Scafe C, Martin C, Nonet M, Podos S, Okamura S, Young R A
Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, Massachusetts 02142.
Mol Cell Biol. 1990 Mar;10(3):1270-5. doi: 10.1128/mcb.10.3.1270-1275.1990.
Conditional mutations in the Saccharomyces cerevisiae RNA polymerase II large subunit, RPB1, were obtained by introducing a mutagenized RPB1 plasmid into yeast cells, selecting for loss of the wild-type RPB1 gene, and screening the cells for heat or cold sensitivity. Sequence analysis of 10 conditional RPB1 mutations and 10 conditional RPB2 mutations revealed that the amino acid residues altered by these distinct mutations are nearly always invariant among eucaryotic RPB1 and RPB2 homologs. These results suggest that RNA polymerase mutants might be obtained in other eucaryotic organisms by alteration of these invariant residues.
通过将诱变的RPB1质粒导入酵母细胞,筛选野生型RPB1基因缺失,并对细胞进行热敏感性或冷敏感性筛选,获得了酿酒酵母RNA聚合酶II大亚基RPB1的条件性突变。对10个RPB1条件性突变和10个RPB2条件性突变进行序列分析,结果显示,这些不同突变所改变的氨基酸残基在真核生物RPB1和RPB2同源物中几乎总是不变的。这些结果表明,通过改变这些不变残基,可能在其他真核生物中获得RNA聚合酶突变体。