Structure of the RNA-dependent RNA polymerase of poliovirus

被引:359
作者
Hansen, JL
Long, AM
Schultz, SC
机构
[1] UNIV COLORADO, DEPT CHEM & BIOCHEM, BOULDER, CO 80309 USA
[2] VERTEX PHARMACEUT, CAMBRIDGE, MA 02139 USA
关键词
oligomerization; picornavirus; replicase; RNA-recognition motif; viral replication;
D O I
10.1016/S0969-2126(97)00261-X
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
Background: The central player in the replication of RNA Viruses is the viral RNA-dependent RNA polymerase. The 53 kDa poliovirus polymerase, together with other viral and possibly host proteins, carries out viral RNA replication in the host cell cytoplasm. RNA-dependent RNA polymerases comprise a distinct category of polymerases that have limited sequence similarity to reverse transcriptases (RNA-dependent DNA polymerases) and perhaps also to DNA-dependent polymerases, Previously reported structures of RNA-dependent DNA polymerases, DNA-dependent DNA polymerases and a DNA-dependent RNA polymerase show that structural and evolutionary relationships exist between the different polymerase categories. Results: We have determined the structure of the RNA-dependent RNA polymerase of poliovirus at 2.6 Angstrom resolution by X-ray crystallography. It has the same overall shape as other polymerases, commonly described by analogy to a right hand. The structures of the 'fingers' and 'thumb' subdomains of poliovirus polymerase differ from those of other polymerases, but the palm subdomain contains a core structure very similar to that of other polymerases. This conserved core structure is composed of four of the amino acid sequence motifs described for RNA-dependent polymerases. Structure-based alignments of these motifs has enabled us to modify and extend previous sequence and structural alignments so as to relate sequence conservation to function. Extensive regions of polymerase-polymerase interactions observed in the crystals suggest an unusual higher order structure that we believe is important for polymerase function. Conclusions: As a first example of a structure of an RNA-dependent RNA polymerase, the poliovirus polymerase structure provides for a better understanding of polymerase structure, function and evolution. In addition, it has yielded insights into an unusual higher order structure that may be critical for poliovirus polymerase function.
引用
收藏
页码:1109 / 1122
页数:14
相关论文
共 61 条
[1]   SIMILARITY IN GENE ORGANIZATION AND HOMOLOGY BETWEEN PROTEINS OF ANIMAL PICORNAVIRUSES AND A PLANT COMOVIRUS SUGGEST COMMON ANCESTRY OF THESE VIRUS FAMILIES [J].
ARGOS, P ;
KAMER, G ;
NICKLIN, MJH ;
WIMMER, E .
NUCLEIC ACIDS RESEARCH, 1984, 12 (18) :7251-7267
[2]   A SEQUENCE MOTIF IN MANY POLYMERASES [J].
ARGOS, P .
NUCLEIC ACIDS RESEARCH, 1988, 16 (21) :9909-9916
[3]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[4]   POLIOVIRUS-INDUCED RNA POLYMERASE AND EFFECTS OF VIRUS-SPECIFIC INHIBITORS ON ITS PRODUCTION [J].
BALTIMORE, D ;
FRANKLIN, RM ;
TAMM, I ;
EGGERS, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1963, 49 (06) :843-&
[5]   STRUCTURAL BASIS FOR THE 3'-5' EXONUCLEASE ACTIVITY OF ESCHERICHIA-COLI DNA-POLYMERASE-I - A 2 METAL-ION MECHANISM [J].
BEESE, LS ;
STEITZ, TA .
EMBO JOURNAL, 1991, 10 (01) :25-33
[6]   STRUCTURE OF DNA-POLYMERASE-I KLENOW FRAGMENT BOUND TO DUPLEX DNA [J].
BEESE, LS ;
DERBYSHIRE, V ;
STEITZ, TA .
SCIENCE, 1993, 260 (5106) :352-355
[7]   RELATIONSHIPS AMONG THE POSITIVE STRAND AND DOUBLE-STRAND RNA VIRUSES AS VIEWED THROUGH THEIR RNA-DEPENDENT RNA-POLYMERASES [J].
BRUENN, JA .
NUCLEIC ACIDS RESEARCH, 1991, 19 (02) :217-226
[8]  
Brunger A. T., 1993, X PLOR MANUAL VERSIO
[9]   ASSESSMENT OF PHASE ACCURACY BY CROSS VALIDATION - THE FREE R-VALUE - METHODS AND APPLICATIONS [J].
BRUNGER, AT .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1993, 49 :24-36
[10]   ROLE OF CYTOPLASMIC MEMBRANES IN POLIOVIRUS BIOSYNTHESIS [J].
CALIGUIRI, LA ;
TAMM, I .
VIROLOGY, 1970, 42 (01) :100-+