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整装原位杂交显示Endo 16是海胆胚胎植物极板区域的一个标记物。

Whole mount in situ hybridization shows Endo 16 to be a marker for the vegetal plate territory in sea urchin embryos.

作者信息

Ransick A, Ernst S, Britten R J, Davidson E H

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125.

出版信息

Mech Dev. 1993 Aug;42(3):117-24. doi: 10.1016/0925-4773(93)90001-e.

Abstract

We have used whole mount in situ hybridization to analyze the pattern of expression of the gene Endo 16 in S. purpuratus embryos. The mRNA is first detectable at 18 h post-fertilization in the cytoplasm of blastomeres derived from the Veg2 6th cleavage tier. The number of Endo 16 positive cells increases gradually through the beginning of gastrulation, and these cell numbers are in agreement with estimates of the number of cells that should be in the vegetal plate at these stages. We conclude that Endo 16 expression is indeed an early vegetal plate marker and that this gene is expressed by all Veg2 tier derivatives while they are part of the vegetal plate. The progressive regionalization of Endo 16 expression that occurs in normal embryos is also seen in lithium chloride induced exogastrulae, leading to the conclusion that genetic regulation of endoderm differentiation is programmed into the vegetal plate cells once they have been specified. Finally, we report a reproducible phenomenon seen in cultures of LiCl exogastrulae, in which the tips of the everted archenterons fuse, followed by the induction of supernumerary pigment cells.

摘要

我们利用整体原位杂交技术分析了紫球海胆胚胎中Endo 16基因的表达模式。受精后18小时,在源自Veg2第六次卵裂层的卵裂球细胞质中首次检测到该mRNA。在原肠胚形成开始阶段,Endo 16阳性细胞数量逐渐增加,这些细胞数量与这些阶段预计位于植物极板的细胞数量一致。我们得出结论,Endo 16表达确实是早期植物极板标记物,并且该基因在所有Veg2层衍生物作为植物极板一部分时表达。正常胚胎中出现的Endo 16表达的渐进区域化在氯化锂诱导的外胚层胚胎中也可见,这导致得出结论,即一旦植物极板细胞被指定,内胚层分化的基因调控就被编入其中。最后,我们报告了在氯化锂外胚层胚胎培养物中观察到的一种可重复现象,即外翻原肠的尖端融合,随后诱导出多余的色素细胞。

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