Literature DB >> 14593742

Cap-dependent translation and control of the cell cycle.

Patrick Cormier1, Stéphane Pyronnet, Patrick Salaün, Odile Mulner-Lorillon, Nahum Sonenberg.   

Abstract

The control of gene expression at the translational level has emerged in the past decade as an important aspect of cell growth, proliferation and malignant transformation. Translation is primarily regulated at the initiation step, and mitogen-dependent signaling pathways converge to modulate the activity of translation initiation factors. In most tumors tested, at least one translation initiation factor is overexpressed and overexpression of translation initiation factors often provokes transformation. Malignant transformation could be caused by the increased translation of a subset of mRNAs encoding important proteins which are required for cell growth and proliferation. These mRNAs usually possess regulatory sequences that render their translation more sensitive to changes in the activity of translation initiation factors. In this chapter, we describe recent advances illustrating the importance of translation in cell cycle progression and cell transformation. Control of translation initiation may represent an excellent target for antitumor drugs.

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Year:  2003        PMID: 14593742

Source DB:  PubMed          Journal:  Prog Cell Cycle Res        ISSN: 1087-2957


  10 in total

1.  Unorthodox mRNA start site to extend the highly structured leader of retrotransposon Tto1 mRNA increases transposition rate.

Authors:  Gudrun Böhmdorfer; Ivo L Hofacker; Karin Garber; Srecko Jelenic; Viktoria Nizhynska; Hirohiko Hirochika; Peter F Stadler; Andreas Bachmair
Journal:  RNA       Date:  2005-08       Impact factor: 4.942

2.  Translation regulation and proteasome mediated degradation cooperate to keep stem-loop binding protein low in G1-phase.

Authors:  Umidahan Djakbarova; William F Marzluff; M Murat Köseoğlu
Journal:  J Cell Biochem       Date:  2014-03       Impact factor: 4.429

3.  Fibroblast growth factor 1 induced during myogenesis by a transcription-translation coupling mechanism.

Authors:  Caroline Conte; Nadera Ainaoui; Aurélie Delluc-Clavières; Marie P Khoury; Rania Azar; Françoise Pujol; Yvan Martineau; Stéphane Pyronnet; Anne-Catherine Prats
Journal:  Nucleic Acids Res       Date:  2009-06-26       Impact factor: 16.971

4.  A UV-responsive internal ribosome entry site enhances serine hydroxymethyltransferase 1 expression for DNA damage repair.

Authors:  Jennifer T Fox; William K Shin; Marie A Caudill; Patrick J Stover
Journal:  J Biol Chem       Date:  2009-09-04       Impact factor: 5.157

Review 5.  Targeting the translational machinery as a novel treatment strategy for hematologic malignancies.

Authors:  Patrick R Hagner; Abraham Schneider; Ronald B Gartenhaus
Journal:  Blood       Date:  2010-01-14       Impact factor: 22.113

Review 6.  Hypoxia-inducible factor signaling in pheochromocytoma: turning the rudder in the right direction.

Authors:  Ivana Jochmanová; Chunzhang Yang; Zhengping Zhuang; Karel Pacak
Journal:  J Natl Cancer Inst       Date:  2013-08-12       Impact factor: 13.506

7.  Cyclin B Translation Depends on mTOR Activity after Fertilization in Sea Urchin Embryos.

Authors:  Héloïse Chassé; Odile Mulner-Lorillon; Sandrine Boulben; Virginie Glippa; Julia Morales; Patrick Cormier
Journal:  PLoS One       Date:  2016-03-10       Impact factor: 3.240

Review 8.  Translation initiation of viral mRNAs.

Authors:  Marcelo López-Lastra; Pablo Ramdohr; Alejandro Letelier; Maricarmen Vallejos; Jorge Vera-Otarola; Fernando Valiente-Echeverría
Journal:  Rev Med Virol       Date:  2010-05       Impact factor: 6.989

9.  A variant mimicking hyperphosphorylated 4E-BP inhibits protein synthesis in a sea urchin cell-free, cap-dependent translation system.

Authors:  Nathalie Oulhen; Sandrine Boulben; Michael Bidinosti; Julia Morales; Patrick Cormier; Bertrand Cosson
Journal:  PLoS One       Date:  2009-03-31       Impact factor: 3.240

10.  Modelization of the regulation of protein synthesis following fertilization in sea urchin shows requirement of two processes: a destabilization of eIF4E:4E-BP complex and a great stimulation of the 4E-BP-degradation mechanism, both rapamycin-sensitive.

Authors:  Sébastien Laurent; Adrien Richard; Odile Mulner-Lorillon; Julia Morales; Didier Flament; Virginie Glippa; Jérémie Bourdon; Pauline Gosselin; Anne Siegel; Patrick Cormier; Robert Bellé
Journal:  Front Genet       Date:  2014-05-06       Impact factor: 4.599

  10 in total

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