Deep Sequencing of the Small RNAs Derived from two Symptomatic Variants of a Chloroplastic Viroid: Implications for their Genesis and for Viroid Pathogenesis (Articolo in rivista)

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  • Deep Sequencing of the Small RNAs Derived from two Symptomatic Variants of a Chloroplastic Viroid: Implications for their Genesis and for Viroid Pathogenesis (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1371/journal.pone.0007539 (literal)
Alternative label
  • Di Serio F.(1); Gisel A.(2); Navarro B.(1), Delgado S.(3); Martínez de Alba Á.E. (3); Donvito G. (4); Flores R. (3) (2009)
    Deep Sequencing of the Small RNAs Derived from two Symptomatic Variants of a Chloroplastic Viroid: Implications for their Genesis and for Viroid Pathogenesis
    in PloS one; Public Library of Science, San Francisco (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Di Serio F.(1); Gisel A.(2); Navarro B.(1), Delgado S.(3); Martínez de Alba Á.E. (3); Donvito G. (4); Flores R. (3) (literal)
Pagina inizio
  • e7539 (literal)
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  • http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0007539 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 4 (literal)
Rivista
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  • doi: 10.1371/journal.pone.0007539 IMPACT FACTOR 2008: 5.00 (literal)
Note
  • ISI Web of Science (WOS) (literal)
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • (1) Istituto di Virologia vegetale del CNR, 70126 Bari, Italy (2) Istituto di Tecnologie Biomediche del CNR, 70126 Bari, Italy. (3) Instituto de Biología Molecular y Celular de Plantas (UPV-CSIC), 46022 Valencia, Spain. (4) Istituto Nazionale di Fisica Nucleare, 70126 Bari, Italy. (literal)
Titolo
  • Deep Sequencing of the Small RNAs Derived from two Symptomatic Variants of a Chloroplastic Viroid: Implications for their Genesis and for Viroid Pathogenesis (literal)
Abstract
  • Northern-blot hybridization and low-scale sequencing have revealed that plants infected by viroids, non-protein-coding RNA replicons, accumulate 21-24 nt viroid-derived small RNAs (vd-sRNAs) similar to the small interfering RNAs, the hallmarks of RNA silencing. These results strongly support that viroids are elicitors and targets of the RNA silencing machinery of their hosts. Low-scale sequencing, however, retrieves partial datasets and may lead to biased interpretations. To overcome this restraint we have examined by deep sequencing (Solexa-Illumina) and computational approaches the vd-sRNAs accumulating in GF-305 peach seedlings infected by two molecular variants of Peach latent mosaic viroid (PLMVd) inciting peach calico (albinism) and peach mosaic. Our results show in both samples multiple PLMVd-sRNAs, with prevalent 21-nt (+) and (-) RNAs presenting a biased distribution of their 5’ nucleotide, and adopting a hotspot profile along the genomic (+) and (-) RNAs. Dicer-like 4 and 2 (DCL4 and DCL2, respectively), which act hierarchically in antiviral defense, most likely also mediate the genesis of the 21- and 22-nt PLMVd-sRNAs. More specifically, because PLMVd replicates in plastids wherein RNA silencing has not been reported, DCL4 and DCL2 should dice the PLMVd genomic RNAs during their cytoplasmic movement or the PLMVd-dsRNAs generated by a cytoplasmic RNA-dependent RNA polymerase (RDR), like RDR6, acting in concert with DCL4 processing. Furthermore, given that vd-sRNAs derived from the 12-14-nt insertion containing the pathogenicity determinant of peach calico are underrepresented, it is unlikely that symptoms may result from the accidental targeting of host mRNAs by vd-sRNAs from this determinant guiding the RNA silencing machinery. (literal)
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