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Acquisition of Hox codes during gastrulation and axial elongation in the mouse embryo.

机译:在小鼠胚胎的胃形成和轴向伸长过程中获取Hox码。

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Early sequential expression of mouse Hox genes is essential for their later function. Analysis of the relationship between early Hox gene expression and the laying down of anterior to posterior structures during and after gastrulation is therefore crucial for understanding the ontogenesis of Hox-mediated axial patterning. Using explants from gastrulation stage embryos, we show that the ability to express 3' and 5' Hox genes develops sequentially in the primitive streak region, from posterior to anterior as the streak extends, about 12 hours earlier than overt Hox expression. The ability to express autonomously the earliest Hox gene, Hoxb1, is present in the posterior streak region at the onset of gastrulation, but not in the anterior region at this stage. However, the posterior region can induce Hoxb1 expression in these anterior region cells. We conclude that tissues are primed to express Hox genes early in gastrulation, concomitant with primitive streak formation and extension, and that Hox gene inducibility is transferred by cell to cell signalling. Axial structures that will later express Hox genes are generated in the node region in the period that Hox expression domains arrive there and continue to spread rostrally. However, lineage analysis showed that definitive Hox codes are not fixed at the node, but must be acquired later and anterior to the node in the neurectoderm, and independently in the mesoderm. We conclude that the rostral progression of Hox gene expression must be modulated by gene regulatory influences from early on in the posterior streak, until the time cells have acquired their stable positions along the axis well anterior to the node.
机译:小鼠Hox基因的早期顺序表达对其后期功能至关重要。因此,分析早期Hox基因表达与在胃形成期间和之后前结构到后结构的沉积之间的关系对于理解Hox介导的轴向模式的本体形成至关重要。使用来自胃泌乳期胚胎的外植体,我们表明表达3'和5'Hox基因的能力在原始条纹区域随着条纹的延伸从后到前顺序发展,比公开的Hox表达早约12小时。自发表达最早的Hox基因Hoxb1的能力存在于胃造瘘开始的后条纹区域中,而在此阶段不存在于前区域。但是,后部区域可以在这些前部区域细胞中诱导Hoxb1表达。我们得出的结论是,组织被预备在胃形成早期表达Hox基因,并伴有原始条痕的形成和延伸,并且Hox基因的诱导能力通过细胞间信号传递。在Hox表达结构域到达那里并继续沿核扩散的期间,在节区域中产生稍后表达Hox基因的轴结构。但是,谱系分析表明,确定性的Hox码不是固定在结点上,而是必须在结节的后部和前部在神经直肠中获得,并且必须在中胚层中独立获得。我们得出的结论是,必须从后条纹的早期开始就通过基因调控影响来调节Hox基因表达的延缓性进展,直到细胞沿结节之前的轴获得其稳定位置为止。

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