后生动物形态发生的耦合循环与调控。

IF 2.8 4区 生物学 Q3 CELL BIOLOGY Cell Division Pub Date : 2020-01-27 eCollection Date: 2020-01-01 DOI:10.1186/s13008-020-0059-3
Saba Rezaei-Lotfi, Ramin M Farahani
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引用次数: 1

摘要

后生动物的特征是不同物种内生物的有限表型异质性(即形态差异),这一特征与植物界观察到的种内形态多样性形成鲜明对比。在后生动物中,形态发生蓝图的强劲出现反映了个体细胞在采用分化等命运结果时受到限制的自主性。在种群水平上,单个细胞的命运与邻近细胞的命运相联系并受其影响。这种耦合是所有自组织系统的共同特性,在没有外部指导力监督的情况下,推动单个细胞之间的简单相互作用产生秩序。作为耦合的结果,器官系统组成细胞之间预期的功能关系在形态发生过程中与多轮细胞分裂同时牢固地建立起来。值得注意的是,形态发生自组织过程中多细胞偶联的分子调控在很大程度上仍未被探索。在这里,我们回顾了关于多细胞自组织的现有文献,特别强调了最近的发现,β-catenin是通过调节单个细胞的同步循环来编程多细胞自组织出现的关键偶联因子。
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Coupled cycling and regulation of metazoan morphogenesis.

Metazoan animals are characterized by restricted phenotypic heterogeneity (i.e. morphological disparity) of organisms within various species, a feature that contrasts sharply with intra-species morphological diversity observed in the plant kingdom. Robust emergence of morphogenic blueprint in metazoan animals reflects restricted autonomy of individual cells in adoption of fate outcomes such as differentiation. Fates of individual cells are linked to and influenced by fates of neighboring cells at the population level. Such coupling is a common property of all self-organising systems and propels emergence of order from simple interactions between individual cells without supervision by external directing forces. As a consequence of coupling, expected functional relationship between the constituent cells of an organ system is robustly established concurrent with multiple rounds of cell division during morphogenesis. Notably, the molecular regulation of multicellular coupling during morphogenic self-organisation remains largely unexplored. Here, we review the existing literature on multicellular self-organisation with particular emphasis on recent discovery that β-catenin is the key coupling factor that programs emergence of multi-cellular self-organisation by regulating synchronised cycling of individual cells.

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来源期刊
Cell Division
Cell Division CELL BIOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
5
审稿时长
>12 weeks
期刊介绍: Cell Division is an open access, peer-reviewed journal that encompasses all the molecular aspects of cell cycle control and cancer, cell growth, proliferation, survival, differentiation, signalling, gene transcription, protein synthesis, genome integrity, chromosome stability, centrosome duplication, DNA damage and DNA repair. Cell Division provides an online forum for the cell-cycle community that aims to publish articles on all exciting aspects of cell-cycle research and to bridge the gap between models of cell cycle regulation, development, and cancer biology. This forum is driven by specialized and timely research articles, reviews and commentaries focused on this fast moving field, providing an invaluable tool for cell-cycle biologists. Cell Division publishes articles in areas which includes, but not limited to: DNA replication, cell fate decisions, cell cycle & development Cell proliferation, mitosis, spindle assembly checkpoint, ubiquitin mediated degradation DNA damage & repair Apoptosis & cell death
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