干扰素对细胞抗细胞作用的线粒体mRNA水平和线粒体功能的抑制。

J Lou, S L Anderson, L Xing, B Y Rubin
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引用次数: 20

摘要

从Daudi细胞中分离的聚腺苷化RNA制备的lambda cDNA文库进行了差异筛选,以分离识别干扰素(IFN)处理后水平降低的mRNA的cDNA。对分离的20个cDNA克隆进行Southern blot和DNA序列分析,发现它们代表线粒体编码的以下蛋白质mrna:细胞色素c氧化酶亚基II和III、atp酶6、细胞色素b和NADH脱氢酶亚基1。利用这些cdna和剩余线粒体编码mrna产生的寡核苷酸进行的Northern blot分析表明,ifn - α处理Daudi细胞介导了所有线粒体编码mrna水平的时间依赖性抑制。这种IFN-mediated效应研究表明:(i)的抑制这些mrna水平依赖于蛋白质合成,(2)它可以观察到发生之前,任何对胸苷公司可检测的影响,(3)的抑制程度与细胞的敏感性anticellular干扰素的作用,及(iv)的抑制这些rna的水平似乎源于影响转录水平而不是这些mrna的稳定性。对IFN处理的Daudi细胞的细胞呼吸水平的研究显示,IFN处理后3小时明显抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Suppression of mitochondrial mRNA levels and mitochondrial function in cells responding to the anticellular action of interferon.

A lambda cDNA library prepared from polyadenylated RNA isolated from Daudi cells was differentially screened to isolate cDNAs that recognize mRNA whose levels are reduced following interferon (IFN) treatment. Southern blot and DNA sequence analysis of 20 cDNA clones that were isolated revealed that they represented mitochondrially encoded mRNAs for the following proteins: cytochrome c oxidase subunits II and III, ATPase 6, cytochrome b, and subunit 1 of the NADH dehydrogenase. Northern blot analysis employing these cDNAs and oligonucleotides generated to the remaining mitochondrially encoded mRNAs demonstrated that IFN-alpha treatment of Daudi cells mediates a time-dependent suppression of the level of all of the mitochondrially encoded mRNAs. Study of this IFN-mediated effect reveals that: (i) the suppression of the level of these mRNAs is dependent on protein synthesis, (ii) it can be observed to occur prior to any detectable effect on thymidine incorporation, (iii) the degree of suppression correlates with the sensitivity of the cells to the anticellular action of IFN, and (iv) the suppression of the level of these RNAs appears to result from an effect on the level of transcription rather than on the stability of these mRNAs. A study of the level of cellular respiration in IFN-treated Daudi cells reveals a clear suppression 3 h following IFN treatment.

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