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鹅膏蕈氨酸和Mix.1抑制短尾相关蛋白的表达,并且是非洲爪蟾头部形成所必需的。

Goosecoid and mix.1 repress Brachyury expression and are required for head formation in Xenopus.

作者信息

Latinkic B V, Smith J C

机构信息

Division of Developmental Biology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.

出版信息

Development. 1999 Apr;126(8):1769-79. doi: 10.1242/dev.126.8.1769.

Abstract

The Xenopus homologue of Brachyury, Xbra, is expressed in the presumptive mesoderm of the early gastrula. Induction of Xbra in animal pole tissue by activin occurs only in a narrow window of activin concentrations; if the level of inducer is too high, or too low, the gene is not expressed. Previously, we have suggested that the suppression of Xbra by high concentrations of activin is due to the action of genes such as goosecoid and Mix.1. Here, we examine the roles played by goosecoid and Mix.1 during normal development, first in the control of Xbra expression and then in the formation of the mesendoderm. Consistent with the model outlined above, inhibition of the function of either gene product leads to transient ectopic expression of Xbra. Such embryos later develop dorsoanterior defects and, in the case of interference with Mix.1, additional defects in heart and gut formation. Goosecoid, a transcriptional repressor, appears to act directly on transcription of Xbra. In contrast, Mix.1, which functions as a transcriptional activator, may act on Xbra indirectly, in part through activation of goosecoid.

摘要

短尾相关蛋白(Brachyury)在非洲爪蟾中的同源物Xbra,在早期原肠胚的预定中胚层中表达。激活素在动物极组织中诱导Xbra的表达仅发生在激活素浓度的狭窄范围内;如果诱导剂水平过高或过低,该基因均不表达。此前,我们曾提出高浓度激活素对Xbra的抑制作用是由于诸如鹅膏蕈氨酸(goosecoid)和Mix.1等基因的作用。在此,我们研究了鹅膏蕈氨酸和Mix.1在正常发育过程中的作用,首先是在Xbra表达的调控方面,然后是在内胚层中胚层的形成方面。与上述模型一致,抑制任一基因产物的功能都会导致Xbra的短暂异位表达。此类胚胎随后会出现背前部缺陷,而在干扰Mix.1的情况下,还会出现心脏和肠道形成方面的额外缺陷。作为转录抑制因子的鹅膏蕈氨酸似乎直接作用于Xbra的转录。相比之下,作为转录激活因子发挥作用的Mix.1可能间接作用于Xbra,部分是通过激活鹅膏蕈氨酸来实现的。

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