Human GLI-2 is a Tat activation response element-independent Tat cofactor

被引:6
作者
Browning, CM
Smith, MJ
Clark, NM
Lane, BR
Parada, C
Montano, M
Kewalramani, VN
Littman, DR
Essex, M
Roeder, RG
Markovitz, DM
机构
[1] Univ Michigan, Med Ctr, Dept Immunol & Microbiol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Ctr, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USA
[3] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10021 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Harvard AIDS Inst, Boston, MA 02115 USA
[5] NYU, Med Ctr, Howard Hughes Med Inst, New York, NY 10016 USA
[6] NYU, Med Ctr, Skirball Inst Biomol Med, New York, NY 10016 USA
关键词
D O I
10.1128/JVI.75.5.2314-2323.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Zinc finger-containing GLI proteins are involved in the development of Caenorhabditis elegans, Xenopus, Drosophila, zebrafish, mice, and humans. In this study, we show that an isoform of human GLI-2 strongly synergizes with the Tat transactivating proteins of human immunodeficiency virus types 1 and 2 (HIV-1 and -2) and markedly stimulates viral replication. GLI-2 also synergizes with the previously described Tat cofactor cyclin T1 to stimulate Tat function. Surprisingly, GLI-2/Tat synergy is not dependent on either a typical GLI DNA binding site or an intact Tat activation response element but does require an intact TATA box. Thus, GLI-2/Tat synergy results from a mechanism of action which is novel both for a GLI protein and for a Tat cofactor. These findings link the GLI family of transcriptional and developmental regulatory proteins to Tat function and HIV replication.
引用
收藏
页码:2314 / 2323
页数:10
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