Structure
Volume 5, Issue 8, 15 August 1997, Pages 1109-1122
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Research Article
Structure of the RNA-dependent RNA polymerase of poliovirus

https://doi.org/10.1016/S0969-2126(97)00261-XGet rights and content
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Abstract

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 Å 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.

Keywords

oligomerization
picornavirus
replicase
RNA-recognition motif
viral replication

Cited by (0)

JL Hansen and SC Schultz, Campus Box 215, Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA.

E-mail address for SC Schultz (corresponding author): [email protected].

AM Long, Vertex Pharmaceuticals, 130 Waverly Street, Cambridge, MA 02139, USA.