Abstract

Evolution is often characterized as a process involving incremental genetic changes that are slowly discovered and fixed in a population through genetic drift and selection. However, a growing body of evidence is finding that changes in the environment frequently induce adaptations that are much too rapid to occur by an incremental genetic search process. Rapid evolution is hypothesized to be facilitated by mutations present within the population that are silent or “cryptic” within the first environment but are co-opted or “exapted” to the new environment, providing a selective advantage once revealed. Although cryptic mutations have recently been shown to facilitate evolution in RNA enzymes, their role in the evolution of complex phenotypes has not been proven. In support of this wider role, this paper describes an unambiguous relationship between cryptic genetic variation and complex phenotypic responses within the immune system. By reviewing the biology of the adaptive immune system through the lens of evolution, we show that T cell adaptive immunity constitutes an exemplary model system where cryptic alleles drive rapid adaptation of complex traits. In naive T cells, normally cryptic differences in T cell receptor reveal diversity in activation responses when the cellular population is presented with a novel environment during infection. We summarize how the adaptive immune response presents a well studied and appropriate experimental system that can be used to confirm and expand upon theoretical evolutionary models describing how seemingly small and innocuous mutations can drive rapid cellular evolution.

Highlights

  • THE ROLE OF CRYPTIC GENETIC VARIATION IN EVOLUTION Cryptic genetic variation (CGV) describes genetic diversity that is hidden within populations that occupy their native habitats but that is revealed as trait diversity within new environments (Gibson and Dworkin, 2004; Le Rouzic and Carlborg, 2008; Schlichting, 2008; McGuigan and Sgrò, 2009)

  • Mutational robustness is believed to facilitate evolvability in two ways: first by establishing genotypic neutral networks from which large numbers of distinct genotypes can be sampled (Wagner, 2008) and second by allowing genetic diversity to arise in a population with subsequent trait differences revealed in an environment-dependent manner (Whitacre, 2012)

  • Thymocytes first begin forming the TCR β chain by the assembling one variable (V), one diversity (D), and one joining (J) gene segment to an invariant constant region (C) from a “library” of V (n = 52), D (n = 2), and J (n = 13) segments that are all initially encoded within each β gene locus (Schatz, 2004)

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Summary

Introduction

THE ROLE OF CRYPTIC GENETIC VARIATION IN EVOLUTION Cryptic genetic variation (CGV) describes genetic diversity that is hidden within populations that occupy their native habitats but that is revealed as trait diversity within new environments (Gibson and Dworkin, 2004; Le Rouzic and Carlborg, 2008; Schlichting, 2008; McGuigan and Sgrò, 2009). Mutational robustness is believed to facilitate evolvability in two ways: first by establishing genotypic neutral networks from which large numbers of distinct genotypes can be sampled (Wagner, 2008) and second by allowing genetic diversity to arise in a population with subsequent trait differences revealed in an environment-dependent manner (Whitacre, 2012).

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