Previous Article | Next Article 
Journal of Virology, June 2004, p. 6517-6526, Vol. 78, No. 12
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.12.6517-6526.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
A Bidirectional SF2/ASF- and SRp40-Dependent Splicing Enhancer Regulates Human Immunodeficiency Virus Type 1 rev, env, vpu, and nef Gene Expression
Massimo Caputi ,1,
,
Marcel Freund,2,
Susanne Kammler,2 Corinna Asang,2 and Heiner Schaal2*
Department of Biology, The Johns Hopkins University, Baltimore, Maryland 21218,1
Institut für Virologie, Heinrich-Heine-Universität Düsseldorf, D-40225 Düsseldorf, Germany2
Received 8 October 2003/
Accepted 18 February 2004
The integrated human immunodeficiency virus type 1 (HIV-1) genome is transcribed in a single pre-mRNA that is alternatively spliced into more than 40 mRNAs. We characterized a novel bidirectional exonic splicing enhancer (ESE) that regulates the expression of the HIV-1 env, vpu, rev, and nef mRNAs. The ESE is localized downstream of the vpu-, env-, and nef-specific 3' splice site no. 5. SF2/ASF and SRp40 activate the ESE and are required for efficient 3' splice site usage and binding of the U1 snRNP to the downstream 5' splice site no. 4. U1 snRNP binding to the 5' splice site no. 4 is required for splicing of the rev and nef mRNAs and to increase expression of the partially spliced env mRNA. Finally, our results indicate that this ESE is necessary for the recruitment of the U1 snRNP to the 5' splice site no. 4, even when the 5' splice site and the U1 snRNA have been mutated to obtain a perfect complementary match. The ESE characterized here is highly conserved in most viral subtypes.
* Corresponding author. Mailing address: Institut für Virologie, Geb. 22.21, Universitätsstr. 1, D-40225 Düsseldorf, Germany. Phone: 49 211-81-12393. Fax: 49 211-81-12227. E-mail:
schaal{at}uni-duesseldorf.de.
M.C. and M.F. contributed equally to this work.
Present address: Biomedical Science Department, Florida Atlantic University, Boca Raton, FL 33431.
Journal of Virology, June 2004, p. 6517-6526, Vol. 78, No. 12
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.12.6517-6526.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Zychlinski, D., Erkelenz, S., Melhorn, V., Baum, C., Schaal, H., Bohne, J.
(2009). Limited complementarity between U1 snRNA and a retroviral 5' splice site permits its attenuation via RNA secondary structure. Nucleic Acids Res
0: gkp694v1-gkp694
[Abstract]
[Full Text]
-
Jablonski, J. A., Caputi, M.
(2009). Role of Cellular RNA Processing Factors in Human Immunodeficiency Virus Type 1 mRNA Metabolism, Replication, and Infectivity. J. Virol.
83: 981-992
[Abstract]
[Full Text]
-
Asang, C., Hauber, I., Schaal, H.
(2008). Insights into the selective activation of alternatively used splice acceptors by the human immunodeficiency virus type-1 bidirectional splicing enhancer. Nucleic Acids Res
36: 1450-1463
[Abstract]
[Full Text]
-
Hovhannisyan, R. H., Carstens, R. P.
(2007). Heterogeneous Ribonucleoprotein M Is a Splicing Regulatory Protein That Can Enhance or Silence Splicing of Alternatively Spliced Exons. J. Biol. Chem.
282: 36265-36274
[Abstract]
[Full Text]
-
Poon, B., Chang, M. A., Chen, I. S. Y.
(2007). Vpr Is Required for Efficient Nef Expression from Unintegrated Human Immunodeficiency Virus Type 1 DNA. J. Virol.
81: 10515-10523
[Abstract]
[Full Text]
-
Schaub, M. C., Lopez, S. R., Caputi, M.
(2007). Members of the Heterogeneous Nuclear Ribonucleoprotein H Family Activate Splicing of an HIV-1 Splicing Substrate by Promoting Formation of ATP-dependent Spliceosomal Complexes. J. Biol. Chem.
282: 13617-13626
[Abstract]
[Full Text]
-
Anderson, J. L., Johnson, A. T., Howard, J. L., Purcell, D. F. J.
(2007). Both Linear and Discontinuous Ribosome Scanning Are Used for Translation Initiation from Bicistronic Human Immunodeficiency Virus Type 1 env mRNAs. J. Virol.
81: 4664-4676
[Abstract]
[Full Text]
-
Heise, T., Sommer, G., Reumann, K., Meyer, I., Will, H., Schaal, H.
(2006). The hepatitis B virus PRE contains a splicing regulatory element. Nucleic Acids Res
34: 353-363
[Abstract]
[Full Text]
-
Wilusz, J. E., Devanney, S. C., Caputi, M.
(2005). Chimeric peptide nucleic acid compounds modulate splicing of the bcl-x gene in vitro and in vivo. Nucleic Acids Res
33: 6547-6554
[Abstract]
[Full Text]
-
Li, X., Wang, J., Manley, J. L.
(2005). Loss of splicing factor ASF/SF2 induces G2 cell cycle arrest and apoptosis, but inhibits internucleosomal DNA fragmentation. Genes Dev.
19: 2705-2714
[Abstract]
[Full Text]
-
Tyson-Capper, A. J., Bailey, J., Krainer, A. R., Robson, S. C., Europe-Finner, G. N.
(2005). The Switch in Alternative Splicing of Cyclic AMP-response Element Modulator Protein CREM{tau}2{alpha} (Activator) to CREM{alpha} (Repressor) in Human Myometrial Cells Is Mediated by SRp40. J. Biol. Chem.
280: 34521-34529
[Abstract]
[Full Text]
-
Freund, M., Hicks, M. J., Konermann, C., Otte, M., Hertel, K. J., Schaal, H.
(2005). Extended base pair complementarity between U1 snRNA and the 5' splice site does not inhibit splicing in higher eukaryotes, but rather increases 5' splice site recognition. Nucleic Acids Res
33: 5112-5119
[Abstract]
[Full Text]