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1.
Science ; 385(6708): eado1663, 2024 Aug 02.
Article de Anglais | MEDLINE | ID: mdl-39088611

RÉSUMÉ

An enduring question in evolutionary biology concerns the degree to which episodes of convergent trait evolution depend on the same genetic programs, particularly over long timescales. In this work, we genetically dissected repeated origins and losses of prickles-sharp epidermal projections-that convergently evolved in numerous plant lineages. Mutations in a cytokinin hormone biosynthetic gene caused at least 16 independent losses of prickles in eggplants and wild relatives in the genus Solanum. Homologs underlie prickle formation across angiosperms that collectively diverged more than 150 million years ago, including rice and roses. By developing new Solanum genetic systems, we leveraged this discovery to eliminate prickles in a wild species and an indigenously foraged berry. Our findings implicate a shared hormone activation genetic program underlying evolutionarily widespread and recurrent instances of plant morphological innovation.


Sujet(s)
Évolution biologique , Cytokinine , Gènes de plante , Épiderme végétal , Solanum , Cytokinine/biosynthèse , Cytokinine/génétique , Évolution moléculaire , Mutation , Oryza/génétique , Phylogenèse , Épiderme végétal/anatomie et histologie , Épiderme végétal/génétique , Solanum/anatomie et histologie , Solanum/génétique
2.
Plant Physiol ; 191(2): 1404-1415, 2023 02 12.
Article de Anglais | MEDLINE | ID: mdl-36449559

RÉSUMÉ

The plant hormone abscisic acid (ABA) plays a central role in the regulation of seed maturation and dormancy. ABA also restrains germination under abiotic-stress conditions. Here, we show in tomato (Solanum lycopersicum) that the ABA importer ABA-IMPORTING TRANSPORTER 1.1 (AIT1.1/NPF4.6) has a role in radicle emergence under salinity conditions. AIT1.1 expression was upregulated following seed imbibition, and CRISPR/Cas9-derived ait1.1 mutants exhibited faster radicle emergence, increased germination and partial resistance to ABA. AIT1.1 was highly expressed in the endosperm, but not in the embryo, and ait1.1 isolated embryos did not show resistance to ABA. On the other hand, loss of AIT1.1 activity promoted the expression of endosperm-weakening-related genes, and seed-coat scarification eliminated the promoting effect of ait1.1 on radicle emergence. Therefore, we propose that imbibition-induced AIT1.1 expression in the micropylar endosperm mediates ABA-uptake into micropylar cells to restrain endosperm weakening. While salinity conditions strongly inhibited wild-type M82 seed germination, high salinity had a much weaker effect on ait1.1 germination. We suggest that AIT1.1 evolved to inhibit germination under unfavorable conditions, such as salinity. Unlike other ABA mutants, ait1.1 exhibited normal seed longevity, and therefore, the ait1.1 allele may be exploited to improve seed germination in crops.


Sujet(s)
Acide abscissique , Solanum lycopersicum , Acide abscissique/pharmacologie , Acide abscissique/métabolisme , Solanum lycopersicum/génétique , Germination/génétique , Graines/génétique , Graines/métabolisme , Salinité , Protéines de transport membranaire/métabolisme , Régulation de l'expression des gènes végétaux
3.
Curr Biol ; 32(2): 329-337.e5, 2022 01 24.
Article de Anglais | MEDLINE | ID: mdl-34847354

RÉSUMÉ

Asymmetric and oriented stem cell divisions enable the continued production of patterned tissues. The molecules that guide these divisions include several "polarity proteins" that are localized to discrete plasma membrane domains, are differentially inherited during asymmetric divisions, and whose scaffolding activities can guide division plane orientation and subsequent cell fates. In the stomatal lineages on the surfaces of plant leaves, asymmetric and oriented divisions create distinct cell types in physiologically optimized patterns. The polarity protein BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) is a major regulator of stomatal lineage division and cell fate asymmetries in Arabidopsis, but its role in the stomatal lineages of other plants is unclear. Here, using phylogenetic and functional assays, we demonstrate that BASL is a eudicot-specific polarity protein. Dicot BASL orthologs can polarize in heterologous systems and rescue the Arabidopsis BASL mutant. The more widely distributed BASL-like proteins, although they share BASL's conserved C-terminal domain, are neither polarized nor do they function in asymmetric divisions of the stomatal lineage. Comparison of BASL protein localization and loss of function BASL phenotypes in Arabidopsis and tomato revealed previously unappreciated differences in how asymmetric cell divisions are employed for pattern formation in different species. This multi-species analysis therefore provides insight into the evolution of a unique polarity regulator and into the developmental choices available to cells as they build and pattern tissues.


Sujet(s)
Protéines d'Arabidopsis , Arabidopsis , Arabidopsis/métabolisme , Protéines d'Arabidopsis/génétique , Protéines d'Arabidopsis/métabolisme , Division cellulaire asymétrique , Protéines du cycle cellulaire/métabolisme , Lignage cellulaire/physiologie , Polarité de la cellule/physiologie , Phylogenèse , Stomates de plante/génétique , Stomates de plante/métabolisme
4.
New Phytol ; 233(3): 1220-1237, 2022 02.
Article de Anglais | MEDLINE | ID: mdl-34758118

RÉSUMÉ

Steroidal glycoalkaloids (SGAs) are protective metabolites constitutively produced by Solanaceae species. Genes and enzymes generating the vast structural diversity of SGAs have been largely identified. Yet, mechanisms of hormone pathways coordinating defence (jasmonate; JA) and growth (gibberellin; GA) controlling SGAs metabolism remain unclear. We used tomato to decipher the hormonal regulation of SGAs metabolism during growth vs defence tradeoff. This was performed by genetic and biochemical characterisation of different JA and GA pathways components, coupled with in vitro experiments to elucidate the crosstalk between these hormone pathways mediating SGAs metabolism. We discovered that reduced active JA results in decreased SGA production, while low levels of GA or its receptor led to elevated SGA accumulation. We showed that MYC1 and MYC2 transcription factors mediate the JA/GA crosstalk by transcriptional activation of SGA biosynthesis and GA catabolism genes. Furthermore, MYC1 and MYC2 transcriptionally regulate the GA signalling suppressor DELLA that by itself interferes in JA-mediated SGA control by modulating MYC activity through protein-protein interaction. Chemical and fungal pathogen treatments reinforced the concept of JA/GA crosstalk during SGA metabolism. These findings revealed the mechanism of JA/GA interplay in SGA biosynthesis to balance the cost of chemical defence with growth.


Sujet(s)
Alcaloïdes , Solanum lycopersicum , Alcaloïdes/métabolisme , Cyclopentanes/métabolisme , Régulation de l'expression des gènes végétaux , Gibbérellines/métabolisme , Solanum lycopersicum/métabolisme , Oxylipines/métabolisme
5.
New Phytol ; 232(5): 1985-1998, 2021 12.
Article de Anglais | MEDLINE | ID: mdl-34541677

RÉSUMÉ

Plants reduce transpiration to avoid dehydration during drought episodes by stomatal closure and inhibition of canopy growth. Previous studies have suggested that low gibberellin (GA) activity promotes these 'drought avoidance' responses. Using genome editing, molecular, physiological and hormone analyses, we examined if drought regulates GA metabolism in tomato (Solanum lycopersicum) guard cells and leaves, and studied how this affects water loss. Water deficiency inhibited the expression of the GA biosynthesis genes GA20 oxidase1 (GA20ox1) and GA20ox2 and induced the GA deactivating gene GA2ox7 in guard cells and leaf tissue, resulting in reduced levels of bioactive GAs. These effects were mediated by abscisic acid-dependent and abscisic acid-independent pathways, and by the transcription factor TINY1. The loss of GA2ox7 attenuated stomatal response to water deficiency and during soil dehydration, ga2ox7 plants closed their stomata later, and wilted faster than wild-type (WT) M82 cv. Mutations in GA20ox1 and GA20ox2, had no effect on stomatal closure, but reduced water loss due to the mutants' smaller canopy areas. The results suggested that drought-induced GA deactivation in guard cells, contributes to stomatal closure at the early stages of soil dehydration, whereas inhibition of GA synthesis in leaves suppresses canopy growth and restricts transpiration area.


Sujet(s)
Solanum lycopersicum , Acide abscissique , Sécheresses , Gibbérellines , Solanum lycopersicum/génétique , Stomates de plante , Eau
6.
Mol Hortic ; 1(1): 15, 2021 Nov 24.
Article de Anglais | MEDLINE | ID: mdl-37789477

RÉSUMÉ

The growth-promoting hormone gibberellin (GA) regulates numerous developmental processes throughout the plant life cycle. It also affects plant response to biotic and abiotic stresses. GA metabolism and signaling in tomato (Solanum lycopersicum) have been studied in the last three decades and major components of the pathways were characterized. These include major biosynthesis and catabolism enzymes and signaling components, such as the three GA receptors GIBBERELLIN INSENSITIVE DWARF 1 (GID1) and DELLA protein PROCERA (PRO), the central response suppressor. The role of these components in tomato plant development and response to the environment have been investigated. Cultivated tomato, similar to many other crop plants, are susceptible to water deficiency. Numerous studies on tomato response to drought have been conducted, including the possible role of GA in tomato drought resistance. Most studies showed that reduced levels or activity of GA improves drought tolerance and drought avoidance. This review aims to provide an overview on GA biosynthesis and signaling in tomato, how drought affects these pathways and how changes in GA activity affect tomato plant response to water deficiency. It also presents the potential of using the GA pathway to generate drought-tolerant tomato plants with improved performance under both irrigation and water-limited conditions.

7.
Plant Physiol ; 184(1): 518-528, 2020 09.
Article de Anglais | MEDLINE | ID: mdl-32576645

RÉSUMÉ

Plants reduce transpiration through stomatal closure to avoid drought stress. While abscisic acid (ABA) has a central role in the regulation of stomatal closure under water-deficit conditions, we demonstrated in tomato (Solanum lycopersicum) that a gibberellin response inhibitor, the DELLA protein PROCERA (PRO), promotes ABA-induced stomatal closure and gene transcription in guard cells. To study how PRO affects stomatal closure, we performed RNA-sequencing analysis of isolated guard cells and identified the ABA transporters ABA-IMPORTING TRANSPORTER1 1 (AIT1 1) and AIT1 2, also called NITRATE TRANSPORTER1/PTR TRANSPORTER FAMILY4 6 in Arabidopsis (Arabidopsis thaliana), as being upregulated by PRO. Tomato has four AIT1 genes, but only AIT1 1 and AIT1 2 were upregulated by PRO, and only AIT1 1 exhibited high expression in guard cells. Functional analysis of AIT1 1 in yeast (Saccharomyces cerevisiae) confirmed its activity as an ABA transporter, possibly an importer. A clustered regularly interspaced short palindromic repeats-Cas9-derived ait1 1 mutant exhibited an increased transpiration, a larger stomatal aperture, and a reduced stomatal response to ABA. Moreover, ait1 1 suppressed the promoting effects of PRO on ABA-induced stomatal closure and gene expression in guard cells, suggesting that the effects of PRO on stomatal aperture and transpiration are AIT1.1-dependent. Previous studies suggest a negative crosstalk between gibberellin and ABA that is mediated by changes in hormone biosynthesis and signaling. The results of this study suggest this crosstalk is also mediated by changes in hormone transport.


Sujet(s)
Protéines d'Arabidopsis/métabolisme , Arabidopsis/métabolisme , Protéines végétales/métabolisme , Stomates de plante/métabolisme , Acide abscissique/pharmacologie , Arabidopsis/effets des médicaments et des substances chimiques , Arabidopsis/génétique , Protéines d'Arabidopsis/génétique , Régulation de l'expression des gènes végétaux/effets des médicaments et des substances chimiques , Régulation de l'expression des gènes végétaux/génétique , Solanum lycopersicum/génétique , Solanum lycopersicum/métabolisme , Protéines végétales/génétique , Stomates de plante/effets des médicaments et des substances chimiques , Stomates de plante/génétique , Transduction du signal/effets des médicaments et des substances chimiques , Transduction du signal/génétique
8.
J Exp Bot ; 71(12): 3603-3612, 2020 06 22.
Article de Anglais | MEDLINE | ID: mdl-32173726

RÉSUMÉ

Low gibberellin (GA) activity in tomato (Solanum lycopersicum) inhibits leaf expansion and reduces stomatal conductance. This leads to lower transpiration and improved water status under transient drought conditions. Tomato has three GIBBERELLIN-INSENSITIVE DWARF1 (GID1) GA receptors with overlapping activities and high redundancy. We tested whether mutation in a single GID1 reduces transpiration without affecting growth and productivity. CRISPR-Cas9 gid1 mutants were able to maintain higher leaf water content under water-deficit conditions. Moreover, while gid1a exhibited normal growth, it showed reduced whole-plant transpiration and better recovery from dehydration. Mutation in GID1a inhibited xylem vessel proliferation, which led to lower hydraulic conductance. In stronger GA mutants, we also found reduced xylem vessel expansion. These results suggest that low GA activity affects transpiration by multiple mechanisms: it reduces leaf area, promotes stomatal closure, and reduces xylem proliferation and expansion, and as a result, xylem hydraulic conductance. We further examined if gid1a performs better than the control M82 in the field. Under these conditions, the high redundancy of GID1s was lost and gid1a plants were semi-dwarf, but their productivity was not affected. Although gid1a did not perform better under drought conditions in the field, it exhibited a higher harvest index.


Sujet(s)
Solanum lycopersicum , Prolifération cellulaire , Gibbérellines , Solanum lycopersicum/génétique , Mutation , Feuilles de plante , Stomates de plante/génétique , Transpiration des plantes , Eau , Xylème/génétique
9.
Plant Cell ; 31(7): 1506-1519, 2019 07.
Article de Anglais | MEDLINE | ID: mdl-31076539

RÉSUMÉ

The pleiotropic and complex gibberellin (GA) response relies on targeted proteolysis of DELLA proteins mediated by a GA-activated GIBBERELLIN-INSENSITIVE DWARF1 (GID1) receptor. The tomato (Solanum lycopersicum) genome encodes for a single DELLA protein, PROCERA (PRO), and three receptors, SlGID1a (GID1a), GID1b1, and GID1b2, that may guide specific GA responses. In this work, clustered regularly interspaced short palindromic repeats (CRISPR) /CRISPR associated protein 9-derived gid1 mutants were generated and their effect on GA responses was studied. The gid1 triple mutant was extremely dwarf and fully insensitive to GA. Under optimal growth conditions, the three receptors function redundantly and the single gid1 mutants exhibited very mild phenotypic changes. Among the three receptors, GID1a had the strongest effects on germination and growth. Yeast two-hybrid assays suggested that GID1a has the highest affinity to PRO. Analysis of lines with a single active receptor demonstrated a unique role for GID1a in protracted response to GA that was saturated only at high doses. When the gid1 mutants were grown in the field under ambient changing environments, they showed phenotypic instability, the high redundancy was lost, and gid1a exhibited dwarfism that was strongly exacerbated by the loss of another GID1b receptor gene. These results suggest that multiple GA receptors contribute to phenotypic stability under environmental extremes.


Sujet(s)
Environnement , Gibbérellines/métabolisme , Protéines végétales/métabolisme , Récepteurs de surface cellulaire/métabolisme , Solanum lycopersicum/métabolisme , Régulation de l'expression des gènes au cours du développement , Régulation de l'expression des gènes végétaux , Mutation/génétique , Phénotype , Développement des plantes , Protéines végétales/génétique , Tiges de plante/croissance et développement
10.
Plant Cell ; 29(12): 3186-3197, 2017 12.
Article de Anglais | MEDLINE | ID: mdl-29150547

RÉSUMÉ

Plants employ stomatal closure and reduced growth to avoid water deficiency damage. Reduced levels of the growth-promoting hormone gibberellin (GA) lead to increased tolerance to water deficit, but the underlying mechanism is unknown. Here, we show that the tomato (Solanum lycopersicum) DELLA protein PROCERA (PRO), a negative regulator of GA signaling, acts in guard cells to promote stomatal closure and reduce water loss in response to water deficiency by increasing abscisic acid (ABA) sensitivity. The loss-of-function pro mutant exhibited increased stomatal conductance and rapid wilting under water deficit stress. Transgenic tomato overexpressing constitutively active stable DELLA proteins (S-della) displayed the opposite phenotype. The effects of S-della on stomatal aperture and water loss were strongly suppressed in the ABA-deficient mutant sitiens, indicating that these effects of S-della are ABA dependent. While DELLA had no effect on ABA levels, guard cell ABA responsiveness was increased in S-della and reduced in pro plants compared with the wild type. Expressing S-della under the control of a guard-cell-specific promoter was sufficient to increase stomatal sensitivity to ABA and to reduce water loss under water deficit stress but had no effect on leaf size. This result indicates that DELLA promotes stomatal closure independently of its effect on growth.


Sujet(s)
Protéines végétales/métabolisme , Stomates de plante/cytologie , Stomates de plante/physiologie , Solanum lycopersicum/métabolisme , Solanum lycopersicum/physiologie , Acide abscissique/pharmacologie , Protéines d'Arabidopsis/métabolisme , Régulation de l'expression des gènes végétaux/effets des médicaments et des substances chimiques , Solanum lycopersicum/génétique , Modèles biologiques , Mutation/génétique , Transpiration des plantes/physiologie , Végétaux génétiquement modifiés , Stress physiologique , Eau
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