Smith M D, Morris P J, Dawson S J, Schwartz M L, Schlaepfer W W, Latchman D S
Department of Molecular Pathology, University College London Medical School, London W1P 6DB, United Kingdom.
J Biol Chem. 1997 Aug 22;272(34):21325-33. doi: 10.1074/jbc.272.34.21325.
The POU domain transcription factor Brn-3a is able to stimulate neurite outgrowth when overexpressed in the neuronal ND7 cell line, whereas the closely related Brn-3b factor does not have this effect. We show that Brn-3a overexpression also enhances the expression of the three neurofilament genes at both the mRNA and protein levels, whereas Brn-3b overexpression has no effect. In addition Brn-3a activates the three neurofilament gene promoters in co-transfection assays in both neuronal and non-neuronal cells. As observed for enhanced neurite outgrowth, the stimulation of neurofilament gene expression and activation of the neurofilament gene promoters is observed with the isolated POU domain of Brn-3a. A single amino acid change in the POU homeodomain of Brn-3a to the equivalent amino acid in Brn-3b abolishes its ability to activate the neurofilament promoters, whereas the reciprocal change converts Brn-3b to an activator of these promoters.
POU结构域转录因子Brn-3a在神经元ND7细胞系中过表达时能够刺激神经突生长,而与之密切相关的Brn-3b因子则没有这种作用。我们发现,Brn-3a过表达还能在mRNA和蛋白质水平上增强三种神经丝基因的表达,而Brn-3b过表达则没有效果。此外,在神经元和非神经元细胞的共转染实验中,Brn-3a激活了三种神经丝基因启动子。正如在增强神经突生长中所观察到的那样,用Brn-3a的分离POU结构域可观察到神经丝基因表达的刺激和神经丝基因启动子的激活。Brn-3a的POU同源结构域中的单个氨基酸突变为Brn-3b中的等效氨基酸会消除其激活神经丝启动子的能力,而反向突变则将Brn-3b转变为这些启动子的激活剂。