نمایش مختصر رکورد

dc.contributor.authorGhanbari Jahromi, Marzieaen_US
dc.contributor.authorRahnama, Hassanen_US
dc.contributor.authorMousavi, Amiren_US
dc.contributor.authorSafarnejad, Mohammad Rezaen_US
dc.contributor.authorKalatejari, Sepideen_US
dc.contributor.authorSoheilivand, Saeeden_US
dc.date.accessioned1399-07-08T23:08:23Zfa_IR
dc.date.accessioned2020-09-29T23:08:23Z
dc.date.available1399-07-08T23:08:23Zfa_IR
dc.date.available2020-09-29T23:08:23Z
dc.date.issued2015-06-01en_US
dc.date.issued1394-03-11fa_IR
dc.date.submitted2014-09-01en_US
dc.date.submitted1393-06-10fa_IR
dc.identifier.citationGhanbari Jahromi, Marziea, Rahnama, Hassan, Mousavi, Amir, Safarnejad, Mohammad Reza, Kalatejari, Sepide, Soheilivand, Saeed. (2015). Transient expression of coding and non-coding regions of PVY confer resistance to virus infection. Progress in Biological Sciences, 5(1), 19-31. doi: 10.22059/pbs.2015.53952en_US
dc.identifier.issn1016-1058
dc.identifier.issn2228-7833
dc.identifier.urihttps://dx.doi.org/10.22059/pbs.2015.53952
dc.identifier.urihttps://pbiosci.ut.ac.ir/article_53952.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/148065
dc.description.abstractOne of the most efficient mechanisms by which plants protect themselves from invading viruses<br />is the specific RNA-dependent silencing pathway termed post-transcriptional gene silencing<br />(PTGS). In this mechanism, resistance to a virus is engineered through the expression of a<br />segment of the virus genomein transgenic plants. Potato VirusY (PVY) is one of the most<br />damaging viruses of potato, infecting most cultivars and causing significant yield losses<br />throughout the world. The present study was performed to compare the efficiency of three<br />construct containing different regions of 3′UTR (UR) and coat protein (CP) against PVY<br />infection. Expression of homologous hairpin RNA to PVY in potato plant was carried out by<br />transient gene expression of constructs with agro-infiltration followed by mechanical viral<br />infection. Results showed that successful production of siRNAs confer resistance to two PVY<br />strain. Comparison between transiently expressed constructs indicated that applying CP+UR<br />PVY hairpin RNA was the most efficient RNAi construct to confer resistance. Resistance was<br />found to have taken the form of immunity, since no viral particle could be detected in the upper<br />leaves as shown by ELISA assay and Northern hybridizations. To the best of our knowledge,<br />this is the first report on the application of 3'non-coding region of PVY in conferring complete<br />resistance against virus in potato.en_US
dc.format.extent481
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherUniversity of Tehran Pressen_US
dc.relation.ispartofProgress in Biological Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22059/pbs.2015.53952
dc.subjectpotatoen_US
dc.subjectPVYen_US
dc.subjectRNA silencingen_US
dc.subjecttransient expressionen_US
dc.subjectbiotechnologyen_US
dc.titleTransient expression of coding and non-coding regions of PVY confer resistance to virus infectionen_US
dc.typeTexten_US
dc.typeOriginal Research Papersen_US
dc.contributor.departmentDepartment of Horticultural Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Tissue Culture and Gene Transformation, Agricultural Biotechnology Research Institute of Iran, Karaj, Iranen_US
dc.contributor.departmentDepartment of Agricultural Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iranen_US
dc.contributor.departmentDepartment of Plant Viruses, Iranian Research Institute of Plant Protection, Tehran, Iranen_US
dc.contributor.departmentDepartment of Horticultural Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Tissue Culture and Gene Transformation, Agricultural Biotechnology Research Institute of Iran, Karaj, Iranen_US
dc.citation.volume5
dc.citation.issue1
dc.citation.spage19
dc.citation.epage31


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