Department of Genetics, North Carolina State University, Raleigh, North Carolina 27650.
Proc Natl Acad Sci U S A. 1980 Feb;77(2):1073-7. doi: 10.1073/pnas.77.2.1073.
The genetic component of variation of enzyme activity in natural populations of Drosophila melanogaster was investigated by using two sets of chromosome substitution lines. The constitution of a line of each type is: i(1)/i(1);+(2)/ +(2);i(3)/i(3) and i(1)/i(1);i(2)/ i(2);+(3)/+(3), where i refers to a chromosome from a highly inbred line and + refers to a chromosome from a natural population. The + but not the i chromosomes vary within a set of lines. By use of a randomized block design to test and estimate components of variance, 50 of the second- and 50 of the third- chromosome substitution lines have been screened for variation in the activity levels of seven enzymes. Six of the seven enzymes show a significant genetic component in at least one set of lines, and five of the seven enzymes show activity variations attributable to factors that are not linked to the structural gene. These unlinked activity modifiers identify possible regulatory elements. Analyses of covariance show that most of the genetic variation of enzyme activities cannot be accounted for by genetic variation of live weight or protein content. These results and the lack of strong correlations between the genetic effects on the activities of different enzymes indicate that the effects are mainly specific for individual enzymes.
利用两套染色体代换系研究了黑腹果蝇自然种群中酶活性变化的遗传成分。各类型的一条代换系的组成如下:i(1)/i(1);+(2)/ +(2);i(3)/i(3)和 i(1)/i(1);i(2)/ i(2);+(3)/+(3),其中 i 指来自高度纯系的染色体,+ 指来自自然种群的染色体。在一套代换系中,只有 + 染色体发生变化,而 i 染色体不变。采用随机区组设计进行检验和估计方差成分,已对 50 条第二代和 50 条第三代染色体代换系进行了七种酶活性水平变化的筛选。七种酶中有六种在至少一套代换系中表现出显著的遗传成分,其中七种酶中有五种的活性变化归因于与结构基因不连锁的因素。这些不连锁的活性修饰因子可鉴定出可能的调控元件。协方差分析表明,大多数酶活性的遗传变异不能用体重或蛋白质含量的遗传变异来解释。这些结果以及不同酶的活性的遗传效应之间缺乏强相关性表明,这些效应主要是针对个别酶的特异性效应。