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通过cDNA.mRNA杂交介导的无细胞蛋白质合成抑制分析mRNA群体

Analysis of mRNA populations by cDNA.mRNA hybrid-mediated inhibition of cell-free protein synthesis.

作者信息

Hastie N D, Held W A

出版信息

Proc Natl Acad Sci U S A. 1978 Mar;75(3):1217-21. doi: 10.1073/pnas.75.3.1217.

Abstract

Hybridization of mRNA to its corresponding cDNA was found to specifically inhibit translation of the mRNA in vitro. Using hybridization of globin cDNA to globin mRNA as a model system, we found that equivalent amounts of cDNA were required both for the saturation of the mRNA hybridization and for complete inhibition of globin synthesis. Also, the rate of inactivation of translation was identical to the rate of hybridization and followed the predicted kinetic form. This assay has been applied to the analysis of a set of abundant mRNAs in mouse liver. Hybridization of liver mRNA with total liver cDNA in slight excess to a low C(0)t value specifically inhibited translation of several major polypeptides. Melting of the hybrids prior to translation restored synthesis of these polypeptides. Moreover, we found that different liver mRNAs are inactivated with different kinetics; the results suggest that the mRNAs for the major urinary polypeptide and for albumin are the most abundant and second most abundant, respectively, in mouse liver. The general applications of this technique are discussed.

摘要

发现mRNA与其相应的cDNA杂交可在体外特异性抑制mRNA的翻译。以珠蛋白cDNA与珠蛋白mRNA杂交作为模型系统,我们发现,mRNA杂交饱和以及完全抑制珠蛋白合成均需要等量的cDNA。此外,翻译失活速率与杂交速率相同,并遵循预测的动力学形式。该分析方法已应用于对小鼠肝脏中一组丰富mRNA的分析。肝脏mRNA与总量略过量的肝脏cDNA在低C(0)t值下杂交,可特异性抑制几种主要多肽的翻译。翻译前杂交体的解链可恢复这些多肽的合成。此外,我们发现不同的肝脏mRNA以不同的动力学失活;结果表明,主要尿蛋白和白蛋白的mRNA分别是小鼠肝脏中最丰富和第二丰富的mRNA。本文讨论了该技术的一般应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b6/411441/2d5bcc601baf/pnas00015-0180-a.jpg

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