Secondary axis specification in sea urchin embryos

C. Bradham, D. McClay
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引用次数: 4

Abstract

Secondary axis specification is a process that relies on asymmetric nuclearization of transcription factors in flies and vertebrates, such that the crucial factor is nuclear and therefore functional only in cells along one side of the embryo. In vertebrates, this transcription factor is β-catenin, which is canonically activated downstream from Wnt signals. However, the sea urchin uses asymmetric β-catenin nuclearization during specification of the primary animal-vegetal axis, rather than the secondary oral-aboral (OA) axis. OA specification relies instead on the asymmetric localization of p38 MAPK, a signaling kinase that directly modulates transcription factor activity. A number of genes are expressed in the oral territory downstream from p38, including Nodal and Goosecoid, both of which are associated with secondary axis specification in vertebrate embryos. Because the p38 asymmetry is the earliest known event in the specification of the OA axis, an outstanding question concerns identifying the apparatus upstream from p38 that regulates its asymmetrical activity. Intriguingly, this may be controlled by reactive oxygen species released from the mitochondria, which are asymmetrically distributed about the OA axis.
海胆胚胎的次轴发育
在果蝇和脊椎动物中,次级轴发育是一个依赖于转录因子非对称核化的过程,因此关键因子是核的,因此只在胚胎一侧的细胞中起作用。在脊椎动物中,这种转录因子是β-catenin,通常在Wnt信号的下游被激活。然而,海胆在主要动物-植物轴的发育过程中使用不对称β-catenin核化,而不是在次级口-口(OA)轴的发育过程中。相反,OA规范依赖于p38 MAPK的不对称定位,p38 MAPK是一种直接调节转录因子活性的信号激酶。许多基因在p38下游的口腔区域表达,包括Nodal和Goosecoid,它们都与脊椎动物胚胎的次级轴发育有关。由于p38不对称是OA轴发育过程中最早已知的事件,因此一个悬而未决的问题是如何确定p38上游调控其不对称活动的装置。有趣的是,这可能是由线粒体释放的活性氧控制的,这些活性氧在OA轴上不对称分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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