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Hox 基因与果蝇的脑发育。

Hox genes and brain development in Drosophila.

机构信息

Biozentrum, University of Basel, Klingelbergstrasse 50, CH-4056 Basel, Switzerland.

出版信息

Adv Exp Med Biol. 2010;689:145-53. doi: 10.1007/978-1-4419-6673-5_11.

Abstract

Hox genes are prominently expressed in the developing brain and ventral ganglia of Drosophila. In the embryonic brain, the Hox genes labial and Deformed are essential for the establishment of regionalized neuronal identity; in their absence cells are generated in the brain but fail to acquire appropriate neuronal features. Genetic analyses reveal that Hox proteins are largely equivalent in their action in embryonic brain development and that their expression is under the control of cross-regulatory interactions among Hox genes that are similar to those found in embryogenesis of trunk segments. Hox genes have a different role in postembryonic brain development. During the larval phase of CNS development, reactivation of specific Hox genes terminates neural proliferation by induction of apoptotic cell death in neural stem cell-like progenitors called neuroblasts. This reactivation process is tightly controlled by epigenetic mechanisms requiring the Polycomb group of genes. Many features of Hox gene action in Drosophila brain development are evolutionarily conserved and are manifest in brain development of vertebrates.

摘要

Hox 基因在果蝇的发育大脑和腹神经节中高度表达。在胚胎大脑中,Hox 基因 labial 和 Deformed 对于建立区域化的神经元身份是必不可少的;在它们缺失的情况下,脑细胞会在大脑中产生,但无法获得适当的神经元特征。遗传分析表明,Hox 蛋白在胚胎大脑发育中的作用基本相同,其表达受 Hox 基因之间交叉调控相互作用的控制,这些相互作用类似于在躯干节胚胎发生中发现的相互作用。Hox 基因在胚胎后大脑发育中具有不同的作用。在中枢神经系统发育的幼虫阶段,特定的 Hox 基因的重新激活通过诱导神经干细胞样祖细胞(称为神经母细胞)的凋亡细胞死亡来终止神经增殖。这个重新激活过程受到表观遗传机制的严格控制,需要 Polycomb 基因群。果蝇大脑发育中 Hox 基因作用的许多特征在进化上是保守的,并在脊椎动物的大脑发育中表现出来。

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