Translation of 5′ leaders is pervasive in genes resistant to eIF2 repression

Eukaryotic cells rapidly reduce protein synthesis in response to various stress conditions. This can be achieved by the phosphorylation-mediated inactivation of a key translation initiation factor, eukaryotic initiation factor 2 (eIF2). However, the persistent translation of certain mRNAs is required for deployment of an adequate stress response. We carried out ribosome profiling of cultured human cells under conditions of severe stress induced with sodium arsenite. Although this led to a 5.4-fold general translational repression, the protein coding open reading frames (ORFs) of certain individual mRNAs exhibited resistance to the inhibition. Nearly all resistant transcripts possess at least one efficiently translated upstream open reading frame (uORF) that represses translation of the main coding ORF under normal conditions. Site-specific mutagenesis of two identified stress resistant mRNAs (PPP1R15B and IFRD1) demonstrated that a single uORF is sufficient for eIF2-mediated translation control in both cases. Phylogenetic analysis suggests that at least two regulatory uORFs (namely, in SLC35A4 and MIEF1) encode functional protein products. DOI: http://dx.doi.org/10.7554/eLife.03971.001

[1]  Ribosome profiling: a Hi‐Def monitor for protein synthesis at the genome‐wide scale , 2017, Wiley interdisciplinary reviews. RNA.

[2]  Vadim N. Gladyshev,et al.  Translation inhibitors cause abnormalities in ribosome profiling experiments , 2014, Nucleic acids research.

[3]  Alan G Hinnebusch,et al.  The scanning mechanism of eukaryotic translation initiation. , 2014, Annual review of biochemistry.

[4]  Gary D Bader,et al.  A draft map of the human proteome , 2014, Nature.

[5]  Nicholas T. Ingolia Ribosome profiling: new views of translation, from single codons to genome scale , 2014, Nature Reviews Genetics.

[6]  Melissa J. Landrum,et al.  RefSeq: an update on mammalian reference sequences , 2013, Nucleic Acids Res..

[7]  Desmond G. Higgins,et al.  GWIPS-viz: development of a ribo-seq genome browser , 2013, Nucleic Acids Res..

[8]  Shigeru Takahashi,et al.  The 5′‐untranslated region regulates ATF5 mRNA stability via nonsense‐mediated mRNA decay in response to environmental stress , 2013, The FEBS journal.

[9]  François-Michel Boisvert,et al.  Direct Detection of Alternative Open Reading Frames Translation Products in Human Significantly Expands the Proteome , 2013, PloS one.

[10]  I. Terenin,et al.  Cap-independent translation initiation of Apaf-1 mRNA based on a scanning mechanism is determined by some features of the secondary structure of its 5′ untranslated region , 2013, Biochemistry (Moscow).

[11]  R. Jackson The current status of vertebrate cellular mRNA IRESs. , 2013, Cold Spring Harbor perspectives in biology.

[12]  Dietmar Rieder,et al.  A novel RB E3 Ubiquitin Ligase (NRBE3) promotes cancer cell proliferation through a regulation loop with RB/E2F1 , 2013 .

[13]  I. Terenin,et al.  The 5′ untranslated region of Apaf‐1 mRNA directs translation under apoptosis conditions via a 5′ end‐dependent scanning mechanism , 2012, FEBS letters.

[14]  Anna M. McGeachy,et al.  The ribosome profiling strategy for monitoring translation in vivo by deep sequencing of ribosome-protected mRNA fragments , 2012, Nature Protocols.

[15]  D. Dinsdale,et al.  Sustained translational repression by eIF2α-P mediates prion neurodegeneration , 2012, Nature.

[16]  R. Wek,et al.  Eukaryotic initiation factor 2 phosphorylation and translational control in metabolism. , 2012, Advances in nutrition.

[17]  Nicholas T. Ingolia,et al.  The translational landscape of mTOR signalling steers cancer initiation and metastasis , 2012, Nature.

[18]  M. Holcik,et al.  IRES-mediated translation of cellular messenger RNA operates in eIF2α- independent manner during stress , 2011, Nucleic acids research.

[19]  Peter F. Stadler,et al.  ViennaRNA Package 2.0 , 2011, Algorithms for Molecular Biology.

[20]  Marcel Martin Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .

[21]  N. Friedman,et al.  Metabolic labeling of RNA uncovers principles of RNA production and degradation dynamics in mammalian cells , 2011, Nature Biotechnology.

[22]  R. Wek,et al.  Phosphorylation of eIF2 Facilitates Ribosomal Bypass of an Inhibitory Upstream ORF to Enhance CHOP Translation*♦ , 2011, The Journal of Biological Chemistry.

[23]  T. Fennell,et al.  Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries , 2011, Genome Biology.

[24]  I. Terenin,et al.  Cap- and IRES-independent scanning mechanism of translation initiation as an alternative to the concept of cellular IRESs , 2010, Molecules and cells.

[25]  A. Komar,et al.  Activities of Ligatin and MCT-1/DENR in eukaryotic translation initiation and ribosomal recycling. , 2010, Genes & development.

[26]  W. Merrick,et al.  GTP-independent tRNA Delivery to the Ribosomal P-site by a Novel Eukaryotic Translation Factor* , 2010, The Journal of Biological Chemistry.

[27]  R. Elkon,et al.  Major role for mRNA stability in shaping the kinetics of gene induction , 2010, BMC Genomics.

[28]  Palash Mandal,et al.  Stress-sensitive Regulation of IFRD1 mRNA Decay Is Mediated by an Upstream Open Reading Frame* , 2010, The Journal of Biological Chemistry.

[29]  Ya-Yun Cheng,et al.  Differential regulation of CHOP translation by phosphorylated eIF4E under stress conditions , 2009, Nucleic acids research.

[30]  Martin Mokrejs,et al.  IRESite—a tool for the examination of viral and cellular internal ribosome entry sites , 2009, Nucleic Acids Res..

[31]  N. Ali,et al.  Initiation Factor eIF2-independent Mode of c-Src mRNA Translation Occurs via an Internal Ribosome Entry Site* , 2009, Journal of Biological Chemistry.

[32]  V. Prassolov,et al.  Differential contribution of the m7G-cap to the 5′ end-dependent translation initiation of mammalian mRNAs , 2009, Nucleic acids research.

[33]  M. Drumm,et al.  Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease , 2009, Nature.

[34]  Nicholas T. Ingolia,et al.  Genome-Wide Analysis in Vivo of Translation with Nucleotide Resolution Using Ribosome Profiling , 2009, Science.

[35]  D. Sabatini,et al.  An ATP-competitive Mammalian Target of Rapamycin Inhibitor Reveals Rapamycin-resistant Functions of mTORC1* , 2009, Journal of Biological Chemistry.

[36]  E. Jan,et al.  An Upstream Open Reading Frame Regulates Translation of GADD34 during Cellular Stresses That Induce eIF2α Phosphorylation* , 2009, Journal of Biological Chemistry.

[37]  A. Hinnebusch,et al.  Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets , 2009, Cell.

[38]  D. Scheuner,et al.  Ppp1r15 gene knockout reveals an essential role for translation initiation factor 2 alpha (eIF2α) dephosphorylation in mammalian development , 2009, Proceedings of the National Academy of Sciences.

[39]  O. Yoo,et al.  New p53 target, phosphatase of regenerating liver 1 (PRL-1) downregulates p53 , 2009, Oncogene.

[40]  Cole Trapnell,et al.  Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.

[41]  J. F. Atkins,et al.  uORFs with unusual translational start codons autoregulate expression of eukaryotic ornithine decarboxylase homologs , 2008, Proceedings of the National Academy of Sciences.

[42]  D. Andreev,et al.  Eukaryotic translation initiation machinery can operate in a bacterial-like mode without eIF2 , 2008, Nature Structural &Molecular Biology.

[43]  C. Hellen,et al.  eIF2‐dependent and eIF2‐independent modes of initiation on the CSFV IRES: a common role of domain II , 2008, The EMBO journal.

[44]  Donghui Zhou,et al.  Phosphorylation of eIF2 Directs ATF5 Translational Control in Response to Diverse Stress Conditions* , 2008, Journal of Biological Chemistry.

[45]  Shigeru Takahashi,et al.  Stress-induced Translation of ATF5 mRNA Is Regulated by the 5′-Untranslated Region* , 2008, Journal of Biological Chemistry.

[46]  Ivan N. Shatsky,et al.  Efficient Translation Initiation Directed by the 900-Nucleotide-Long and GC-Rich 5′ Untranslated Region of the Human Retrotransposon LINE-1 mRNA Is Strictly Cap Dependent Rather than Internal Ribosome Entry Site Mediated , 2007, Molecular and Cellular Biology.

[47]  Carito Guziolowski,et al.  Algorithms for Molecular Biology , 2007 .

[48]  F. Bouillaud,et al.  Translation control of UCP2 synthesis by the upstream open reading frame , 2006, Cellular and Molecular Life Sciences.

[49]  H. Prokisch,et al.  The Nfs1 interacting protein Isd11 has an essential role in Fe/S cluster biogenesis in mitochondria , 2006, The EMBO journal.

[50]  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.

[51]  M. Brostrom,et al.  Reversible phosphorylation of eukaryotic initiation factor 2α in response to endoplasmic reticular signaling , 1993, Molecular and Cellular Biochemistry.

[52]  P. Angel,et al.  AP-1 subunits: quarrel and harmony among siblings , 2004, Journal of Cell Science.

[53]  D. Ron,et al.  Translation reinitiation at alternative open reading frames regulates gene expression in an integrated stress response , 2004, The Journal of cell biology.

[54]  R. Wek,et al.  Reinitiation involving upstream ORFs regulates ATF4 mRNA translation in mammalian cells. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[55]  G. Crooks,et al.  WebLogo: a sequence logo generator. , 2004, Genome research.

[56]  D. Ron,et al.  Inhibition of a constitutive translation initiation factor 2α phosphatase, CReP, promotes survival of stressed cells , 2003, The Journal of cell biology.

[57]  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.

[58]  John Quackenbush Microarray data normalization and transformation , 2002, Nature Genetics.

[59]  D. Weil,et al.  In Vivo Kinetics of mRNA Splicing and Transport in Mammalian Cells , 2002, Molecular and Cellular Biology.

[60]  F. Urano,et al.  Inhibition of CHOP translation by a peptide encoded by an open reading frame localized in the chop 5'UTR. , 2001, Nucleic acids research.

[61]  D. Ron,et al.  Feedback Inhibition of the Unfolded Protein Response by GADD34-Mediated Dephosphorylation of eIF2α , 2001, The Journal of cell biology.

[62]  Z. Xia,et al.  Arsenite-Induced Apoptosis in Cortical Neurons Is Mediated by c-Jun N-Terminal Protein Kinase 3 and p38 Mitogen-Activated Protein Kinase , 2000, The Journal of Neuroscience.

[63]  P. Sarnow,et al.  Initiation of Protein Synthesis from the A Site of the Ribosome , 2000, Cell.

[64]  S. Mukherjee,et al.  Increased phosphorylation of eukaryotic initiation factor 2alpha at the G2/M boundary in human osteosarcoma cells correlates with deglycosylation of p67 and a decreased rate of protein synthesis. , 1999, Experimental cell research.

[65]  Weiya Ma,et al.  Arsenic induces apoptosis through a c-Jun NH2-terminal kinase-dependent, p53-independent pathway. , 1999, Cancer research.

[66]  F S Fay,et al.  Visualization of single RNA transcripts in situ. , 1998, Science.

[67]  J. L. Quesne,et al.  C-Myc 5′ untranslated region contains an internal ribosome entry segment , 1998, Oncogene.

[68]  A. Hinnebusch,et al.  Translational Regulation of Yeast GCN4 , 1997, The Journal of Biological Chemistry.

[69]  B. Roizman,et al.  The γ134.5 protein of herpes simplex virus 1 complexes with protein phosphatase 1α to dephosphorylate the α subunit of the eukaryotic translation initiation factor 2 and preclude the shutoff of protein synthesis by double-stranded RNA-activated protein kinase , 1997 .

[70]  B. Roizman,et al.  The gamma(1)34.5 protein of herpes simplex virus 1 complexes with protein phosphatase 1alpha to dephosphorylate the alpha subunit of the eukaryotic translation initiation factor 2 and preclude the shutoff of protein synthesis by double-stranded RNA-activated protein kinase. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[71]  M. Sachs,et al.  Translational regulation in response to changes in amino acid availability in Neurospora crassa , 1995, Molecular and cellular biology.

[72]  Y. Murakami,et al.  Ornithine decarboxylase antizyme in kidneys of male and female mice. , 1988, The Biochemical journal.

[73]  A. Sobel,et al.  The Journal of Biological Chemistry. , 2009, Nutrition reviews.

[74]  A. B. Stone A simplified method for preparing sucrose gradients. , 1974, The Biochemical journal.

[75]  A. B. Stone A simplified method for preparing sucrose gradients (Short Communication) , 1974 .