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蛋白质合成的抑制会破坏裂殖酵母粟酒裂殖酵母中的高尔基体。

Inhibition of protein synthesis disrupts the Golgi apparatus in the fission yeast, Schizosaccharomyces pombe.

作者信息

Ayscough K, Warren G

机构信息

Cell Biology Laboratory, Imperial Cancer Research Fund, London, U.K.

出版信息

Yeast. 1994 Jan;10(1):1-11. doi: 10.1002/yea.320100102.

Abstract

Schizosaccharomyces pombe was treated with either cycloheximide or anisomycin at levels sufficient to inhibit > 95% of protein synthesis for periods upon to 3 h, equivalent to one cell cycle. Treatment for as little as 1 h caused significant loss of the Golgi apparatus by both immunofluorescence and electron microscopy. The loss was quantitated by stereology on electron micrographs. Nearly 90% of the stacked Golgi was lost over a 3 h period. No other intracellular membrane compartment seemed to be affected. Measurement of enzyme activities confirmed these observations. The activity of a resident of the Golgi apparatus, alpha-1,2 galactosyltransferase, was reduced over this time, whereas the endoplasmic reticulum marker, BiP, and the cytoplasmic enzyme, hexokinase, were unaffected. The morphological changes associated with cycloheximide addition were reversed on its removal, though there was a lag before cells recommenced growth or secretion of the enzyme, acid phosphatase.

摘要

用足以抑制95%以上蛋白质合成的放线菌酮或茴香霉素处理粟酒裂殖酵母长达3小时,这相当于一个细胞周期。仅处理1小时,通过免疫荧光和电子显微镜观察就发现高尔基体有显著损失。通过对电子显微镜照片进行体视学分析对损失进行了定量。在3小时内,近90%的堆叠式高尔基体消失。似乎没有其他细胞内膜区室受到影响。酶活性的测定证实了这些观察结果。在此期间,高尔基体驻留酶α-1,2半乳糖基转移酶的活性降低,而内质网标记物BiP和细胞质酶己糖激酶不受影响。添加放线菌酮后出现的形态变化在去除该药物后逆转,不过在细胞重新开始生长或分泌酸性磷酸酶之前有一段延迟期。

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