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Cell Host Microbe. 2007 Jul 12;2(1):41-53.

Identification of human MVB12 proteins as ESCRT-I subunits that function in HIV budding.

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1
Department of Biochemistry, University of Utah, Salt Lake City, UT 84112-5650, USA.

Abstract

Human ESCRT-I is a multiprotein complex that plays essential roles in HIV budding and endosomal protein sorting. All ESCRT-I complexes contain three common subunits (TSG101, VPS28, and VPS37), and a fourth subunit of yeast ESCRT-I was recently identified (Mvb12p). We now demonstrate that two related human proteins (MVB12A and MVB12B) constitute the fourth class of metazoan ESCRT-I subunits, despite lacking identifiable sequence homology to Mvb12p. Hydrodynamic studies indicate that soluble human ESCRT-I complexes contain one copy of each of the four subunit types. MVB12 subunits associate with the core region of the binary TSG101-VPS37 complex through conserved C-terminal sequence elements. Both MVB12 depletion and overexpression inhibit HIV-1 infectivity and induce unusual viral assembly defects, including aberrant virion morphologies and altered viral Gag protein processing. Taken together, these studies define the composition of human ESCRT-I complexes and indicate that the MVB12 subunits play a unique role in regulating ESCRT-mediated virus budding.

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PMID:
18005716
PMCID:
PMC2034311
DOI:
10.1016/j.chom.2007.06.003
[Indexed for MEDLINE]
Free PMC Article

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