Modification and improvement of a plasmid vector for the production of antigenic molecules in GM tobacco, for veterinary use
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Data di Pubblicazione:
2008
Citazione:
Modification and improvement of a plasmid vector for the production of antigenic molecules in GM tobacco, for veterinary use / M. Festa, L. Militano, F. Sala, B. Basso. ((Intervento presentato al 4. convegno EPSO Conference tenutosi a Toulon nel 2008.
Abstract:
The production of important molecules (as subunit vaccines) in plants is increasingly
considered for relevant advantages: low costs of production, purification and delivery, no risks of
contamination by pathogens and high scale production, but improvement and enhancement of
transformation techniques are needed. MAR/SARs (Matrix/Scaffold Attachment Regions) are
DNA sequences that have been reported to create a network with the proteinaceous fibrils of
nuclear matrix, organizing chromatin into a series of topologically isolated loop domains of 5-200
kb. These sequences may influence the conformation of transgenes and their expression, possibly
reducing or eliminating some forms of gene silencing.
Our research is addressed at the production of plant derived antigens, to be used in veterinary
prophylaxis. In this field, the optimisation of transgene expression is crucial, also because of the
necessity of plant containment during the whole cultivation period.
In particular, we sub-cloned Rb7, a MAR sequence from Nicotiana tabacum, in the binary
vector pAMPAT, inside t-DNA close to LB and RB terminations, in its two possible orientations.
The vector expression cassette carries a 511 bp portion of Fib, encoding Fibrinogen Binding
Protein, from Staphylococcus aureus, under the control of 35SS constitutive promoter. The Fib
protein fragment was proved to be effective against S. aureus mastitis in dairy cattle. Nicotiana
tabacum, var. Samsun was transformed via Agrobacterium tumefaciens with the four constructs
carrying Rb7 elements in all their possible combinations. Statistical analysis was performed after
four different experiments, showing an enhanced transformation efficiency for MAR-containing
constructs (higher shoot number and shorter shooting time). Molecular and immunological analysis
on transformed plants are now in progress, to define the transgene copy number and the resulting
protein expression level.
Tipologia IRIS:
14 - Intervento a convegno non pubblicato
Elenco autori:
M. Festa, L. Militano, F. Sala, B. Basso
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