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Pejman mehr, M., Ebadi, A., Moosavi, A., McDavid, D., R. Walker, A. (2015). Designing, construction and transformation of silencing constructs for F3´H and F3´5´H genes in grapevine cv. Shiraz. , 46(1), 1-16. doi: 10.22059/ijhs.2015.54120
Maryam Pejman mehr; Ali Ebadi; Amir Moosavi; Debra McDavid; Amanda R. Walker. "Designing, construction and transformation of silencing constructs for F3´H and F3´5´H genes in grapevine cv. Shiraz". , 46, 1, 2015, 1-16. doi: 10.22059/ijhs.2015.54120
Pejman mehr, M., Ebadi, A., Moosavi, A., McDavid, D., R. Walker, A. (2015). 'Designing, construction and transformation of silencing constructs for F3´H and F3´5´H genes in grapevine cv. Shiraz', , 46(1), pp. 1-16. doi: 10.22059/ijhs.2015.54120
Pejman mehr, M., Ebadi, A., Moosavi, A., McDavid, D., R. Walker, A. Designing, construction and transformation of silencing constructs for F3´H and F3´5´H genes in grapevine cv. Shiraz. , 2015; 46(1): 1-16. doi: 10.22059/ijhs.2015.54120

Designing, construction and transformation of silencing constructs for F3´H and F3´5´H genes in grapevine cv. Shiraz

علوم باغبانی ایران
Article 1, Volume 46, Issue 1, May 2015, Pages 1-16    PDF (1.49 M)
Document Type: Full Paper
DOI: 10.22059/ijhs.2015.54120
Authors
Maryam Pejman mehr* 1; Ali Ebadi2; Amir Moosavi3; Debra McDavid4; Amanda R. Walker4
1Post Graduate Student and Professor, University College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
2. Post Graduate Student and Professor, University College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
3. Associate Professor, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
4. Researcher and Professor in CSIRO Plant Industries, Adelaide, Australia
Abstract
abstract
 In order to study F3´5´H and F3´H function and their intraction in the grapevine flavonoids biosynthetic pathway, designing and constraction of suitable constructs encoding ihpRNA was performed and transgenic lines containing silencing construct of F3´H and simultaneous silencing construct of F3´5´H and F3´H were created. For this purpose, fragments were selected from both genes and inserted into pHANNIBAL vector as inverted repeats. Using binary vector system, each construct inserted into p27 mod GFP 4a vector and were used for Agrobacterium transformation. Embryogenic calli, drived from anther culture, were co-cultivated with Agrobacterium for transformation. Expression of GFP gene was detected in transgenic embryogenic calli, 5 days after inoculation using microscope. Finally, 42 and 34 lines were generated from single (F3´H) and simultaneous silencing (F3´5´H and F3´H) cultures, respectively. PCR analysis confirmed 36 single (F3´H) silencing line and 27 simultaneous silencing (F3´5´H and F3´H) lines, showing high efficacy of regeneration and transformation methods.
Keywords
Vitis vinifera; gene construct; silencing; F3´H; F3´5´H
References
 

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