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在对干扰素的抗细胞作用产生反应的细胞中,线粒体mRNA水平和线粒体功能受到抑制。

Suppression of mitochondrial mRNA levels and mitochondrial function in cells responding to the anticellular action of interferon.

作者信息

Lou J, Anderson S L, Xing L, Rubin B Y

机构信息

Department of Biological Sciences, Fordham University, Bronx, NY 10458.

出版信息

J Interferon Res. 1994 Feb;14(1):33-40. doi: 10.1089/jir.1994.14.33.

Abstract

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.

摘要

从Daudi细胞中分离的聚腺苷酸化RNA构建的λ cDNA文库经过差异筛选,以分离那些能识别在干扰素(IFN)处理后水平降低的mRNA的cDNA。对分离得到的20个cDNA克隆进行Southern印迹和DNA序列分析,结果显示它们代表了以下蛋白质的线粒体编码mRNA:细胞色素c氧化酶亚基II和III、ATP酶6、细胞色素b以及NADH脱氢酶亚基1。利用这些cDNA以及针对其余线粒体编码mRNA生成的寡核苷酸进行Northern印迹分析,结果表明,用IFN-α处理Daudi细胞可介导所有线粒体编码mRNA水平的时间依赖性抑制。对这种IFN介导的效应的研究表明:(i)这些mRNA水平的抑制依赖于蛋白质合成;(ii)在对胸苷掺入产生任何可检测到的影响之前就能观察到这种抑制;(iii)抑制程度与细胞对IFN抗细胞作用的敏感性相关;(iv)这些RNA水平的抑制似乎是由于对转录水平的影响,而不是对这些mRNA稳定性的影响。对IFN处理的Daudi细胞中的细胞呼吸水平进行研究发现,IFN处理3小时后细胞呼吸明显受到抑制。

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