Mechanism of Plum pox virus resistance in transgenic Prunus domestica L.
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027006%3A_____%2F06%3A1485" target="_blank" >RIV/00027006:_____/06:1485 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Mechanism of Plum pox virus resistance in transgenic Prunus domestica L.
Popis výsledku v původním jazyce
RNA silencing (posttranscriptional gene silencing-PTGS in plant) is a sequence-specific RNA degradation mechanism first discovered in transgenic plants functions as an adaptive immune system targeted against viruses. The hal1marks of RNA silencing, siRNAs (21 nt short and 27 nt long) were detected in transgenic plum, Prunus domestica clone C-5, resistant to Plum pox virus (PPV). The duplex siRNA (21-27-nt) were detected in non-inoculated healthy C5 plums. No such siRNAs were detected in healthy susceptible transgenic plum clone C-6 plums. When C6 plants were inoculated with PPV the 21-nt siRNA was clearly present. Similar short of21 nt was detected in a PPV infected C-5 (a single C5 plum was infected with PPV out of 30 PPV inoculated plants). However,PPV inoculated virus free clone C-5 showed the double banding pattern of siRNA (21-27-nt) as non-inoculated C5. The association of short (21 nt) and long (27nt) siRNA with PPV resistance is correspond with reports in herbaceous plant mode
Název v anglickém jazyce
Mechanism of Plum pox virus resistance in transgenic Prunus domestica L.
Popis výsledku anglicky
RNA silencing (posttranscriptional gene silencing-PTGS in plant) is a sequence-specific RNA degradation mechanism first discovered in transgenic plants functions as an adaptive immune system targeted against viruses. The hal1marks of RNA silencing, siRNAs (21 nt short and 27 nt long) were detected in transgenic plum, Prunus domestica clone C-5, resistant to Plum pox virus (PPV). The duplex siRNA (21-27-nt) were detected in non-inoculated healthy C5 plums. No such siRNAs were detected in healthy susceptible transgenic plum clone C-6 plums. When C6 plants were inoculated with PPV the 21-nt siRNA was clearly present. Similar short of21 nt was detected in a PPV infected C-5 (a single C5 plum was infected with PPV out of 30 PPV inoculated plants). However,PPV inoculated virus free clone C-5 showed the double banding pattern of siRNA (21-27-nt) as non-inoculated C5. The association of short (21 nt) and long (27nt) siRNA with PPV resistance is correspond with reports in herbaceous plant mode
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
EE - Mikrobiologie, virologie
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2006
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
Book of Proceedings of the "Eufrin Plum and Prune Working Group Meeting"
ISBN
80-902636-9-0
ISSN
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e-ISSN
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Počet stran výsledku
9
Strana od-do
61-69
Název nakladatele
Research and Breeding Institute of Pomology Holovousy Ltd.
Místo vydání
Holovousy
Místo konání akce
Hradec Králové - Holovousy
Datum konání akce
31. 8. 2006
Typ akce podle státní příslušnosti
WRD - Celosvětová akce
Kód UT WoS článku
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