2011
DOI: 10.4161/rna.8.2.15663
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RNA virus replication, transcription and recombination

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Cited by 23 publications
(15 citation statements)
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“…This is consistent with the literature showing that differences in coverage of overlapping sequences can lead to the split of supposedly contiguous sequences into different contigs [19]. This is a problem mainly when assembling viral genomes from RNAs since viral genes can show different transcription profiles [37,38]. To overcome this limitation, we decided to use contigs derived from the "meta" strategy as trusted contigs trying to extend these contiguous sequences.…”
Section: Resultssupporting
confidence: 75%
“…This is consistent with the literature showing that differences in coverage of overlapping sequences can lead to the split of supposedly contiguous sequences into different contigs [19]. This is a problem mainly when assembling viral genomes from RNAs since viral genes can show different transcription profiles [37,38]. To overcome this limitation, we decided to use contigs derived from the "meta" strategy as trusted contigs trying to extend these contiguous sequences.…”
Section: Resultssupporting
confidence: 75%
“…Worobey and Holmes [ 43 ] mention that segmental exchange recombination in phi6 RNA virus is impossible or very rare. They go on to state that template switching by viral replicase may be inhibited by physical constraints such as the ribonucleoprotein packaging in the case of negative-strand RNA viruses, also corroborated by White et al [ 42 ] as mentioned earlier. However, one other physical constraint mentioned by them, viz., the extent of sequence dissimilarity between potentially recombining genomes, is obviated in our case by our imposed condition that potential matches ensure identical sequences between parent and daughter segments.…”
Section: Introductionmentioning
confidence: 58%
“…Homologous recombination is well documented in the case of eukaryote and bacterial genomes [ 29 ], but is controversial in cases of negative stranded RNA viruses [ 18 ]. Such viruses are believed to be rapidly packed with ribonucleoprotein after being transcribed and it then becomes difficult, but perhaps not impossible, for RNA polymerase to ‘jump’ from one strand to another to search for similar sequences [ 42 ]. In mammalian genes and chromosomes, recombination can take place through one or more cross-overs during replication [ 29 ].…”
Section: Introductionmentioning
confidence: 99%
“…The majority of viruses infecting animals are RNA viruses. All RNA virus replication proceeds through a RNA strand complimentary intermediate, except for in retroviruses where the intermediate is DNA [ 66 ]. Despite differences in genomic features and replication strategies, immediately after virus infection, all RNA viruses trigger evolutionarily conserved innate immune responses that serve as a first line of defense against infection.…”
Section: Intracellular Immune Ecosystem Of Virus-infected Cellsmentioning
confidence: 99%