pain response was shorter and more powerful in the case of physical stress than in the case of chemical stress, which lasted longer.

Advocating for Humane Treatment

“It is a given that all animals need some kind of pain system to cope by avoiding danger. I don’t think we need to test all species of crustaceans, as they have a similar structure and therefore similar nervous systems. We can assume that shrimps, crayfish and lobsters can also send external signals about painful stimuli to their brain which will process this information,” says Kasiouras.

The researchers point out that we need to find more humane ways to handle and even kill crustaceans. At present, it is allowed to cut up a crustacean alive, unlike the mammals we eat.

“We need more research to find less painful ways to kill shellfish,” says Sneddon.

Reference: “Putative Nociceptive Responses in a Decapod Crustacean: The Shore Crab (Carcinus maenas)” by Eleftherios Kasiouras, Peter C. Hubbard, Albin Gräns and Lynne U. Sneddon, 21 October 2024, Biology.
DOI: 10.3390/biology13110851

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