Processing of a cellular polypeptide by 3CD proteinase is required for poliovirus ribonucleoprotein complex formation

Journal of Virology

Volumn 71, Issue 1, 1997, Pages 578-585

  Roehl, Holger H ^a   Parsley, Todd B ^a   Ho, Tri V ^a   Semler, Bert L ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; COMPLEMENTARY DNA; POLYPEPTIDE; PROTEINASE; RIBONUCLEOPROTEIN; VIRUS RNA;

ARTICLE; BINDING AFFINITY; COMPLEX FORMATION; CONTROLLED STUDY; GENE DELETION; HELA CELL; HUMAN; HUMAN CELL; MOLECULAR WEIGHT; NONHUMAN; POLIOMYELITIS VIRUS; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN MODIFICATION; PROTEIN PROCESSING; PROTEIN RNA BINDING; RNA REPLICATION; VIRUS CELL INTERACTION; VIRUS REPLICATION;

EID: 0031060513     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/jvi.71.1.578-585.1997     Document Type: Article

References (44)

1. Andino, R., G. E. Rieckhof, and D. Baltimore. 1990. A functional ribonucleoprotein complex forms around the 5′ end of poliovirus RNA. Cell 63:369-380.
2. Audino, R., G. E. Rieckhof, P. L. Achacoso, and D. Baltimore. 1993. Poliovirus RNA synthesis utilizes an RNP complex formed around the 5′-end of viral RNA. EMBO J. 12:3587-3598.
3. Bernstein, H. D., N. Sonenberg, and D. Baltimore. 1985. Poliovirus mutant that does not selectively inhibit host cell protein synthesis. Mol. Cell. Biol. 5:2913-2923.
4. Blair, W. S., X. Li, and B. L. Semler. 1993. A cellular cofactor facilitates efficient 3CD cleavage of the poliovirus P1 precursor. J. Virol. 67:2336-2343.
5. Blair, W. S., J. H. C. Nguyen, T. B. Parsley, and B. L. Semler. 1996. Mutations in the poliovirus 3CD proteinase S1-specificity pocket affect substrate recognition and RNA binding. Virology 218:1-13.
6. Blyn, L. B., K. M. Swiderek, O. C. Richards, D. C. Stahl, B. L. Semler, and E. Ehrenfeld. 1996. Poly (rC) binding protein 2 binds to stem-loop IV of the poliovirus RNA 5′ noncoding region: identification by automated LC-tandem mass spectrometry. Proc. Natl. Acad. Sci. USA 93:11115-11120.
7. Buckley, B., and E. Ehrenfeld. 1987. The cap-binding protein complex in uninfected and poliovirus-infccted HeLa cells. J. Biol. Chem. 262:13599-13606.
8. Charini, W. A., C. C. Burns, E. Ehrenfeld, and B. L. Semler. 1991. trans rescue of a mutant poliovirus RNA polymerase function. J. Virol. 65:2655-2665.
9. Clark, M. E., T. Hämmerle, E. Wimmer, and A. Dasgupta. 1991. Poliovirus proteinase 3C converts an active form of transcription factor IIIC to an inactive form: a mechanism for inhibition of host cell polymerase III transcription by poliovirus. EMBO J. 10:2941-2947.
10. Clark, M. E., P. M. Lieberman, A. J. Berk, and A. Dasgupta. 1993. Direct cleavage of human TATA-binding protein by poliovirus protease 3C in vivo and in vitro. Mol. Cell. Biol. 13:1232-1237.
11. Dewalt, P. G., and B. L. Semler. 1987. Site-directed mutagenesis of proteinase 3C results in a poliovirus deficient in synthesis of viral RNA polymerase. J. Virol. 61:2162-2170.
12. Etchison, D., S. C. Milburn, I. Edery, N. Sonenberg, and J. W. Hershey. 1982. Inhibition of HeLa cell protein synthesis following poliovirus infection correlates with the proteolysis of a 220,000-dalton polypeptide associated with eucaryotic initiation factor 3 and a cap binding protein complex. J. Biol. Chem. 257:14806-14810.
13. Falk, M. M., P. R. Grigera, I. E. Bergmann, A. Zibert, G. Multhaup, and E. Beck. 1990. Foot-and-mouth disease virus protease 3C induces specific proteolytic cleavage of host cell histone H3. J. Virol. 64:748-756.
14. Favaloro, J., R. Treisman, and R. Kamen. 1980. Transcription maps of polyoma virus-specific RNA: analysis by two-dimensional nuclease S1 gel mapping. Methods Enzymol. 65:718-749.
15. Furuya, T., and M. M. Lai. 1993. Three different cellular proteins bind to complementary sites on the 5′-end-positive and 3′-end-negative strands of mouse hepatitis virus RNA. J. Virol. 67:7215-7222.
16. Haller, A. A., and B. L. Semler. 1992. Linker scanning mutagenesis of the internal ribosome entry site of poliovirus RNA. J. Virol. 66:5075-5086.
17. Haller, A. A., J. H. C. Nguyen, and B. L. Semler. 1993. Minimum internal ribosome entry site required for poliovirus infectivity. J. Virol. 67:7461-7471.
18. Harris, K. S., W. Xiang, L. Alexander, W. S. Lane, A. V. Paul, and E. Wimmer. 1994. Interaction of poliovirus polypeptide 3CDpro with the 5′ and 3′ termini of the poliovirus genome. Identification of viral and cellular cofactors needed for efficient binding. J. Biol. Chem. 269:27004-27014.
19. Joachims, M., K. S. Harris, and D. Etchison. 1995. Poliovirus protease 3C mediates cleavage of microtubule-associated protein 4. Virology 211:451-461.
20. Kaariainen, L., and M. Ranki. 1984. Inhibition of cell functions by RNA-virus infections. Annu. Rev. Microbiol. 38:91-109.
21. Kräusslich, H. G., M. J. Nicklin, H. Toyoda, D. Etchison, and E. Wimmer. 1987. Poliovirus proteinase 2A induces cleavage of eucaryotic initiation factor 4F polypeptide p220. J. Virol. 61:2711-2718.
22. La Monica, N., C. Meriam, and V. R. Racaniello. 1986. Mapping of sequences required for mouse neurovirulence of poliovirus type 2 Lansing. J. Virol. 57:515-525.
23. Leffers, H., K. Dejgaard, and J. E. Celis. 1995. Characterisation of two major cellular poly(rC)-binding human proteins, each containing three K-homologous (KH) domains. Eur. J. Biochem. 230:447-453.
24. Liebig, H. D., E. Ziegler, R. Yan, K. Hartmuth, H. Klump, H. Kowalski, D. Blaas, W. Sommergruber, L. Frasel, B. Lamphear, R. Rhoads, E. Kuechler, and T. Skern. 1993. Purification of two picornaviral 2A proteinases: interaction with eIF-4 gamma and influence on in vitro translation. Biochemistry 32:7581-7588.
25. Lloyd, R. E., M. J. Grubman, and E. Ehrenfeld. 1988. Relationship of p220 cleavage during picornavirus infection to 2A proteinase sequences. J. Virol. 62:4216-4223.
26. Nguyen, J. H. C., and B. L. Semler. Unpublished data.
27. Parsley, T. B., L. B. Blyn, E. Ehrenfeld, and B. L. Semler. Unpublished data.
28. Pelletier, J., G. Kaplan, V. R. Racaniello, and N. Sonenberg. 1988. Cap-independent translation of poliovirus mRNA is conferred by sequence elements within the 5′ noncoding region. Mol. Cell. Biol. 8:1103-1112.
29. Pelletier, J., and N. Sonenberg. 1988. Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA. Nature 334:320-325.
30. Racaniello, V. R., and C. Meriam. 1986. Poliovirus temperature-sensitive mutant containing a single nucleotide deletion in the 5′-noncoding region of the viral RNA. Virology 155:498-507.
31. Rivera, V. M., J. D. Welsh, and J. V. Maizel. 1988. Comparative sequence analysis of the 5′ noncoding region of the enteroviruses and rhinoviruses. Virology 165:42-50.
32. Roehl, H. H., M. M. Anderson, C. S. Mehigh, and S. E. Conrad. 1993. Regulation of the cellular thymidine kinase gene promoter in simian virus 40-infected cells. J. Virol. 67:4964-4971.
33. Roehl, H. H., and B. L. Semler. 1994. In vitro biochemical methods for investigating RNA-protein interactions in picornaviruses, p. 169-182. In K. W. Adolph (ed.), Methods in Molecular Genetics, vol. 4. Academic Press, Inc., Orlando, Fla.
34. Roehl, H. H., and B. L. Semler. 1995. Poliovirus infection enhances the formation of two ribonucleoprotein complexes at the 3′ end of viral negative-strand RNA. J. Virol. 69:2954-2961.
35. Roehl, H. H., J. S. Towner, and B. L. Semler. Unpublished data.
36. Rubinstein, S. J., and A. Dasgupta. 1989. Inhibition of rRNA synthesis by poliovirus: specific inactivation of transcription factors. J. Virol. 63:4689-4696.
37. Sarnow, P. 1989. Translation of glucose-regulated protein 78/immunoglobulin heavy-chain binding protein mRNA is increased in poliovirus-infected cells at a time when cap-dependent translation of cellular mRNAs is inhibited. Proc. Natl. Acad. Sci. USA 86:5795-5799.
38. Semler, B. L., V. H. Johnson, P. G. Dewalt, and M. F. Ypma-Wong. 1987. Site-specific mutagenesis of cDNA clones expressing a poliovirus proteinase. J. Cell Biochem. 33:39-51.
39. Simoes, E. A., and P. Sarnow. 1991. An RNA hairpin at the extreme 5′ end of the poliovirus RNA genome modulates viral translation in human cells. J. Virol. 65:913-921.
40. Skinner, M. A., V. R. Racaniello, G. Dunn, J. Cooper, P. D. Minor, and J. W. Almond. 1989. New model for the secondary structure of the 5′ noncoding RNA of poliovirus is supported by biochemical and genetic data that also show that RNA secondary structure is important in neurovirulence. J. Mol. Biol. 207:379-392.
41. Tesar, M., and O. Marquardt. 1990. Foot-and-mouth disease virus protease 3C inhibits cellular transcription and mediates cleavage of histone H3. Virology 174:364-374.
42. Trono, D., R. Andino, and D. Baltimore. 1988. An RNA sequence of hundreds of nucleotides at the 5′ end of poliovirus RNA is involved in allowing viral protein synthesis. J. Virol. 62:2291-2299.
43. Walker, C., M. Selby, A. Erickson, D. Cataldo, J. P. Valensi, and G. V. Van Nest. 1992. Cationic lipids direct a viral glycoprotein into the class I major histocompatibility complex antigen-presentation pathway. Proc. Natl. Acad. Sci. USA 89:7915-7918.
44. Zuker, M. 1989. On finding all suboptimal foldings of an RNA molecule. Science 244:48-52.