微管和肌动蛋白丝在马氏囊孢子细胞极化过程中指导核运动。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2024-10-15 Epub Date: 2024-07-23 DOI:10.1242/dev.202823
Sarah T Attrill, Hugh Mulvey, Clément Champion, Liam Dolan
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引用次数: 0

摘要

陆生植物的多细胞单倍体阶段是由减数分裂产生的单倍体细胞--孢子发育而成的。这些孢子从非极性状态开始,形成极性,进行不对称分裂,并建立第一对称轴。在这里,我们展示了在 Marchantia polymorpha 孢子细胞极化过程中,细胞核从细胞中心点迁移到基极。细胞核前缘的微管组织中心启动了核表面与基极皮层之间的微管阵列。与此同时,皮层微管从顶端半球消失,但在基部半球继续存在。与此同时,在细胞核和基极皮层之间形成了密集的细肌动蛋白丝网络。微管或肌动蛋白丝的实验性解聚会破坏细胞的不对称性。这些数据表明,细胞骨架在孢子极化过程中会重组,并控制着细胞核向基极的定向迁移。细胞核在基极的存在为非对称细胞分裂提供了细胞不对称性,从而建立了植物的顶-基轴。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microtubules and actin filaments direct nuclear movement during the polarisation of Marchantia spore cells.

The multicellular haploid stage of land plants develops from a single haploid cell produced by meiosis - the spore. Starting from a non-polar state, these spores develop polarity, divide asymmetrically and establish the first axis of symmetry. Here, we show that the nucleus migrates from the cell centroid to the basal pole during polarisation of the Marchantia polymorpha spore cell. A microtubule organising centre on the leading edge of the nucleus initiates a microtubule array between the nuclear surface and the cortex at the basal pole. Simultaneously, cortical microtubules disappear from the apical hemisphere but persist in the basal hemisphere. This is accompanied by the formation a dense network of fine actin filaments between the nucleus and the basal pole cortex. Experimental depolymerisation of either microtubules or actin filaments disrupts cellular asymmetry. These data demonstrate that the cytoskeleton reorganises during spore polarisation and controls the directed migration of the nucleus to the basal pole. The presence of the nucleus at the basal pole provides the cellular asymmetry for the asymmetric cell division that establishes the apical-basal axis of the plant.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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