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    fbf-2 Fem-3 mRNA-binding factor 2 [ Caenorhabditis elegans ]

    Gene ID: 174017, updated on 9-Dec-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    COP9 signalosome component CSN-5 stabilizes PUF proteins FBF-1 and FBF-2 in Caenorhabditis elegans germline stem and progenitor cells.

    COP9 signalosome component CSN-5 stabilizes PUF proteins FBF-1 and FBF-2 in Caenorhabditis elegans germline stem and progenitor cells.
    Osterli E, Ellenbecker M, Wang X, Terzo M, Jacobson K, Cuello D, Voronina E.,

    06/3/2024
    Antagonistic control of Caenorhabditis elegans germline stem cell proliferation and differentiation by PUF proteins FBF-1 and FBF-2.

    Antagonistic control of Caenorhabditis elegans germline stem cell proliferation and differentiation by PUF proteins FBF-1 and FBF-2.
    Wang X, Ellenbecker M, Hickey B, Day NJ, Osterli E, Terzo M, Voronina E., Free PMC Article

    02/13/2021
    LST-1 weakens FBF-2 binding affinity for short and long motifs, which may increase target selectivity.

    A crystal structure of a collaborative RNA regulatory complex reveals mechanisms to refine target specificity.
    Qiu C, Bhat VD, Rajeev S, Zhang C, Lasley AE, Wine RN, Campbell ZT, Hall TMT., Free PMC Article

    02/8/2020
    Data indicate that a 10-amino-acid region in germline development defective-3 (GLD-3) is required for fem-3 binding factor (FBF) binding, while a 7-amino-acid loop in FBF between PUF repeats 7 and 8 is necessary for GLD-3 binding.

    A protein.protein interaction platform involved in recruitment of GLD-3 to the FBF.fem-3 mRNA complex.
    Wu J, Campbell ZT, Menichelli E, Wickens M, Williamson JR., Free PMC Article

    04/6/2013
    Data show that CPB-1 (cytoplasmic polyadenylation element binding protein homolog-1) alters the affinity of FBF (fem-3 mRNA binding factor) for specific RNA sequences.

    Biochemical characterization of the Caenorhabditis elegans FBF.CPB-1 translational regulation complex identifies conserved protein interaction hotspots.
    Menichelli E, Wu J, Campbell ZT, Wickens M, Williamson JR., Free PMC Article

    04/6/2013
    findings show FBF-1 and FBF-2 have different effects on target mRNAs; FBF-2 prevents translation; FBF-2 activity depends on PGL-1; PGL-1 is required to localize FBF-2 to perinuclear P granules and for efficient binding of FBF-2 to its mRNA targets

    The P granule component PGL-1 promotes the localization and silencing activity of the PUF protein FBF-2 in germline stem cells.
    Voronina E, Paix A, Seydoux G., Free PMC Article

    12/8/2012
    Data suggest that the FBF-2/GLD-2 protein directed polyadenylation of the endogenous mRNA, compensating for that mRNA's natural deadenylation.

    Targeted translational regulation using the PUF protein family scaffold.
    Cooke A, Prigge A, Opperman L, Wickens M., Free PMC Article

    12/17/2011
    The Puf RNA-binding proteins FBF-1 and FBF-2 inhibit the expression of synaptonemal complex proteins in germline stem cells.

    The Puf RNA-binding proteins FBF-1 and FBF-2 inhibit the expression of synaptonemal complex proteins in germline stem cells.
    Merritt C, Seydoux G., Free PMC Article

    06/14/2010
    fbf-2 regulates the size of the mitotic region in helminth germ cells.

    FBF-1 and FBF-2 regulate the size of the mitotic region in the C. elegans germline.
    Lamont LB, Crittenden SL, Bernstein D, Wickens M, Kimble J.

    01/21/2010
    FBF may coordinately repress sperm-specifying mRNAs to direct oogenesis and it represses the fog-1 mRNA to maintain FOG-1 at a low level appropriate for proliferation

    Dose-dependent control of proliferation and sperm specification by FOG-1/CPEB.
    Thompson BE, Bernstein DS, Bachorik JL, Petcherski AG, Wickens M, Kimble J., Free PMC Article

    01/21/2010
    Fbf-2 redundantly inhibits primary vulval cell fate specification in two distinct pathways acting in the soma and in the germline

    Distinct roles of the Pumilio and FBF translational repressors during C. elegans vulval development.
    Walser CB, Battu G, Hoier EF, Hajnal A.

    01/21/2010
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