POSITIONALLY INDEPENDENT AND EXCHANGEABLE LATE BUDDING FUNCTIONS OF THE ROUS-SARCOMA VIRUS AND HUMAN-IMMUNODEFICIENCY-VIRUS GAG PROTEINS

被引:229
作者
PARENT, LJ
BENNETT, RP
CRAVEN, RC
NELLE, TD
KRISHNA, NK
BOWZARD, JB
WILSON, CB
PUFFER, BA
MONTELARO, RC
WILLS, JW
机构
[1] PENN STATE UNIV,COLL MED,DEPT MICROBIOL & IMMUNOL,HERSHEY,PA 17033
[2] UNIV PITTSBURGH,SCH MED,DEPT MOLEC GENET & BIOCHEM,PITTSBURGH,PA 15261
关键词
D O I
10.1128/JVI.69.9.5455-5460.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Gag proteins of Rous sarcoma virus and human immunodeficiency virus (HIV) each contain a function involved in a late step in budding, defects in which result in the accumulation of these molecules at the plasma membrane. In the Rous sarcoma virus Gag protein (pr76(gag)), this assembly domain is associated with a PPPY motif, which is located at an internal position between the MA and CA sequences. This motif is not contained anywhere within the HIV Gag protein (pr55(gag)), and the MA sequence is linked directly to CA. Instead, a late assembly function of HIV has been associated with the p6 sequence situated at the C terminus of Gag. Here we demonstrate the remarkable finding that the late assembly domains from these two unrelated Gag proteins are exchangeable between retroviruses and can function in a positionally independent manner.
引用
收藏
页码:5455 / 5460
页数:6
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