Riccardo Aiese Cigliano

Dr. Riccardo Aiese Cigliano

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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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17 November 2015 in Nucleic Acids Research
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APAndreu Paytuví
Andreu Paytuví
TPToni Hermoso Pulido
Toni Hermoso Pulido
ILIrantzu Anzar Martínez de Lagrán
Irantzu Anzar Martínez de Lagrán
WSWalter Sanseverino
Walter Sanseverino
RCRiccardo Aiese Cigliano
Riccardo Aiese Cigliano
Long non-coding RNAs (lncRNAs) are functional non-translated molecules greater than 200 nt. Their roles are diverse and they are usually involved in transcriptional regulation. LncRNAs still remain largely uninvestigated in plants with few exceptions. Experimentally validated plant lncRNAs have been shown to regulate important agronomic traits such as phosphate starvation response, flowering time and interaction with symbiotic organisms, making them of great interest in plant biology and in breeding. There is still a lack of lncRNAs in most sequenced plant species, and in those where they have been annotated, different methods have been used, so making the lncRNAs less useful in comparisons within and between species. We developed a pipeline to annotate lncRNAs and applied it to 37 plant species and six algae, resulting in the annotation of more than 120 000 lncRNAs. To facilitate the study of lncRNAs for the plant research community, the information gathered is organised in the Green Non-Coding Database (GreeNC, http://greenc.sciencedesigners.com/).

14 June 2019 in Science
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RSRaquel Sánchez-Pérez
Raquel Sánchez-Pérez
Stefano PavanStefano Pavan
Stefano Pavan
RMRosa Mazzeo
Rosa Mazzeo
CMC. Moldovan
C. Moldovan
RCRiccardo Aiese Cigliano
Riccardo Aiese Cigliano
BMBirger Lindbergi Møller
Birger Lindbergi Møller
How to make almonds palatable: The domesticated almond tree has been feeding humans for millennia. Derivation from the wild, bitter, and toxic almond required loss of the cyanogenic diglucoside amygdalin. Sánchez-Pérez et al. sequenced the almond genome and analyzed the genomic region responsible for this shift. The key change turned out to be a point mutation in a transcription factor that regulates production of P450 monooxygenases in the biosynthetic pathway for the toxic compound. Science , this issue p. 1095

1 October 2019 in Progress in Lipid Research
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CMChristian Morabito
Christian Morabito
CBCaroline Bournaud
Caroline Bournaud
CMCécile Maës
Cécile Maës
MSMartin Schuler
Martin Schuler
RCRiccardo Aiese Cigliano
Riccardo Aiese Cigliano
FRFabrice Rébeillé
Fabrice Rébeillé

14 April 2015 in The Plant Cell
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RARiccardo Aversano
Riccardo Aversano
FCFelice Contaldi
Felice Contaldi
MEMaria Raffaella Ercolano
Maria Raffaella Ercolano
VGValentina Grosso
Valentina Grosso
MIMassimo Iorizzo
Massimo Iorizzo
DCDomanico Carputo
Domanico Carputo
Here, we report the draft genome sequence of Solanum commersonii, which consists of ∼830 megabases with an N50 of 44,303 bp anchored to 12 chromosomes, using the potato (Solanum tuberosum) genome sequence as a reference. Compared with potato, S. commersonii shows a striking reduction in heterozygosity (1.5% versus 53 to 59%), and differences in genome sizes were mainly due to variations in intergenic sequence length. Gene annotation by ab initio prediction supported by RNA-seq data produced a catalog of 1703 predicted microRNAs, 18,882 long noncoding RNAs of which 20% are shown to target cold-responsive genes, and 39,290 protein-coding genes with a significant repertoire of nonredundant nucleotide binding site-encoding genes and 126 cold-related genes that are lacking in S. tuberosum. Phylogenetic analyses indicate that domesticated potato and S. commersonii lineages diverged ∼2.3 million years ago. Three duplication periods corresponding to genome enrichment for particular gene families related to response to salt stress, water transport, growth, and defense response were discovered. The draft genome sequence of S. commersonii substantially increases our understanding of the domesticated germplasm, facilitating translation of acquired knowledge into advances in crop stability in light of global climate and environmental changes.

16 November 2017 in Nucleic Acids Research
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COCristina M Osuna-Cruz
Cristina M Osuna-Cruz
APAndreu Paytuví
Andreu Paytuví
ADAntimo Di Donato
Antimo Di Donato
VSVicky Sundesha
Vicky Sundesha
GAGiuseppe Andolfo
Giuseppe Andolfo
MEMaria Raffaella Ercolano
Maria Raffaella Ercolano
The Plant Resistance Genes database (PRGdb; http://prgdb.org) has been redesigned with a new user interface, new sections, new tools and new data for genetic improvement, allowing easy access not only to the plant science research community but also to breeders who want to improve plant disease resistance. The home page offers an overview of easy-to-read search boxes that streamline data queries and directly show plant species for which data from candidate or cloned genes have been collected. Bulk data files and curated resistance gene annotations are made available for each plant species hosted. The new Gene Model view offers detailed information on each cloned resistance gene structure to highlight shared attributes with other genes. PRGdb 3.0 offers 153 reference resistance genes and 177 072 annotated candidate Pathogen Receptor Genes (PRGs). Compared to the previous release, the number of putative genes has been increased from 106 to 177 K from 76 sequenced Viridiplantae and algae genomes. The DRAGO 2 tool, which automatically annotates and predicts (PRGs) from DNA and amino acid with high accuracy and sensitivity, has been added. BLAST search has been implemented to offer users the opportunity to annotate and compare their own sequences. The improved section on plant diseases displays useful information linked to genes and genomes to connect complementary data and better address specific needs. Through, a revised and enlarged collection of data, the development of new tools and a renewed portal, PRGdb 3.0 engages the plant science community in developing a consensus plan to improve knowledge and strategies to fight diseases that afflict main crops and other plants.

26 April 2017 in Scientific Reports
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Pasquale Luca CurciPasquale Luca Curci
Pasquale Luca Curci
RCRiccardo Aiese Cigliano
Riccardo Aiese Cigliano
Diana L. ZuluagaDiana L. Zuluaga
Diana L. Zuluaga
MJMichela Janni
Michela Janni
WSWalter Sanseverino
Walter Sanseverino
Gabriella SonnanteGabriella Sonnante
Gabriella Sonnante
Nitrogen (N) is a key macronutrient representing a limiting factor for plant growth and development and affects productivity in wheat. In this study, durum wheat response to N chronic starvation during grain filling was investigated through a transcriptomic approach in roots, leaves/stems, flag leaf and spikes of cv. Svevo. Nitrogen stress negatively influenced plant height, tillering, flag leaf area, spike and seed traits, and total N content. RNA-seq data revealed 4,626 differentially expressed genes (DEGs). Most transcriptomic changes were observed in roots, with 3,270 DEGs, while 963 were found in leaves/stems, 470 in flag leaf, and 355 in spike tissues. A total of 799 gene ontology (GO) terms were identified, 180 and 619 among the upregulated and downregulated genes, respectively. Among the most addressed GO categories, N compound metabolism, carbon metabolism, and photosynthesis were mostly represented. Interesting DEGs, such as N transporters, genes involved in N assimilation, along with transcription factors, protein kinases and other genes related to stress were highlighted. These results provide valuable information about the transcriptomic response to chronic N stress in durum wheat, which could be useful for future improvement of N use efficiency.