This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hardy, R. W.
Right arrow Articles by Rice, C. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hardy, R. W.
Right arrow Articles by Rice, C. M.

 Previous Article  |  Next Article 

Journal of Virology, April 2005, p. 4630-4639, Vol. 79, No. 8
0022-538X/05/$08.00+0     doi:10.1128/JVI.79.8.4630-4639.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Requirements at the 3' End of the Sindbis Virus Genome for Efficient Synthesis of Minus-Strand RNA

Richard W. Hardy1* and Charles M. Rice2

Department of Biology, Indiana University, Bloomington, Indiana,1 Laboratory of Virology and Infectious Disease, Center for the Study of Hepatitis C, The Rockefeller University, New York, New York2

Received 26 October 2004/ Accepted 3 December 2004

The 3'-untranslated region of the Sindbis virus genome is 0.3 kb in length with a 19-nucleotide conserved sequence element (3' CSE) immediately preceding the 3'-poly(A) tail. The 3' CSE and poly(A) tail have been assumed to constitute the core promoter for minus-strand RNA synthesis during genome replication; however, their involvement in this process has not been formally demonstrated. Utilizing both in vitro and in vivo analyses, we have examined the role of these elements in the initiation of minus-strand RNA synthesis. The major findings of this study with regard to efficient minus-strand RNA synthesis are the following: (i) the wild-type 3' CSE and the poly(A) tail are required, (ii) the poly(A) tail must be a minimum of 11 to 12 residues in length and immediately follow the 3' CSE, (iii) deletion or substitution of the 3' 13 nucleotides of the 3' CSE severely inhibits minus-strand RNA synthesis, (iv) templates possessing non-wild-type 3' sequences previously demonstrated to support virus replication do not program efficient RNA synthesis, and (v) insertion of uridylate residues between the poly(A) tail and a non-wild-type 3' sequence can restore promoter function to a limited extent. This study shows that the optimal structure of the 3' component of the minus-strand promoter is the wild-type 3' CSE followed a poly(A) tail of at least 11 residues. Our findings also show that insertion of nontemplated bases can restore function to an inactive promoter.


* Corresponding author. Mailing address: Department of Biology, Indiana University, 1001 E. Third St., Bloomington, IN 47405. Phone: (812) 856-0652. Fax: (812) 855-6705. E-mail: rhardy{at}bio.indiana.edu.


Journal of Virology, April 2005, p. 4630-4639, Vol. 79, No. 8
0022-538X/05/$08.00+0     doi:10.1128/JVI.79.8.4630-4639.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Kulasegaran-Shylini, R., Atasheva, S., Gorenstein, D. G., Frolov, I. (2009). Structural and Functional Elements of the Promoter Encoded by the 5' Untranslated Region of the Venezuelan Equine Encephalitis Virus Genome. J. Virol. 83: 8327-8339 [Abstract] [Full Text]  
  • Zhai, Y.-g., Wang, H.-Y., Sun, X.-h., Fu, S.-h., Wang, H.-q., Attoui, H., Tang, Q., Liang, G.-d. (2008). Complete sequence characterization of isolates of Getah virus (genus Alphavirus, family Togaviridae) from China. J. Gen. Virol. 89: 1446-1456 [Abstract] [Full Text]  
  • Garneau, N. L., Sokoloski, K. J., Opyrchal, M., Neff, C. P., Wilusz, C. J., Wilusz, J. (2008). The 3' Untranslated Region of Sindbis Virus Represses Deadenylation of Viral Transcripts in Mosquito and Mammalian Cells. J. Virol. 82: 880-892 [Abstract] [Full Text]  
  • Attoui, H., Sailleau, C., Mohd Jaafar, F., Belhouchet, M., Biagini, P., Cantaloube, J. F., de Micco, P., Mertens, P., Zientara, S. (2007). Complete nucleotide sequence of Middelburg virus, isolated from the spleen of a horse with severe clinical disease in Zimbabwe. J. Gen. Virol. 88: 3078-3088 [Abstract] [Full Text]  
  • Li, W., Wong, S.-M. (2007). Host-dependent effects of the 3' untranslated region of turnip crinkle virus RNA on accumulation in Hibiscus and Arabidopsis. J. Gen. Virol. 88: 680-687 [Abstract] [Full Text]  
  • Tomar, S., Hardy, R. W., Smith, J. L., Kuhn, R. J. (2006). Catalytic Core of Alphavirus Nonstructural Protein nsP4 Possesses Terminal Adenylyltransferase Activity.. J. Virol. 80: 9962-9969 [Abstract] [Full Text]  
  • van Leeuwen, H. C., Liefhebber, J. M. P., Spaan, W. J. M. (2006). Repair and Polyadenylation of a Naturally Occurring Hepatitis C Virus 3' Nontranslated Region-Shorter Variant in Selectable Replicon Cell Lines. J. Virol. 80: 4336-4343 [Abstract] [Full Text]