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裂殖酵母细胞中Cdr2节点模式的设计原则。

Design principles of Cdr2 node patterns in fission yeast cells.

作者信息

Opalko Hannah, Geng Shuhan, Hall Aaron R, Vavylonis Dimitrios, Moseley James B

机构信息

Department of Biochemistry and Cell Biology, The Geisel School of Medicine at Dartmouth, Hanover, NH.

Department of Physics, Lehigh University, Bethlehem, PA.

出版信息

bioRxiv. 2023 Jul 21:2023.04.19.537536. doi: 10.1101/2023.04.19.537536.

Abstract

Pattern forming networks have diverse roles in cell biology. Rod-shaped fission yeast cells use pattern formation to control the localization of mitotic signaling proteins and the cytokinetic ring. During interphase, the kinase Cdr2 forms membrane-bound multiprotein complexes termed nodes, which are positioned in the cell middle due in part to the node inhibitor Pom1 enriched at cell tips. Node positioning is important for timely cell cycle progression and positioning of the cytokinetic ring. Here, we combined experimental and modeling approaches to investigate pattern formation by the Pom1-Cdr2 system. We found that Cdr2 nodes accumulate near the nucleus, and Cdr2 undergoes nucleocytoplasmic shuttling when cortical anchoring is reduced. We generated particle-based simulations based on tip inhibition, nuclear positioning, and cortical anchoring. We tested model predictions by investigating Pom1-Cdr2 localization patterns after perturbing each positioning mechanism, including in both anucleate and multinucleated cells. Experiments show that tip inhibition and cortical anchoring alone are sufficient for the assembly and positioning of nodes in the absence of the nucleus, but that the nucleus and Pom1 facilitate the formation of unexpected node patterns in multinucleated cells. These findings have implications for spatial control of cytokinesis by nodes and for spatial patterning in other biological systems.

摘要

模式形成网络在细胞生物学中具有多种作用。杆状裂殖酵母细胞利用模式形成来控制有丝分裂信号蛋白和细胞分裂环的定位。在间期,激酶Cdr2形成称为节点的膜结合多蛋白复合物,这些节点部分由于富集在细胞顶端的节点抑制剂Pom1而定位在细胞中部。节点定位对于细胞周期的及时进展和细胞分裂环的定位很重要。在这里,我们结合实验和建模方法来研究Pom1-Cdr2系统的模式形成。我们发现Cdr2节点在细胞核附近积累,并且当皮层锚定减少时Cdr2会进行核质穿梭。我们基于顶端抑制、核定位和皮层锚定生成了基于粒子的模拟。我们通过研究在干扰每种定位机制后Pom1-Cdr2的定位模式来测试模型预测,包括在无核细胞和多核细胞中。实验表明,在没有细胞核的情况下,单独的顶端抑制和皮层锚定足以使节点组装和定位,但细胞核和Pom1有助于在多核细胞中形成意想不到的节点模式。这些发现对节点对胞质分裂的空间控制以及其他生物系统中的空间模式形成具有启示意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d97e/10364205/cdbe3bafd5dc/nihpp-2023.04.19.537536v2-f0001.jpg

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