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Cadmium modification of nucleolar ultrastructure and RNA synthesis in Physarum polycephalum

机译:镉修饰多头绒泡菌核仁超微结构及RNa合成

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摘要

Exposure of the acellular slime mold Physarum polycephalum to cadmium resulted in distortion of nucleolar structure and in inhibition of RNA synthesis. The extent of these lesions was dependent on concentration of cadmium, as well as duration and timing of exposure in the cell cycle. A 30-min exposure to 5 x 10-4 m CdSO4, initiated just as DNA synthesis began, inhibited RNA synthesis by 50% and caused subtle nucleolar changes: eccentric placement of nucleoli in nuclei, and the appearance of multiple nucleolar bodies in low incidence. Exposure to either 5 x 10-4 m or 1.5 x 10-3 m CdSO4 for 4 hr depressed RNA synthesis to 20-25% of control values and caused ring-shaped nucleoli. In electron micrographs of cadmium-treated cells, nucleoli appeared as electron dense rings of nucleolar material enclosing less intensely staining central zones, in contrast to control nucleoli which appeared as uniformly dense, nearly spherical bodies. Three-dimensional reconstructions showed that the "ring" was, in actuality, a sphere of nucleolar material completely surrounding a central cavity. A 4-hr exposure to 5 x 10-4 or 1.5 x 10-3 m CdSO4 after postmitotic reconstruction was complete and DNA synthesis had been underway for 2 hr or more inhibited RNA synthesis by 50%, but nucleolar rings were not formed. These observations identify the nucleus as a target for cadmium, or for effectors which mediate cadmium toxicity, and they suggest that disruption of nucleolar function (i.e., synthesis of RNA) and/or of nucleolar structure may be underlying mechanisms of cadmium toxicity.
机译:暴露于幼苗的无细胞粘液模子生理骨髓,导致核仁结构的扭曲和RNA合成的抑制作用。这些病变的程度依赖于镉的浓度,以及细胞周期中暴露的持续时间和时间。 30分钟暴露于5×10-4米CDSO4,就像DNA合成开始一样,抑制RNA合成50%并导致细微的核仁变化:核细胞中核仁的偏心放置,以及多种核心在低发病率下的外观。暴露于5×10-4m或1.5×10 -3 m CDSO4,4小时抑制RNA合成至20-25%的对照值并引起环形核仁。在镉处理细胞的电子显微照片中,核仁出现为核磁材料的电子致密环,其封闭着较少强烈的染色中央区域,以控制核仁,其出现为均匀致密的,几乎球形的体。三维重建表明,“环”实际上是完全围绕中心腔的核仁材料球体。在后关染案重建后,4小时暴露于5×10-4或1.5×10 -3 M CDSO4完成,并且在2小时或更高抑制的RNA合成的情况下,DNA合成抑制了50%,但未形成核仁环。这些观察结果将细胞核鉴定为镉的靶标,或用于介导镉毒性的效果,并且他们表明核仁函数的破坏(即RNA的合成)和/或核仁结构的破坏可能是镉毒性的潜在机制。

著录项

  • 作者

    J.F. Sina; B. Chin;

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  • 年度 1978
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  • 正文语种 en_us
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