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放线菌素D抑制后转录的恢复情况

On the recovery of transcription after inhibition by actinomycin D.

作者信息

Sawicki S G, Godman G C

出版信息

J Cell Biol. 1972 Nov;55(2):299-309. doi: 10.1083/jcb.55.2.299.

DOI:10.1083/jcb.55.2.299
PMID:4627744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2108806/
Abstract

After pulse exposure to concentrations of actinomycin D (AMD) sufficient to abolish transcription, Vero cells recover RNA synthesis much more rapidly than most other cell types. This is only in part attributable to the remarkable capacity of Vero very promptly to excrete bound AMD, elimination of which, although necessary, is not a sufficient condition for resurgence of RNA synthesis. After elimination of higher concentrations of AMD from Vero, although over-all RNA synthesis resumes a normal rate within 24 hr, protein synthesis lags, and a long period of division-delay ensues. Division-delay lasting 2-3 days results from exposure of Vero to doses of AMD greater than those that suppress RNA synthesis by greater than 90% (e.g. 1 microg/ml for 2 hr) but not by lower doses, which permit almost immediate reentry into the cell cycle. In contrast, although L cells recover over-all RNA synthesis very slowly after pulse treatment with AMD, resumption of protein synthesis or cell division is not comparably delayed thereafter. These and other data suggest that the early restoration of RNA synthesis in Vero after relief of inhibition by AMD is qualitatively imperfect. The results reported herein are explainable by the hypothesis that the synthesis of those species of RNA which are involved, directly or indirectly, in reactivating the transcription of genes controlling progression in the cell cycle is relatively resistant to suppression by AMD. Decay of such RNA templates and their products, which differs in different cell types during inhibition by AMD, determines the duration of division-delay.

摘要

在用足以阻断转录的放线菌素D(AMD)脉冲处理后,Vero细胞恢复RNA合成的速度比大多数其他细胞类型快得多。这部分归因于Vero细胞迅速排泄结合的AMD的显著能力,虽然消除AMD是RNA合成恢复的必要条件,但并非充分条件。从Vero细胞中消除较高浓度的AMD后,尽管总体RNA合成在24小时内恢复正常速率,但蛋白质合成滞后,随后会出现长时间的分裂延迟。持续2至3天的分裂延迟是由于Vero细胞暴露于高于能将RNA合成抑制90%以上的剂量的AMD(例如,1微克/毫升处理2小时),而较低剂量则不会导致这种情况,较低剂量允许细胞几乎立即重新进入细胞周期。相比之下,尽管L细胞在用AMD脉冲处理后恢复总体RNA合成非常缓慢,但此后蛋白质合成或细胞分裂的恢复并没有类似的延迟。这些以及其他数据表明,Vero细胞在AMD抑制解除后RNA合成的早期恢复在质量上是不完美的。本文报道的结果可以用以下假说来解释:那些直接或间接参与重新激活控制细胞周期进程的基因转录的RNA种类的合成相对抗AMD的抑制。这种RNA模板及其产物的降解在AMD抑制期间在不同细胞类型中有所不同,决定了分裂延迟的持续时间。

相似文献

1
On the recovery of transcription after inhibition by actinomycin D.放线菌素D抑制后转录的恢复情况
J Cell Biol. 1972 Nov;55(2):299-309. doi: 10.1083/jcb.55.2.299.
2
On the differential cytotoxicity of actinomycin D.论放线菌素D的差异细胞毒性。
J Cell Biol. 1971 Sep;50(3):746-61. doi: 10.1083/jcb.50.3.746.
3
Study on the reinitiation of transcription in 37 RC cells after actinomycin D inhibition. Spectrum of major RNA species resynthesized after maximal suppression by the drug.放线菌素D抑制后37 RC细胞中转录再起始的研究。药物最大抑制后重新合成的主要RNA种类谱。
J Cell Biol. 1975 Dec;67(3):538-50. doi: 10.1083/jcb.67.3.538.
4
Resistance of African green monkey kidney cell lines to actinomycin D: drug uptake in 37 RC cells after persistent inhibition of transcription.非洲绿猴肾细胞系对放线菌素D的抗性:转录持续抑制后37 RC细胞中的药物摄取
Antimicrob Agents Chemother. 1979 Feb;15(2):300-12. doi: 10.1128/AAC.15.2.300.
5
37RC cells rapidly recover their RNA synthesis after inhibition with high doses of actinomycin D.37RC细胞在用高剂量放线菌素D抑制后能迅速恢复其RNA合成。
J Cell Biol. 1972 Jan;52(1):171-4. doi: 10.1083/jcb.52.1.171.
6
Sequential irreversible, actinomycin D-sensitive, and cycloheximide-sensitive steps prior to cortisol inhibition of uridine utilization by P1798 tumor lymphocytes.在皮质醇抑制P1798肿瘤淋巴细胞的尿苷利用之前,存在连续的不可逆步骤,这些步骤对放线菌素D敏感且对环己酰亚胺敏感。
Cancer Res. 1975 Aug;35(8):2145-53.
7
Schedule-dependent effects of two consecutive, divided, low doses of actinomycin D on translocation of protein B23, inhibition of cell growth and RNA synthesis in HeLa cells.连续两次低剂量放线菌素D对HeLa细胞中蛋白质B23转位、细胞生长抑制及RNA合成的时间依赖性效应。
Int J Cancer. 1992 Sep 9;52(2):317-22. doi: 10.1002/ijc.2910520227.
8
Actinomycin D binding to 37 RC and HeLa cell lines.放线菌素D与37 RC和HeLa细胞系的结合。
Biochim Biophys Acta. 1972 Dec 6;287(2):330-9. doi: 10.1016/0005-2787(72)90382-6.
9
The effects of low concentrations of actinomycin D upon nucleic acid synthesis in different cell types.低浓度放线菌素D对不同细胞类型核酸合成的影响。
Experientia. 1973 Nov 15;29(11):1390-2. doi: 10.1007/BF01922836.
10
Short exposure to actinomycin D induces "reversible" translocation of protein B23 as well as "reversible" inhibition of cell growth and RNA synthesis in HeLa cells.短时间暴露于放线菌素D会诱导HeLa细胞中蛋白质B23的“可逆”易位以及细胞生长和RNA合成的“可逆”抑制。
Cancer Res. 1990 Sep 15;50(18):5987-91.

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Resistance of African green monkey kidney cell lines to actinomycin D: drug uptake in 37 RC cells after persistent inhibition of transcription.非洲绿猴肾细胞系对放线菌素D的抗性:转录持续抑制后37 RC细胞中的药物摄取
Antimicrob Agents Chemother. 1979 Feb;15(2):300-12. doi: 10.1128/AAC.15.2.300.

本文引用的文献

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37RC cells rapidly recover their RNA synthesis after inhibition with high doses of actinomycin D.37RC细胞在用高剂量放线菌素D抑制后能迅速恢复其RNA合成。
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