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抗增殖基因TIS21在神经发生开始时的表达可识别出从增殖性分裂转变为神经元生成性分裂的单个神经上皮细胞。

Expression of the antiproliferative gene TIS21 at the onset of neurogenesis identifies single neuroepithelial cells that switch from proliferative to neuron-generating division.

作者信息

Iacopetti P, Michelini M, Stuckmann I, Oback B, Aaku-Saraste E, Huttner W B

机构信息

Department of Neurobiology, University of Heidelberg, Im Neuenheimer Feld 364, D-69120 Heidelberg, Germany.

出版信息

Proc Natl Acad Sci U S A. 1999 Apr 13;96(8):4639-44. doi: 10.1073/pnas.96.8.4639.

Abstract

At the onset of mammalian neurogenesis, neuroepithelial (NE) cells switch from proliferative to neuron-generating divisions. Understanding the molecular basis of this switch requires the ability to distinguish between these two types of division. Here we show that in the mouse ventricular zone, expression of the mRNA of the antiproliferative gene TIS21 (PC3, BTG2) (i) starts at the onset of neurogenesis, (ii) is confined to a subpopulation of NE cells that increases in correlation with the progression of neurogenesis, and (iii) is not detected in newborn neurons. Expression of the TIS21 mRNA in the NE cells occurs transiently during the cell cycle, i.e., in the G1 phase. In contrast to the TIS21 mRNA, the TIS21 protein persists through the division of NE cells and is inherited by the neurons, where it remains detectable during neuronal migration and the initial phase of differentiation. Our observations indicate that the TIS21 gene is specifically expressed in those NE cells that, at their next division, will generate postmitotic neurons, but not in proliferating NE cells. Using TIS21 as a marker, we find that the switch from proliferative to neuron-generating divisions is initiated in single NE cells rather than in synchronized neighboring cells.

摘要

在哺乳动物神经发生开始时,神经上皮(NE)细胞从增殖性分裂转变为生成神经元的分裂。要理解这种转变的分子基础,需要有能力区分这两种分裂类型。在这里,我们表明,在小鼠脑室区,抗增殖基因TIS21(PC3,BTG2)的mRNA表达:(i)在神经发生开始时启动;(ii)局限于NE细胞的一个亚群,该亚群随着神经发生的进展而增加;(iii)在新生神经元中未检测到。NE细胞中TIS21 mRNA的表达在细胞周期中短暂出现,即在G1期。与TIS21 mRNA不同,TIS21蛋白在NE细胞分裂过程中持续存在,并由神经元继承,在神经元迁移和分化初始阶段仍可检测到。我们的观察结果表明,TIS21基因在那些下一次分裂将产生有丝分裂后神经元的NE细胞中特异性表达,但在增殖的NE细胞中不表达。使用TIS21作为标记,我们发现从增殖性分裂到生成神经元的分裂的转变是在单个NE细胞中启动的,而不是在同步的相邻细胞中启动的。

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