Dario Paolo

Dr. Dario Paolo

CNR - IBBA
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 April 2017 in PLOS Genetics
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JRJ. Irepan Reyes-Olalde
J. Irepan Reyes-Olalde
VZVíctor M. Zúñiga-Mayo
Víctor M. Zúñiga-Mayo
JSJoanna Serwatowska
Joanna Serwatowska
RMRicardo A. Chávez Montes
Ricardo A. Chávez Montes
PLPaulina Lozano-Sotomayor
Paulina Lozano-Sotomayor
SFStefan De Folter
Stefan De Folter
Fruits and seeds are the major food source on earth. Both derive from the gynoecium and, therefore, it is crucial to understand the mechanisms that guide the development of this organ of angiosperm species. In Arabidopsis, the gynoecium is composed of two congenitally fused carpels, where two domains: medial and lateral, can be distinguished. The medial domain includes the carpel margin meristem (CMM) that is key for the production of the internal tissues involved in fertilization, such as septum, ovules, and transmitting tract. Interestingly, the medial domain shows a high cytokinin signaling output, in contrast to the lateral domain, where it is hardly detected. While it is known that cytokinin provides meristematic properties, understanding on the mechanisms that underlie the cytokinin signaling pattern in the young gynoecium is lacking. Moreover, in other tissues, the cytokinin pathway is often connected to the auxin pathway, but we also lack knowledge about these connections in the young gynoecium. Our results reveal that cytokinin signaling, that can provide meristematic properties required for CMM activity and growth, is enabled by the transcription factor SPATULA (SPT) in the medial domain. Meanwhile, cytokinin signaling is confined to the medial domain by the cytokinin response repressor ARABIDOPSIS HISTIDINE PHOSPHOTRANSFERASE 6 (AHP6), and perhaps by ARR16 (a type-A ARR) as well, both present in the lateral domains (presumptive valves) of the developing gynoecia. Moreover, SPT and cytokinin, probably together, promote the expression of the auxin biosynthetic gene TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOPSIS 1 (TAA1) and the gene encoding the auxin efflux transporter PIN-FORMED 3 (PIN3), likely creating auxin drainage important for gynoecium growth. This study provides novel insights in the spatiotemporal determination of the cytokinin signaling pattern and its connection to the auxin pathway in the young gynoecium. Most of our food comes from fruits and seeds, derived from a fertilized gynoecium. Therefore, understanding the mechanisms that control gynoecium development is of crucial importance. The Arabidopsis gynoecium has two fused carpels, with a medial domain between them, and a lateral domain consisting of the carpel walls. All the tissues that are involved in reproduction arise from the carpel margin meristem in the medial domain. The phytohormone cytokinin provides meristematic activity to cells, and interestingly, in a young gynoecium, the medial, but not the lateral, domain presents strong cytokinin signaling. One question that comes to mind is how this pattern is defined. This work demonstrates that the transcription factor SPATULA enables cytokinin signaling at the medial domain, while cytokinin signaling repressors are present in the lateral domain. A second question is whether and how cytokinin in the medial domain communicates with auxin, an important phytohormone for tissue differentiation. We found that cytokinin and SPT activate auxin biosynthesis and transport genes. The integration of these findings gives the first gene regulatory network acting during early gynoecium development. This network is most likely conserved in flowering plants, and can provide insights of molecular processes that are key for food production.

6 February 2015 in Plant Reproduction
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GOGregorio Orozco-Arroyo
Gregorio Orozco-Arroyo
Dario PaoloDario Paolo
Dario Paolo
IEIgnacio Ezquer
Ignacio Ezquer
LCLucia Colombo
Lucia Colombo

18 December 2014 in PLOS Genetics
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Chiara MizzottiChiara Mizzotti
Chiara Mizzotti
IEIgnacio Ezquer
Ignacio Ezquer
Dario PaoloDario Paolo
Dario Paolo
PRPaloma Rueda-Romero
Paloma Rueda-Romero
RGRosalinda Fiorella Guerra
Rosalinda Fiorella Guerra
LCLucia Colombo
Lucia Colombo
The role of secondary metabolites in the determination of cell identity has been an area of particular interest over recent years, and studies strongly indicate a connection between cell fate and the regulation of enzymes involved in secondary metabolism. In Arabidopsis thaliana, the maternally derived seed coat plays pivotal roles in both the protection of the developing embryo and the first steps of germination. In this regard, a characteristic feature of seed coat development is the accumulation of proanthocyanidins (PAs - a class of phenylpropanoid metabolites) in the innermost layer of the seed coat. Our genome-wide transcriptomic analysis suggests that the ovule identity factor SEEDSTICK (STK) is involved in the regulation of several metabolic processes, providing a strong basis for a connection between cell fate determination, development and metabolism. Using phenotypic, genetic, biochemical and transcriptomic approaches, we have focused specifically on the role of STK in PA biosynthesis. Our results indicate that STK exerts its effect by direct regulation of the gene encoding BANYULS/ANTHOCYANIDIN REDUCTASE (BAN/ANR), which converts anthocyanidins into their corresponding 2,3-cis-flavan-3-ols. Our study also demonstrates that the levels of H3K9ac chromatin modification directly correlate with the active state of BAN in an STK-dependent way. This is consistent with the idea that MADS-domain proteins control the expression of their target genes through the modification of chromatin states. STK might thus recruit or regulate histone modifying factors to control their activity. In addition, we show that STK is able to regulate other BAN regulators. Our study demonstrates for the first time how a floral homeotic gene controls tissue identity through the regulation of a wide range of processes including the accumulation of secondary metabolites. Plant secondary metabolites accumulate in seeds to protect the developing embryo. Using an RNA sequencing approach in conjunction with enrichment analyses we identified the homeotic MADS-domain gene SEEDSTICK (STK) as a regulator of metabolic processes during seed development. We analyzed the role of STK as a key regulator of the production of proanthocyanidins, compounds which are important for the pigmentation of the seed. STK directly regulates a network of metabolic genes, and is also implicated in changes occurring in the chromatin landscape. Our work demonstrates that a key homeotic transcription factor not only determines the identity of ovules but also controls metabolic processes that occur subsequent to the initial identity determination process, thus suggesting a link between identity determination and cell-specific (metabolic) processes.

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Raffaella BalestriniRaffaella Balestrini
Raffaella Balestrini
Cecilia BrunettiCecilia Brunetti
Cecilia Brunetti
Maria CammareriMaria Cammareri
Maria Cammareri
Sofia CarettoSofia Caretto
Sofia Caretto
VCValeria Cavallaro
Valeria Cavallaro
ZEZampieri Elisa
Zampieri Elisa
Plant specialized metabolites (SMs) play an important role in the interaction with the environment and are part of the plant defense response. These natural products are volatile, semi-volatile and non-volatile compounds produced from common building blocks deriving from primary metabolic pathways and rapidly evolved to allow a better adaptation of plants to environmental cues. Specialized metabolites include terpenes, flavonoids, alkaloids, glucosinolates, tannins, resins, etc. that can be used as phytochemicals, food additives, flavoring agents and pharmaceutical compounds. This review will be focused on Mediterranean crop plants as a source of SMs, with a special attention on the strategies that can be used to modulate their production, including abiotic stresses, interaction with beneficial soil microorganisms and novel genetic approaches.

27 August 2020 in Frontiers in Plant Science
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Federico ColomboFederico Colombo
Federico Colombo
Dario PaoloDario Paolo
Dario Paolo
ECEleonora Cominelli
Eleonora Cominelli
FSFrancesca Sparvoli
Francesca Sparvoli
ENErik Nielsen
Erik Nielsen
Roberto PILURoberto PILU
Roberto PILU
Phytic acid (PA) represents the major storage form of seed phosphate (P). During seed maturation, it accumulates as phytate salts chelating various mineral cations, therefore reducing their bioavailability. During germination, phytase dephosphorylates PA releasing both P and cations which in turn can be used for the nutrition of the growing seedling. Animals do not possess phytase, thus monogastric animals assimilate only 10% of the phytate ingested with feed, whilst 90% is excreted and may contribute to cause P pollution of the environment. To overcome this double problem, nutritional and environmental, in the last four decades, many low phytic acid (lpa) mutants (most of which affect the PA-MRP transporters) have been isolated and characterized in all major crops, showing that the lpa trait can increase the nutritional quality of foods and feeds and improve P management in agriculture. Nevertheless, these mutations are frequently accompanied by negative pleiotropic effects leading to agronomic defects which may affect either seed viability and germination or plant development or in some cases even increase the resistance to cooking, thus limiting the interest of breeders. Therefore, although some significant results have been reached, the isolation of lpa mutants improved for their nutritional quality and with a good field performance remains a goal so far not fully achieved for many crops. Here, we will summarize the main pleiotropic effects that have been reported to date in lpa mutants affected in PA-MRP transporters in five productive agronomic species, as well as addressing some of the possible challenges to overcome these hurdles and improve the breeding efforts for lpa mutants.

1 November 2019 in Food Chemistry
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Dario PaoloDario Paolo
Dario Paolo
GBGiulia Bianchi
Giulia Bianchi
CMCarlo Francesco Morelli
Carlo Francesco Morelli
GSGiovanna Speranza
Giovanna Speranza
GCGabriele Campanelli
Gabriele Campanelli
RSRoberto Lo Scalzo
Roberto Lo Scalzo