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R11: a cis-regulatory node of the sea urchin embryo gene network that controls early expression of SpDelta in micromeres

机译:R11:海胆胚胎基因网络的顺式调控节点,可控制SpDelta在微粒子中的早期表达

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摘要

A gene regulatory network (GRN) controls the process by which the endomesoderm of the sea urchin embryo is specified. In this GRN, the program of gene expression unique to the skeletogenic micromere lineage is set in train by activation of the pmar1 gene. Through a double repression system, this gene is responsible for localization of expression of downstream regulatory and signaling genes to cells of this lineage. One of these genes, delta, encodes a Notch ligand, and its expression in the right place and time is crucial to the specification of the endomesoderm. Here we report a cis-regulatory element R11 that is responsible for localizing the expression of delta by means of its response to the pmar1 repression system. R11 was identified as an evolutionarily conserved genomic sequence located about 13 kb downstream of the last exon of the delta gene. We demonstrate here that this cis-regulatory element is able to drive the expression of a reporter gene in the same cells and at the same time that the endogenous delta gene is expressed, and that temporally, spatially, and quantitatively it responds to the pmar1 repression system just as predicted for the delta gene in the endomesoderm GRN. This work illustrates the application of cis-regulatory analysis to the validation of predictions of the GRN model. In addition, we introduce new methodological tools for quantitative measurement of the output of expression constructs that promise to be of general value for cis-regulatory analysis in sea urchin embryos. (C) 2004 Elsevier Inc. All rights reserved.
机译:基因调控网络(GRN)控制着指定海胆胚胎的内胚层的过程。在此GRN中,通过激活pmar1基因来设置仅针对生成骨骼的微纤维谱系的基因表达程序。通过双重阻抑系统,该基因负责将下游调控和信号传导基因的表达定位到该谱系的细胞中。这些基因之一,δ,编码一个Notch配体,其在正确的位置和时间表达对于内胚层的规格至关重要。在这里,我们报告一个顺式调控元件R11,它通过对pmar1阻遏系统的反应来负责delta表达的定位。 R11被鉴定为位于delta基因最后一个外显子下游约13 kb处的进化保守基因组序列。我们在这里证明了这种顺式调控元件能够驱动报告基因在相同细胞中的表达,并同时表达内源性δ基因,并且在时间,空间和数量上对pmar1的抑制作出反应。系统与内胚层GRN中的delta基因相同。这项工作说明了顺式调控分析在GRN模型预测验证中的应用。此外,我们引入了用于定量测量表达构建体输出的新方法学工具,这些工具有望对海胆胚胎的顺式调控分析具有一般价值。 (C)2004 Elsevier Inc.保留所有权利。

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