Karl Claudia, Couillard-Despres Sebastien, Prang Peter, Munding Matthias, Kilb Werner, Brigadski Tanja, Plötz Sonja, Mages Wolfgang, Luhmann Heiko, Winkler Jürgen, Bogdahn Ulrich, Aigner Ludwig
Volkswagen-Foundation-Research Group, University of Regensburg, Regensburg, Germany.
J Neurochem. 2005 Jan;92(2):264-82. doi: 10.1111/j.1471-4159.2004.02879.x.
The doublecortin (DCX) gene encodes a 40-kDa microtubule-associated protein specifically expressed in neuronal precursors of the developing and adult CNS. Due to its specific expression pattern, attention was drawn to DCX as a marker for neuronal precursors and neurogenesis, thereby underscoring the importance of its promoter identification and promoter analysis. Here, we analysed the human DCX regulatory sequence and confined it to a 3.5-kb fragment upstream of the ATG start codon. We demonstrate by transient transfection experiments that this fragment is sufficient and specific to drive expression of reporter genes in embryonic and adult neuronal precursors. The activity of this regulatory fragment overlapped with the expression of endogenous DCX and with the young neuronal markers class III beta-tubulin isotype and microtubule-associated protein Map2ab but not with glial or oligodendroglial markers. Electrophysiological data further confirmed the immature neuronal nature of these cells. Deletions within the 3.5-kb region demonstrated the relevance of specific regions containing transcription factor-binding sites. Moreover, application of neurogenesis-related growth factors in the neuronal precursor cultures suggested the lack of direct signalling of these factors on the DCX promoter construct.
双皮质素(DCX)基因编码一种40 kDa的微管相关蛋白,该蛋白在发育中和成年中枢神经系统的神经元前体细胞中特异性表达。由于其特定的表达模式,DCX作为神经元前体细胞和神经发生的标志物受到关注,从而凸显了其启动子鉴定和启动子分析的重要性。在此,我们分析了人类DCX调控序列,并将其定位到ATG起始密码子上游3.5 kb的片段。我们通过瞬时转染实验证明,该片段足以且特异性地驱动报告基因在胚胎和成年神经元前体细胞中的表达。该调控片段的活性与内源性DCX的表达以及年轻神经元标志物III类β-微管蛋白亚型和微管相关蛋白Map2ab的表达重叠,但与神经胶质或少突胶质细胞标志物不重叠。电生理数据进一步证实了这些细胞的未成熟神经元特性。3.5 kb区域内的缺失表明了包含转录因子结合位点的特定区域的相关性。此外,在神经元前体细胞培养物中应用与神经发生相关的生长因子表明,这些因子对DCX启动子构建体缺乏直接信号传导作用。