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中脑-后脑边界的模式形成和形态发生受多种 Grainy head-like 2 依赖性途径的调节。

Midbrain-hindbrain boundary patterning and morphogenesis are regulated by diverse grainy head-like 2-dependent pathways.

机构信息

Department of Medicine, Monash University Central Clinical School, Prahran VIC 3181, Australia.

出版信息

Development. 2012 Feb;139(3):525-36. doi: 10.1242/dev.066522.

Abstract

The isthmic organiser located at the midbrain-hindbrain boundary (MHB) is the crucial developmental signalling centre responsible for patterning mesencephalic and metencephalic regions of the vertebrate brain. Formation and maintenance of the MHB is characterised by a hierarchical program of gene expression initiated by fibroblast growth factor 8 (Fgf8), coupled with cellular morphogenesis, culminating in the formation of the tectal-isthmo-cerebellar structures. Here, we show in zebrafish that one orthologue of the transcription factor grainy head-like 2 (Grhl2), zebrafish grhl2b plays a central role in both MHB maintenance and folding by regulating two distinct, non-linear pathways. Loss of grhl2b expression induces neural apoptosis and extinction of MHB markers, which are rescued by re-expression of engrailed 2a (eng2a), an evolutionarily conserved target of the Grhl family. Co-injection of sub-phenotypic doses of grhl2b and eng2a morpholinos reproduces the apoptosis and MHB marker loss, but fails to substantially disrupt formation of the isthmic constriction. By contrast, a novel direct grhl2b target, spec1, identified by phylogenetic analysis and confirmed by ChIP, functionally cooperates with grhl2b to induce MHB morphogenesis, but plays no role in apoptosis or maintenance of MHB markers. Collectively, these data show that MHB maintenance and morphogenesis are dissociable events regulated by grhl2b through diverse transcriptional targets.

摘要

中脑-后脑边界(MHB)处的峡部组织者是负责模式化脊椎动物脑的中脑和后脑区域的关键发育信号中心。MHB 的形成和维持的特点是由成纤维细胞生长因子 8(Fgf8)引发的基因表达的层次程序,与细胞形态发生相结合,最终形成小脑顶盖-峡部-小脑结构。在这里,我们在斑马鱼中表明,转录因子颗粒头样 2(Grhl2)的一个同源物,斑马鱼 grhl2b 通过调节两个不同的、非线性途径,在 MHB 的维持和折叠中起着核心作用。grhl2b 表达的丧失诱导神经细胞凋亡和 MHB 标志物的消失,而 engrailed 2a(eng2a)的重新表达,即 Grhl 家族的一个进化保守的靶标,可以挽救这种情况。grhl2b 和 eng2a 形态发生素的亚表型剂量的共注射重现了凋亡和 MHB 标志物的丧失,但未能显著破坏峡部的收缩形成。相比之下,通过系统发育分析鉴定并通过 ChIP 确认的一个新的直接 grhl2b 靶标 spec1,与 grhl2b 协同作用诱导 MHB 形态发生,但在凋亡或 MHB 标志物的维持中不起作用。总的来说,这些数据表明,MHB 的维持和形态发生是由 grhl2b 通过不同的转录靶标调节的可分离事件。

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