HnRNP H and hnRNP F complex with Fox2 to silence fibroblast growth factor receptor 2 Exon IIIc
被引:98
作者:
Mauger, David M.
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Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Duke Univ, Med Ctr, Ctr RNA Biol, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Mauger, David M.
[1
,2
]
Lin, Carolina
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机构:
Duke Univ, Med Ctr, Cell & Mol Biol Program, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Lin, Carolina
[3
]
Garcia-Blanco, Mariano A.
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Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Duke Univ, Med Ctr, Ctr RNA Biol, Durham, NC 27710 USA
Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Garcia-Blanco, Mariano A.
[1
,2
,4
]
机构:
[1] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Ctr RNA Biol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Cell & Mol Biol Program, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
The heterogeneous nuclear ribonucleoprotein H (hnRNP) family of proteins has been shown to activate exon inclusion by binding intronic G triplets. Much less is known, however, about how hnRNP H and hnRNP F silence exons. In this study, we identify hnRNP H and hnRNP F proteins as being novel silencers of fibroblast growth factor receptor 2 exon IIIc. In cells that normally include this exon, we show that the overexpression of either hnRNP H1 or hnRNP F resulted in the dramatic silencing of exon IIIc. In cells that normally skip exon IIIc, skipping was disrupted when RNA interference was used to knock down both hnRNP H and hnRNP F. We show that an exonic GGG motif overlapped a critical exonic splicing enhancer, which was predicted to bind the SR protein ASF/SF2. Furthermore, the expression of ASF/SF2 reversed the silencing of exon IIIc caused by the expression of hnRNP H1. We show that hnRNP H and hnRNP F proteins are present in a complex with Fox2 and that the presence of Fox allows hnRNP H1 to better compete with ASF/SF2 for binding to exon IIIc. These results establish hnRNP H and hnRNP F as being repressors of exon inclusion and suggest that Fox proteins enhance their ability to antagonize ASF/SF2.
机构:
Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Howard Hughes Med Inst, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
机构:Univ Calif Santa Cruz, Dept Mol & Cellular & Dev Biol, Santa Cruz, CA 95064 USA
Caputi, M
Zahler, AM
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Univ Calif Santa Cruz, Dept Mol & Cellular & Dev Biol, Santa Cruz, CA 95064 USAUniv Calif Santa Cruz, Dept Mol & Cellular & Dev Biol, Santa Cruz, CA 95064 USA
机构:
Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Howard Hughes Med Inst, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
机构:Univ Calif Santa Cruz, Dept Mol & Cellular & Dev Biol, Santa Cruz, CA 95064 USA
Caputi, M
Zahler, AM
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h-index: 0
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Univ Calif Santa Cruz, Dept Mol & Cellular & Dev Biol, Santa Cruz, CA 95064 USAUniv Calif Santa Cruz, Dept Mol & Cellular & Dev Biol, Santa Cruz, CA 95064 USA