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Inherent properties not conserved in other tenuiviruses increase priming and realignment cycles during transcription of Rice stripe virus
- Source :
- Virology, 496, 287-298, Virology 496 (2016)
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Two tenuiviruses Rice stripe virus (RSV) and Rice grassy stunt virus (RGSV) were found to co-infect rice with the same reovirus Rice ragged stunt virus (RRSV). During the co-infection, both tenuiviruses recruited 10-21 nucleotides sized capped-RNA leaders from the RRSV. A total of 245 and 102 RRSV-RGSV and RRSV-RSV chimeric mRNA clones, respectively, were sequenced. An analysis of the sequences suggested a scenario consistent with previously reported data on related viruses, in which capped leader RNAs having a 3' end complementary to the viral template are preferred and upon base pairing the leaders prime processive transcription directly or after one to several cycles of priming and realignment (repetitive prime-and-realign). Interestingly, RSV appeared to have a higher tendency to use repetitive prime-and-realign than RGSV even with the same leader derived from the same RRSV RNA. Combining with relevant data reported previously, this points towards an intrinsic feature of RSV.
- Subjects :
- 0301 basic medicine
Transcription, Genetic
Base pair
viruses
Laboratory of Virology
Plant-infecting reovirus
Cap snatching
Laboratorium voor Virologie
Evolution, Molecular
03 medical and health sciences
Transcription (biology)
Virology
RNA, Messenger
Rice grassy stunt virus
Tenuivirus
Plant Diseases
Base Sequence
biology
Coinfection
Prime-and-realign
food and beverages
RNA
Oryza
Rice stripe virus
Cap-snatching
Rice ragged stunt virus
biology.organism_classification
Co-infection
030104 developmental biology
RNA, Viral
EPS
5' Untranslated Regions
Subjects
Details
- ISSN :
- 00426822
- Volume :
- 496
- Database :
- OpenAIRE
- Journal :
- Virology
- Accession number :
- edsair.doi.dedup.....150d7ebef60e6713a18a2987190e2c71
- Full Text :
- https://doi.org/10.1016/j.virol.2016.06.018