Abstract
Cucumber mosaic virus (CMV) contains four major RNA species (RNAs 1,2,3 and 4) the largest three of which are necessary for infectivity [ 1,2] . RNA 4 serves as a messenger for synthesis of coat protein in a wheat embryo cell-free system [3] . The nucleotide sequence of RNA 4 must also be present in RNA 3 since it is known that RNA 3 carries the information for coat protein synthesis in vivo [4,5] . In addition to the genome RNAs and RNA 4, a fifth RNA component (RNA 5) of low molecular weight (100 000) has been detected in CMV preparations [ 1,6] . Interest in RNA 5 was enhanced by the finding that, even though the small RNA is apparently dependent upon the CMV genome RNAs for replication [7] , the relative proportions of RNA 5 and RNA l-4 is tied to the nature of the plant host of viral propagation and, furthermore, the presence of RNA 5 can dramatically alter the response of certain hosts to CMV infection [8,9]. The above findings make it unlikely that RNA 5 is a host RNA normally present in the plant which is entrapped during virus assembly, but they do not in themselves permit us to distinguish between two further possibilities: (1) RNA 5 originates from the CMV RNA but is nonessential for infectivity, i.e., a deletion fragment or partial transcription product of one of the genome RNAs, or (2) RNA 5 is a ‘satellite’ RNA, that is, a parasite RNA with little or no sequence homology with the helper genome. As a prelude to a more detailed sequence analysis, we have determined some of the properties of RNA 5. In particular, the 5’ and 3’ extremities of the RNA
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