Law R H, Devenish R J
Department of Biochemistry, Monash University, Clayton, Victoria, Australia.
Biochem Int. 1988 Oct;17(4):673-9.
The utility of antisense RNA as a means of regulating gene expression in yeast has been explored by inserting into a high copy number yeast expression vector an ADE1 gene fragment in such an orientation so as to produce antisense RNA in vivo which could hybridize to natural ADE1 mRNA. Northern blotting analysis of total cellular RNA extracted from transformed yeast cells confirmed the presence of high levels of antisense RNA to ADE1 mRNA within cells. However the high level of expression of antisense RNA did not result in production of Ade- cells.
通过将ADE1基因片段以特定方向插入高拷贝数酵母表达载体,使其在体内产生可与天然ADE1 mRNA杂交的反义RNA,来探索反义RNA作为调节酵母基因表达手段的效用。对从转化酵母细胞中提取的总细胞RNA进行Northern印迹分析,证实细胞内存在高水平的针对ADE1 mRNA的反义RNA。然而,反义RNA的高表达水平并未导致产生Ade-细胞。