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甲酰胺诱导的中心体改变会导致异常纺锤极形成。

Centrosome alterations induced by formamide cause abnormal spindle pole formations.

作者信息

Schatten H, Hueser C N, Chakrabarti A

机构信息

Department of Veterinary Pathobiology, University of Missouri-Columbia, 1600 East Rollins Street, Columbia, MO 65211, USA.

出版信息

Cell Biol Int. 2000;24(9):611-20. doi: 10.1006/cbir.2000.0537.

Abstract

The formation of the bipolar mitotic apparatus depends on accurate centrosome organization which is crucial for the separation of the genome during cell division. While it has been shown that mutations and overexpression of centrosome proteins (Brinkley and Goepfert, 1998; Pihan et al., 1998) can cause abnormal spindle pole formation, here we report that damages to centrosome structure caused by the chaotropic agent formamide will cause multipolar mitoses upon recovery from the effect when applied at first cell division in sea urchin eggs. Formamide was used as a chemical tool to manipulate centrosome structure and to investigate the effects on microtubule organization. When 1-1.5 m formamide was administered for 30 min at prometaphase of first cell division, microtubules were disassembled and centrosomes compacted into dense spheres around highly condensed chromatin. Upon recovery from formamide, centrosomes decompacted and attempted to form various mitotic organizations. Normal recovery (and attempts of recovery) to bipolarity was possible in five percent of cells treated with 1-1.5 m formamide for 30 min, but abnormal patterns of spindle formation were observed in all other cells, which included mono- (20%), tri (45%), and multipolar (30%) formations organized by mono-, tri-, and multipolar centrosome clusters. When cells were treated with 1.5 m formamide for 90 min, centrosomes became pulverized and fragmented and only monopolar mitotic formations were observed upon recovery. These results are highly reproducible and reveal that abnormalities in centrosome structure can lead to abnormal mitosis which is not caused by mutation or overexpression of centrosome proteins.

摘要

双极有丝分裂装置的形成依赖于精确的中心体组织,这对于细胞分裂过程中基因组的分离至关重要。虽然已经表明中心体蛋白的突变和过表达(Brinkley和Goepfert,1998年;Pihan等人,1998年)会导致异常的纺锤体极形成,但在此我们报告,当在海胆卵的第一次细胞分裂时施加离液剂甲酰胺对中心体结构造成损伤后,在从其影响中恢复时会导致多极有丝分裂。甲酰胺被用作一种化学工具来操纵中心体结构并研究其对微管组织的影响。当在第一次细胞分裂的前中期用1 - 1.5 M甲酰胺处理30分钟时,微管被拆解,中心体围绕高度浓缩的染色质压缩成致密的球体。从甲酰胺处理中恢复后,中心体解压缩并试图形成各种有丝分裂组织。在用1 - 1.5 M甲酰胺处理30分钟的细胞中,5%的细胞有可能正常恢复(以及恢复尝试)成双极性,但在所有其他细胞中都观察到了异常的纺锤体形成模式,其中包括由单极、三极和多极中心体簇组织的单极(20%)、三极(45%)和多极(30%)形成。当用1.5 M甲酰胺处理细胞90分钟时,中心体变得粉碎和破碎,恢复时仅观察到单极有丝分裂形成。这些结果具有高度可重复性,表明中心体结构异常可导致异常有丝分裂,这并非由中心体蛋白的突变或过表达引起。

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