Selective Translation Complex Profiling Reveals Staged Initiation and Co-translational Assembly of Initiation Factor Complexes
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
Wellcome Trust - United Kingdom
090812/B/09/Z
Wellcome Trust - United Kingdom
PubMed
32589964
PubMed Central
PMC7447980
DOI
10.1016/j.molcel.2020.06.004
PII: S1097-2765(20)30389-0
Knihovny.cz E-zdroje
- Klíčová slova
- ATF4, GCN4, Ribo-seq, TCP-seq, UTR, co-translational assembly, eIF2, eIF3, gene expression, mRNA, ribosome, ribosome profiling, translational control,
- MeSH
- 5' nepřekládaná oblast MeSH
- eukaryotický iniciační faktor 2 genetika metabolismus MeSH
- eukaryotický iniciační faktor 3 genetika metabolismus MeSH
- HEK293 buňky MeSH
- iniciační faktory genetika metabolismus MeSH
- kodon iniciační MeSH
- lidé MeSH
- malé podjednotky ribozomu eukaryotické genetika metabolismus MeSH
- multiproteinové komplexy genetika metabolismus MeSH
- proteosyntéza * MeSH
- ribozomy genetika metabolismus MeSH
- Saccharomyces cerevisiae - proteiny genetika metabolismus MeSH
- Saccharomyces cerevisiae genetika MeSH
- transkripční faktor ATF4 genetika metabolismus MeSH
- transkripční faktory bZIP genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 5' nepřekládaná oblast MeSH
- ATF4 protein, human MeSH Prohlížeč
- eukaryotický iniciační faktor 2 MeSH
- eukaryotický iniciační faktor 3 MeSH
- GCN4 protein, S cerevisiae MeSH Prohlížeč
- iniciační faktory MeSH
- kodon iniciační MeSH
- multiproteinové komplexy MeSH
- Saccharomyces cerevisiae - proteiny MeSH
- transkripční faktor ATF4 MeSH
- transkripční faktory bZIP MeSH
Translational control targeting the initiation phase is central to the regulation of gene expression. Understanding all of its aspects requires substantial technological advancements. Here we modified yeast translation complex profile sequencing (TCP-seq), related to ribosome profiling, and adapted it for mammalian cells. Human TCP-seq, capable of capturing footprints of 40S subunits (40Ss) in addition to 80S ribosomes (80Ss), revealed that mammalian and yeast 40Ss distribute similarly across 5'TRs, indicating considerable evolutionary conservation. We further developed yeast and human selective TCP-seq (Sel-TCP-seq), enabling selection of 40Ss and 80Ss associated with immuno-targeted factors. Sel-TCP-seq demonstrated that eIF2 and eIF3 travel along 5' UTRs with scanning 40Ss to successively dissociate upon AUG recognition; notably, a proportion of eIF3 lingers on during the initial elongation cycles. Highlighting Sel-TCP-seq versatility, we also identified four initiating 48S conformational intermediates, provided novel insights into ATF4 and GCN4 mRNA translational control, and demonstrated co-translational assembly of initiation factor complexes.
Zobrazit více v PubMed
Anders S., Pyl P.T., Huber W. HTSeq--a Python framework to work with high-throughput sequencing data. Bioinformatics. 2015;31:166–169. PubMed PMC
Archer S.K., Shirokikh N.E., Beilharz T.H., Preiss T. Dynamics of ribosome scanning and recycling revealed by translation complex profiling. Nature. 2016;535:570–574. PubMed
Asano K., Phan L., Anderson J., Hinnebusch A.G. Complex formation by all five homologues of mammalian translation initiation factor 3 subunits from yeast Saccharomyces cerevisiae. J. Biol. Chem. 1998;273:18573–18585. PubMed
Asano K., Phan L., Valásek L., Schoenfeld L.W., Shalev A., Clayton J., Nielsen K., Donahue T.F., Hinnebusch A.G. A multifactor complex of eIF1, eIF2, eIF3, eIF5, and tRNA(i)Met promotes initiation complex assembly and couples GTP hydrolysis to AUG recognition. Cold Spring Harb. Symp. Quant. Biol. 2001;66:403–415. PubMed
Asano K., Shalev A., Phan L., Nielsen K., Clayton J., Valásek L., Donahue T.F., Hinnebusch A.G. Multiple roles for the C-terminal domain of eIF5 in translation initiation complex assembly and GTPase activation. EMBO J. 2001;20:2326–2337. PubMed PMC
Beznosková P., Cuchalová L., Wagner S., Shoemaker C.J., Gunišová S., von der Haar T., Valášek L.S. Translation initiation factors eIF3 and HCR1 control translation termination and stop codon read-through in yeast cells. PLoS Genet. 2013;9:e1003962. PubMed PMC
Beznosková P., Wagner S., Jansen M.E., von der Haar T., Valášek L.S. Translation initiation factor eIF3 promotes programmed stop codon readthrough. Nucleic Acids Res. 2015;43:5099–5111. PubMed PMC
Bhushan S., Gartmann M., Halic M., Armache J.P., Jarasch A., Mielke T., Berninghausen O., Wilson D.N., Beckmann R. α-Helical nascent polypeptide chains visualized within distinct regions of the ribosomal exit tunnel. Nat. Struct. Mol. Biol. 2010;17:313–317. PubMed
Bohlen J., Fenzi K., Kramenr G., Bukau B., Teleman A.A. Selective 40S Footprinting Reveals Cap-Tethered Ribosome Scanning in Human Cells. Mol. Cell. 2020;79:561–574. PubMed
Cate J.H. Human eIF3: from ‘blobology’ to biological insight. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2017;372:20160176. PubMed PMC
Cigan A.M., Foiani M., Hannig E.M., Hinnebusch A.G. Complex formation by positive and negative translational regulators of GCN4. Mol. Cell. Biol. 1991;11:3217–3228. PubMed PMC
Dennis M.D., Person M.D., Browning K.S. Phosphorylation of plant translation initiation factors by CK2 enhances the in vitro interaction of multifactor complex components. J. Biol. Chem. 2009;284:20615–20628. PubMed PMC
Gomes-Duarte A., Lacerda R., Menezes J., Romão L. eIF3: a factor for human health and disease. RNA Biol. 2018;15:26–34. PubMed PMC
Grant C.M., Miller P.F., Hinnebusch A.G. Requirements for intercistronic distance and level of eukaryotic initiation factor 2 activity in reinitiation on GCN4 mRNA vary with the downstream cistron. Mol. Cell. Biol. 1994;14:2616–2628. PubMed PMC
Gunišová S., Valášek L.S. Fail-safe mechanism of GCN4 translational control--uORF2 promotes reinitiation by analogous mechanism to uORF1 and thus secures its key role in GCN4 expression. Nucleic Acids Res. 2014;42:5880–5893. PubMed PMC
Gunišová S., Beznosková P., Mohammad M.P., Vlčková V., Valášek L.S. In-depth analysis of cis-determinants that either promote or inhibit reinitiation on GCN4 mRNA after translation of its four short uORFs. RNA. 2016;22:542–558. PubMed PMC
Gunišová S., Hronová V., Mohammad M.P., Hinnebusch A.G., Valášek L.S. Please do not recycle! Translation reinitiation in microbes and higher eukaryotes. FEMS Microbiol. Rev. 2018;42:165–192. PubMed PMC
Guydosh N.R., Green R. Dom34 rescues ribosomes in 3′ untranslated regions. Cell. 2014;156:950–962. PubMed PMC
Hellen C.U.T. Translation Termination and Ribosome Recycling in Eukaryotes. Cold Spring Harb. Perspect. Biol. 2018;10:a032656. PubMed PMC
Hinnebusch A.G. Translational regulation of GCN4 and the general amino acid control of yeast. Annu. Rev. Microbiol. 2005;59:407–450. PubMed
Hinnebusch A.G. The scanning mechanism of eukaryotic translation initiation. Annu. Rev. Biochem. 2014;83:779–812. PubMed
Hinnebusch A.G. Structural Insights into the Mechanism of Scanning and Start Codon Recognition in Eukaryotic Translation Initiation. Trends Biochem. Sci. 2017;42:589–611. PubMed
Hronová V., Mohammad M.P., Wagner S., Pánek J., Gunišová S., Zeman J., Poncová K., Valášek L.S. Does eIF3 promote reinitiation after translation of short upstream ORFs also in mammalian cells? RNA Biol. 2017;14:1660–1667. PubMed PMC
Hunter J.D. Matplotlib: A 2D Graphics Environment. Comput. Sci. Eng. 2007;9:90–95.
Ingolia N.T. Genome-wide translational profiling by ribosome footprinting. Methods Enzymol. 2010;470:119–142. PubMed
Ingolia N.T., Ghaemmaghami S., Newman J.R.S., Weissman J.S. Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling. Science. 2009;324:218–223. PubMed PMC
Ingolia N.T., Brar G.A., Rouskin S., McGeachy A.M., Weissman J.S. The ribosome profiling strategy for monitoring translation in vivo by deep sequencing of ribosome-protected mRNA fragments. Nat. Protoc. 2012;7:1534–1550. PubMed PMC
Ingolia N.T., Hussmann J.A., Weissman J.S. Ribosome Profiling: Global Views of Translation. Cold Spring Harb. Perspect. Biol. 2019;11:a032698. PubMed PMC
Langmead B., Salzberg S.L. Fast gapped-read alignment with Bowtie 2. Nat. Methods. 2012;9:357–359. PubMed PMC
Langmead B., Trapnell C., Pop M., Salzberg S.L. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009;10:R25. PubMed PMC
Lareau L.F., Hite D.H., Hogan G.J., Brown P.O. Distinct stages of the translation elongation cycle revealed by sequencing ribosome-protected mRNA fragments. eLife. 2014;3:e01257. PubMed PMC
Li H., Handsaker B., Wysoker A., Fennell T., Ruan J., Homer N., Marth G., Abecasis G., Durbin R., 1000 Genome Project Data Processing Subgroup The Sequence Alignment/Map format and SAMtools. Bioinformatics. 2009;25:2078–2079. PubMed PMC
Lin Y., Li F., Huang L., Duan H., Fang J., Sun L., Xin X., Tian G., Cheng Y., Yang X., Wolf D.A. eIF3 associates with 80S ribosomes to promote translation elongation, mitochondrial homeostasis, and muscle health. Mol. Cell. 2020;79:575–587. PubMed
Llácer J.L., Hussain T., Marler L., Aitken C.E., Thakur A., Lorsch J.R., Hinnebusch A.G., Ramakrishnan V. Conformational Differences between Open and Closed States of the Eukaryotic Translation Initiation Complex. Mol. Cell. 2015;59:399–412. PubMed PMC
Llácer J.L., Hussain T.1., Gordiyenko Y., Lorsch J.R., Hinnebusch A.G., Ramakrishnan V. The beta propellers of eIF3b and eIF3i relocate together to the ribosomal intersubunit interface during translation initiation. bioRxiv. 2018 doi: 10.1101/453688. DOI
Lu P.D., Harding H.P., Ron D. Translation reinitiation at alternative open reading frames regulates gene expression in an integrated stress response. J. Cell Biol. 2004;167:27–33. PubMed PMC
McGlincy N.J., Ingolia N.T. Transcriptome-wide measurement of translation by ribosome profiling. Methods. 2017;126:112–129. PubMed PMC
Mohammad M.P., Munzarová Pondelícková V., Zeman J., Gunišová S., Valášek L.S. In vivo evidence that eIF3 stays bound to ribosomes elongating and terminating on short upstream ORFs to promote reinitiation. Nucleic Acids Res. 2017;45:2658–2674. PubMed PMC
Munzarová V., Pánek J., Gunišová S., Dányi I., Szamecz B., Valášek L.S. Translation reinitiation relies on the interaction between eIF3a/TIF32 and progressively folded cis-acting mRNA elements preceding short uORFs. PLoS Genet. 2011;7:e1002137. PubMed PMC
Nielsen K.H., Valásek L., Sykes C., Jivotovskaya A., Hinnebusch A.G. Interaction of the RNP1 motif in PRT1 with HCR1 promotes 40S binding of eukaryotic initiation factor 3 in yeast. Mol. Cell. Biol. 2006;26:2984–2998. PubMed PMC
Park H.S., Himmelbach A., Browning K.S., Hohn T., Ryabova L.A. A plant viral “reinitiation” factor interacts with the host translational machinery. Cell. 2001;106:723–733. PubMed
Phan L., Zhang X., Asano K., Anderson J., Vornlocher H.P., Greenberg J.R., Qin J., Hinnebusch A.G. Identification of a translation initiation factor 3 (eIF3) core complex, conserved in yeast and mammals, that interacts with eIF5. Mol. Cell. Biol. 1998;18:4935–4946. PubMed PMC
Pisarev A.V., Hellen C.U.T., Pestova T.V. Recycling of eukaryotic posttermination ribosomal complexes. Cell. 2007;131:286–299. PubMed PMC
Pizzinga M., Bates C., Lui J., Forte G., Morales-Polanco F., Linney E., Knotkova B., Wilson B., Solari C.A., Berchowitz L.E. Translation factor mRNA granules direct protein synthetic capacity to regions of polarized growth. J. Cell Biol. 2019;218:1564–1581. PubMed PMC
R Core Team . R Foundation for Statistical Computing; 2018. R: A language and environment for statistical computing.
Robichaud N., Sonenberg N. Translational control and the cancer cell response to stress. Curr. Opin. Cell Biol. 2017;45:102–109. PubMed
Shiber A., Döring K., Friedrich U., Klann K., Merker D., Zedan M., Tippmann F., Kramer G., Bukau B. Cotranslational assembly of protein complexes in eukaryotes revealed by ribosome profiling. Nature. 2018;561:268–272. PubMed PMC
Shieh Y.W., Minguez P., Bork P., Auburger J.J., Guilbride D.L., Kramer G., Bukau B. Operon structure and cotranslational subunit association direct protein assembly in bacteria. Science. 2015;350:678–680. PubMed
Shirokikh N.E., Preiss T. Translation initiation by cap-dependent ribosome recruitment: Recent insights and open questions. Wiley Interdiscip. Rev. RNA. 2018;9:e1473. PubMed
Shirokikh N.E., Archer S.K., Beilharz T.H., Powell D., Preiss T. Translation complex profile sequencing to study the in vivo dynamics of mRNA-ribosome interactions during translation initiation, elongation and termination. Nat. Protoc. 2017;12:697–731. PubMed
Shirokikh N.E., Dutikova Y.S., Staroverova M.A., Hannan R.D., Preiss T. Migration of Small Ribosomal Subunits on the 5′ Untranslated Regions of Capped Messenger RNA. Int. J. Mol. Sci. 2019;20:E4464. PubMed PMC
Simonetti A., Brito Querido J., Myasnikov A.G., Mancera-Martinez E., Renaud A., Kuhn L., Hashem Y. eIF3 Peripheral Subunits Rearrangement after mRNA Binding and Start-Codon Recognition. Mol. Cell. 2016;63:206–217. PubMed
Skabkin M.A., Skabkina O.V., Hellen C.U., Pestova T.V. Reinitiation and other unconventional posttermination events during eukaryotic translation. Mol. Cell. 2013;51:249–264. PubMed PMC
Smith M.D., Arake-Tacca L., Nitido A., Montabana E., Park A., Cate J.H. Assembly of eIF3 Mediated by Mutually Dependent Subunit Insertion. Structure. 2016;24:886–896. PubMed PMC
Sokabe M., Fraser C.S., Hershey J.W.B. The human translation initiation multi-factor complex promotes methionyl-tRNAi binding to the 40S ribosomal subunit. Nucleic Acids Res. 2012;40:905–913. PubMed PMC
Sonenberg N., Hinnebusch A.G. Regulation of translation initiation in eukaryotes: mechanisms and biological targets. Cell. 2009;136:731–745. PubMed PMC
Szamecz B., Rutkai E., Cuchalová L., Munzarová V., Herrmannová A., Nielsen K.H., Burela L., Hinnebusch A.G., Valásek L. eIF3a cooperates with sequences 5′ of uORF1 to promote resumption of scanning by post-termination ribosomes for reinitiation on GCN4 mRNA. Genes Dev. 2008;22:2414–2425. PubMed PMC
Valásek L.S. ‘Ribozoomin’--translation initiation from the perspective of the ribosome-bound eukaryotic initiation factors (eIFs) Curr. Protein Pept. Sci. 2012;13:305–330. PubMed PMC
Valásek L., Nielsen K.H., Hinnebusch A.G. Direct eIF2-eIF3 contact in the multifactor complex is important for translation initiation in vivo. EMBO J. 2002;21:5886–5898. PubMed PMC
Valásek L., Nielsen K.H., Zhang F., Fekete C.A., Hinnebusch A.G. Interactions of eukaryotic translation initiation factor 3 (eIF3) subunit NIP1/c with eIF1 and eIF5 promote preinitiation complex assembly and regulate start codon selection. Mol. Cell. Biol. 2004;24:9437–9455. PubMed PMC
Valásek L., Szamecz B., Hinnebusch A.G., Nielsen K.H. In vivo stabilization of preinitiation complexes by formaldehyde cross-linking. Methods Enzymol. 2007;429:163–183. PubMed
Valášek L.S., Zeman J., Wagner S., Beznosková P., Pavlíková Z., Mohammad M.P., Hronová V., Herrmannová A., Hashem Y., Gunišová S. Embraced by eIF3: structural and functional insights into the roles of eIF3 across the translation cycle. Nucleic Acids Res. 2017;45:10948–10968. PubMed PMC
van Rossum G. 1995. Python Tutorial, CWI Report CS-R9526.https://gvanrossum.github.io/Publications.html
Vattem K.M., Wek R.C. Reinitiation involving upstream ORFs regulates ATF4 mRNA translation in mammalian cells. Proc. Natl. Acad. Sci. USA. 2004;101:11269–11274. PubMed PMC
Wagner S., Herrmannová A., Malík R., Peclinovská L., Valášek L.S. Functional and biochemical characterization of human eukaryotic translation initiation factor 3 in living cells. Mol. Cell. Biol. 2014;34:3041–3052. PubMed PMC
Wagner S., Herrmannová A., Šikrová D., Valášek L.S. Human eIF3b and eIF3a serve as the nucleation core for the assembly of eIF3 into two interconnected modules: the yeast-like core and the octamer. Nucleic Acids Res. 2016;44:10772–10788. PubMed PMC
Wu C.C., Zinshteyn B., Wehner K.A., Green R. High-Resolution Ribosome Profiling Defines Discrete Ribosome Elongation States and Translational Regulation during Cellular Stress. Mol. Cell. 2019;73:959–970.e5. PubMed PMC
Young D.J., Makeeva D.S., Zhang F., Anisimova A.S., Stolboushkina E.A., Ghobakhlou F., Shatsky I.N., Dmitriev S.E., Hinnebusch A.G., Guydosh N.R. Tma64/eIF2D, Tma20/MCT-1, and Tma22/DENR Recycle Post-termination 40S Subunits In Vivo. Mol. Cell. 2018;71:761–774.e5. PubMed PMC
Zeman J., Itoh Y., Kukačka Z., Rosůlek M., Kavan D., Kouba T., Jansen M.E., Mohammad M.P., Novák P., Valášek L.S. Binding of eIF3 in complex with eIF5 and eIF1 to the 40S ribosomal subunit is accompanied by dramatic structural changes. Nucleic Acids Res. 2019;47:8282–8300. PubMed PMC
Zhang F., Hinnebusch A.G. An upstream ORF with non-AUG start codon is translated in vivo but dispensable for translational control of GCN4 mRNA. Nucleic Acids Res. 2011;39:3128–3140. PubMed PMC