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The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation.

The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Research Abstract Details 

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  • The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Abstract Text:

    vincent r gerbasiVincent R Gerbasi,andrew j linkAndrew J Link,

    The 5'-untranslated region of the ornithine decarboxylase (ODC) mRNA contains an internal ribosomal entry site (IRES). Mutational analysis of the ODC IRES has led to the identification of sequences necessary for cap-independent translation of the ODC mRNA. To discover novel IRES trans-acting factors (ITAFs), we performed a proteomics screen for proteins that regulate ODC translation using the wild-type ODC mRNA and a mutant version with an inactive IRES. We identified two RNA-binding proteins that associate with the wild-type ODC IRES but not the mutant IRES. One of these RNA-binding proteins, PCBP2, is an established activator of viral and cellular IRESs. The second protein, ZNF9 (myotonic dystrophy type 2 protein), has not been shown previously to bind IRES-like elements. Using a series of biochemical assays, we validated the interaction of these proteins with ODC mRNA. Interestingly ZNF9 and PCBP2 biochemically associated with each other and appeared to function as part of a larger holo-ITAF ribonucleoprotein complex. Our functional studies showed that PCBP2 and ZNF9 stimulate translation of the ODC IRES. Importantly these results may provide insight into the normal role of ZNF9 and why ZNF9 mutations cause myotonic dystrophy.

    The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Publishing Authors By Initials

    vr gerbasiVR Gerbasi,aj linkAJ Link,

    For similar cells: cellular structures: intracellular space: cytoplasm: cytoplasmic structures: organelles: ribosomes research abstracts see: cells: cellular structures: intracellular space: cytoplasm: cytoplasmic structures: organelles: ribosomes research

    PUBMED ID PMID:

    MEDLINE DATE:

    The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Molecular & cellular proteomics : MCP

    VOLUME: 6

    Page Numbers: 1049-58

    Journal Abbreviation: Mol. Cell Proteomics

    ISSN: 1535-9476

    DAY: 26

    MONTH: 02

    YEAR: 2007

    The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101125647

    The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Keywords Mesh Terms:

    KEYWORDS: Ribosomes

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Information

    Substance Name: Ornithine Decarboxylase

    Registry Number: EC 4.1.1.17

    Grant and Affiliation Information for The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation.

    AFFILIATION: Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: T32 CA009385

    ACRONYM: CA

    MEDLINETA: Mol Cell Proteomics

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    DATABASENAME:

    ACCESSION NUMBER:

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