The excretory systems of closely related worm species have distinct morphological and functional features. A new study now shows that evolutionary gain of lin-48 expression in the excretory duct cell in Caenorhabditis elegans is responsible for the unique excretory system innovations present in this species.
The genetic basis of phenotypic evolution is one of the most intriguing questions in biology1,2,3. Much of our recent progress in this field has used the candidate gene approach (Fig. 1). This approach leverages the power of model experimental systems by placing gene function in a historical context. Comparative analysis of gene expression, combined with the knowledge of gene function in a model organism, can be used to deduce the role of a gene in the origin of new phenotypes. But the final proof that the candidate gene does what we think it does cannot be obtained without a functional test: a genetic cross or, where crossing is impossible, transgenic analysis. On page 231, Wang and Chamberlin4 show how gene replacement can be used to distinguish between different models of phenotypic evolution.
C. elegans is distinguished from its nearest relatives by two unique features of its excretory system: a short excretory duct and high salt tolerance. Phylogenetic analysis showed that both features were derived and appeared only recently in C. elegans evolution (Fig. 1b)4. The development of derived traits in C. elegans depends on the expression of the zinc finger transcription factor lin-48 in the excretory duct cell. In lin-48 mutants, both excretory duct morphology and salt tolerance revert to the ancestral condition (Fig. 1a)5. This prompted Wang and Chamberlin to examine lin-48 expression and function in other worm species. The results were notable. In the relatives of C. elegans that have long excretory ducts and low salt tolerance, lin-48 was not expressed in the excretory duct cell (Fig. 1b), and lin-48 transgenes from any of these species could restore the development of derived features in C. elegans lin-48 mutants (Fig. 1c). Together, these results suggested that evolutionary changes in the expression, but not the function, of lin-48 had a key role in the origin of new morphological and physiological traits.
The exact nature of this role would not have become clear were it not for Wang and Chamberlin's asking the question: Would forcing the more primitive species to express lin-48 in excretory duct cells be sufficient to confer the derived traits? The answer was both yes and no. Expression of lin-48 in the duct cell in C. briggsae, the closest relative of C. elegans, resulted in a C. elegans–like excretory duct morphology but did not give C. briggsae a higher salt tolerance (Fig. 1c). A probable historical scenario is that a regulatory change in a single gene, lin-48, led to the evolution of new morphology, but other loci had to change before the worm could acquire greater salt tolerance.
Single genes, big effects
These results send both a promise and a note of caution to scientists who study the evolution of development. By the very nature of their discipline, developmental biologists are inclined to believe in, and look for, individual genes that account for a large proportion of phenotypic differences between species. Wang and Chamberlin's paper confirms once more that this is not a fool's errand: not only do such major-effect genes exist, but their existence can be proven conclusively by functional tests. At the same time, we are cautioned about the dangers of making historical inferences based solely on mutant phenotypes and gene expression patterns. Without the gene replacement tests, we would not have learned that the morphology and physiology of the worm excretory system are separable and follow different modes of evolution (monogenic versus polygenic).
Although the field of evolutionary developmental genetics is still too young to make sweeping generalizations, major-effect genes seem to be a common feature in morphological evolution. Sometimes, one such gene may completely account for the phenotypic differences between taxa. This is especially common for relatively simple traits, such as body pigmentation and cuticular decorations in insects and vertebrates6,7,8,9. More frequently, morphological differences involve several major-effect genes as well as weaker modifiers8,10,11,12. The existence of major-effect genes makes the evolution of animal morphology much more tractable at the molecular level than it would be under a highly polygenic model.
Lest we start believing in hopeful monsters13, we should keep in mind the distinction between major-effect genes and major-effect mutations. A single locus may exert a substantial effect on the phenotype in interspecific genetic crosses or in transgenic animals. But there is no reason to think that this difference appeared all at once as a single mutation event. Rather, a gradual accumulation of many mutations, each with only a slight effect on the phenotype, may eventually turn a locus into what we perceive, in retrospect, to be a major-effect gene. When Wang and Chamberlin compared the cis-regulatory sequences of lin-48 between C. elegans and its relative species4, they found extensive differences, including multiple nucleotide substitutions and deletions that affect putative binding sites for Ces-2, an important upstream regulator of lin-48 (ref. 5). We do not know which of these molecular changes were responsible for the new expression pattern acquired by lin-48 in the C. elegans lineage, but we are probably looking at a cumulative effect of multiple mutations.
The existence of major-effect genes tells us more about development than about evolution. There may simply be a limited number of developmental mechanisms that an animal can use to achieve a given phenotype9,14. Only a close synthesis of developmental biology with evolutionary and population genetics can help us understand how evolution explores these limited possibilities. Groups of closely related species of worms and flies have become a fertile ground for this synthesis15 and will no doubt continue to produce exciting results.
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Kopp, A. Making a better worm. Nat Genet 36, 213–214 (2004). https://doi.org/10.1038/ng0304-213