Mario A. Pagnotta

Prof. Dr. Mario A. Pagnotta

Department of Sciences and Technology for Agriculture, Forest, Environment and Energy, Università degli Studi della Tuscia, 01100 Viterbo, Italy
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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

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

Representative Publications

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6 August 2009 in Diversity
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Journal Article
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LMLinda Mondini
Linda Mondini
ANArshiya Noorani
Arshiya Noorani
Mario A. PagnottaMario A. Pagnotta
Mario A. Pagnotta
This paper is an overview of the diverse, predominantly molecular techniques, used in assessing plant genetic diversity. In recent years, there has been a significant increase in the application of molecular genetic methods for assessing the conservation and use of plant genetic resources. Molecular techniques have been applied in the analysis of specific genes, as well as to increase understanding of gene action, generate genetic maps and assist in the development of gene transfer technologies. Molecular techniques have also had critical roles in studies of phylogeny and species evolution, and have been applied to increase our understanding of the distribution and extent of genetic variation within and between species. These techniques are well established and their advantages as well as limitations have been realized and described in this work. Recently, a new class of advanced techniques has emerged, primarily derived from a combination of earlier, more basic techniques. Advanced marker techniques tend to amalgamate advantageous features of several basic techniques, in order to increase the sensitivity and resolution to detect genetic discontinuity and distinctiveness. Some of the advanced marker techniques utilize newer classes of DNA elements, such as retrotransposons, mitochondrial and chloroplast based microsatellites, thereby revealing genetic variation through increased genome coverage. Techniques such as RAPD and AFLP are also being applied to cDNA-based templates to study patterns of gene expression and uncover the genetic basis of biological responses. The most important and recent advances made in molecular marker techniques are discussed in this review, along with their applications, advantages and limitations applied to plant sciences.

1 October 1998 in Theoretical and Applied Genetics
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ABAntonio Blanco
Antonio Blanco
MBM. P. Bellomo
M. P. Bellomo
ACAlberto Cenci
Alberto Cenci
CGC. De Giovanni
C. De Giovanni
RDR. D’ovidio
R. D’ovidio
OTO. A. Tanzarella
O. A. Tanzarella

1 February 2001 in Theoretical and Applied Genetics
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Journal Article
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MNM. M. Nachit
M. M. Nachit
IEI. Elouafi
I. Elouafi
Mario A. PagnottaMario A. Pagnotta
Mario A. Pagnotta
Ahmad ALSALEHAhmad ALSALEH
Ahmad ALSALEH
EIE. Iacono
E. Iacono
MSM. E. Sorrells
M. E. Sorrells

5 August 2015 in BMC Genomic Data
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TOTemesgen Magule Olango
Temesgen Magule Olango
BTBizuayehu Tesfaye
Bizuayehu Tesfaye
Mario A. PagnottaMario A. Pagnotta
Mario A. Pagnotta
MPMario Enrico Pè
Mario Enrico Pè
MCMarcello Catellani
Marcello Catellani
Enset (Ensete ventricosum (Welw.) Cheesman; Musaceae) is a multipurpose drought-tolerant food security crop with high conservation and improvement concern in Ethiopia, where it supplements the human calorie requirements of around 20 million people. The crop also has an enormous potential in other regions of Sub-Saharan Africa, where it is known only as a wild plant. Despite its potential, genetic and genomic studies supporting breeding programs and conservation efforts are very limited. Molecular methods would substantially improve current conventional approaches. Here we report the development of the first set of SSR markers from enset, their cross-transferability to Musa spp., and their application in genetic diversity, relationship and structure assessments in wild and cultivated enset germplasm. SSR markers specific to E. ventricosum were developed through pyrosequencing of an enriched genomic library. Primer pairs were designed for 217 microsatellites with a repeat size > 20 bp from 900 candidates. Primers were validated in parallel by in silico and in vitro PCR approaches. A total of 67 primer pairs successfully amplified specific loci and 59 showed polymorphism. A subset of 34 polymorphic SSR markers were used to study 70 both wild and cultivated enset accessions. A large number of alleles were detected along with a moderate to high level of genetic diversity. AMOVA revealed that intra-population allelic variations contributed more to genetic diversity than inter-population variations. UPGMA based phylogenetic analysis and Discriminant Analysis of Principal Components show that wild enset is clearly separated from cultivated enset and is more closely related to the out-group Musa spp. No cluster pattern associated with the geographical regions, where this crop is grown, was observed for enset landraces. Our results reaffirm the long tradition of extensive seed-sucker exchange between enset cultivating communities in Southern Ethiopia. The first set of genomic SSR markers were developed in enset. A large proportion of these markers were polymorphic and some were also transferable to related species of the genus Musa. This study demonstrated the usefulness of the markers in assessing genetic diversity and structure in enset germplasm, and provides potentially useful information for developing conservation and breeding strategies in enset.

21 October 2014 in Molecular Genetics and Genomics
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Journal Article
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LMLinda Mondini
Linda Mondini
MNMiloudi Mikael Nachit
Miloudi Mikael Nachit
Mario A. PagnottaMario A. Pagnotta
Mario A. Pagnotta

5 August 2008 in Genetic Resources and Crop Evolution
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Mario A. PagnottaMario A. Pagnotta
Mario A. Pagnotta
LMLinda Mondini
Linda Mondini
PCPasquale Codianni
Pasquale Codianni
CFClara Fares
Clara Fares