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体节发生的微阵列分析揭示了体节中胚层不同WNT信号通路的新靶点。

Microarray analysis of somitogenesis reveals novel targets of different WNT signaling pathways in the somitic mesoderm.

作者信息

Buttitta Laura, Tanaka Tetsuya S, Chen Alice E, Ko Minoru S H, Fan Chen-Ming

机构信息

Carnegie Institution of Washington, Department of Embryology, Baltimore, MD 21210, USA.

出版信息

Dev Biol. 2003 Jun 1;258(1):91-104. doi: 10.1016/s0012-1606(03)00116-7.

Abstract

WNT signaling plays a major role in patterning the dermomyotome of the somitic mesoderm. However, knowledge of downstream target genes and their regulation is limited. To identify new genes involved in the development and early patterning of the somite, we performed a comparison of gene expression by microarray between the presomitic mesoderm and the 5 most recently formed somites of the mouse at embryonic day 9.5. We identified 207 genes upregulated and 120 genes downregulated in somite formation. Expression analysis and functional categorization of these genes demonstrate this to be a diverse pool that provides a valuable resource for studying somite development. Thus far, we have found three genes expressed in the dermomyotome of the early somite. Consistent with their expression patterns, these genes are transcriptional targets of WNT signals, but display differential activation by different WNTs. We further demonstrate that 1 of these genes, Troy, is a direct target of canonical WNT signaling, while the other 2 genes, Selp and Arl4, are not. Thus, our microarray study using microdissected tissues not only provides global information on gene expression during somite development, it also provides novel targets to study the inductive signaling pathways that direct somite patterning.

摘要

WNT信号通路在体节中胚层的生皮节模式形成中起主要作用。然而,对其下游靶基因及其调控的了解有限。为了鉴定参与体节发育和早期模式形成的新基因,我们在胚胎第9.5天对小鼠的前体节中胚层和最近形成的5个体节进行了基因芯片表达比较。我们鉴定出在体节形成过程中207个基因上调,120个基因下调。对这些基因的表达分析和功能分类表明,这是一个多样化的基因库,为研究体节发育提供了宝贵资源。到目前为止,我们已经发现三个基因在早期体节的生皮节中表达。与它们的表达模式一致,这些基因是WNT信号的转录靶标,但对不同的WNT显示出不同的激活作用。我们进一步证明,这些基因中的一个,Troy,是经典WNT信号的直接靶标,而另外两个基因,Selp和Arl4,则不是。因此,我们使用显微切割组织进行的基因芯片研究不仅提供了体节发育过程中基因表达的全局信息,还为研究指导体节模式形成的诱导信号通路提供了新的靶标。

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