| Literature DB >> 10334034 |
S Liu1, R W Briddon, I D Bedford, M S Pinner, P G Markham.
Abstract
The inability to transmit progeny virus resulting from the cloned components of an isolate of African cassava mosaic virus originating from Kenya (ACMV-K) has been shown to be due to defects in both genomic components. This was achieved by the production of infectious pseudorecombinants between ACMV-K and the cloned components of a whitefly-transmissible ACMV isolate originating from Nigeria (ACMV-NOg). The exchange of gene fragments between ACMV-K and ACMV-NOg has been used to demonstrate that the defects responsible for lack of transmissibility reside on the coat protein and DNA B C1 gene of ACMV-K. The significance of these finding with respect to the present understanding of the function of these gene products are discussed.Entities:
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Year: 1999 PMID: 10334034 DOI: 10.1023/a:1008017017020
Source DB: PubMed Journal: Virus Genes ISSN: 0920-8569 Impact factor: 2.332