Vourc'h Patrick, Dessay Sabine, Mbarek Olivier, Marouillat Védrine Sylviane, Müh Jean-Pierre, Andres Christian
Génétique de l'autisme et de la déficience mentale, INSERM U 316, 2 bis, Boulevard Tonnellé, 37032 Tours Cedex, France.
Brain Res Dev Brain Res. 2003 Sep 10;144(2):159-68. doi: 10.1016/s0165-3806(03)00167-6.
Oligodendrocyte-myelin glycoprotein (OMgp) is expressed on the surface of oligodendrocytes and neurones and is thought to inhibit axonal regeneration after brain injury in adult, like Nogo and myelin-associated glycoprotein (MAG). We previously observed that the OMgp gene locus on chromosome 17 could be associated with autism, a developmental disorder. The aim of the present study was to characterise the developmental expression of OMgp mRNA in the central nervous system. First we determined the rat OMgp gene sequence and compared it with the human and mouse sequences. Several regions, putative sites for the fixation of transcription factors, are conserved between these three species in the unique intron of this gene. Using quantitative and semi-quantitative RT-PCR, we studied OMgp gene expression in rat brain during post-natal development. We found that OMgp mRNA expression was developmentally regulated, with a peak of expression in the late stages of myelination. We observed a similar profile in oligodendrocyte cultures, in absence of neurones, suggesting that OMgp mRNA expression by oligodendrocytes was independent of axonal influence. Our observations suggest that OMgp is a late marker of myelination, which could be implicated in the arrest of oligodendrocyte proliferation, arrest of myelination or compaction of myelin.
少突胶质细胞髓磷脂糖蛋白(OMgp)表达于少突胶质细胞和神经元表面,与Nogo及髓磷脂相关糖蛋白(MAG)一样,被认为在成体脑损伤后抑制轴突再生。我们之前观察到17号染色体上的OMgp基因座可能与自闭症(一种发育障碍)相关。本研究的目的是描述OMgp mRNA在中枢神经系统中的发育表达情况。首先,我们确定了大鼠OMgp基因序列,并将其与人类和小鼠序列进行比较。在该基因唯一的内含子中,这三个物种之间存在几个保守区域,这些区域是转录因子固定的假定位点。使用定量和半定量逆转录聚合酶链反应(RT-PCR),我们研究了大鼠出生后发育过程中脑内OMgp基因的表达。我们发现OMgp mRNA表达受到发育调控,在髓鞘形成后期表达达到峰值。在没有神经元的少突胶质细胞培养物中,我们观察到了类似的表达模式,这表明少突胶质细胞中OMgp mRNA的表达独立于轴突的影响。我们的观察结果表明,OMgp是髓鞘形成的晚期标志物,可能与少突胶质细胞增殖的停滞、髓鞘形成的停滞或髓磷脂的压实有关。