The teleost agouti-related protein 2 gene is an ohnolog gone missing from the tetrapod genome.

A central question in evolutionary genomics is how morphological differences between taxa arise from differences in gene repertoire. Answers require rigorous orthology assignments. Recent work (1) illuminated the mechanism of background adaptation in teleost fishes by investigating the function of agoutirelated protein 2 (agrp2), a gene so far found only in teleosts. Agouti family proteins antagonize melanocortin receptors, function in energy homeostasis, and regulate pigmentation. The authors (1) proposed a neurocrine axis in which zebrafish Agrp2 is expressed exclusively in the pineal gland, where it binds to the melanocortin 1 receptor and thereby, controls expression of melanin-concentrating hormones; this causes melanosome contraction in melanophores and adaptation to light backgrounds (1). These findings intriguingly implied that the acquisition of agrp2 in teleosts enabled the evolution of background adaptation by regulation through the pineal. Tetrapods have two agouti family members [Agouti signaling protein (Asip) and Agrp], but teleosts have four (asip1, asip2, agrp1, and agrp2). Published studies (1, 2) vaguely suggest that agrp2 is a paralog of agrp1 generated during the teleost-specific genome duplication (TSGD). Phylogenetic analyses, however, remain ambiguous regarding vertebrate agouti gene relationships (2) (Fig. 1A). Our investigation of this gene family using synteny data clearly reveals that the teleost agrp2 chromosomal region shares syntenies neither with the teleost agrp1 region nor with the tetrapod Agrp region (Fig. 1B), contradicting the current gene nomenclature (2). In contrast, teleost agrp2 and asip2 regions show conserved synteny to a region on human chromosome 8 (Hsa8) (Fig. 1C). Furthermore, we find at least three regions of paralogy in the human genome (Fig. 1D)—Hsa16 (AGRP region), Hsa8, and Hsa20 (ASIP region)—most likely derived from a single Asip/Agrp region on ancestral vertebrate protochromosome B (3). The ASIP region on Hsa20 shares more paralogies with the region on Hsa8 (Fig. 1D). According to our model (Fig. 1E), an ancestral Asip/Agrp precursor gene was duplicated two times during the two rounds of vertebrate genome duplication (R1 and R2). After R2, Asip and Agrp were retained in all bony vertebrates, but a third ohnolog (4) went missing in the tetrapod lineage. This gene was retained, however, in the rayfin fish lineage, giving rise to agrp2 and asip2 after the TSGD. Our results support a revision of agouti family nomenclature (Fig. 1E). Importantly, our model suggests that the genetic basis of teleost background adaptation may not root in the agouti family expansion during the TSGD but to R2, far deeper in vertebrate evolution (Fig. 1E). It is unlikely that zebrafish agrp2 (new name: asip2b) newly evolved its single pineal-specific function after the TSGD (as suggested by ref. 1), because asip2 (asip2a) is absent in zebrafish but present in other teleosts. The interesting findings of Zhang et al. (1) should, thus, spur research on the function of asip2a/b in other teleosts and agouti genes in basal rayfin fishes, basal lobefins like lungfish and coelacanth, background-adapting tetrapods, and more basal vertebrates in the light of our rigorous phylogenetic framework (Fig. 1E).