Programme (final)
Download programme: word.doc |
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| SATURDAY June 12 | |
14.45-18.00 |
Registration |
18.15-18.30 |
Opening of the Workshop |
INTRODUCTORY LECTURES |
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18.30-19.10 |
RNA conformational shifts control translation and replication of Turnip crinkle virus (O1) |
19.10-19.50 |
Defense, counter-defense and counter-counter-defense: a never ending tale of RNA silencing (O2) |
20.30 |
Dinner |
22.00-23.00 |
Mounting of posters |
SUNDAY June 13
SESSION: REPLICATION AND TRANSLATION
Chair: K. Andrew White
8.30 |
Tombusvirus recruitment of the host translational machinery via the 3’UTR (O3) |
8.55 |
Viroid replication: recent insights on the enzymes and ribozymes involved (O4) |
9.20 |
Geminivirus infection and plant cell cycle controls (O5) |
9.45 |
Host factors required for plant susceptibility to viruses: targets to improve plant resistance to viruses (O6) |
10.10 |
Post-translational modifications of TYMV polymerase |
10.45-11.15 |
Coffe break |
11.15-12.15 |
Four short talks (15 min each) |
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Specific Interaction with Viral RNA Reveals a Novel Role of Hsp90 in the Initiation of Plant Virus Replication (P3) |
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Quantitation of Potato virus A gene expression under various conditions gives new insights into the regulation of viral translation and replication (P4) |
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The Cauliflower mosaic virus reinitiation factor TAV controls the TOR signalling pathway (P8) |
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Viral-induced systemic necrosis in plants involves both programmed cell death and the inhibition of viral multiplication, which are regulated by independent pathways (P40) |
12.30-14.00 |
Lunch (buffet) |
14.00-15.30 |
Poster session (P1-P20) Presenters standing near their poster |
SESSION: PLANT RESPONSE (part I)
Chair: Savithramma P. Dinesh-Kumar
15.30 |
Emerging perspectives on the antiviral innate immune response (O8) |
15.55 |
Massive production of small RNAs from a non-coding region as a decoy strategy of Cauliflower mosaic virus to counteract gene silencing (O9) |
16.20 |
RNA silencing suppressors and potyviral infections: a complex tale (O10) |
16.45-17.15 |
Coffee break |
17.15 |
Multiple effects of silencing the RDR1 gene of tobacco (O11) |
17.40 |
Toward understanding the mechanisms of tobamovirus replication complex formation (O12) |
18.15 |
Bus leaving for the Visit to the Fortress of Fenestrelle |
20.30 |
Dinner in the Fortress, with music entertainment |
MONDAY June 14
SESSION: PLANT RESPONSE (part II)
Chair: Jari P.T. Valkonen
8.45 |
Viral Class 1 RNase III enzymes as suppressors of RNA silencing (O13) |
9.10 |
The role of TYLCV V2 in suppression of RNA silencing (O14) |
9.35 |
Mechanisms of argonaute targeting viral suppressors of RNA silencing (O15) |
10.00 |
Viral secondary siRNAs in antiviral silencing (O16) |
10.25 |
Organ-specific transcriptional response in tomato systemically infected by Tomato spotted wilt virus (O17) |
11.00-11-30 |
Coffee break |
11.30-13.00 |
Six short talks (15 min each) |
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A new potyvirus virulence determinant: the CI C-terminus modulates pathogenicity of Lettuce mosaic virus in lettuce (P18) |
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Virus-derived small RNAs and their potential to control the outcome of plant-virus interactions (P23) |
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Plant virus mediated induction of miR168 is associated with repression of ARGONAUTE1 accumulation (P19) |
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Structural and functional analysis of viral siRNAs (P30) G. Szittya |
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Role of C2 during Geminivirus infection: effect on the CSN and the SCF complexes (P36) |
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RNA silencing in plant-viroid interactions: insights from deep sequencing of the small RNAs from plants infected by nuclear- and chloroplast-replicating viroids (P17) |
13.15-14.45 |
Lunch (buffet) |
SESSION: VIRUS / VECTOR INTERACTIONS
Chair: Juan José López-Moya
15.00 |
Vector transmission mechanisms in two genera of the family Potyviridae: differences between potyviruses and ipomoviruses (O18) |
15.25 |
How can a plant virus “sense” the feeding of its insect vector on the infected plant and immediately relocate within the cell and increase its chances of acquisition? (O19) |
15.50 |
Microarray-based analysis of interactions between Tomato yellow leaf curl virus and its vector the whitefly Bemisia tabaci (O20) |
16.30-17.00 |
Coffee break |
17.00-17.30 |
Two short talks (15 min each) |
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What’s new in polerovirus transmission ? (P43) |
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Facilitation of Bemisia tabaci transmission of Tomato yellow leaf curl virus by a single symbiotic bacterium (P44) |
17.40-18.20 |
EMBO Science & Society Lecture: Communicating science: people and biology, hopes, expectations and fears |
18.30 |
Poster session (P21-P42) Presenters standing near their poster |
20.30 |
Dinner |
22.00 |
Presentation of the next EMBO Workshop |
TUESDAY June 15
SESSION: MOVEMENT AND TRAFFICKING
Chair: Andrew J. Maule
8.45 |
Plasmodesmata - Gateways to local and systemic virus infection (O21) |
9.10 |
The cell nucleus and plant virus movement (O22) |
9.35 |
Structural and functional insights into tubule-guided virus movement (O23) |
10.00 |
Couple-skating Abutilon mosaic virus movement proteins (O24) |
10.25 |
Phloem tropism of poleroviruses does not hinge only upon Dicer-like activity (O25) |
11.00-11-30 |
Coffee break |
11.30-13.00 |
Poster session (P43-P66) Presenters standing near their poster |
13.00 |
Lunch (buffet) |
14.30 |
Departure from Pracatinat to Torino: visit to the town centre and dinner |
22.00 |
Bus departure from Torino to Pracatinat |
WEDNESDAY June 16
SESSION: RECOMBINATION AND EVOLUTION
Chair: Fernando García-Arenal
8.30 |
Mechanisms and genetic regulation of plant tolerance to virus infection (O26) |
8.55 |
Adaptation process of Rice yellow mottle virus to two alleles of the eIF(iso)4G-mediated rice resistance (O27) |
9.20 |
Variability and evolution rate of plant viruses with a single-stranded DNA genome (O28) |
9.45 |
A systems biology approach to dissect the roles of host proteins |
10.30-11.00 |
Coffee break |
11.00-12.30 |
Six short talks (15 min each) |
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The cytosolic nucleoprotein of the plant-infecting bunyavirus Tomato spotted wilt is able to recruit ER-resident proteins to ER export sites (P50) |
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The intra- and intercellular movement of Melon necrotic spot virus (MNSV) depends on an active secretory pathway (P51) |
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Genetic and functional characterization of the RTM-mediated resistance (P52) |
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Biological and cellular evaluation of the association of the movement protein of Tobacco mosaic virus to biological membranes (P53) |
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Nuclear and chloroplastic viroids replicate with different mutation rates (P59) |
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VPg and HCpro: central players in potyvirus-host interactions (P29) |
13.00 |
Lunch (buffet) |
14.00 |
Departure of shuttle buses for Torino (airport and city centre) |
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