Human immunodeficiency virus type 1 envelope proteins traffic toward virion assembly sites via a TBC1D20/Rab1-regulated pathway

Dikla Nachmias, Ella H. Sklan*, Marcelo Ehrlich, Eran Bacharach

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background: The cellular activity of many factors and pathways is required to execute the complex replication cycle of the human immunodeficiency virus type 1 (HIV-1). To reveal these cellular components, several extensive RNAi screens have been performed, listing numerous 'HIV-dependency factors'. However, only a small overlap between these lists exists, calling for further evaluation of the relevance of specific factors to HIV-1 replication and for the identification of additional cellular candidates. TBC1D20, the GTPase-activating protein (GAP) of Rab1, regulates endoplasmic reticulum (ER) to Golgi trafficking, was not identified in any of these screens, and its involvement in HIV-1 replication cycle is tested here.Findings: Excessive TBC1D20 activity perturbs the early trafficking of HIV-1 envelope protein through the secretory pathway. Overexpression of TBC1D20 hampered envelope processing and reduced its association with detergent-resistant membranes, entailing a reduction in infectivity of HIV-1 virion like particles (VLPs).Conclusions: These findings add TBC1D20 to the network of host factors regulating HIV replication cycle.

Original languageEnglish
Article number7
JournalRetrovirology
Volume9
DOIs
StatePublished - 19 Jan 2012

Funding

FundersFunder number
Ela Kodesz Institute for Research on Cancer Development and Prevention
Parkinson Diseases Research
Israel Science Foundation169/09
Tel Aviv University

    Keywords

    • Assembly
    • Envelope
    • HIV-1
    • Rab1
    • Secretory pathway
    • TBCID20

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