Schaffrath R, Meinhardt F, Meacock P A
Department of Genetics, University of Leicester, Leicester, UK.
Mol Gen Genet. 1996 Feb 25;250(3):286-94. doi: 10.1007/BF02174386.
A k2/k1 plasmid gene shuffle system has been used to investigate linear plasmid promoter function in Kluyveromyces lactis. By transplacing various ORF5 deletion constructs from the larger plasmid k2 onto k1, and analysing trans-complementation of an ORF5(0) deletion on k2, a 40 bp k2 fragment, including the UCS motif of ORF5 (UCS5), has been identified as a cis-acting promoter element essential for ORF5 gene function. Qualitative and quantitative transcript analyses of a UCS5-ScLEU2 fusion gene using Northern blot analysis and phosphor image technology revealed a plasmid-dependent LEU2 transcript distinct in size (1.55 kb) and regulation from its nuclear counterpart (1.35 kb): cytoplasmic, UCS5-driven expression of the marker gene was non-repressible by leucine and reduced five- to eight-fold compared to fully derepressed nuclear K1LEU2 mRNA levels. Thus, the killer plasmids k2 and k1 appear to express low levels of transcript overall, when relative gene copy numbers (one for the nuclear allele versus 50-100 copies for the plasmid-borne LEU2 gene) are taken into account.
一种k2/k1质粒基因洗牌系统已被用于研究乳酸克鲁维酵母中线性质粒启动子的功能。通过将来自较大质粒k2的各种ORF5缺失构建体转位到k1上,并分析k2上ORF5(0)缺失的反式互补,一个40 bp的k2片段,包括ORF5的UCS基序(UCS5),已被鉴定为ORF5基因功能所必需的顺式作用启动子元件。使用Northern印迹分析和磷图像技术对UCS5-ScLEU2融合基因进行定性和定量转录分析,发现一种依赖于质粒的LEU2转录本,其大小(1.55 kb)和调控与核内对应物(1.35 kb)不同:标记基因在细胞质中由UCS5驱动的表达不受亮氨酸抑制,与完全去阻遏的核K1LEU2 mRNA水平相比降低了五至八倍。因此,考虑到相对基因拷贝数(核等位基因一个,而质粒携带的LEU2基因有50-100个拷贝),杀伤质粒k2和k1总体上似乎表达低水平的转录本。