Kaneko K
Department of Pure and Applied Sciences, College of Arts and Sciences, University of Tokyo, Komaba, Meguro-ku, Tokyo, 153 Japan.
J Biol Phys. 2002 Dec;28(4):781-92. doi: 10.1023/A:1021211410988.
The origin of heredity is studied as a recursive state in a replicatingprotocell consisting of many molecule species in mutually catalyzingreaction networks. Protocells divide when the number of molecules, increasing due to replication, exceeds a certain threshold. We study how the chemicals in a catalytic network can form recursive production states in the presence of errors in the replication process. Depending on the balance between the total number of molecules in a cell and the number of molecule species, we have found three phases; a phase without a recursive production state, a phase with itinerancy over a few recursive states, and a phase with fixedrecursive production states. Heredity is realized in the latter two phaseswhere molecule species that are population-wise in the minority are preserved and control the phenotype of the cell. It is shown that evolvability is realized in the itinerancy phase, where a change in the number of minority molecules controls a change of the chemical state.
遗传的起源被作为一种递归状态来研究,该状态存在于一个由相互催化反应网络中的多种分子物种组成的复制原始细胞中。当由于复制而增加的分子数量超过某个阈值时,原始细胞就会分裂。我们研究了在复制过程中存在错误的情况下,催化网络中的化学物质如何形成递归产生状态。根据细胞中分子总数与分子物种数量之间的平衡,我们发现了三个阶段:一个没有递归产生状态的阶段、一个在几个递归状态之间循环的阶段以及一个具有固定递归产生状态的阶段。在后两个阶段中实现了遗传,其中在数量上占少数的分子物种得以保留并控制细胞的表型。结果表明,在循环阶段实现了可进化性,其中少数分子数量的变化控制着化学状态的变化。