Piper P W, Curran B P
Department of Biochemistry, University College London, UK.
Curr Genet. 1990 Feb;17(2):119-23. doi: 10.1007/BF00312855.
This study demonstrates how varying the promoter strength of an essential gene on a yeast 2 mu ORI-STB YEp multicopy vector can influence vector copy levels. A phosphoglycerate kinase gene (PGK) on this plasmid was made essential for fermentative growth by transformation into a pgk- yeast strain. When in these PGK+ transformants the requirement for PGK expression was the sole selective criterion for plasmid maintenance, PGK promoter activity was inversely related to vector copy levels. Plasmids with an efficiently-transcribed PGK gene were maintained at approximately one copy per cell, whereas those lacking the UAS that normally directs high basal PGK transcription levels were present at up to 10-15 copies. All cultures of these PGK+ transformants contained only a low proportion of pgk- cells. Since mitotic loss of the plasmid arrests growth through loss of a functional PGK allele, PGK confers high stability to the YEp vector in such a pgk- genetic background. In this system YEp vector levels are probably influenced by PGK transcription because high expression of PGK is needed in rapid fermentative growth. Remarkably, low plasmid PGK promoter activity caused PGK mRNA levels slightly higher than those found in yeast with normal PGK regulation. A higher plasmid copy number is therefore not the only factor counteracting the effects of low PGK transcription, and it is possible that PGK mRNA becomes more stable in response to inefficient PGK transcription.
本研究展示了在酵母2μ ORI - STB YEp多拷贝载体上改变必需基因的启动子强度如何影响载体拷贝数水平。通过转化到pgk⁻酵母菌株中,使该质粒上的磷酸甘油酸激酶基因(PGK)对于发酵生长至关重要。在这些PGK⁺转化体中,当对PGK表达的需求是质粒维持的唯一选择标准时,PGK启动子活性与载体拷贝数水平呈负相关。具有高效转录的PGK基因的质粒维持在每个细胞约一个拷贝,而那些缺乏通常指导高基础PGK转录水平的上游激活序列(UAS)的质粒则以高达10 - 15个拷贝存在。这些PGK⁺转化体的所有培养物中仅含有低比例的pgk⁻细胞。由于质粒的有丝分裂丢失会通过功能性PGK等位基因的丢失而阻止生长,因此在这种pgk⁻遗传背景下,PGK赋予YEp载体高稳定性。在这个系统中,YEp载体水平可能受PGK转录影响,因为在快速发酵生长中需要高表达的PGK。值得注意的是,低质粒PGK启动子活性导致PGK mRNA水平略高于正常PGK调控的酵母中的水平。因此,较高的质粒拷贝数不是抵消低PGK转录影响的唯一因素,并且有可能PGK mRNA会因低效的PGK转录而变得更稳定。