TL;DR
This paper demonstrates how recognition sites coupled to moving targets can rapidly evolve increased complexity, larger code length, and lower density, driven by an adaptive ratchet mechanism in dynamic environments.
Contribution
It introduces a model showing recognition site evolution with a time-dependent target, revealing a ratchet process that enhances molecular complexity and adaptation speed.
Findings
Recognition sites evolve larger code length and lower density with dynamic targets.
Adaptive ratchet mechanism drives complexity increase and faster adaptation.
Application to immune system antigen recognition illustrates real-world relevance.
Abstract
Biological systems have evolved to amazingly complex states, yet we do not understand in general how evolution operates to generate increasing genetic and functional complexity. Molecular recognition sites are short genome segments or peptides binding a cognate recognition target of sufficient sequence similarity. Such sites are simple, ubiquitous modules of sequence information, cellular function, and evolution. Here we show that recognition sites, if coupled to a time-dependent target, can rapidly evolve to complex states with larger code length and smaller coding density than sites recognising a static target. The underlying fitness model contains selection for recognition, which depends on the sequence similarity between site and target, and a uniform cost per unit of code length. Site sequences are shown to evolve in a specific adaptive ratchet, which produces selection of…
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