Newman B J, Grindley N D
Cell. 1984 Sep;38(2):463-9. doi: 10.1016/0092-8674(84)90501-4.
The resolvase protein encoded by the gamma delta transposon has two functions. It catalyzes a site-specific recombination, and it negatively regulates the expression of two transposon genes. Both functions involve the action of resolvase at the res site. To define regions of resolvase that are involved specifically in the recombination reaction, we have isolated and characterized mutants that are defective in cointegrate resolution but retain the ability to bind to res (as measured by regulatory activity). Nine independent mutants were found to contain six different amino acid substitutions among just four distinct residues. The altered residues all lie within the 140 amino acid amino-terminal domain of resolvase and fall within two clusters of amino acids that are highly conserved in other related recombinases. The regulatory properties of the mutants suggest that one of these clusters may be involved in the interaction of the catalytic domain with the crossover site.
由γδ转座子编码的解离酶蛋白具有两种功能。它催化位点特异性重组,并负向调节两个转座子基因的表达。这两种功能都涉及解离酶在res位点的作用。为了确定解离酶中专门参与重组反应的区域,我们分离并鉴定了在共整合体解离方面有缺陷但保留与res结合能力的突变体(通过调节活性来衡量)。发现九个独立的突变体在仅四个不同的残基中包含六个不同的氨基酸替换。改变的残基都位于解离酶的140个氨基酸的氨基末端结构域内,并且落在其他相关重组酶中高度保守的两个氨基酸簇内。突变体的调节特性表明,这些簇中的一个可能参与催化结构域与交叉位点的相互作用。