间接编码的多细胞生物的发育和复制的基因组的进化增长

S. Nichele, G. Tufte
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引用次数: 13

摘要

生物有机体的基因组在大小上不是固定的。它们进化并分化成不同的物种,获得新的基因,因此具有不同的长度。在某种程度上,生物基因组是一个自组装过程的结果,在这个过程中,更复杂的表型可以通过拥有更大的基因组来生存和适应。在人工领域,进化和发展系统通常具有静态大小的基因组,例如,由系统设计者通过试错预先选择或使用复杂的启发式先验估计。因此,最大可进化的复杂性是预先确定的,这与自然界的开放式进化形成了鲜明对比。在本文中,我们认为人工基因组也可能在进化过程中不断扩大规模,以逐步产生高维解决方案。我们提出了一种间接编码的人工细胞生物基因组表示的进化增长。基因组从单个基因开始,并在必要时获取新的基因,从而增加了自由度,扩大了可用的搜索空间。细胞自动机(CA)被用作两个不同问题的试验台:复制和形态发生。所选择的CA编码是一个标准的开发表和基于指令的方法。结果表明,所提出的基因组进化生长方法能够产生紧凑有效的基因组,而不需要指定全套的调控配置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolutionary growth of genomes for the development and replication of multicellular organisms with indirect encoding
The genomes of biological organisms are not fixed in size. They evolved and diverged into different species acquiring new genes and thus having different lengths. In a way, biological genomes are the result of a self-assembly process where more complex phenotypes could benefit by having larger genomes in order to survive and adapt. In the artificial domain, evolutionary and developmental systems often have static size genomes, e.g. chosen beforehand by the system designer by trial and error or estimated a priori with complicated heuristics. As such, the maximum evolvable complexity is predetermined, in contrast to open-ended evolution in nature. In this paper, we argue that artificial genomes may also grow in size during evolution to produce high-dimensional solutions incrementally. We propose an evolutionary growth of genome representations for artificial cellular organisms with indirect encodings. Genomes start with a single gene and acquire new genes when necessary, thus increasing the degrees of freedom and expanding the available search-space. Cellular Automata (CA) are used as test bed for two different problems: replication and morphogenesis. The chosen CA encodings are a standard developmental table and an instruction based approach. Results show that the proposed evolutionary growth of genomes' method is able to produce compact and effective genomes, without the need of specifying the full set of regulatory configurations.
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