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  • Title: Human synapsin I mediates the function of nuclear respiratory factor 1 in neurite outgrowth in neuroblastoma IMR-32 cells.
    Author: Wang JL, Chang WT, Tong CW, Kohno K, Huang AM.
    Journal: J Neurosci Res; 2009 Aug 01; 87(10):2255-63. PubMed ID: 19301426.
    Abstract:
    Nuclear respiratory factor (NRF)-1 is a transcription factor with a novel function in neurite outgrowth. Synapsin I protein is a well-known phosphoprotein in neuronal terminals and has been implicated in neuronal differentiation. Human synapsin I gene promoter has a putative NRF-1 responsive element (NRE), but it is not known whether this NRE is functional. We hypothesized that synapsin I is downstream of NRF-1 and mediates its function in neurite outgrowth. Gel electrophoretic mobility shift assays, chromatin immunoprecipitation, site-directed mutagenesis, and promoter studies indicated that NRF-1 is a positive regulator of synapsin I promoter. Exogenous NRF-1 overexpression increased synapsin I protein levels in IMR-32 and HEK293T cells. Serum deprivation, which induces neurite outgrowth in IMR-32 cells, increased the binding activity of NRF-1 to synapsin I NRE and induced alternating synapsin I protein expression. Down-regulating synapsin I expression markedly decreased the percentage of neurite-bearing cells and the length of the longest neurite in IMR-32 cells that stably or transiently overexpressed NRF-1. We conclude that the human synapsin I gene is positively regulated by NRF-1 and mediates the function of NRF-1 in neurite outgrowth.
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