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大雌异水霉游动孢子形成过程中细胞核位置的建立与维持:细胞骨架的作用

Establishment and maintenance of nuclear position during zoospore formation in allomyces macrogynus: roles of the cytoskeleton.

作者信息

Lowry DS, Fisher KE, Roberson RW

机构信息

Department of Plant Biology, Arizona State University, Tempe, Arizona, 85287-1601, USA.

出版信息

Fungal Genet Biol. 1998 Jun;24(1-2):34-44. doi: 10.1006/fgbi.1998.1060.

DOI:10.1006/fgbi.1998.1060
PMID:9742191
Abstract

The involvement of the microtubule (MT) and actin microfilament (MF) cytoskeletons in establishing nuclear positions during zoosporogenesis in Allomyces macrogynus was assessed using selective cytoskeletal disrupting treatments and documented with light microscopy. These experiments were coupled with low-speed centrifugation studies to determine the degree to which cytoskeletal elements anchor nuclear position. At the onset of zoospore formation, nuclei were positioned only in cortical cytoplasmic regions of the zoosporangia (ZS). Immunofluorescence microscopy revealed that MTs primarily emanated from centrosomal regions into the surrounding cytoplasm at this stage. During delimitation of the cytoplasm into individual uninucleate zoospores, nuclei migrated from cortical regions to become distributed throughout the cytoplasm. Coincident with nuclear migrations, MTs were primarily organized at and emanated from nuclear surfaces, forming extensive perinuclear arrays. Nuclear migrations were suppressed in ZS induced to sporulate in the presence of cytochalasin D, an actin MF inhibiting compound. Disruption of MTs with nocodazole did not block nuclear migrations, although resultant nuclear spacing was irregular. Centrifugation treatments of control and drug-treated ZS demonstrated that nuclear positions were stabilized by perinuclear MT arrays. The results indicate that nuclear motility in ZS of A. macrogynus is the result of an actin-based system while perinuclear MTs arrays function to establish and fix nuclear position during zoospore formation. Copyright 1998 Academic Press.

摘要

利用选择性细胞骨架破坏处理方法,评估了大雌异水霉游动孢子形成过程中微管(MT)和肌动蛋白微丝(MF)细胞骨架在确定细胞核位置方面的作用,并通过光学显微镜进行记录。这些实验与低速离心研究相结合,以确定细胞骨架成分锚定细胞核位置的程度。在游动孢子形成开始时,细胞核仅位于游动孢子囊(ZS)的皮质细胞质区域。免疫荧光显微镜显示,在此阶段,微管主要从中心体区域延伸到周围细胞质中。在将细胞质分隔成单个单核游动孢子的过程中,细胞核从皮质区域迁移并分布于整个细胞质中。与细胞核迁移同时发生的是,微管主要在核表面组织并从核表面延伸出来,形成广泛的核周阵列。在存在细胞松弛素D(一种肌动蛋白微丝抑制化合物)的情况下诱导形成游动孢子的游动孢子囊中,细胞核迁移受到抑制。用诺考达唑破坏微管并没有阻止细胞核迁移,尽管最终的核间距不规则。对对照和药物处理的游动孢子囊进行离心处理表明,核周微管阵列稳定了细胞核位置。结果表明,大雌异水霉游动孢子囊中细胞核的运动是基于肌动蛋白的系统作用的结果,而核周微管阵列在游动孢子形成过程中起到建立和固定细胞核位置的作用。版权所有1998年学术出版社。

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