Szathmáry E
Laboratory of Mathematical Biology, MRC National Institute for Medical Research, Mill Hill, London, England.
Genetics. 1993 Jan;133(1):127-32. doi: 10.1093/genetics/133.1.127.
Metabolic control theory is used to derive conditions under which two deleterious mutations affecting the dynamics of a metabolic pathway act synergistically. It is found that two mutations tend to act mostly synergistically when they reduce the activity of the same enzyme. If the two mutations affect different enzymes, the conclusion depends on the way that fitness is determined by aspects of the pathway. The cases analyzed are: selection for (1) maximal flux, (2) maximal equilibrium concentration (pool size) of an intermediate, (3) optimal flux, (4) optimal pool size. The respective types of epistasis found are: (1) antagonistic, (2) partly synergistic, (3-4) synergism is likely to predominate over antagonism. This results in somewhat different predictions concerning the effect of metabolic mutations on fitness in prokaryotes and eukaryotes. The fact that bacteria are largely clonal but have often a mosaic gene structure is consistent with expectations from the model.
代谢控制理论用于推导影响代谢途径动力学的两个有害突变协同作用的条件。研究发现,当两个突变降低同一种酶的活性时,它们往往大多表现为协同作用。如果这两个突变影响不同的酶,结论则取决于适合度由途径各方面决定的方式。所分析的情况有:(1)最大通量选择,(2)中间产物的最大平衡浓度(库大小)选择,(3)最佳通量选择,(4)最佳库大小选择。所发现的相应上位性类型有:(1)拮抗,(2)部分协同,(3 - 4)协同作用可能占主导地位。这导致了关于代谢突变对原核生物和真核生物适合度影响的一些不同预测。细菌在很大程度上是克隆的,但通常具有嵌合基因结构这一事实与该模型的预期相符。