Journal
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE
Volume 11, Issue 7, Pages -Publisher
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/cshperspect.a038497
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Funding
- Japan Society for the Promotion of Science (JSPS) Grant-in-Aid for Challenging Research (Exploratory) [19K22529]
- JSPS Grant-in-Aid for Scientific Research (B) [20H03494]
- JSPS Core-to-Core Program A, the Advanced Research Networks
- Ministry of Education, Culture, Sports, Science and Technology (MEXT) Grant-in-Aid for Scientific Research on Innovative Area [19H04831]
- Japan Agency for Medical Research and Development (AMED) Research Program on Emerging and Re-emerging Infectious Disease grants [19fk0108113, 20fk0108270h0001]
- Grant for Joint Research Projects of the Institute of Medical Science, University of Tokyo
- Joint Usage/Research Center program of the Institute for Frontier Life and Medical Sciences Kyoto University,
- Daiichi Sankyo Foundation of Life Science
- Uehara Memorial Foundation
- Takeda Science Foundation
- Grants-in-Aid for Scientific Research [20H03494, 19K22529, 19H04831] Funding Source: KAKEN
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The genome of influenza A virus consists of eight segmented RNAs, which are now believed to be selectively packaged through interactions mediated by segment-specific genome packaging signals. Studies suggest that these interactions are facilitated by their specific RNA characteristics.
The genome of influenza Avirus (IAV) comprises eight segmented, single-stranded, negative-sense RNAs. The genome packaging mechanism of IAV was a long-standing enigma, but it is now widely accepted that IAV packages one copy of each of the eight viral RNA (vRNA) segments in a selective manner. Accumulating evidence over the last decade suggests that the eight unique vRNAs are selected via intersegment interactions mediated by their segment-specific genome packaging signals; however, the characteristics of these RNA-based interactions largely remain unknown. This review summarizes our current knowledge of IAV selective genome packaging and the possible mechanisms underlying the selection of the eight unique vRNAs.
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