Suppr超能文献

一种扩展的Notch-Delta模型,具有长程模式形成并纳入了微小RNA调控。

An expanded Notch-Delta model exhibiting long-range patterning and incorporating MicroRNA regulation.

作者信息

Chen Jerry S, Gumbayan Abygail M, Zeller Robert W, Mahaffy Joseph M

机构信息

Computational Science Research Center, San Diego State University, San Diego, California, United States of America; Department of Biology, San Diego State University, San Diego, California, United States of America.

Department of Biology, San Diego State University, San Diego, California, United States of America.

出版信息

PLoS Comput Biol. 2014 Jun 19;10(6):e1003655. doi: 10.1371/journal.pcbi.1003655. eCollection 2014 Jun.

Abstract

Notch-Delta signaling is a fundamental cell-cell communication mechanism that governs the differentiation of many cell types. Most existing mathematical models of Notch-Delta signaling are based on a feedback loop between Notch and Delta leading to lateral inhibition of neighboring cells. These models result in a checkerboard spatial pattern whereby adjacent cells express opposing levels of Notch and Delta, leading to alternate cell fates. However, a growing body of biological evidence suggests that Notch-Delta signaling produces other patterns that are not checkerboard, and therefore a new model is needed. Here, we present an expanded Notch-Delta model that builds upon previous models, adding a local Notch activity gradient, which affects long-range patterning, and the activity of a regulatory microRNA. This model is motivated by our experiments in the ascidian Ciona intestinalis showing that the peripheral sensory neurons, whose specification is in part regulated by the coordinate activity of Notch-Delta signaling and the microRNA miR-124, exhibit a sparse spatial pattern whereby consecutive neurons may be spaced over a dozen cells apart. We perform rigorous stability and bifurcation analyses, and demonstrate that our model is able to accurately explain and reproduce the neuronal pattern in Ciona. Using Monte Carlo simulations of our model along with miR-124 transgene over-expression assays, we demonstrate that the activity of miR-124 can be incorporated into the Notch decay rate parameter of our model. Finally, we motivate the general applicability of our model to Notch-Delta signaling in other animals by providing evidence that microRNAs regulate Notch-Delta signaling in analogous cell types in other organisms, and by discussing evidence in other organisms of sparse spatial patterns in tissues where Notch-Delta signaling is active.

摘要

Notch-Delta信号传导是一种基本的细胞间通讯机制,它控制着许多细胞类型的分化。现有的大多数Notch-Delta信号传导数学模型都基于Notch和Delta之间的反馈回路,导致对相邻细胞的侧向抑制。这些模型产生一种棋盘状的空间模式,即相邻细胞表达相反水平的Notch和Delta,导致细胞命运交替。然而,越来越多的生物学证据表明,Notch-Delta信号传导会产生其他非棋盘状的模式,因此需要一个新模型。在这里,我们提出了一个扩展的Notch-Delta模型,该模型基于先前的模型构建,增加了一个影响长程模式形成的局部Notch活性梯度和一种调控性微小RNA的活性。我们在海鞘Ciona intestinalis中的实验激发了这个模型,该实验表明,其特化部分受Notch-Delta信号传导和微小RNA miR-124协同活性调控的外周感觉神经元呈现出一种稀疏的空间模式,即连续的神经元可能相隔十几个细胞。我们进行了严格的稳定性和分岔分析,并证明我们的模型能够准确解释和重现Ciona中的神经元模式。通过对我们的模型进行蒙特卡罗模拟以及miR-124转基因过表达实验,我们证明miR-124的活性可以纳入我们模型的Notch衰减率参数中。最后,我们通过提供证据表明微小RNA在其他生物体的类似细胞类型中调节Notch-Delta信号传导,并通过讨论其他生物体中Notch-Delta信号传导活跃的组织中稀疏空间模式的证据,来激发我们的模型对其他动物Notch-Delta信号传导的普遍适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c37c/4063677/b35e3a4cad39/pcbi.1003655.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验