The interplay between cis- and trans-acting factors drives selective mRNA translation initiation in eukaryotes

被引:6
作者
Tidu, Antonin [1 ]
Martin, Franck [1 ]
机构
[1] Univ Strasbourg, Inst Biol & Mol Cellulaire, Architecture & Reactivite ARN, CNRS UPR9002, 2 Allee Konrad Roentgen, F-67084 Strasbourg, France
关键词
5'UTR; Translation; Ribosome; IRES; uORF; IRES-MEDIATED TRANSLATION; START CODON RECOGNITION; HOST PROTEIN-SYNTHESIS; CAP-BINDING-PROTEIN; P-I RELEASE; NUCLEOTIDE EXCHANGE; PREINITIATION COMPLEX; HELICASE ACTIVITY; MAMMALIAN TARGET; ALPHA-SUBUNIT;
D O I
10.1016/j.biochi.2023.09.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Translation initiation consists in the assembly of the small and large ribosomal subunits on the start codon. This important step directly modulates the general proteome in living cells. Recently, genome wide studies revealed unexpected translation initiation events from unsuspected novel open reading frames resulting in the synthesis of a so-called 'dark proteome'. Indeed, the identification of the start codon by the translation machinery is a critical step that defines the translational landscape of the cell. Therefore, translation initiation is a highly regulated process in all organisms. In this review, we focus on the various cis- and trans -acting factors that rule the regulation of translation initiation in eukaryotes. Recent discoveries have shown that the guidance of the translation machinery for the choice of the start codon require sophisticated molecular mechanisms. In particular, the 5'UTR and the coding sequences contain cis -acting elements that trigger the use of AUG codons but also non-AUG codons to initiate protein synthesis. The use of these alternative start codons is also largely influenced by numerous transacting elements that drive selective mRNA translation in response to environmental changes. (c) 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY -NC -ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:20 / 30
页数:11
相关论文
共 144 条
[1]   The structural basis of translational control by eIF2 phosphorylation [J].
Adomavicius, Tomas ;
Guaita, Margherita ;
Zhou, Yu ;
Jennings, Martin D. ;
Latif, Zakia ;
Roseman, Alan M. ;
Pavitt, Graham D. .
NATURE COMMUNICATIONS, 2019, 10 (1)
[2]   False-positive IRESes from Hoxa9 and other genes resulting from errors in mammalian 5′ UTR annotations [J].
Akirtava, Christina ;
May, Gemma E. ;
McManus, C. Joel .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2022, 119 (36)
[3]   Translation inhibitory elements from Hoxa3 and Hoxa11 mRNAs use uORFs for translation inhibition [J].
Alghoul, Fatima ;
Laure, Schaeffer ;
Eriani, Gilbert ;
Martin, Franck .
ELIFE, 2021, 10
[4]   Pi release from elF2, not GTP hydrolysis, is the step controlled by start-site selection during eukaryotic translation initiation [J].
Algire, MA ;
Maag, D ;
Lorsch, JR .
MOLECULAR CELL, 2005, 20 (02) :251-262
[5]   Dynamics of ribosome scanning and recycling revealed by translation complex profiling [J].
Archer, Stuart K. ;
Shirokikh, Nikolay E. ;
Beilharz, Traude H. ;
Preiss, Thomas .
NATURE, 2016, 535 (7613) :570-+
[6]   A multifactor complex of eukaryotic initiation factors, eIE1, eIF2, eIF3, eIF5, and initiator tRNAMet is an important translation initiation intermediate in vivo [J].
Asano, K ;
Clayton, J ;
Shalev, A ;
Hinnebusch, AG .
GENES & DEVELOPMENT, 2000, 14 (19) :2534-2546
[7]   mRNA regions where 80S ribosomes pause during translation elongation in vivo interact with protein uS19, a component of the decoding site [J].
Babaylova, Elena S. ;
Gopanenko, Alexander, V ;
Bulygin, Konstantin N. ;
Tupikin, Alexey E. ;
Kabilov, Marsel R. ;
Malygin, Alexey A. ;
Karpova, Galina G. .
NUCLEIC ACIDS RESEARCH, 2020, 48 (02) :912-923
[8]   A dual inhibitory mechanism restricts msl-2 mRNA translation for dosage compensation in Drosophila [J].
Beckmann, K ;
Grskovic, M ;
Gebauer, F ;
Hentze, MW .
CELL, 2005, 122 (04) :529-540
[9]   Foot-and-mouth disease virus 3C protease induces cleavage of translation initiation factors eIF4A and eIF4G within infected cells [J].
Belsham, GJ ;
McInerney, GM ;
Ross-Smith, N .
JOURNAL OF VIROLOGY, 2000, 74 (01) :272-280
[10]   Dynamics of uS19 C-Terminal Tail during the Translation Elongation Cycle in Human Ribosomes [J].
Bhaskar, Varun ;
Graff-Meyer, Alexandra ;
Schenk, Andreas D. ;
Cavadini, Simone ;
von Loeffelholz, Ottilie ;
Natchiar, S. Kundhavai ;
Artus-Revel, Caroline G. ;
Hotz, Hans-Rudolf ;
Bretones, Gabriel ;
Klaholz, Bruno P. ;
Chao, Jeffrey A. .
CELL REPORTS, 2020, 31 (01)