Paradoxical interactions between human delta hepatitis agent RNA and the cellular protein kinase PKR

被引:48
作者
Robertson, HD [1 ]
Manche, L [1 ]
Mathews, MB [1 ]
机构
[1] COLD SPRING HARBOR LAB, COLD SPRING HARBOR, NY 11724 USA
关键词
D O I
10.1128/JVI.70.8.5611-5617.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome of the human delta hepatitis agent is a circular, highly structured single-stranded RNA lacking regular runs of RNA-RNA duplex longer than 15 bp. We have tested the ability of delta agent RNA to participate in reactions with a protein containing a motif which confers the ability to bind double-stranded RNA (dsRNA). Surprisingly, highly purified delta agent RNA preparations from which all traces of contaminating dsRNA have been removed activate PKR, the dsRNA-dependent protein kinase activity of mammalian cells (also known as DAI, P1-eIF-2, and p68 kinase). This behavior is in marked contrast to the interaction of PKR with a number of other highly structured viral single-stranded RNAs, which inhibit, rather than stimulate, activation of this kinase. PKR activation leads to inhibition of protein synthesis in the rabbit reticulocyte lysate system. Paradoxically, delta RNA failed to elicit the expected PKR-mediated inhibition of cell-free translation. Instead, delta RNA interfered with PKR activation and the translational block induced by dsRNA. We conclude that the interaction of PKR and delta agent RNA may represent a new category of protein-RNA interactions involving the dsRNA binding motif.
引用
收藏
页码:5611 / 5617
页数:7
相关论文
共 52 条
[1]   BINDING-PROPERTIES OF NEWLY IDENTIFIED XENOPUS PROTEINS CONTAINING DSRNA-BINDING MOTIFS [J].
BASS, BL ;
HURST, SR ;
SINGER, JD .
CURRENT BIOLOGY, 1994, 4 (04) :301-314
[2]   EFFICIENT TRANS-CLEAVAGE AND A COMMON STRUCTURAL MOTIF FOR THE RIBOZYMES OF THE HUMAN HEPATITIS-DELTA AGENT [J].
BRANCH, AD ;
ROBERTSON, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :10163-10167
[3]   AN ULTRAVIOLET-SENSITIVE RNA STRUCTURAL ELEMENT IN A VIROID-LIKE DOMAIN OF THE HEPATITIS DELTA VIRUS [J].
BRANCH, AD ;
BENENFELD, BJ ;
BAROUDY, BM ;
WELLS, FV ;
GERIN, JL ;
ROBERTSON, HD .
SCIENCE, 1989, 243 (4891) :649-652
[4]  
BRANCH AD, 1989, METHOD ENZYMOL, V180, P418
[5]  
BRANCH AD, 1984, SCIENCE, V223, P450, DOI 10.1126/science.6197756
[6]  
BRANCH AD, 1990, SEMIN VIROL, V1, P143
[7]   STRUCTURE AND REPLICATION OF THE GENOME OF THE HEPATITIS DELTA-VIRUS [J].
CHEN, PJ ;
KALPANA, G ;
GOLDBERG, J ;
MASON, W ;
WERNER, B ;
GERIN, J ;
TAYLOR, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (22) :8774-8778
[8]  
CIRCLE DA, UNPUB
[9]   TRANSLATIONAL CONTROL BY THE EPSTEIN-BARR-VIRUS SMALL RNA EBER-1 - REVERSAL OF THE DOUBLE-STRANDED RNA-INDUCED INHIBITION OF PROTEIN-SYNTHESIS IN RETICULOCYTE LYSATES [J].
CLARKE, PA ;
SHARP, NA ;
CLEMENS, MJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 193 (03) :635-641
[10]  
CLARKE PA, 1995, RNA, V1, P7