220
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      DENR•MCT-1 Promotes Translation Reinitiation Downstream of uORFs to Control Tissue Growth

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          During cap-dependent eukaryotic translation initiation, ribosomes scan mRNA from the 5′ end to the first AUG start codon with favorable sequence context 1, 2 . For many mRNAs this AUG belongs to a short upstream open reading frame (uORF) 3 , and translation of the main downstream ORF requires reinitiation, an incompletely understood process 1, 4- 6 . Reinitiation is thought to involve the same factors as standard initiation 1, 5, 7 . It is unknown if any factors specifically affect translation reinitiation without affecting standard cap-dependent translation. We uncover here the non-canonical initiation factors Density Regulated Protein (DENR) and Multiple Copies in T-cell Lymphoma-1 (MCT-1) as the first selective regulators of eukaryotic reinitiation. mRNAs containing upstream Open Reading Frames with strong Kozak sequences (stuORFs) selectively require DENR•MCT-1 for their proper translation, yielding a novel class of mRNAs that can be co-regulated and that is enriched for regulatory proteins such as oncogenic kinases. Collectively, our data reveal that cells have a previously unappreciated translational control system with a key role in supporting proliferation and tissue growth.

          Related collections

          Most cited references27

          • Record: found
          • Abstract: found
          • Article: not found

          Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans.

          Upstream ORFs (uORFs) are mRNA elements defined by a start codon in the 5' UTR that is out-of-frame with the main coding sequence. Although uORFs are present in approximately half of human and mouse transcripts, no study has investigated their global impact on protein expression. Here, we report that uORFs correlate with significantly reduced protein expression of the downstream ORF, based on analysis of 11,649 matched mRNA and protein measurements from 4 published mammalian studies. Using reporter constructs to test 25 selected uORFs, we estimate that uORFs typically reduce protein expression by 30-80%, with a modest impact on mRNA levels. We additionally identify polymorphisms that alter uORF presence in 509 human genes. Finally, we report that 5 uORF-altering mutations, detected within genes previously linked to human diseases, dramatically silence expression of the downstream protein. Together, our results suggest that uORFs influence the protein expression of thousands of mammalian genes and that variation in these elements can influence human phenotype and disease.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Molecular mechanisms of translational control

            Key Points Translational regulation can be global or mRNA specific, and most examples of translational regulation that have been described so far affect the rate-limiting initiation step. Global control of translation is frequently exerted by regulating the phosphorylation or availability of initiation factors. Two of the most well-known examples are the regulation of eukaryotic initiation factor (eIF)4E availability by 4E-binding proteins (4E-BPs), and the modulation of the levels of active ternary complex by eIF2α phosphorylation. mRNA-specific translational control is driven by RNA sequences and/or structures that are commonly located in the untranslated regions of the transcript. These features are usually recognized by regulatory proteins or micro RNAs (miRNAs). Quasi-circularization of mRNAs can be mediated by the cap structure and the poly(A) tail via the eIF4E–eIF4G–polyA-binding-protein (PABP) interaction. Such interactions between the 5′ and the 3′ ends of mRNAs could provide a spatial framework for the action of regulatory factors that bind to the 3′ untranslated region (UTR). However, other forms of 5′–3′-end interactions are likely to occur as well. Many regulatory proteins target the stable association of the small ribosomal subunit with the mRNA. These factors function by steric hindrance (for example, iron-regulatory protein; IRP), by interfering with the eIF4F complex (for example, Maskin, Bicoid, Cup) or by as-yet-unknown, distinct mechanisms to control translation initiation (sex-lethal; SXL). Other regulatory molecules modulate the joining of the large ribosomal subunit (hnRNP K and E1) or, potentially, post-initiation translation steps (miRNAs). General translation factors can regulate the expression of specific mRNAs. An illustrative example is the stimulation of translation of the mRNA that encodes the GCN4 transcriptional activator by eIF2α phosphorylation.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The elongation, termination, and recycling phases of translation in eukaryotes.

              This work summarizes our current understanding of the elongation and termination/recycling phases of eukaryotic protein synthesis. We focus here on recent advances in the field. In addition to an overview of translation elongation, we discuss unique aspects of eukaryotic translation elongation including eEF1 recycling, eEF2 modification, and eEF3 and eIF5A function. Likewise, we highlight the function of the eukaryotic release factors eRF1 and eRF3 in translation termination, and the functions of ABCE1/Rli1, the Dom34:Hbs1 complex, and Ligatin (eIF2D) in ribosome recycling. Finally, we present some of the key questions in translation elongation, termination, and recycling that remain to be answered.
                Bookmark

                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                9 May 2014
                06 July 2014
                14 August 2014
                14 February 2015
                : 512
                : 7513
                : 208-212
                Affiliations
                [1 ]German Cancer Research Center (DKFZ), Heidelberg, Germany
                [2 ]Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany
                [3 ]Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany
                Author notes
                [* ]equal contribution and correspondence: kent.duncan@ 123456zmnh.uni-hamburg.de & a.teleman@ 123456dkfz.de tel/fax:+49 40 7410 56274 / +49 40 7410 53436 tel/fax:+49 6221 42-1620 / +49 6221 42-1629

                Author Contributions S.S. performed most experiments, except as indicated below. K.S. analyzed histoblast proliferation, EcR and InR protein levels and signaling in cells and animals, and performed EcR/InR rescue experiments in vivo. P.C.J. assessed proliferation, translation, rRNA and tRNA levels, as well as polysome profiles of DENR-KD S2 cells, and performed in vitro translation assays. T.K. established inducible reporter assays in proliferating and quiescent cells ( ED Figs. 7a-f, 10c). K.K.M. performed DENR-MCT-1co-IP assays ( ED Fig. 10b). K.H. performed DENR RNA-IP assays ( ED Fig. 4g). Y.S.C analyzed MCT-1 levels and phosphorylation ( ED Fig. 10d’). K.K. established in vitro translation assays from S2 cells. A.A.T. performed the bioinformatic analyses.

                K.E.D. and A.A.T designed the study and wrote the paper with input from G.S. All authors interpreted data, discussed results, and contributed to writing the manuscript.

                Article
                EMS58242
                10.1038/nature13401
                4134322
                25043021
                3b854226-d2f5-4c0a-b509-a9298f68ece0
                History
                Categories
                Article

                Uncategorized
                translational control,uorf,reinitiation,coordinated regulation,drosophila,development,tissue growth,cell proliferation

                Comments

                Comment on this article