Early developmental patterning sets the stage for brain evolution.

T he evolution of brain structure and function has long fascinated biologists. This fascination was initially prompted by the observation that allometric relationships exist between the size of the brain—or brain region—and body size across a wide range of vertebrates (1). Besides random drift, two main ideas have been advanced to explain how brains evolve, and both have found considerable support. From a purely adaptationist point of view, selection on a specific set of behavior patterns or sensory specializations is thought to result in “mosaic” changes in only the brain regions that mediate these processes (2). In contrast, selection on any single brain region would cause the brain to change as a whole unit owing to developmental constraints and processes that regulate the formation and growth of a range of brain regions overall (3). Beyond the “just so” stories that often characterize the interpretation of the causes and origins of brain diversity (4), two problems have vexed this line of research. First, it is not at all obvious how an increase in (relative) size would give rise to functional differences (e.g., increased cognitive abilities, novel sensory specializations, or behavioral complexity). Although a larger number of neurons and/or synapses might well result in greater processing power and/or speed, there is no clear relationship between such measures and behavioral or cognitive outcomes. Second, our understanding of the developmental mechanisms that give rise to the observed variation in brain structure is still very limited, and most studies have suggested that neurogenesis later in development generates diversity, which might result in the differential expansion of various brain areas (3). In this context it is also important to keep in mind that differences in brain structure and function can be as much a consequence of genetic and/ or developmental control as they can be the result of (developmental) plasticity in response to the environment (5, 6). It is this developmental problem for which a new study (7) establishes a ground-breaking paradigm. Similar to the basic patterning processes that specify the main body axes across all metazoans, the overall spatial and temporal activity patterns of transcription factor networks that establish the main compartments during early brain development are highly conserved (8). Could small variations in these expression profiles potentially result in large changes in overall brain structure? Surprisingly, this possibility has not yet been explored within an evolutionary developmental framework. The new study elegantly applies this “evo-devo” approach to gain insights into the developmental processes that might give rise to brain diversity by examining the activity of several of the genes that delineate compartments very early during the development of the nervous system. The authors exploit the remarkable phenotypic diversity found in the cichlid fishes from east Africa’s Great Lakes region, which provide an ideal model system for uncovering the ecological and behavioral forces that sculpt neural phenotypes. Cichlids display the most rapid and extensive adaptive radiations known for vertebrates (9), yet they have produced an astonishing array of phenotypes with little genetic diversification (10, 11). The extraordinary ecological (e.g., habitat, feeding specialization) and behavioral (e.g., color preferences by females, mating and parental care systems) diversity is correlated with variation in brain structure of a magnitude that exceeds that of all mammals and facilitates comparisons across large social and physical gradients in closely related species of cichlids (12, 13). The new study (7) takes advantage of this “natural mutant screen” (9) by investigating brain development across a range of ecologically distinct cichlids from Lake Malawi. Specifically, the authors examine the expression patterns of a gene regulatory circuit involving WNT signaling that is important across vertebrates for specifying the anterior–posterior orientation of the developing brain and for determining the boundaries between its major compartments. There is considerable variation in the expression patterns of these genes between rock-dwelling mbuna and sand-dwelling nonmbuna cichlids, consistent with the differences observed in the relative size of foreand midbrain structures in adult fish. When the WNT signaling pathway is chemically perturbed in the developing embryo, alterations in this coexpression network are sufficient to give rise to the observed differences in brain development, resulting for instance in a rockdweller with the forebrain shaped and sized like that of a sand-dweller. Finally, a SNP in the irx1b gene, which mediates WNT signaling and is required for proper foreand midbrain development, is fixed between rockand sand-dwelling cichlids. Although it is not yet clear whether this substitution causes the observed shift in the developing brain compartments, it is likely the result of natural selection, because the vast majority of SNPs in Malawi cichlids are not fixed (11). These neuroanatomical, developmental, and genomic results strongly support the conclusion that evolutionary changes in the patterning of developing brain compartments can establish ecologically and behaviorally relevant differences in the brain. Variation in subsequent neurogenesis, which until now has been thought to be the main source of variation in brain structure across species, can then elaborate the construction of diverse brains. Variation in Brain Natural/Sexual Selection, Drift