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小鼠体节形成的机制。

The mechanism of somite formation in mice.

机构信息

Division of Mammalian Development, National institute of Genetics and Department of Genetics, SOKENDAI, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.

出版信息

Curr Opin Genet Dev. 2012 Aug;22(4):331-8. doi: 10.1016/j.gde.2012.05.004. Epub 2012 Jun 27.

Abstract

Somitogenesis is a series of dynamic morphogenetic events that involve cyclical signaling. The periodicity of somitogenesis is controlled by segmentation clock operating in the presomitic mesoderm (PSM), the precursor of somites. Notch signaling plays important roles not only in the segmentation clock mechanism but also as an output signal of the clock to induce Mesp2 transcription that controls somite formation. In the present review, recent advances in the understanding of the molecular mechanisms underlying the translation of clock information into the spatial patterning of segmental somites in mice are discussed. Particular attention is paid to the interplay between two the distinct signaling pathways of Notch and FGF and the Mesp2 transcription factor acting as an effector molecule during mouse somitogenesis.

摘要

体节发生是一系列涉及周期性信号转导的动态形态发生事件。体节发生的周期性由在体节前体中起作用的节段时钟控制。Notch 信号不仅在节段时钟机制中起重要作用,而且作为时钟的输出信号诱导控制体节形成的 Mesp2 转录。在本综述中,讨论了对将时钟信息翻译成小鼠分段体节的空间模式的分子机制的理解的最新进展。特别关注 Notch 和 FGF 两个不同信号通路与作为小鼠体节发生过程中的效应分子的 Mesp2 转录因子之间的相互作用。

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