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Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/1370
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Elayabalan, S., Kalaiponmani, K., Subramanian, S., Selvarajan,R., Panchanathan, R.,Muthuvelayutham,R.,Kumar,K.K. and Balasubramanian,P | en_US |
dc.date.accessioned | 2017-01-12T10:02:32Z | - |
dc.date.available | 2017-01-12T10:02:32Z | - |
dc.date.issued | 2013-04-01 | - |
dc.identifier.citation | 11 | en_US |
dc.identifier.uri | http://krishi.icar.gov.in/jspui/handle/123456789/1370 | - |
dc.description | Banana crop faces numerous environmental challenges, particularly with fungal and bacterial pathogens as well as the major threatening disease like banana bunchy top virus (Hu et al. 1996). The problem is aggravated by the limited diversity of banana cultivars around the world. Conventional breeding methods have limited success due to low female fertility, sterility, ploidy levels and poor seed set, besides the process is time consuming. These problems point to the necessity of developing alternate strategies for banana improvement. | en_US |
dc.description.abstract | One of the most severe viral diseases of hill banana is caused by banana bunchy top virus (BBTV), a nanovirus transmitted by the aphid Pentalonia nigronervosa. In this study, we reported the Agrobacterium-mediated transformation on a highly valued hill banana cultivar Virupakshi (AAB) for resistance to BBTV disease. The target of the RNA interference (RNAi) is the rep gene, encoded by the BBTV-DNA1. In order to develop RNAi construct targeting the BBTV rep gene, the full-length rep gene of 870 bp was polymerase chain reaction amplified from BBTV infected hill banana sample DNA, cloned and confirmed by DNA sequencing. The partial rep gene fragment was cloned in sense and anti sense orientation in the RNAi intermediate vector, pSTARLING-A. After cloning in pSTARLING-A, the cloned RNAi gene cassette was released by NotI enzyme digestion and cloned into the NotI site of binary vector, pART27. Two different explants, embryogenic cells and embryogenic cell suspension derived microcalli were used for co-cultivation. Selection was done in presence of 100 mg/L kanamycin. In total, 143 putative transgenic hill banana lines were generated and established in green house condition. The presence of the transgenes was confirmed in the selected putative transgenic hill banana lines by PCR and reverse transcription PCR analyses. Transgenic hill banana plants expressing RNAi-BBTV rep were obtained and shown to resist infection by BBTV. The transformed plants are symptomless, and the replication of challenge BBTV almost completely suppressed. Hence, the RNAi mediating resistances were shown to be effective management of BBTV in hill banana. | en_US |
dc.language.iso | English | en_US |
dc.publisher | Springer Link | en_US |
dc.subject | Banana bunchy top virus, BBTV, RNAi- BBTV, rep,Transgenic, hill banana, Virupakshi AAB, Research Paper 2013, ICAR NRCB | en_US |
dc.title | Development of agrobacterium-mediated transformation of highly valued hill banana cultivar Virupakshi (AAB) for resistance to BBTV disease. | en_US |
dc.type | Research Paper | en_US |
dc.publication.journalname | World Journal of Microbiology and Biotechnology | en_US |
dc.publication.volumeno | 29(4) | en_US |
dc.publication.pagenumber | 589-96 | en_US |
dc.publication.divisionUnit | Virology | en_US |
dc.publication.sourceUrl | http://link.springer.com/article/10.1007/s11274-012-1214-z | en_US |
dc.publication.naasrating | 8.48 | en_US |
Appears in Collections: | HS-NRCB-Publication |
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File | Description | Size | Format | |
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art%3A10.1007%2Fs11274-012-1214-z.pdf | 698.88 kB | Adobe PDF | View/Open |
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