TY - JOUR
T1 - Analysis of transitive RNA silencing after grafting in transgenic plants with the coat protein gene of Sweet potato feathery mottle virus
AU - Haque, A. K.M.N.
AU - Tanaka, Yoshikazu
AU - Sonoda, Shoji
AU - Nishiguchi, Masamichi
N1 - Funding Information:
Acknowledgements The authors would like to thank David Baulcombe (The Sainsbury Laboratory, Norwich, UK) and his other lab members for kindly providing the PVX vector and specific comments on the crossing of N. benthamiana. They are also grateful to Sk. Md. Fazle Akbar (School of Medicine, Ehime University, Japan) and Thangavelu U. Arumugam (Faculty of Agriculture, Ehime University) for critical reading of the manuscript, and Charles Lecellier (Institut de Biologie Moleculaire des Plantes - CNRS UPR2357, France) for suggestions concerning the siRNA detection experiment. This work was financially supported in part by Ministry of Education, Culture, Sports, Science and Technology of Japan and by Ministry of Agriculture, Forestry and Fisheries of Japan.
PY - 2007/1
Y1 - 2007/1
N2 - We have previously reported the graft transmission of target specificity for RNA silencing using transgenic Nicotiana benthamiana plants expressing the coat protein gene (CP, including the 3′ non-translated region) of Sweet potato feathery mottle virus. Transgenic plants carrying the 5′ 200 and 400 bp regions of CP were newly produced. From these plants, two silenced and two non-silenced lines were selected to investigate the manifestation of transitive RNA silencing by graft experiments. Non-silenced scions carrying the entire transgene were grafted onto either 5′ or 3′ silencing inducer rootstocks. When non-silenced scions were grafted onto 5′ silencing inducer rootstocks, RNA silencing was induced in the non-silenced scions and spread toward the 3′ region of the transgene mRNA. Similarly, when non-silenced scions were grafted onto 3′ silencing inducer rootstocks, RNA silencing was induced in the non-silenced scions, but was restricted to the 3′ region of the transgene and did not spread to the 5′ region. In addition, results from crossing experiments, involving non-silenced and 3′ silencing inducer plants, confirmed the above finding. This indicates that RNA silencing spreads in the 5′-3′ direction, not in the 3′-5′ direction, along the transgene mRNA.
AB - We have previously reported the graft transmission of target specificity for RNA silencing using transgenic Nicotiana benthamiana plants expressing the coat protein gene (CP, including the 3′ non-translated region) of Sweet potato feathery mottle virus. Transgenic plants carrying the 5′ 200 and 400 bp regions of CP were newly produced. From these plants, two silenced and two non-silenced lines were selected to investigate the manifestation of transitive RNA silencing by graft experiments. Non-silenced scions carrying the entire transgene were grafted onto either 5′ or 3′ silencing inducer rootstocks. When non-silenced scions were grafted onto 5′ silencing inducer rootstocks, RNA silencing was induced in the non-silenced scions and spread toward the 3′ region of the transgene mRNA. Similarly, when non-silenced scions were grafted onto 3′ silencing inducer rootstocks, RNA silencing was induced in the non-silenced scions, but was restricted to the 3′ region of the transgene and did not spread to the 5′ region. In addition, results from crossing experiments, involving non-silenced and 3′ silencing inducer plants, confirmed the above finding. This indicates that RNA silencing spreads in the 5′-3′ direction, not in the 3′-5′ direction, along the transgene mRNA.
KW - Coat protein gene (CP)
KW - Grafting
KW - Nicotiana benthamiana
KW - Post-transcriptional gene silencing
KW - RNA silencing
KW - Sweet potato feathery mottle virus
KW - siRNA
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U2 - 10.1007/s11103-006-9070-6
DO - 10.1007/s11103-006-9070-6
M3 - Article
C2 - 17160454
AN - SCOPUS:33845643721
SN - 0167-4412
VL - 63
SP - 35
EP - 47
JO - Plant Molecular Biology
JF - Plant Molecular Biology
IS - 1
ER -