Molecular architecture of the ribosome-bound Hepatitis C Virus internal ribosomal entry site RNA

. 2015 Dec 14 ; 34 (24) : 3042-58. [epub] 20151124

Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid26604301

Internal ribosomal entry sites (IRESs) are structured cis-acting RNAs that drive an alternative, cap-independent translation initiation pathway. They are used by many viruses to hijack the translational machinery of the host cell. IRESs facilitate translation initiation by recruiting and actively manipulating the eukaryotic ribosome using only a subset of canonical initiation factor and IRES transacting factors. Here we present cryo-EM reconstructions of the ribosome 80S- and 40S-bound Hepatitis C Virus (HCV) IRES. The presence of four subpopulations for the 80S•HCV IRES complex reveals dynamic conformational modes of the complex. At a global resolution of 3.9 Å for the most stable complex, a derived atomic model reveals a complex fold of the IRES RNA and molecular details of its interaction with the ribosome. The comparison of obtained structures explains how a modular architecture facilitates mRNA loading and tRNA binding to the P-site. This information provides the structural foundation for understanding the mechanism of HCV IRES RNA-driven translation initiation.

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Adams PD, Afonine PV, Bunkoczi G, Chen VB, Davis IW, Echols N, Headd JJ, Hung LW, Kapral GJ, Grosse‐Kunstleve RW, McCoy AJ, Moriarty NW, Oeffner R, Read RJ, Richardson DC, Richardson JS, Terwilliger TC, Zwart PH (2010) PHENIX: a comprehensive Python‐based system for macromolecular structure solution. Acta Crystallogr D Biol Crystallogr 66: 213–221 PubMed PMC

Anger AM, Armache JP, Berninghausen O, Habeck M, Subklewe M, Wilson DN, Beckmann R (2013) Structures of the human and Drosophila 80S ribosome. Nature 497: 80–85 PubMed

Asnani M, Kumar P, Hellen CU (2015) Widespread distribution and structural diversity of Type IV IRESs in members of Picornaviridae. Virology 478: 61–74 PubMed PMC

Babaylova E, Graifer D, Malygin A, Stahl J, Shatsky I, Karpova G (2009) Positioning of subdomain IIId and apical loop of domain II of the hepatitis C IRES on the human 40S ribosome. Nucleic Acids Res 37: 1141–1151 PubMed PMC

Behrmann E, Loerke J, Budkevich TV, Yamamoto K, Schmidt A, Penczek PA, Vos MR, Burger J, Mielke T, Scheerer P, Spahn CM (2015) Structural snapshots of actively translating human ribosomes. Cell 161: 845–857 PubMed PMC

Ben‐Shem A, Garreau de Loubresse N, Melnikov S, Jenner L, Yusupova G, Yusupov M (2011) The structure of the eukaryotic ribosome at 3.0 A resolution. Science 334: 1524–1529 PubMed

Berry KE, Waghray S, Doudna JA (2010) The HCV IRES pseudoknot positions the initiation codon on the 40S ribosomal subunit. RNA 16: 1559–1569 PubMed PMC

Berry KE, Waghray S, Mortimer SA, Bai Y, Doudna JA (2011) Crystal structure of the HCV IRES central domain reveals strategy for start‐codon positioning. Structure 19: 1456–1466 PubMed PMC

Bhat P, Shwetha S, Sharma DK, Joseph AP, Srinivasan N, Das S (2015) The beta hairpin structure within ribosomal protein S5 mediates interplay between domains II and IV and regulates HCV IRES function. Nucleic Acids Res 43: 2888–2901 PubMed PMC

Boehringer D, Thermann R, Ostareck‐Lederer A, Lewis JD, Stark H (2005) Structure of the hepatitis C virus IRES bound to the human 80S ribosome: remodeling of the HCV IRES. Structure 13: 1695–1706 PubMed

Boerneke MA, Dibrov SM, Gu J, Wyles DL, Hermann T (2014) Functional conservation despite structural divergence in ligand‐responsive RNA switches. Proc Natl Acad Sci USA 111: 15952–15957 PubMed PMC

Budkevich T, Giesebrecht J, Altman RB, Munro JB, Mielke T, Nierhaus KH, Blanchard SC, Spahn CM (2011) Structure and dynamics of the mammalian ribosomal pretranslocation complex. Mol Cell 44: 214–224 PubMed PMC

Budkevich TV, Giesebrecht J, Behrmann E, Loerke J, Ramrath DJ, Mielke T, Ismer J, Hildebrand PW, Tung CS, Nierhaus KH, Sanbonmatsu KY, Spahn CM (2014) Regulation of the mammalian elongation cycle by subunit rolling: a eukaryotic‐specific ribosome rearrangement. Cell 158: 121–131 PubMed PMC

Cate JH, Yusupov MM, Yusupova GZ, Earnest TN, Noller HF (1999) X‐ray crystal structures of 70S ribosome functional complexes. Science 285: 2095–2104 PubMed

Chen JZ, Grigorieff N (2007) SIGNATURE: a single‐particle selection system for molecular electron microscopy. J Struct Biol 157: 168–173 PubMed

Devaraj A, Shoji S, Holbrook ED, Fredrick K (2009) A role for the 30S subunit E site in maintenance of the translational reading frame. RNA 15: 255–265 PubMed PMC

Dibrov SM, Ding K, Brunn ND, Parker MA, Bergdahl BM, Wyles DL, Hermann T (2012) Structure of a hepatitis C virus RNA domain in complex with a translation inhibitor reveals a binding mode reminiscent of riboswitches. Proc Natl Acad Sci USA 109: 5223–5228 PubMed PMC

Dibrov SM, Parsons J, Carnevali M, Zhou S, Rynearson KD, Ding K, Garcia Sega E, Brunn ND, Boerneke MA, Castaldi MP, Hermann T (2014) Hepatitis C virus translation inhibitors targeting the internal ribosomal entry site. J Med Chem 57: 1694–1707 PubMed PMC

Easton LE, Locker N, Lukavsky PJ (2009) Conserved functional domains and a novel tertiary interaction near the pseudoknot drive translational activity of hepatitis C virus and hepatitis C virus‐like internal ribosome entry sites. Nucleic Acids Res 37: 5537–5549 PubMed PMC

Emsley P, Lohkamp B, Scott WG, Cowtan K (2010) Features and development of Coot. Acta Crystallogr D Biol Crystallogr 66: 486–501 PubMed PMC

Filbin ME, Kieft JS (2011) HCV IRES domain IIb affects the configuration of coding RNA in the 40S subunit's decoding groove. RNA 17: 1258–1273 PubMed PMC

Filbin ME, Vollmar BS, Shi D, Gonen T, Kieft JS (2013) HCV IRES manipulates the ribosome to promote the switch from translation initiation to elongation. Nat Struct Mol Biol 20: 150–158 PubMed PMC

Frank J, Radermacher M, Penczek P, Zhu J, Li Y, Ladjadj Leith A (1996) SPIDER and WEB: processing and visualization of images in 3D electron microscopy and related fields. J Struct Biol 116: 190–199 PubMed

Fuchs G, Petrov AN, Marceau CD, Popov LM, Chen J, O'Leary SE, Wang R, Carette JE, Sarnow P, Puglisi JD (2015) Kinetic pathway of 40S ribosomal subunit recruitment to hepatitis C virus internal ribosome entry site. Proc Natl Acad Sci USA 112: 319–325 PubMed PMC

Fukushi S, Okada M, Stahl J, Kageyama T, Hoshino FB, Katayama K (2001) Ribosomal protein S5 interacts with the internal ribosomal entry site of hepatitis C virus. J Biol Chem 276: 20824–20826 PubMed

Hajarizadeh B, Grebely J, Dore GJ (2013) Epidemiology and natural history of HCV infection. Nat Rev Gastroenterol Hepatol 10: 553–562 PubMed

Hashem Y, des Georges A, Dhote V, Langlois R, Liao HY, Grassucci RA, Pestova TV, Hellen CU, Frank J (2013) Hepatitis‐C‐virus‐like internal ribosome entry sites displace eIF3 to gain access to the 40S subunit. Nature 503: 539–543 PubMed PMC

Hellen CU, de Breyne S (2007) A distinct group of hepacivirus/pestivirus‐like internal ribosomal entry sites in members of diverse picornavirus genera: evidence for modular exchange of functional noncoding RNA elements by recombination. J Virol 81: 5850–5863 PubMed PMC

Hohn M, Tang G, Goodyear G, Baldwin PR, Huang Z, Penczek PA, Yang C, Glaeser RM, Adams PD, Ludtke SJ (2007) SPARX, a new environment for Cryo‐EM image processing. J Struct Biol 157: 47–55 PubMed

Honda M, Brown EA, Lemon SM (1996) Stability of a stem‐loop involving the initiator AUG controls the efficiency of internal initiation of translation on hepatitis C virus RNA. RNA 2: 955–968 PubMed PMC

Jackson RJ, Hellen CU, Pestova TV (2010) The mechanism of eukaryotic translation initiation and principles of its regulation. Nat Rev Mol Cell Biol 11: 113–127 PubMed PMC

Ji H, Fraser CS, Yu Y, Leary J, Doudna JA (2004) Coordinated assembly of human translation initiation complexes by the hepatitis C virus internal ribosome entry site RNA. Proc Natl Acad Sci USA 101: 16990–16995 PubMed PMC

Joseph AP, Bhat P, Das S, Srinivasan N (2014) Re‐analysis of cryoEM data on HCV IRES bound to 40S subunit of human ribosome integrated with recent structural information suggests new contact regions between ribosomal proteins and HCV RNA. RNA Biol 11: 891–905 PubMed PMC

Jubin R (2001) Hepatitis C IRES: translating translation into a therapeutic target. Curr Opin Mol Ther 3: 278–287 PubMed

Kalliampakou KI, Psaridi‐Linardaki L, Mavromara P (2002) Mutational analysis of the apical region of domain II of the HCV IRES. FEBS Lett 511: 79–84 PubMed

Keating KS, Pyle AM (2012) RCrane: semi‐automated RNA model building. Acta Crystallogr D Biol Crystallogr 68: 985–995 PubMed PMC

Khatter H, Myasnikov AG, Natchiar SK, Klaholz BP (2015) Structure of the human 80S ribosome. Nature 520: 640–645 PubMed

Kieft JS, Zhou K, Jubin R, Murray MG, Lau JY, Doudna JA (1999) The hepatitis C virus internal ribosome entry site adopts an ion‐ dependent tertiary fold. J Mol Biol 292: 513–529 PubMed

Kieft JS, Zhou K, Jubin R, Doudna JA (2001) Mechanism of ribosome recruitment by hepatitis C IRES RNA. RNA 7: 194–206 PubMed PMC

Kieft JS, Zhou K, Grech A, Jubin R, Doudna JA (2002) Crystal structure of an RNA tertiary domain essential to HCV IRES‐mediated translation initiation. Nat Struct Biol 9: 370–374 PubMed

Klinck R, Westhof E, Walker S, Afshar M, Collier A, Aboul‐Ela F (2000) A potential RNA drug target in the hepatitis C virus internal ribosomal entry site. RNA 6: 1423–1431 PubMed PMC

Kolupaeva VG, Pestova TV, Hellen CU (2000) An enzymatic footprinting analysis of the interaction of 40S ribosomal subunits with the internal ribosomal entry site of hepatitis C virus. J Virol 74: 6242–6250 PubMed PMC

Kucukelbir A, Sigworth FJ, Tagare HD (2014) Quantifying the local resolution of cryo‐EM density maps. Nat Methods 11: 63–65 PubMed PMC

Laing C, Schlick T (2009) Analysis of four‐way junctions in RNA structures. J Mol Biol 390: 547–559 PubMed PMC

Laletina E, Graifer D, Malygin A, Ivanov A, Shatsky I, Karpova G (2006) Proteins surrounding hairpin IIIe of the hepatitis C virus internal ribosome entry site on the human 40S ribosomal subunit. Nucleic Acids Res 34: 2027–2036 PubMed PMC

Lancaster AM, Jan E, Sarnow P (2006) Initiation factor‐independent translation mediated by the hepatitis C virus internal ribosome entry site. RNA 12: 894–902 PubMed PMC

Landry DM, Hertz MI, Thompson SR (2009) RPS25 is essential for translation initiation by the Dicistroviridae and hepatitis C viral IRESs. Genes Dev 23: 2753–2764 PubMed PMC

Locker N, Easton LE, Lukavsky PJ (2007) HCV and CSFV IRES domain II mediate eIF2 release during 80S ribosome assembly. EMBO J 26: 795–805 PubMed PMC

Loerke J, Giesebrecht J, Spahn CM (2010) Multiparticle cryo‐EM of ribosomes. Methods Enzymol 483: 161–177 PubMed

Lukavsky PJ, Otto GA, Lancaster AM, Sarnow P, Puglisi JD (2000) Structures of two RNA domains essential for hepatitis C virus internal ribosome entry site function. Nat Struct Biol 7: 1105–1110 PubMed

Lukavsky PJ, Kim I, Otto GA, Puglisi JD (2003) Structure of HCV IRES domain II determined by NMR. Nat Struct Biol 10: 1033–1038 PubMed

Lukavsky PJ (2009) Structure and function of HCV IRES domains. Virus Res 139: 166–171 PubMed PMC

Luttermann C, Meyers G (2009) The importance of inter‐ and intramolecular base pairing for translation reinitiation on a eukaryotic bicistronic mRNA. Genes Dev 23: 331–344 PubMed PMC

Malygin AA, Kossinova OA, Shatsky IN, Karpova GG (2013a) HCV IRES interacts with the 18S rRNA to activate the 40S ribosome for subsequent steps of translation initiation. Nucleic Acids Res 41: 8706–8714 PubMed PMC

Malygin AA, Shatsky IN, Karpova GG (2013b) Proteins of the human 40S ribosomal subunit involved in hepatitis C IRES binding as revealed from fluorescent labeling. Biochemistry 78: 53–59 PubMed

Matsuda D, Mauro VP (2014) Base pairing between hepatitis C virus RNA and 18S rRNA is required for IRES‐dependent translation initiation in vivo . Proc Natl Acad Sci USA 111: 15385–15389 PubMed PMC

Mindell JA, Grigorieff N (2003) Accurate determination of local defocus and specimen tilt in electron microscopy. J Struct Biol 142: 334–347 PubMed

Muhs M, Yamamoto H, Ismer J, Takaku H, Nashimoto M, Uchiumi T, Nakashima N, Mielke T, Hildebrand PW, Nierhaus KH, Spahn CM (2011) Structural basis for the binding of IRES RNAs to the head of the ribosomal 40S subunit. Nucleic Acids Res 39: 5264–5275 PubMed PMC

Munro JB, Sanbonmatsu KY, Spahn CM, Blanchard SC (2009) Navigating the ribosome's metastable energy landscape. Trends Biochem Sci 34: 390–400 PubMed PMC

Murshudov GN, Skubak P, Lebedev AA, Pannu NS, Steiner RA, Nicholls RA, Winn MD, Long F, Vagin AA (2011) REFMAC5 for the refinement of macromolecular crystal structures. Acta Crystallogr D Biol Crystallogr 67: 355–367 PubMed PMC

Odreman‐Macchioli F, Baralle FE, Buratti E (2001) Mutational analysis of the different bulge regions of hepatitis C virus domain II and their influence on internal ribosome entry site translational ability. J Biol Chem 276: 41648–41655 PubMed

Otto GA, Lukavsky PJ, Lancaster AM, Sarnow P, Puglisi JD (2002) Ribosomal proteins mediate the hepatitis C virus IRES‐HeLa 40S interaction. RNA 8: 913–923 PubMed PMC

Otto GA, Puglisi JD (2004) The pathway of HCV IRES‐mediated translation initiation. Cell 119: 369–380 PubMed

Passmore LA, Schmeing TM, Maag D, Applefield DJ, Acker MG, Algire MA, Lorsch JR, Ramakrishnan V (2007) The eukaryotic translation initiation factors eIF1 and eIF1A induce an open conformation of the 40S ribosome. Mol Cell 26: 41–50 PubMed

Penczek PA, Frank J, Spahn CM (2006) A method of focused classification, based on the bootstrap 3D variance analysis, and its application to EF‐G‐dependent translocation. J Struct Biol 154: 184–194 PubMed

Perard J, Leyrat C, Baudin F, Drouet E, Jamin M (2013) Structure of the full‐length HCV IRES in solution. Nat Commun 4: 1612 PubMed

Pestova TV, Shatsky IN, Fletcher SP, Jackson RJ, Hellen CU (1998) 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. Genes Dev 12: 67–83 PubMed PMC

Pestova TV, de Breyne S, Pisarev AV, Abaeva IS, Hellen CU (2008) eIF2‐dependent and eIF2‐independent modes of initiation on the CSFV IRES: a common role of domain II. EMBO J 27: 1060–1072 PubMed PMC

Pettersen EF, Goddard TD, Huang CC, Couch GS, Greenblatt DM, Meng EC, Ferrin TE (2004) UCSF Chimera–a visualization system for exploratory research and analysis. J Comput Chem 25: 1605–1612 PubMed

Pisarev AV, Unbehaun A, Hellen CU, Pestova TV (2007) Assembly and analysis of eukaryotic translation initiation complexes. Methods Enzymol 430: 147–177 PubMed

Pisarev AV, Kolupaeva VG, Yusupov MM, Hellen CU, Pestova TV (2008) Ribosomal position and contacts of mRNA in eukaryotic translation initiation complexes. EMBO J 27: 1609–1621 PubMed PMC

Quade N, Boehringer D, Leibundgut M, van den Heuvel J, Ban N (2015) Cryo‐EM structure of Hepatitis C virus IRES bound to the human ribosome at 3.9‐A resolution. Nat Commun 6: 7646 PubMed PMC

Ratje AH, Loerke J, Mikolajka A, Brunner M, Hildebrand PW, Starosta AL, Donhofer A, Connell SR, Fucini P, Mielke T, Whitford PC, Onuchic JN, Yu Y, Sanbonmatsu KY, Hartmann RK, Penczek PA, Wilson DN, Spahn CM (2010) Head swivel on the ribosome facilitates translocation by means of intra‐subunit tRNA hybrid sites. Nature 468: 713–716 PubMed PMC

Reynolds JE, Kaminski A, Carroll AR, Clarke BE, Rowlands DJ, Jackson RJ (1996) Internal initiation of translation of hepatitis C virus RNA: the ribosome entry site is at the authentic initiation codon. RNA 2: 867–878 PubMed PMC

Schuler M, Connell SR, Lescoute A, Giesebrecht J, Dabrowski M, Schroeer B, Mielke T, Penczek PA, Westhof E, Spahn CM (2006) Structure of the ribosome‐bound cricket paralysis virus IRES RNA. Nat Struct Mol Biol 13: 1092–1096 PubMed

Siridechadilok B, Fraser CS, Hall RJ, Doudna JA, Nogales E (2005) Structural roles for human translation factor eIF3 in initiation of protein synthesis. Science 310: 1513–1515 PubMed

Sizova DV, Kolupaeva VG, Pestova TV, Shatsky IN, Hellen CU (1998) Specific interaction of eukaryotic translation initiation factor 3 with the 5′ nontranslated regions of hepatitis C virus and classical swine fever virus RNAs. J Virol 72: 4775–4782 PubMed PMC

Spahn CM, Kieft JS, Grassucci RA, Penczek PA, Zhou K, Doudna JA, Frank J (2001) Hepatitis C virus IRES RNA‐induced changes in the conformation of the 40s ribosomal subunit. Science 291: 1959–1962 PubMed

Spahn CM, Jan E, Mulder A, Grassucci RA, Sarnow P, Frank J (2004) Cryo‐EM visualization of a viral internal ribosome entry site bound to human ribosomes: the IRES functions as an RNA‐based translation factor. Cell 118: 465–475 PubMed

Suloway C, Pulokas J, Fellmann D, Cheng A, Guerra F, Quispe J, Stagg S, Potter CS, Carragher B (2005) Automated molecular microscopy: the new Leginon system. J Struct Biol 151: 41–60 PubMed

Terenin IM, Dmitriev SE, Andreev DE, Shatsky IN (2008) Eukaryotic translation initiation machinery can operate in a bacterial‐like mode without eIF2. Nat Struct Mol Biol 15: 836–841 PubMed

Visweswaraiah J, Pittman Y, Dever TE, Hinnebusch AG (2015) The beta‐hairpin of 40S exit channel protein Rps5/uS7 promotes efficient and accurate translation initiation in vivo . Elife 4: e07939 PubMed PMC

Voorhees RM, Fernandez IS, Scheres SH, Hegde RS (2014) Structure of the mammalian ribosome‐Sec61 complex to 3.4 A resolution. Cell 157: 1632–1643 PubMed PMC

Wang C, Le SY, Ali N, Siddiqui A (1995) An RNA pseudoknot is an essential structural element of the internal ribosome entry site located within the hepatitis C virus 5′ noncoding region. RNA 1: 526–537 PubMed PMC

Whitford PC, Ahmed A, Yu Y, Hennelly SP, Tama F, Spahn CM, Onuchic JN, Sanbonmatsu KY (2011) Excited states of ribosome translocation revealed through integrative molecular modeling. Proc Natl Acad Sci USA 108: 18943–18948 PubMed PMC

Willcocks MM, Locker N, Gomwalk Z, Royall E, Bakhshesh M, Belsham GJ, Idamakanti N, Burroughs KD, Reddy PS, Hallenbeck PL, Roberts LO (2011) Structural features of the Seneca Valley virus internal ribosome entry site (IRES) element: a picornavirus with a pestivirus‐like IRES. J Virol 85: 4452–4461 PubMed PMC

Xue S, Tian S, Fujii K, Kladwang W, Das R, Barna M (2015) RNA regulons in Hox 5′ UTRs confer ribosome specificity to gene regulation. Nature 517: 33–38 PubMed PMC

Yamamoto H, Unbehaun A, Loerke J, Behrmann E, Collier M, Burger J, Mielke T, Spahn CM (2014) Structure of the mammalian 80S initiation complex with initiation factor 5B on HCV‐IRES RNA. Nat Struct Mol Biol 21: 721–727 PubMed

Yusupova G, Jenner L, Rees B, Moras D, Yusupov M (2006) Structural basis for messenger RNA movement on the ribosome. Nature 444: 391–394 PubMed

Zinoviev A, Hellen CU, Pestova TV (2015) Multiple mechanisms of reinitiation on bicistronic calicivirus mRNAs. Mol Cell 57: 1059–1073 PubMed PMC

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. 2016 Aug 15 ; 16 (1) : 187. [epub] 20160815

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