APOBEC4 Enhances the Replication of HIV-1

被引:26
|
作者
Marino, Daniela [1 ,2 ]
Perkovic, Mario [1 ,2 ,7 ]
Hain, Anika [1 ]
Vasudevan, Ananda A. Jaguva [1 ]
Hofmann, Henning [1 ,2 ,8 ]
Hanschmann, Kay-Martin [3 ]
Muehlebach, Michael D. [2 ,4 ]
Schumann, Gerald G. [2 ]
Koenig, Renate [5 ,6 ]
Cichutek, Klaus [2 ]
Haeussinger, Dieter [1 ]
Muenk, Carsten [1 ,2 ]
机构
[1] Univ Dusseldorf, Fac Med, Clin Gastroenterol Hepatol & Infectiol, Dusseldorf, Germany
[2] Paul Ehrlich Inst, Div Med Biotechnol, Langen, Germany
[3] Paul Ehrlich Inst, Biostat, Langen, Germany
[4] Paul Ehrlich Inst, Prod Testing Immunol Med Prod Vet Uses, Langen, Germany
[5] Paul Ehrlich Inst, Host Pathogen Interact, Langen, Germany
[6] Sanford Burnham Prebys Med Discovery Inst, Immun & Pathogenesis Program, La Jolla, CA USA
[7] Johannes Gutenberg Univ Mainz, TRON Translat Oncol Univ Med Ctr, D-55122 Mainz, Germany
[8] Robert Koch Inst, Div HIV & Other Retroviruses, Berlin, Germany
来源
PLOS ONE | 2016年 / 11卷 / 06期
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; RNA EDITING ENZYME; B MESSENGER-RNA; CYTIDINE DEAMINASE AID; CLASS SWITCH RECOMBINATION; MALE GENITAL-TRACT; VIF PROTEIN; IN-SITU; ANTIRETROVIRAL THERAPY; MOLECULAR-CLONING;
D O I
10.1371/journal.pone.0155422
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
APOBEC4 (A4) is a member of the AID/APOBEC family of cytidine deaminases. In this study we found a high mRNA expression of A4 in human testis. In contrast, there were only low levels of A4 mRNA detectable in 293T, HeLa, Jurkat or A3.01 cells. Ectopic expression of A4 in HeLa cells resulted in mostly cytoplasmic localization of the protein. To test whether A4 has antiviral activity similar to that of proteins of the APOBEC3 (A3) subfamily, A4 was co-expressed in 293T cells with wild type HIV-1 and HIV-1 luciferase reporter viruses. We found that A4 did not inhibit the replication of HIV-1 but instead enhanced the production of HIV-1 in a dose-dependent manner and seemed to act on the viral LTR. A4 did not show detectable cytidine deamination activity in vitro and weakly interacted with single-stranded DNA. The presence of A4 in virus producer cells enhanced HIV-1 replication by transiently transfected A4 or stably expressed A4 in HIV-susceptible cells. APOBEC4 was capable of similarly enhancing transcription from a broad spectrum of promoters, regardless of whether they were viral or mammalian. We hypothesize that A4 may have a natural role in modulating host promoters or endogenous LTR promoters.
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页数:23
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