TAT-RESPONSIVE REGION RNA OF HUMAN IMMUNODEFICIENCY VIRUS-1 CAN PREVENT ACTIVATION OF THE DOUBLE-STRANDED-RNA-ACTIVATED PROTEIN-KINASE

被引:135
作者
GUNNERY, S [1 ]
RICE, AP [1 ]
ROBERTSON, HD [1 ]
MATHEWS, MB [1 ]
机构
[1] CORNELL UNIV,MED CTR,COLL MED,DEPT BIOCHEM,NEW YORK,NY 10021
关键词
eukaryotic initiation factor 2 kinase; interferon; phosphorylation; translational control;
D O I
10.1073/pnas.87.22.8687
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
Transcription from the human immunodeficiency virus type 1 promoter gives rise to short cytoplasmic transcripts of ≃60 nucleotides as well as to longer mRNAs. These RNAs contain the Tat-responsive region sequence, which is capable of assuming a stem-loop structure and has been implicated in the regulation of both transcription and translation. It has been reported that Tat-responsive region RNA inhibits translation in vitro through activation of an interferon-induced protein kinase, the double-stranded-RNA-activated inhibitor, which phosphorylates eukaryotic initiation factor 2. We show that the activation property is due to double-stranded RNA that often contaminates RNA synthesized in vitro using bacteriophage RNA polymerases. After purification, high concentrations of Tat-responsive region RNA inhibit the activation of double-stranded RNA-activated inhibitor, suggesting that it may serve to protect human immunodeficiency virus type 1 infection from a cellular defense mechanism.
引用
收藏
页码:8687 / 8691
页数:5
相关论文
共 58 条
[11]   ACTIVATION OF DOUBLE-STRANDED RNA-DEPENDENT KINASE (DSL) BY THE TAR REGION OF HIV-1 MESSENGER-RNA - A NOVEL TRANSLATIONAL CONTROL MECHANISM [J].
EDERY, I ;
PETRYSHYN, R ;
SONENBERG, N .
CELL, 1989, 56 (02) :303-312
[12]   HIV-1 TAT TRANS-ACTIVATION REQUIRES THE LOOP SEQUENCE WITHIN TAR [J].
FENG, S ;
HOLLAND, EC .
NATURE, 1988, 334 (6178) :165-167
[14]   HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 LTR TATA AND TAR REGION SEQUENCES REQUIRED FOR TRANSCRIPTIONAL REGULATION [J].
GARCIA, JA ;
HARRICH, D ;
SOULTANAKIS, E ;
WU, F ;
MITSUYASU, R ;
GAYNOR, RB .
EMBO JOURNAL, 1989, 8 (03) :765-778
[15]   OMPT ENCODES THE ESCHERICHIA-COLI OUTER-MEMBRANE PROTEASE THAT CLEAVES T7-RNA POLYMERASE DURING PURIFICATION [J].
GRODBERG, J ;
DUNN, JJ .
JOURNAL OF BACTERIOLOGY, 1988, 170 (03) :1245-1253
[16]  
JOHNSTON MI, 1984, INTERFERON MECHANISM, V3, P189
[17]   ANTI-TERMINATION OF TRANSCRIPTION WITHIN THE LONG TERMINAL REPEAT OF HIV-1 BY TAT GENE-PRODUCT [J].
KAO, SY ;
CALMAN, AF ;
LUCIW, PA ;
PETERLIN, BM .
NATURE, 1987, 330 (6147) :489-493
[18]   THE PHOSPHORYLATION STATE OF EUKARYOTIC INITIATION FACTOR-II ALTERS TRANSLATIONAL EFFICIENCY OF SPECIFIC MESSENGER-RNAS [J].
KAUFMAN, RJ ;
DAVIES, MV ;
PATHAK, VK ;
HERSHEY, JWB .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) :946-958
[19]   TRANSLATIONAL CONTROL MEDIATED BY EUKARYOTIC INITIATION FACTOR-II IS RESTRICTED TO SPECIFIC MESSENGER-RNAS IN TRANSFECTED CELLS [J].
KAUFMAN, RJ ;
MURTHA, P .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (04) :1568-1571
[20]   AN ADENOVIRUS MUTANT UNABLE TO EXPRESS VAI-RNA DISPLAYS DIFFERENT GROWTH-RESPONSES AND SENSITIVITY TO INTERFERON IN VARIOUS HOST-CELL LINES [J].
KITAJEWSKI, J ;
SCHNEIDER, RJ ;
SAFER, B ;
SHENK, T .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (12) :4493-4498