果蝇神经发育过程中Notch动力学的数学建模。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fly Pub Date : 2022-12-01 DOI:10.1080/19336934.2021.1953363
Tetsuo Yasugi, Makoto Sato
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引用次数: 2

摘要

Notch信号是一种保守的信号通路,通过细胞间通讯调节细胞命运。Notch信号传导的一个典型特征是“侧抑制”,即两个具有相同分化状态的相邻细胞获得不同的细胞命运。最近,数学和计算方法已经解决了果蝇神经发育中的Notch动力学。在胚胎中的神经干细胞和胸腔中的感觉器官前体中观察到典型的侧抑制。在眼盘发育过程中,Notch信号通路与其他信号通路共同决定感光细胞均匀分布的位置。Notch与表皮生长因子受体信号传导之间的相互作用调节了视叶神经干细胞分化的时间。本文综述了国内外对Notch动力学的理论研究,并讨论了数学模型与生物实验相结合的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mathematical modeling of Notch dynamics in <i>Drosophila</i> neural development.

Mathematical modeling of Notch dynamics in <i>Drosophila</i> neural development.

Mathematical modeling of Notch dynamics in <i>Drosophila</i> neural development.

Mathematical modeling of Notch dynamics in Drosophila neural development.

Notch signalling is a well-conserved signalling pathway that regulates cell fate through cell-cell communication. A typical feature of Notch signalling is 'lateral inhibition', whereby two neighbouring cells of equivalent state of differentiation acquire different cell fates. Recently, mathematical and computational approaches have addressed the Notch dynamics in Drosophila neural development. Typical examples of lateral inhibition are observed in the specification of neural stem cells in the embryo and sensory organ precursors in the thorax. In eye disc development, Notch signalling cooperates with other signalling pathways to define the evenly spaced positioning of the photoreceptor cells. The interplay between Notch and epidermal growth factor receptor signalling regulates the timing of neural stem cell differentiation in the optic lobe. In this review, we summarize the theoretical studies that have been conducted to elucidate the Notch dynamics in these systems and discuss the advantages of combining mathematical models with biological experiments.

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来源期刊
Fly
Fly 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
>12 weeks
期刊介绍: Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions. Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.
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