Perlman D, Raney P, Halvorson H O
Mol Cell Biol. 1984 Sep;4(9):1682-8. doi: 10.1128/mcb.4.9.1682-1688.1984.
A single structural gene, SUC2, encodes both secreted and cytoplasmic invertase in Saccharomyces cerevisiae. It is known that the unprocessed polypeptides which differ by a secretion signal sequence are encoded by separate mRNAs. This unusual transcriptional organization raises the question as to the degree to which the transcripts can be independently regulated. To define a system for studying this problem, we examined invertase transcription after various physiological perturbations of cells: rapid catabolite derepression, heat shock, and cell cycle arrest. With each treatment, fluctuations in mRNA levels for both cytoplasmic and secreted invertase were observed. We concluded that (i) catabolite-derepressed synthesis of the mRNAs occurs rapidly after a drop in glucose, is a sustained response, and does not require de novo protein synthesis; (ii) heat shock transcription of both invertase mRNAs is, in contrast, a brief and transient response requiring de novo protein synthesis; and (iii) alpha-mating hormone treatment (G1 phase arrest and release) results in regular and coordinated synthesis of both mRNAs midway between rounds of histone mRNA synthesis. We propose that invertase mRNA regulation involves constitutively synthesized transcriptional factors (observed during catabolite derepression) and transient factors (observed during heat shock and possibly during synchronous growth). Moreover, the mRNA levels for secreted and cytoplasmic invertase can be independently regulated.
酿酒酵母中的一个结构基因SUC2编码分泌型和胞质型两种转化酶。已知由分泌信号序列不同的未加工多肽由不同的mRNA编码。这种不寻常的转录组织引发了一个问题,即转录本在多大程度上可以独立调节。为了定义一个研究这个问题的系统,我们在细胞经历各种生理扰动后检测了转化酶的转录:快速碳源分解代谢物阻遏解除、热休克和细胞周期停滞。每种处理后,都观察到胞质型和分泌型转化酶的mRNA水平波动。我们得出以下结论:(i)在葡萄糖水平下降后,mRNA的碳源分解代谢物阻遏解除合成迅速发生,是一种持续反应,且不需要从头合成蛋白质;(ii)相反,两种转化酶mRNA的热休克转录是一种短暂的瞬时反应,需要从头合成蛋白质;(iii)α-交配激素处理(G1期停滞和释放)导致两种mRNA在组蛋白mRNA合成轮次之间的中间阶段有规律且协调地合成。我们提出,转化酶mRNA的调节涉及组成型合成的转录因子(在碳源分解代谢物阻遏解除期间观察到)和瞬时因子(在热休克期间以及可能在同步生长期间观察到)。此外,分泌型和胞质型转化酶的mRNA水平可以独立调节。