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Journal of Virology, September 2003, p. 9173-9182, Vol. 77, No. 17
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.17.9173-9182.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Tsg101 Control of Human Immunodeficiency Virus Type 1 Gag Trafficking and Release

A. Goff,1 L. S. Ehrlich,1 S. N. Cohen,2 and C. A. Carter1*

Department of Molecular Genetics and Microbiology, State University of New York at Stony Brook, Stony Brook, New York 11794-5222,1 Department of Genetics, Stanford University School of Medicine, Stanford, California 94305-51202

Received 6 June 2002/ Accepted 29 May 2003

The structural precursor polyprotein of human immunodeficiency virus type 1, Pr55gag, contains a proline-rich motif (PTAP) called the "late domain" in its C-terminal p6 region that directs release of mature virus-like particles (VLPs) from the plasma membranes of gag-transfected COS-1 cells. The motif binds Tsg101 (vacuolar protein-sorting protein 23, or Vps23), which functions in endocytic trafficking. Here, we show that accumulation of the wild-type (wt) Gag precursor in a fraction of COS-1 cytoplasm enriched in multivesicular bodies and small particulate components of the plasma membrane (P100) is p6 dependent. Cleavage intermediates and mature CA mainly partitioned with more rapidly sedimenting larger material enriched in components of lysosomes and early endosomes (P27), and this also was p6 dependent. Expression of truncated or full-length Tsg101 proteins interfered with VLP assembly and Gag accumulation in the P100 fraction. This correlated with reduced accumulation of Gag tagged with green fluorescent protein (Gag-GFP) at the plasma membrane and colocalization with the tagged Tsg101 in perinuclear early endosomes, as visualized by confocal microscopy. Fractionation analysis and confocal examination both indicated that the N-terminal region of Tsg101, which contains binding sites for PTAP and ubiquitin (Ub), was required for Gag trafficking to the plasma membrane. Expression of FLAG-tagged Tsg101 with a deletion in the Ub-binding pocket inhibited VLP release almost completely and to a significantly greater extent than expression of the wt tagged Tsg101 protein or Tsg101-FLAG containing a deletion in the PTAP-binding region. The results demonstrate that Gag associates with endosomal trafficking compartments and indicate that efficient release of virus particles from the plasma membrane requires both the PTAP- and Ub-binding functions of Tsg101 to recruit the cellular machinery required for budding.

* Corresponding author. Mailing address: Department of Molecular Genetics and Microbiology, State University of New York at Stony Brook, Life Sciences Bldg., Rm. 248, Stony Brook, NY 11794-5222. Phone: (631) 632-8801. Fax: (631) 632-9797. E-mail: ccarter{at}ms.cc.sunysb.edu.

Journal of Virology, September 2003, p. 9173-9182, Vol. 77, No. 17
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.17.9173-9182.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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