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Interaction of the phospholipid scramblase 1 with HIV-1 Tat results in the repression of Tat-dependent transcription
被引:23
|作者:
Kusano, Shuichi
[1
]
Eizuru, Yoshito
[1
]
机构:
[1] Kagoshima Univ, Div Persistent & Oncogen Viruses, Ctr Chron Viral Dis, Grad Sch Med & Dent Sci, Kagoshima 8908544, Japan
关键词:
Phospholipid scramblase 1;
HIV-1;
Tat;
Transcription;
PROTEINS SPECIFICALLY INTERACT;
VIRUS-REPLICATION;
DOMAIN PROTEINS;
INTERFERON;
TRANSACTIVATION;
IDENTIFICATION;
REPEATS;
CELLS;
GAMMA;
NOTCH;
D O I:
10.1016/j.bbrc.2013.02.098
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Human phospholipid scramblase 1 (PLSCR1) is an interferon (IFN)-stimulated gene and possesses an IFN-mediated antiviral function. We show here that PLSCR1 directly interacts with human immunodeficiency virus type-1 (HIV-1) Tat. This interaction occurs both in vitro and in vivo through amino acids 160-250 of PLSCR1. Overexpression of PLSCR1 efficiently represses the Tat-dependent transactivation of the HIV-1 long terminal repeat (LTR) and reduces the nuclear translocation of Tat. In addition, shRNA-mediated suppression of endogenous PLSCR1 expression enhances the levels of gag mRNA in an HIV-1-infected T-cell line. These findings indicate that PLSCR1 negatively regulates the Tat-dependent transactivation of the HIV-1 LTR during HIV-1 infection. (C) 2013 Elsevier Inc. All rights reserved.
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页码:438 / 444
页数:7
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