The S40 residue in HIV-1 Gag p6 impacts local and distal budding determinants, revealing additional late domain activities

• Published in: Retrovirology Vol. 10; no. 1; p. 143
• Main Authors: Watanabe, Susan M, Chen, Min-Huei, Khan, Mahfuz, Ehrlich, Lorna, Kemal, Kimdar Sherefa, Weiser, Barbara, Shi, Binshan, Chen, Chaoping, Powell, Michael, Anastos, Kathryn, Burger, Harold, Carter, Carol A
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 21.11.2013; BioMed Central
• Subjects: Amino Acid Substitution; Amino acids; Analysis; Animals; Calcium-Binding Proteins - metabolism; Care and treatment; Cell Cycle Proteins - metabolism; Cercopithecus aethiops; COS Cells; DNA-Binding Proteins - metabolism; Endosomal Sorting Complexes Required for Transport - metabolism; gag Gene Products, Human Immunodeficiency Virus - genetics; gag Gene Products, Human Immunodeficiency Virus - metabolism; Gene mutations; HIV; HIV (Viruses); HIV-1 - genetics; HIV-1 - physiology; Host-Pathogen Interactions; Human immunodeficiency virus; Human immunodeficiency virus 1; Medical research; Medicine; Microscopy; Microscopy, Electron; Mutant Proteins - genetics; Mutant Proteins - metabolism; Mutation; Physiological aspects; Protein Binding; Retroviruses; Risk factors; Studies; Transcription Factors - metabolism; Two-Hybrid System Techniques; Virus Release
• ISSN: 1742-4690; 1742-4690
• DOI: 10.1186/1742-4690-10-143

HIV-1 budding is directed primarily by two motifs in Gag p6 designated as late domain-1 and -2 that recruit ESCRT machinery by binding Tsg101 and Alix, respectively, and by poorly characterized determinants in the capsid (CA) domain. Here, we report that a conserved Gag p6 residue, S40, impacts budding mediated by all of these determinants. Whereas budding normally results in formation of single spherical particles ~100 nm in diameter and containing a characteristic electron-dense conical core, the substitution of Phe for S40, a change that does not alter the amino acids encoded in the overlapping pol reading frame, resulted in defective CA-SP1 cleavage, formation of strings of tethered particles or filopodia-like membrane protrusions containing Gag, and diminished infectious particle formation. The S40F-mediated release defects were exacerbated when the viral-encoded protease (PR) was inactivated or when L domain-1 function was disrupted or when budding was almost completely obliterated by the disruption of both L domain-1 and -2. S40F mutation also resulted in stronger Gag-Alix interaction, as detected by yeast 2-hybrid assay. Reducing Alix binding by mutational disruption of contact residues restored single particle release, implicating the perturbed Gag-Alix interaction in the aberrant budding events. Interestingly, introduction of S40F partially rescued the negative effects on budding of CA NTD mutations EE75,76AA and P99A, which both prevent membrane curvature and therefore block budding at an early stage. The results indicate that the S40 residue is a novel determinant of HIV-1 egress that is most likely involved in regulation of a critical assembly event required for budding in the Tsg101-, Alix-, Nedd4- and CA N-terminal domain affected pathways.