Increasing Rate of Cleavage at Boundary between Non-structural Proteins 4B and 5A Inhibits Replication of Hepatitis C Virus*

Background: Hepatitis C virus replication requires that non-structural (NS) proteins be derived from a cleavable polyprotein precursor. Results: Increasing the rate of processing at an NS cleavage boundary inhibits replication. Conclusion: Some transient NS precursors have a time-dependent function. Significance: The findings are a key reference point for future investigations establishing NS precursor function. In hepatitis C virus, non-structural proteins are cleaved from the viral polyprotein by viral encoded proteases. Although proteolytic processing goes to completion, the rate of cleavage differs between different boundaries, primarily due to the sequence at these positions. However, it is not known whether slow cleavage is important for viral replication or a consequence of restrictions on sequences that can be tolerated at the cleaved ends of non-structural proteins. To address this question, mutations were introduced into the NS4B side of the NS4B5A boundary, and their effect on replication and polyprotein processing was examined in the context of a subgenomic replicon. Single mutations that modestly increased the rate of boundary processing were phenotypically silent, but a double mutation, which further increased the rate of boundary cleavage, was lethal. Rescue experiments relying on viral RNA polymerase-induced error failed to identify second site compensatory mutations. Use of a replicon library with codon degeneracy did allow identification of second site compensatory mutations, some of which fell exclusively within the NS5A side of the boundary. These mutations slowed boundary cleavage and only enhanced replication in the context of the original lethal NS4B double mutation. Overall, the data indicate that slow cleavage of the NS4B5A boundary is important and identify a previously unrecognized role for NS4B5A-containing precursors requiring them to exist for a minimum finite period of time.

[1]  J. Mackenzie,et al.  A Conserved Peptide in West Nile Virus NS4A Protein Contributes to Proteolytic Processing and Is Essential for Replication , 2011, Journal of Virology.

[2]  T. Logan,et al.  A Major Determinant of Cyclophilin Dependence and Cyclosporine Susceptibility of Hepatitis C Virus Identified by a Genetic Approach , 2010, PLoS pathogens.

[3]  F. Penin,et al.  An Amphipathic α-Helix at the C Terminus of Hepatitis C Virus Nonstructural Protein 4B Mediates Membrane Association , 2009, Journal of Virology.

[4]  R. Bartenschlager,et al.  Essential Role of Cyclophilin A for Hepatitis C Virus Replication and Virus Production and Possible Link to Polyprotein Cleavage Kinetics , 2009, PLoS pathogens.

[5]  F. Penin,et al.  Hepatitis C Virus NS5A Protein Is a Substrate for the Peptidyl-prolyl cis/trans Isomerase Activity of Cyclophilins A and B* , 2009, Journal of Biological Chemistry.

[6]  John McLauchlan,et al.  The Hepatitis C Virus NS4B Protein Can trans-Complement Viral RNA Replication and Modulates Production of Infectious Virus , 2008, Journal of Virology.

[7]  J. Arnold,et al.  Picornavirus Genome Replication , 2008, Journal of Biological Chemistry.

[8]  Volker Brass,et al.  Structural determinants for membrane association and dynamic organization of the hepatitis C virus NS3-4A complex , 2008, Proceedings of the National Academy of Sciences.

[9]  K. Blight,et al.  A Genetic Interaction between Hepatitis C Virus NS4B and NS3 Is Important for RNA Replication , 2008, Journal of Virology.

[10]  R. Striker,et al.  Sensitivity of hepatitis C virus to cyclosporine A depends on nonstructural proteins NS5A and NS5B , 2007, Hepatology.

[11]  Yuqiong Liang,et al.  Disruption of innate immunity due to mitochondrial targeting of a picornaviral protease precursor , 2007, Proceedings of the National Academy of Sciences.

[12]  Ralf Bartenschlager,et al.  The Non-structural Protein 4A of Dengue Virus Is an Integral Membrane Protein Inducing Membrane Alterations in a 2K-regulated Manner* , 2007, Journal of Biological Chemistry.

[13]  D. Rowlands,et al.  Tagging of NS5A expressed from a functional hepatitis C virus replicon. , 2006, The Journal of general virology.

[14]  X. Tong,et al.  Trans-complementation of HCV replication by non-structural protein 5A. , 2006, Virus research.

[15]  D. Rowlands,et al.  A link between translation of the hepatitis C virus polyprotein and polymerase function; possible consequences for hyperphosphorylation of NS5A. , 2006, The Journal of general virology.

[16]  Ralf Bartenschlager,et al.  Quantitative Analysis of the Hepatitis C Virus Replication Complex , 2005, Journal of Virology.

[17]  J. McLauchlan,et al.  Mobility of the hepatitis C virus NS4B protein on the endoplasmic reticulum membrane and membrane-associated foci. , 2005, The Journal of general virology.

[18]  R. Bartenschlager,et al.  Efficient Rescue of Hepatitis C Virus RNA Replication by trans-Complementation with Nonstructural Protein 5A , 2005, Journal of Virology.

[19]  C. Rice,et al.  Genetic Interactions between Hepatitis C Virus Replicons , 2004, Journal of Virology.

[20]  S. Lemon,et al.  Conserved C-Terminal Threonine of Hepatitis C Virus NS3 Regulates Autoproteolysis and Prevents Product Inhibition , 2004, Journal of Virology.

[21]  C. Rice,et al.  Amphipathic Helix-Dependent Localization of NS5A Mediates Hepatitis C Virus RNA Replication , 2003, Journal of Virology.

[22]  G. von Heijne,et al.  Topology of the Membrane-Associated Hepatitis C Virus Protein NS4B , 2003, Journal of Virology.

[23]  L. Bianchi,et al.  Expression of Hepatitis C Virus Proteins Induces Distinct Membrane Alterations Including a Candidate Viral Replication Complex , 2002, Journal of Virology.

[24]  Volker Brass,et al.  An Amino-terminal Amphipathic α-Helix Mediates Membrane Association of the Hepatitis C Virus Nonstructural Protein 5A* , 2002, The Journal of Biological Chemistry.

[25]  D. Rowlands,et al.  Efficient delivery and regulable expression of hepatitis C virus full-length and minigenome constructs in hepatocyte-derived cell lines using baculovirus vectors. , 2002, The Journal of general virology.

[26]  B. Malcolm,et al.  Effect of naturally occurring active site mutations on hepatitis C virus NS3 protease specificity , 2001, Proteins.

[27]  S. Jang,et al.  In vivo determination of substrate specificity of hepatitis C virus NS3 protease: genetic assay for site-specific proteolysis. , 2000, Analytical biochemistry.

[28]  Y. Kusov,et al.  Improving Proteolytic Cleavage at the 3A/3B Site of the Hepatitis A Virus Polyprotein Impairs Processing and Particle Formation, and the Impairment Can Be Complemented intrans by 3AB and 3ABC , 1999, Journal of Virology.

[29]  S. Back,et al.  Subcellular localization of hepatitis C viral proteins in mammalian cells , 1999, Archives of Virology.

[30]  B. Semler,et al.  Rescue of Defective Poliovirus RNA Replication by 3AB-Containing Precursor Polyproteins , 1998, Journal of Virology.

[31]  R. Cortese,et al.  Potent peptide inhibitors of human hepatitis C virus NS3 protease are obtained by optimizing the cleavage products. , 1998, Biochemistry.

[32]  H. Kräusslich,et al.  Sequential Steps in Human Immunodeficiency Virus Particle Maturation Revealed by Alterations of Individual Gag Polyprotein Cleavage Sites , 1998, Journal of Virology.

[33]  S. Raybuck,et al.  Mechanistic role of an NS4A peptide cofactor with the truncated NS3 protease of hepatitis C virus: elucidation of the NS4A stimulatory effect via kinetic analysis and inhibitor mapping. , 1997, Biochemistry.

[34]  W. Windsor,et al.  Probing the substrate specificity of hepatitis C virus NS3 serine protease by using synthetic peptides , 1997, Journal of virology.

[35]  P. Mui,et al.  Enhancement of hepatitis C virus NS3 proteinase activity by association with NS4A-specific synthetic peptides: identification of sequence and critical residues of NS4A for the cofactor activity. , 1996, Virology.

[36]  J. Galama,et al.  Mutagenesis of the coxsackie B3 virus 2B/2C cleavage site: determinants of processing efficiency and effects on viral replication , 1996, Journal of virology.

[37]  H. Langen,et al.  Hepatitis C virus core protein: carboxy-terminal boundaries of two processed species suggest cleavage by a signal peptide peptidase. , 1996, Virology.

[38]  A. Urbani,et al.  Activity of purified hepatitis C virus protease NS3 on peptide substrates , 1996, Journal of virology.

[39]  A. Kaplan,et al.  The p2 domain of human immunodeficiency virus type 1 Gag regulates sequential proteolytic processing and is required to produce fully infectious virions , 1994, Journal of virology.

[40]  C. Rice,et al.  Hepatitis C virus NS3 serine proteinase: trans-cleavage requirements and processing kinetics , 1994, Journal of virology.

[41]  K. Shimotohno,et al.  Hepatitis C virus polyprotein processing: kinetics and mutagenic analysis of serine proteinase-dependent cleavage , 1994, Journal of virology.

[42]  C. Rice,et al.  Specificity of the hepatitis C virus NS3 serine protease: effects of substitutions at the 3/4A, 4A/4B, 4B/5A, and 5A/5B cleavage sites on polyprotein processing , 1994, Journal of virology.

[43]  K. Shimotohno,et al.  Two hepatitis C virus glycoprotein E2 products with different C termini , 1994, Journal of virology.

[44]  C. Rice,et al.  Processing in the hepatitis C virus E2-NS2 region: identification of p7 and two distinct E2-specific products with different C termini , 1994, Journal of virology.

[45]  R. Bartenschlager,et al.  Kinetic and structural analyses of hepatitis C virus polyprotein processing , 1994, Journal of virology.

[46]  R. Francesco,et al.  Both NS3 and NS4A are required for proteolytic processing of hepatitis C virus nonstructural proteins , 1994, Journal of virology.

[47]  C. Rice,et al.  A second hepatitis C virus-encoded proteinase. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[48]  N. Kato,et al.  Two distinct proteinase activities required for the processing of a putative nonstructural precursor protein of hepatitis C virus , 1993, Journal of virology.

[49]  R. De Francesco,et al.  NS3 is a serine protease required for processing of hepatitis C virus polyprotein , 1993, Journal of virology.

[50]  C. Rice,et al.  Characterization of the hepatitis C virus-encoded serine proteinase: determination of proteinase-dependent polyprotein cleavage sites , 1993, Journal of virology.

[51]  C. Rice,et al.  Expression and identification of hepatitis C virus polyprotein cleavage products , 1993, Journal of virology.

[52]  N. Kato,et al.  Gene mapping of the putative structural region of the hepatitis C virus genome by in vitro processing analysis. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[53]  J. Tobias,et al.  Universality and structure of the N-end rule. , 1989, The Journal of biological chemistry.

[54]  A. Varshavsky,et al.  In vivo half-life of a protein is a function of its amino-terminal residue. , 1986, Science.