Bergkamp-Steffens G K, Hoekstra R, Planta R J
Laboratorium voor Biochemie en Moleculaire Biologie, Vrije Universiteit, Amsterdam, The Netherlands.
Yeast. 1992 Nov;8(11):903-22. doi: 10.1002/yea.320081102.
The transcription of the majority of the ribosomal protein (rp) genes of Saccharomyces cerevisiae is activated by cis-acting elements, designated RPG boxes, which specifically bind the multifunctional protein RAP1 in vitro. To investigate to what extent this global system of transcription regulation has been conserved, we have isolated a number of rp genes of the related yeast species Kluyveromyces lactis and Kluyveromyces marxianus, whose counterparts in Saccharomyces are controlled by RAP1. The coding regions of these genes showed a sequence similarity of about 90% when compared to their Saccharomyces counterparts. In contrast, little or no sequence similarity was found between the upstream regions and the intervening sequences of Kluyveromyces and Saccharomyces homologs. However, the occurrence and the position of the introns is conserved. The sequence data also show that the physical linkage that exists in S. cerevisiae between the rp genes encoding RP59 (CRY1), S24 and L46 is conserved in Kluyveromyces. Northern analysis demonstrated that each of the isolated Kluyveromyces genes is transcriptionally active. By sequence comparison we identified a number of conserved sequences in the upstream region of each of the Kluyveromyces rp genes, which we designated the X, Z and RPGK boxes. The last one is highly similar, though not identical, to the S. cerevisiae RPG box. Functional analysis of the intergenic region between the genes encoding Kluyveromyces ribosomal proteins S24 and L46 showed that the RPGK box (+Z box) functions as a transcriptional activator, while the X box acts as a transcriptional repressor. Band-shift assays confirmed the existence of a RAP1-like protein in Kluyveromyces that binds to the RPGK box but not to the S. cerevisiae RPG box. In contrast, S. cerevisiae RAP1 did recognize the RPGK box.
酿酒酵母大多数核糖体蛋白(rp)基因的转录由顺式作用元件(称为RPG框)激活,这些元件在体外能特异性结合多功能蛋白RAP1。为了研究这种全局转录调控系统在多大程度上得以保留,我们分离了相关酵母物种乳酸克鲁维酵母和马克斯克鲁维酵母的多个rp基因,酿酒酵母中其对应基因受RAP1调控。与酿酒酵母的对应基因相比,这些基因的编码区序列相似性约为90%。相比之下,克鲁维酵母和酿酒酵母同源物的上游区域和间隔序列之间几乎没有序列相似性。然而,内含子的出现和位置是保守的。序列数据还表明,酿酒酵母中编码RP59(CRY1)、S24和L46的rp基因之间存在的物理连锁在克鲁维酵母中是保守的。Northern分析表明,每个分离的克鲁维酵母基因都具有转录活性。通过序列比较,我们在每个克鲁维酵母rp基因的上游区域鉴定出了一些保守序列,我们将其命名为X、Z和RPGK框。最后一个与酿酒酵母的RPG框高度相似,但并不相同。对克鲁维酵母核糖体蛋白S24和L46编码基因之间的基因间区域进行功能分析表明,RPGK框(+Z框)作为转录激活因子起作用,而X框作为转录抑制因子起作用。凝胶迁移试验证实,克鲁维酵母中存在一种与RAP1样蛋白结合的蛋白,该蛋白能与RPGK框结合,但不能与酿酒酵母的RPG框结合。相比之下,酿酒酵母的RAP1确实能识别RPGK框。