2004
DOI: 10.1099/vir.0.80029-0
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Splicing of Cauliflower mosaic virus 35S RNA serves to downregulate a toxic gene product

Abstract: Alternative splicing usually leads to an increase in the number of gene products that can be derived from a single transcript. Here, a different and novel use of alternative splicing -as a means to control the amount of a potentially toxic gene product in the plant pararetrovirus Cauliflower mosaic virus (CaMV) -is reported. About 70 % of the CaMV 35S RNA, which serves as a substrate for both reverse transcription and polycistronic mRNA, is spliced into four additional RNA species. Splicing occurs between four… Show more

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Cited by 20 publications
(31 citation statements)
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“…This plasmid is not infectious when inoculated into turnip plants unless the stop codon reverts to a coding nucleotide triplet; that infectious revertants appear spontaneously upon Top-S inoculation has been reported previously (13). Several infectious revertants were characterized and are described in Results.…”
Section: Methodsmentioning
confidence: 72%
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“…This plasmid is not infectious when inoculated into turnip plants unless the stop codon reverts to a coding nucleotide triplet; that infectious revertants appear spontaneously upon Top-S inoculation has been reported previously (13). Several infectious revertants were characterized and are described in Results.…”
Section: Methodsmentioning
confidence: 72%
“…Laboratory colonies of all aphid species were initiated from a single viviparous aptera collected on cauliflower (B. Plasmid construction and mutagenesis. Clone pCa37 is the reference clone for the CaMV isolate Cabb-S (12); clone ⌬II-S, where the entire coding sequence of gene II is replaced by the unique restriction site SpeI, was described elsewhere (13).…”
Section: Methodsmentioning
confidence: 99%
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“…The shunt mechanism allows ribosomes to reach the start codon of gene VII. The subsequent expression of genes I through V on the 35S RNA involves alternative mechanisms, including transactivation of the translation of genes I through V by the CaMV gene VI product (18,44) and splicing (14,28).…”
mentioning
confidence: 99%