Lyu Yi Lisa, Wang James C
Department of Molecular and Cellular Biology, Harvard University, 7 Divinity Avenue, Cambridge, MA 02138, USA.
Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):7123-8. doi: 10.1073/pnas.1232376100. Epub 2003 May 28.
We have examined corticogenesis in mouse embryos lacking DNA topoisomerase IIbeta (IIbeta) in the brain or in all tissues. The absence of IIbeta, a type II DNA topoisomerase normally expressed in postmitotic cells in the developing cortex, severely affects cerebral stratification: no subplate is discernible, and neurons born at later stages of corticogenesis fail to migrate to the superficial layers. This abnormal pattern of neuron positioning in the cerebral cortex is reminiscent of that observed in mouse mutants defective in the reelin-signaling pathway. Significantly, the level of reelin in the neocortex is much reduced when IIbeta is absent. These results implicate a role of IIbeta in brain development. The enzyme may be required in implementing particular genetic programs in postmitotic cells, such as reelin expression in Cajal-Retzius cells, perhaps through its action on nucleoprotein structure of particular chromosomal regions.
我们研究了大脑或所有组织中缺乏DNA拓扑异构酶IIβ(IIβ)的小鼠胚胎的皮质发生。IIβ是一种II型DNA拓扑异构酶,通常在发育中的皮质的有丝分裂后细胞中表达,其缺失严重影响大脑分层:无法识别出亚板,并且在皮质发生后期产生的神经元无法迁移到表层。大脑皮质中这种异常的神经元定位模式让人联想到在瑞连蛋白信号通路有缺陷的小鼠突变体中观察到的情况。值得注意的是,当缺乏IIβ时,新皮质中瑞连蛋白的水平会大幅降低。这些结果表明IIβ在大脑发育中起作用。该酶可能是在有丝分裂后细胞中执行特定遗传程序所必需的,比如在Cajal-Retzius细胞中表达瑞连蛋白,这可能是通过其对特定染色体区域的核蛋白结构的作用来实现的。