Medical Journals

The Leader Region of Laminin B1 Mrna Confers Cap-independent Translation.

Authors:
  • Petz Michaela
  • Kozina Daniela
  • Huber Heidemarie
  • Siwiec Tanja
  • Seipelt Joachim
  • Sommergruber Wolfgang
  • Mikulits Wolfgang

From: Department of Medicine I, Division Institute of Cancer Research, Medical University of Vienna, Borschke-Gasse 8a, A-1090 Vienna, Boehringer Ingelheim Austria.

Nucleic acids research

  • Publish Date: 2007
  • ISSN: 1362-4962
  • Volume: 35
  • Issue: 8
  • Pages: 2473-82
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Petz Michaela, Kozina Daniela, Huber Heidemarie, et al. The Leader Region of Laminin B1 Mrna Confers Cap-independent Translation.. Nucleic Acids Res. 2007;35:2473-82

Abstract

Translation initiation of eukaryotic mRNAs generally occurs by cap-dependent ribosome scanning. However, certain mRNAs contain internal ribosome entry sites (IRES) allowing cap-independent translation. Several of these IRES-competent transcripts and their corresponding proteins are involved in tumourigenesis. This study focused on IRES-driven translation control during the epithelial to mesenchymal transition (EMT) of hepatocytes that reflects crucial aspects of carcinoma progression. Expression profiling of EMT revealed Laminin B1 (LamB1) to be translationally upregulated. The 5’-untranslated region (UTR) of LamB1 was potent to direct IRES-dependent mRNA utilization of a bicistronic reporter construct. Stringent assays for cryptic promoter and splice sites showed no aberrantly expressed transcripts, suggesting that the reporter activity provided by the leader region of LamB1 mRNA exclusively depends on IRES. In accordance, LamB1 expression increased upon negative interference with cap-dependent translation by expression of human rhinovirus 2A protease or heat shock of cells. Finally, the enhanced expression of LamB1 during EMT correlated with an elevated IRES activity. Together, these data provide first evidence that the 5’-UTR of LamB1 contains a bona fide IRES that directs translational upregulation of LamB1 during stress conditions and neoplastic progression of hepatocytes.

Mesh Headings (Keywords): 5’ Untranslated Regions, Animals, Cell Line, Cysteine Endopeptidases, Epithelium, Genes, Reporter, Heat-Shock Response, Hepatocytes, Humans, Laminin, Mesoderm, Mice, Peptide Chain Initiation, Translational, Promoter Regions (Genetics), RNA Caps, RNA Splice Sites, Up-Regulation, Viral Proteins


Check for Full Text / PubMed Unique Identifier (PMID): 17395640


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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