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合子基因组激活(XIC)对于Siamois活性和背前部发育是必需的。

XIC is required for Siamois activity and dorsoanterior development.

作者信息

Snider Lauren, Tapscott Stephen J

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA 98109-1024, USA.

出版信息

Mol Cell Biol. 2005 Jun;25(12):5061-72. doi: 10.1128/MCB.25.12.5061-5072.2005.

Abstract

Siamois is the transcriptional mediator of the dorsal Wnt signaling pathway and is necessary for formation of the Spemann organizer and dorsoanterior development in Xenopus. We have determined that XIC, a Xenopus I-mfa domain protein that regulates Tcf3 binding, is required for dorsoaxial development and specifically for Siamois activity in establishing the dorsal organizer. In loss-of-function studies, we found that embryos injected with a morpholino to XIC mRNA (XIC morphpolino) are missing head structures, neural tube, notochord, and paraxial mesoderm as well as NCAM and XMyoD expression. Although Siamois, Twin, and Xnr3 expression is normal in morpholino-injected embryos, levels of downstream organizer factors, including goosecoid, Xnot, Cerberus, and chordin, are severely reduced. Ectopic axis formation induced by Siamois is repressed by injection of the XIC morpholino and further repressed by coinjection of beta-catenin or a constitutively active Tcf3/HMG/G4A fusion. Activation of reporters driven by the Siamois-responsive proximal element of the goosecoid promoter is inhibited in the presence of the morpholino and can be rescued by murine I-mfa and by a dominant-negative Tcf3. The data indicate a role for XIC in limiting Tcf3-dependent repression of Siamois activities that are required for goosecoid transcription and for dorsal organizer formation.

摘要

暹罗蛋白是背侧Wnt信号通路的转录调节因子,对非洲爪蟾中斯佩曼组织者的形成和背前部发育至关重要。我们已经确定,XIC(一种调节Tcf3结合的非洲爪蟾I-mfa结构域蛋白)对于背轴发育是必需的,并且在建立背侧组织者时对暹罗蛋白的活性具有特异性作用。在功能缺失研究中,我们发现注射针对XIC mRNA的吗啉代寡核苷酸(XIC吗啉代寡核苷酸)的胚胎缺失头部结构、神经管、脊索和近轴中胚层,以及神经细胞黏附分子(NCAM)和XMyoD的表达。尽管在注射吗啉代寡核苷酸的胚胎中暹罗蛋白、孪生蛋白和Xnr3的表达正常,但包括 goosecoid、Xnot、Cerberus和脊索蛋白在内的下游组织者因子的水平却严重降低。由暹罗蛋白诱导的异位轴形成被注射XIC吗啉代寡核苷酸所抑制,并被共注射β-连环蛋白或组成型活性Tcf3/HMG/G4A融合蛋白进一步抑制。在存在吗啉代寡核苷酸的情况下,由goosecoid启动子的暹罗蛋白反应性近端元件驱动的报告基因的激活受到抑制,并且可以被小鼠I-mfa和显性负性Tcf3挽救。这些数据表明XIC在限制Tcf3对暹罗蛋白活性的依赖性抑制中发挥作用,而暹罗蛋白活性是goosecoid转录和背侧组织者形成所必需的。

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