Structural requirements of adenovirus VAI RNA for its translation enhancement function
- PMID: 3982415
- PMCID: PMC366693
- DOI: 10.1128/mcb.5.1.187-196.1985
Structural requirements of adenovirus VAI RNA for its translation enhancement function
Abstract
Recently, by genetic and biochemical approaches, it has been shown that adenovirus VAI RNA is required for efficient translation of viral mRNAs at late times after infection. To understand the nucleotide sequences and the domains of the VAI RNA that are responsible for the role of VAI RNA in enhancement of translation, a mutational analysis of the VAI gene was undertaken. Deletion, substitution, and insertion mutations covering most of the nucleotide sequences of VAI RNA were introduced into the VAI gene at the plasmid level. These mutant genes were then reintroduced into the virus, and growth properties of the mutant viruses were studied. The majority of the mutants retained normal or nearly normal levels of biological function. Mutations in the region between +43 and +53 and between +107 and the 3' end of the gene resulted in a considerable loss of activity. These mutants, however, grew significantly better than did an adenovirus type 5 mutant lacking both functional VAI and VAII genes, indicating that they retain a portion of their activity. Because no one mutation was able to completely abolish the function, we suggest that the VAI RNA may have multiple functional sites for its translation modulation function. These multiple sites may be short oligonucleotide sequences that may interact with cellular or viral components or both during translation.
Similar articles
-
Construction and analysis of additional adenovirus substitution mutants confirm the complementation of VAI RNA function by two small RNAs encoded by Epstein-Barr virus.J Virol. 1985 Dec;56(3):750-6. doi: 10.1128/JVI.56.3.750-756.1985. J Virol. 1985. PMID: 2999431 Free PMC article.
-
Adenovirus mutants with DNA sequence perturbations in the intragenic promoter of VAI RNA gene allow the enhanced transcription of VAII RNA gene in HeLa cells.Nucleic Acids Res. 1984 Oct 11;12(19):7377-88. doi: 10.1093/nar/12.19.7377. Nucleic Acids Res. 1984. PMID: 6493978 Free PMC article.
-
Functional dissection of adenovirus VAI RNA.J Virol. 1989 Aug;63(8):3423-34. doi: 10.1128/JVI.63.8.3423-3434.1989. J Virol. 1989. PMID: 2746735 Free PMC article.
-
Adenovirus virus-associated RNA and translation control.J Virol. 1991 Nov;65(11):5657-62. doi: 10.1128/JVI.65.11.5657-5662.1991. J Virol. 1991. PMID: 1920611 Free PMC article. Review. No abstract available.
-
Release of viruses and viral DNA from nucleus to cytoplasm of HeLa cells at late stages of productive adenovirus infection as revealed by electron microscope in situ hybridization.Biol Cell. 1998 Jan;90(1):5-38. doi: 10.1016/s0248-4900(98)80230-x. Biol Cell. 1998. PMID: 9691424 Review.
Cited by
-
Characterization of a low-molecular-weight virus-associated (VA) RNA encoded by simian adenovirus type 7 which functionally can substitute for adenovirus type 5 VA RNAI.J Virol. 1986 Nov;60(2):635-44. doi: 10.1128/JVI.60.2.635-644.1986. J Virol. 1986. PMID: 3773054 Free PMC article.
-
In vitro analysis of virus-associated RNA I (VAI RNA): inhibition of the double-stranded RNA-activated protein kinase PKR by VAI RNA mutants correlates with the in vivo phenotype and the structural integrity of the central domain.J Virol. 1994 Jul;68(7):4137-51. doi: 10.1128/JVI.68.7.4137-4151.1994. J Virol. 1994. PMID: 7911532 Free PMC article.
-
Posttranscriptional regulation of hsp70 expression in human cells: effects of heat shock, inhibition of protein synthesis, and adenovirus infection on translation and mRNA stability.Mol Cell Biol. 1987 Dec;7(12):4357-68. doi: 10.1128/mcb.7.12.4357-4368.1987. Mol Cell Biol. 1987. PMID: 3437893 Free PMC article.
-
A MicroRNA Derived from Adenovirus Virus-Associated RNAII Promotes Virus Infection via Posttranscriptional Gene Silencing.J Virol. 2019 Jan 4;93(2):e01265-18. doi: 10.1128/JVI.01265-18. Print 2019 Jan 15. J Virol. 2019. PMID: 30355689 Free PMC article.
-
Persistently adenovirus-infected lymphoid cells express microRNAs derived from the viral VAI and especially VAII RNA.Virology. 2013 Dec;447(1-2):140-5. doi: 10.1016/j.virol.2013.08.024. Epub 2013 Sep 26. Virology. 2013. PMID: 24210108 Free PMC article.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources