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酿酒酵母中核糖体蛋白基因与生长相关的表达

Growth-related expression of ribosomal protein genes in Saccharomyces cerevisiae.

作者信息

Kraakman L S, Griffioen G, Zerp S, Groeneveld P, Thevelein J M, Mager W H, Planta R J

机构信息

Department of Biochemistry and Molecular Biology, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

Mol Gen Genet. 1993 May;239(1-2):196-204. doi: 10.1007/BF00281618.

Abstract

The rate of ribosomal protein gene (rp-gene) transcription in yeast is accurately adjusted to the cellular requirement for ribosomes under various growth conditions. However, the molecular mechanisms underlying this co-ordinated transcriptional control have not yet been elucidated. Transcriptional activation of rp-genes is mediated through two different multifunctional transacting factors, ABF1 and RAP1. In this report, we demonstrate that changes in cellular rp-mRNA levels during varying growth conditions are not parallelled by changes in the in vitro binding capacity of ABF1 or RAP1 for their cognate sequences. In addition, the nutritional upshift response of rp-genes observed after addition of glucose to a culture growing on a non-fermentative carbon source turns out not to be the result of increased expression of the ABF1 and RAP1 genes or of elevated DNA-binding activity of these factors. Therefore, growth rate-dependent transcription regulation of rp-genes is most probably not mediated by changes in the efficiency of binding of ABF1 and RAP1 to the upstream activation sites of these genes, but rather through other alterations in the efficiency of transcription activation. Furthermore, we tested the possibility that cAMP may play a role in elevating rp-gene expression during a nutritional shift-up. We found that the nutritional upshift response occurs normally in several mutants defective in cAMP metabolism.

摘要

酵母中核糖体蛋白基因(rp基因)的转录速率在各种生长条件下都能精确地根据细胞对核糖体的需求进行调节。然而,这种协调转录控制的分子机制尚未阐明。rp基因的转录激活是通过两种不同的多功能反式作用因子ABF1和RAP1介导的。在本报告中,我们证明了在不同生长条件下细胞rp-mRNA水平的变化与ABF1或RAP1与其同源序列的体外结合能力的变化并不平行。此外,在向以非发酵碳源生长的培养物中添加葡萄糖后观察到的rp基因的营养上调反应,并非ABF1和RAP1基因表达增加或这些因子的DNA结合活性升高的结果。因此,rp基因的生长速率依赖性转录调控很可能不是由ABF1和RAP1与这些基因上游激活位点的结合效率变化介导的,而是通过转录激活效率的其他改变。此外,我们测试了cAMP在营养上调过程中可能在提高rp基因表达中发挥作用的可能性。我们发现,在几种cAMP代谢缺陷的突变体中,营养上调反应正常发生。

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