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

被引:92
作者
Morita, Eiji
Sandrin, Virginie
Alam, Steven L.
Eckert, Debra M.
Gygi, Steven P.
Sundquist, Wesley I. [1 ]
机构
[1] Univ Utah, Dept Biochem, Salt Lake City, UT 84112 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.chom.2007.06.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human ESCRT-1 is a multiprotein complex that plays essential roles in HIV budding and endosomal protein sorting. All ESCRT-1 complexes contain three common subunits (TSG101, VPS28, and VPS37), and a fourth subunit of yeast ESCRT-1 was recently identified (Mvb12p). We now demonstrate that two related human proteins (MVB12A and MVB12B) constitute the fourth class of metazoan ESCRT-1 subunits, despite lacking identifiable sequence homology to Mvb12p. Hydrodynamic studies indicate that soluble human ESCRT-1 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-1 complexes and indicate that the MVB12 subunits play a unique role in regulating ESCRT-mediated virus budding.
引用
收藏
页码:41 / 53
页数:13
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