粗神经孢子虫5S rRNA基因与5S rRNA结合核糖体蛋白同源基因的非坐标调控。

I de la Serna, T P Cujec, Y Shi, B M Tyler
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引用次数: 2

摘要

在真核生物中,核糖体蛋白的水平在不同的营养条件和不同的发育阶段受到协调调节。关于核糖体蛋白水平如何与rRNA水平耦合,我们所知甚少。由5S rRNA和核糖体蛋白组成的核糖核蛋白颗粒的形成是核糖体组装的早期步骤。为了研究这两种核糖体成分在粗神经孢子虫中是如何被调控的,我们克隆了5S rRNA结合核糖体蛋白(crp-4)的编码基因,并利用源自40S前体RNA的报告RNA建立了一种新的系统来测量体内5S rRNA的相对转录率。报告RNA是在体内从5S rRNA中切割出来的,因此我们可以区分5S rRNA转录率和5S rRNA稳定性的变化。利用该系统,我们发现在碳上升或碳下降过程中,5S rRNA的转录是组成性的,与crp-4 mRNA或40S rRNA的水平不协调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-coordinate regulation of 5S rRNA genes and the gene encoding the 5S rRNA-binding ribosomal protein homolog in Neurospora crassa.

In eukaryotes, the levels of ribosomal proteins are coordinately regulated under varying nutritional conditions and at different developmental stages. Little is known about how ribosomal protein levels are coupled to the levels of rRNA. The formation of a ribonucleoprotein particle composed of 5S rRNA and a ribosomal protein is an early step in ribosome assembly. To investigate how these two ribosomal components are regulated in Neurospora crassa, we cloned the gene encoding the 5S rRNA-binding ribosomal protein (crp-4) and developed a novel system for measuring relative 5S rRNA transcriptional rates in vivo, using a reporter RNA derived from the 40S precursor RNA. The reporter RNA is cleaved from the 5S rRNA in vivo and therefore allows us to distinguish between changes in the 5S rRNA transcription rate and 5S rRNA stability. Using this system, we found that transcription of 5S rRNA is constitutive and is not coordinated with the levels of crp-4 mRNA or with 40S rRNA levels during a carbon upshift or a carbon downshift.

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