Abstract
Gemin4 is a ubiquitously expressed multifunctional protein that is involved in U snRNP assembly, apoptosis, nuclear/cytoplasmic transportation, transcription, and RNAi pathways. Gemin4 is one of the core components of the Gemin-complex, which also contains survival motor neuron (SMN), the seven Gemin proteins (Gemin2-8), and Unrip. Mutations in the SMN1 gene cause the autosomal recessive disorder spinal muscular atrophy (SMA). Although the functions assigned to Gemin4 predominantly occur in the nucleus, the mechanisms that mediate the nuclear import of Gemin4 remain unclear. Here, using a novel panel of Gemin4 constructs we identify a canonical nuclear import sequence (NLS) in the N-terminus of Gemin4. The Gemin4 NLS is necessary and independently sufficient to mediate nuclear import of Gemin4. This is the first functional NLS identified within the SMN-Gemin complex.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Active Transport, Cell Nucleus
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Cell Nucleus / metabolism
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Cyclic AMP Response Element-Binding Protein / genetics
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Cyclic AMP Response Element-Binding Protein / metabolism
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Cytoplasm / metabolism
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HeLa Cells
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Humans
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Minor Histocompatibility Antigens
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Mutation
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / metabolism
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Nuclear Localization Signals / genetics
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Nuclear Localization Signals / metabolism*
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RNA-Binding Proteins / genetics
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RNA-Binding Proteins / metabolism
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Ribonucleoproteins, Small Nuclear / genetics
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Ribonucleoproteins, Small Nuclear / metabolism*
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SMN Complex Proteins
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Survival of Motor Neuron 1 Protein
Substances
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Cyclic AMP Response Element-Binding Protein
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GEMIN4 protein, human
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Minor Histocompatibility Antigens
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Nerve Tissue Proteins
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Nuclear Localization Signals
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RNA-Binding Proteins
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Ribonucleoproteins, Small Nuclear
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SMN Complex Proteins
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SMN1 protein, human
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Survival of Motor Neuron 1 Protein