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轴旁中胚层的图案生成。

Generation of patterns in the paraxial mesoderm.

机构信息

Institute of Bioengineering, School of Life Sciences, Swiss Federal Institute of Technology Lausanne EPFL, Switzerland.

Institute of Bioengineering, School of Life Sciences, Swiss Federal Institute of Technology Lausanne EPFL, Switzerland.

出版信息

Curr Top Dev Biol. 2024;159:372-405. doi: 10.1016/bs.ctdb.2023.11.001. Epub 2023 Nov 30.

DOI:10.1016/bs.ctdb.2023.11.001
PMID:38729682
Abstract

The Segmentation Clock is a tissue-level patterning system that enables the segmentation of the vertebral column precursors into transient multicellular blocks called somites. This patterning system comprises a set of elements that are essential for correct segmentation. Under the so-called "Clock and Wavefront" model, the system consists of two elements, a genetic oscillator that manifests itself as traveling waves of gene expression, and a regressing wavefront that transforms the temporally periodic signal encoded in the oscillations into a permanent spatially periodic pattern of somite boundaries. Over the last twenty years, every new discovery about the Segmentation Clock has been tightly linked to the nomenclature of the "Clock and Wavefront" model. This constrained allocation of discoveries into these two elements has generated long-standing debates in the field as what defines molecularly the wavefront and how and where the interaction between the two elements establishes the future somite boundaries. In this review, we propose an expansion of the "Clock and Wavefront" model into three elements, "Clock", "Wavefront" and signaling gradients. We first provide a detailed description of the components and regulatory mechanisms of each element, and we then examine how the spatiotemporal integration of the three elements leads to the establishment of the presumptive somite boundaries. To be as exhaustive as possible, we focus on the Segmentation Clock in zebrafish. Furthermore, we show how this three-element expansion of the model provides a better understanding of the somite formation process and we emphasize where our current understanding of this patterning system remains obscure.

摘要

节段时钟是一种组织水平的模式系统,能够将脊椎前体分割成称为体节的短暂多细胞块。这个模式系统包括一组对于正确的分割是必不可少的元素。在所谓的“时钟和波前”模型下,该系统由两个元素组成,一个是表现为基因表达传播波的遗传振荡器,另一个是退行波前,它将在振荡中编码的时间周期性信号转化为体节边界的永久空间周期性模式。在过去的二十年中,关于节段时钟的每一个新发现都与“时钟和波前”模型的命名紧密相关。这种将发现严格分配到这两个元素中的做法在该领域引发了长期的争论,即什么定义了波前的分子特性,以及两个元素之间的相互作用是如何以及在何处建立未来的体节边界的。在这篇综述中,我们提出将“时钟和波前”模型扩展为三个元素,即“时钟”、“波前”和信号梯度。我们首先详细描述了每个元素的组成部分和调节机制,然后研究了三个元素的时空整合如何导致假定体节边界的建立。为了尽可能详尽,我们专注于斑马鱼的节段时钟。此外,我们展示了这个模型的三元素扩展如何提供对体节形成过程的更好理解,并强调了我们对这个模式系统的当前理解仍然模糊的地方。

相似文献

1
Generation of patterns in the paraxial mesoderm.轴旁中胚层的图案生成。
Curr Top Dev Biol. 2024;159:372-405. doi: 10.1016/bs.ctdb.2023.11.001. Epub 2023 Nov 30.
2
Signalling dynamics in vertebrate segmentation.脊椎动物分节中的信号动态。
Nat Rev Mol Cell Biol. 2014 Nov;15(11):709-21. doi: 10.1038/nrm3891.
3
Modelling Delta-Notch perturbations during zebrafish somitogenesis.在斑马鱼体节生成过程中模拟 Delta-Notch 干扰。
Dev Biol. 2013 Jan 15;373(2):407-21. doi: 10.1016/j.ydbio.2012.10.014. Epub 2012 Oct 16.
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A multi-cell, multi-scale model of vertebrate segmentation and somite formation.脊椎动物分节和体节形成的多细胞多尺度模型。
PLoS Comput Biol. 2011 Oct;7(10):e1002155. doi: 10.1371/journal.pcbi.1002155. Epub 2011 Oct 6.
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Molecular mechanism for cyclic generation of somites: Lessons from mice and zebrafish.体节循环生成的分子机制:来自小鼠和斑马鱼的启示
Dev Growth Differ. 2016 Jan;58(1):31-42. doi: 10.1111/dgd.12249. Epub 2015 Dec 17.
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Somite boundary determination in normal and clock-less vertebrate embryos.体节边界在正常和无时钟脊椎动物胚胎中的确定。
Dev Growth Differ. 2020 Apr;62(3):177-187. doi: 10.1111/dgd.12655. Epub 2020 Feb 28.
7
Analysis of her1 and her7 mutants reveals a spatio temporal separation of the somite clock module.分析 her1 和 her7 突变体揭示了体节时钟模块的时空分离。
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Periodic inhibition of Erk activity drives sequential somite segmentation.周期性抑制 Erk 活性驱动连续体节的分段。
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Cellular and molecular control of vertebrate somitogenesis.脊椎动物体节形成的细胞和分子控制。
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Noise in the Vertebrate Segmentation Clock Is Boosted by Time Delays but Tamed by Notch Signaling.脊椎动物分节时钟的噪声通过时间延迟增强,但受到 Notch 信号的抑制。
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NOTCH1 S2513 is critical for the regulation of NICD levels impacting the segmentation clock in hiPSC-derived PSM cells and somitoids.NOTCH1 S2513对于调节NICD水平至关重要,而NICD水平会影响人诱导多能干细胞衍生的体节中胚层细胞和拟体节中的体节时钟。
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