Identification of Critical Motifs within HIV-1 Integrase Required for Importin α3 Interaction and Viral cDNA Nuclear Import

被引:25
作者
Jayappa, Kallesh Danappa [1 ]
Ao, Zhujun [1 ]
Yang, Ming [2 ]
Wang, Junzhi [3 ]
Yao, Xiaojian [1 ]
机构
[1] Univ Manitoba, Lab Mol Human Retrovirol, Dept Med Microbiol, Fac Med, Winnipeg, MB R3E 0J9, Canada
[2] Peking Univ Hlth Sci Ctr, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
[3] Natl Inst Control Pharmaceut & Biol Prod, Beijing 100050, Peoples R China
基金
加拿大健康研究院;
关键词
integrase; importin alpha 3; HIV-1 nuclear import; nuclear localization signal; NLS binding grooves; HUMAN-IMMUNODEFICIENCY-VIRUS; CENTRAL DNA FLAP; AMINO-ACID-RESIDUES; REVERSE TRANSCRIPTION COMPLEXES; CATALYTIC CORE DOMAIN; TYPE-1; INTEGRASE; NONDIVIDING CELLS; LOCALIZATION SIGNAL; MATRIX PROTEIN; PREINTEGRATION COMPLEX;
D O I
10.1016/j.jmb.2011.04.011
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
The viral cDNA nuclear import is an important requirement for human immunodeficiency virus type 1 (HIV-1) replication in dividing and nondividing cells. Our recent study identified a specific interaction of importin alpha 3 (Imp alpha 3) with HIV-1 integrase (IN) and its involvement in viral cDNA nuclear import. In this study, we have performed a more detailed investigation on the molecular mechanism of how HIV-1 IN interacts with Imp alpha 3. Our results revealed a reduced interaction between the two IN mutants lNKK215,9AA(IN215,9) and INRK263,4AA (IN263,4) with Imp alpha 3, while an IN double mutant, IN215,9/263,4,was severely impaired for its Imp alpha 3-binding ability, even though it was still found interacting with other cofactors, IN interactor I and Transportin3. Immunostaining and fractionation analysis have shown that YFP-IN215,9/263,4 failed to localize in the nucleus of transfected cells. Also, we found that both major and minor nuclear localization signal binding grooves of Imp alpha 3 are involved in interaction with IN. All of these results suggest a cargo protein import receptor type of interaction. Finally, the effect of IN215,9/263,4 mutations on HIV-1 replication was evaluated, and real-time quantitative PCR analysis showed that, while mutant virus (v215,9/263,4) had a slightly lowered total viral DNA, the 2-long-terminal-repeat DNA, a marker for nuclear import, was greatly reduced during v215,9/263,4 infection in both dividing and nondividing cells. Also, by cell fractionation assay, we found that a significant proportion of viral cDNA was still retained in cytoplasmic fraction of v215,9/263,4-infected cells. Overall, our study provides strong evidence that (211)KELQKQITK and (262)RRKAK regions of IN C-terminal domain are required for Imp alpha 3 interaction and HIV-1 cDNA nuclear import. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:847 / 862
页数:16
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