Eukaryotic translation initiation machinery can operate in a prokaryotic-like mode without eIF2

[1]  N. Sonenberg,et al.  La Autoantigen Is Necessary for Optimal Function of the Poliovirus and Hepatitis C Virus Internal Ribosome Entry Site In Vivo and In Vitro , 2004, Molecular and Cellular Biology.

[2]  I. Shatsky,et al.  Conversion of 48S translation preinitiation complexes into 80S initiation complexes as revealed by toeprinting , 2003, FEBS letters.

[3]  C. Hellen,et al.  The joining of ribosomal subunits in eukaryotes requires eIF5B , 2000, Nature.

[4]  B. Safer,et al.  Role of eukaryotic initiation factor 5 in the formation of 80 S initiation complexes. , 1979, Journal of Biological Chemistry.

[5]  J. Doudna,et al.  Coordinated assembly of human translation initiation complexes by the hepatitis C virus internal ribosome entry site RNA. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[6]  C. Gualerzi,et al.  Initiation factors in the early events of mRNA translation in bacteria. , 2001, Cold Spring Harbor symposia on quantitative biology.

[7]  R. Jackson,et al.  Phosphorylation of initiation factor eIF-2 and the control of reticulocyte protein synthesis , 1977, Cell.

[8]  R. Jackson,et al.  A prokaryotic-like mode of cytoplasmic eukaryotic ribosome binding to the initiation codon during internal translation initiation of hepatitis C and classical swine fever virus RNAs. , 1998, Genes & development.

[9]  Nicolas Locker,et al.  HCV and CSFV IRES domain II mediate eIF2 release during 80S ribosome assembly , 2007, The EMBO journal.

[10]  Matthew H. Brush,et al.  Growth Arrest and DNA Damage-Inducible Protein GADD34 Targets Protein Phosphatase 1α to the Endoplasmic Reticulum and Promotes Dephosphorylation of the α Subunit of Eukaryotic Translation Initiation Factor 2 , 2003, Molecular and Cellular Biology.

[11]  Zhenming Xu,et al.  Triple Decoding of Hepatitis C Virus RNA by Programmed Translational Frameshifting , 2003, Molecular and Cellular Biology.

[12]  D. Ron,et al.  Perk is essential for translational regulation and cell survival during the unfolded protein response. , 2000, Molecular cell.

[13]  Joseph D. Puglisi,et al.  The Pathway of HCV IRES-Mediated Translation Initiation , 2004, Cell.

[14]  B. Safer,et al.  Binding and release of radiolabeled eukaryotic initiation factors 2 and 3 during 80 S initiation complex formation. , 1979, The Journal of biological chemistry.

[15]  A. Koromilas,et al.  PKR-Dependent Mechanisms of Gene Expression from a Subgenomic Hepatitis C Virus Clone , 2002, Journal of Virology.

[16]  J. Pelletier,et al.  Initiation of protein synthesis by hepatitis C virus is refractory to reduced eIF2.GTP.Met-tRNA(i)(Met) ternary complex availability. , 2006, Molecular biology of the cell.

[17]  W. Merrick,et al.  Promotion of met-tRNAiMet binding to ribosomes by yIF2, a bacterial IF2 homolog in yeast. , 1998, Science.

[18]  P. Sarnow,et al.  Initiation factor-independent translation mediated by the hepatitis C virus internal ribosome entry site. , 2006, RNA.

[19]  Randal J. Kaufman,et al.  Heme-regulated Inhibitor Kinase-mediated Phosphorylation of Eukaryotic Translation Initiation Factor 2 Inhibits Translation, Induces Stress Granule Formation, and Mediates Survival upon Arsenite Exposure* , 2005, Journal of Biological Chemistry.

[20]  I. Terenin,et al.  A Leaderless mRNA Can Bind to Mammalian 80S Ribosomes and Direct Polypeptide Synthesis in the Absence of Translation Initiation Factors , 2006, Molecular and Cellular Biology.

[21]  J. Hershey,et al.  2 The Pathway and Mechanism of Initiation of Protein Synthesis , 2000 .

[22]  S. E. Dmitriev,et al.  A Cross-Kingdom Internal Ribosome Entry Site Reveals a Simplified Mode of Internal Ribosome Entry , 2005, Molecular and Cellular Biology.