Virus-derived small RNAs in tomato plants infected by Tomato yellow leaf curl Sardinia virus analysed by deep sequencing (Abstract/Comunicazione in atti di convegno)

Type
Label
  • Virus-derived small RNAs in tomato plants infected by Tomato yellow leaf curl Sardinia virus analysed by deep sequencing (Abstract/Comunicazione in atti di convegno) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Alternative label
  • MIOZZI L., PANTALEO V., NORIS E., BURGYAN J. & ACCOTTO G.P. (2011)
    Virus-derived small RNAs in tomato plants infected by Tomato yellow leaf curl Sardinia virus analysed by deep sequencing
    in SIV 2011, Orvieto, September, 11-14, 2011
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • MIOZZI L., PANTALEO V., NORIS E., BURGYAN J. & ACCOTTO G.P. (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • oral communication (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
  • INTERVENTO ORALE (literal)
Note
  • Comunicazione (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • ML; PV; NE; BJ; AGP: IVV CNR (literal)
Titolo
  • Virus-derived small RNAs in tomato plants infected by Tomato yellow leaf curl Sardinia virus analysed by deep sequencing (literal)
Abstract
  • Background: The begomovirus Tomato yellow leaf curl Sardinia virus (TYLCSV) induces a devastating disease of tomato crops in the Mediterranean region. TYLCSV has a 2.7 kb circular single-stranded DNA genome that includes a bidirectional promoter driving the synthesis of viral RNA transcripts. These are recognised by the plant RNA silencing machinery as foreign RNAs that generate viral small interfering RNAs (v-siRNAs). Methods: A cDNA library of small RNAs was obtained from TYLCSV-infected tomato plants and sequenced on Solexa/Illumina platform. The subset of v-siRNAs was identified and characterized. Results: TYLCSV-derived siRNAs, mainly of 21-22 nt, spanned the entire viral genome but were discontinuously distributed throughout it. Viral-siRNAs from the non-coding region were poorly represented; the most abundant v-siRNAs were from the coat protein and the Rep/C4 genes and were mainly of sense polarity. The major hot spots were experimentally validated by reverse oligo dot blot analysis. Conclusions: The first high-resolution v-siRNA map for TYLCSV is reported. The mechanism/s of v-siRNA biogenesis and their role in antiviral plant response are discussed. (literal)
Prodotto di
Autore CNR
Insieme di parole chiave

Incoming links:


Autore CNR di
Prodotto
Insieme di parole chiave di
data.CNR.it