4.8 Article

Spiny and soft-rayed fin domains in acanthomorph fish are established through a BMP-gremlin-shh signaling network

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2101783118

Keywords

fin spine; acanthomorph; evolutionary key innovation; evo-devo; exaptation

Funding

  1. Deutsche Forschungsgemeinschaft [WO-2165/2-1]
  2. Young Scholar Fund of the University of Konstanz
  3. European Research Council (ERC) [293700]

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With over 18,000 species, Acanthomorpha fishes form the largest and most diverse radiation of vertebrates, with their evolutionary success attributed to the spiny rays in their fins. By studying the differentiation of fin domains in Astatotilapia burtoni, researchers identified distinct transcription factor signatures and mechanisms such as BMP inhibition and shh secretion that contribute to the establishment of spiny and soft-ray domains. This research suggests a repeated exaptation of developmental programs contributing to the convergent evolution of spiny fin elements in fishes.
With over 18,000 species, the Acanthomorpha, or spiny-rayed fishes, form the largest and arguably most diverse radiation of vertebrates. One of the key novelties that contributed to their evolutionary success are the spiny rays in their fins that serve as a defense mechanism. We investigated the patterning mechanisms underlying the differentiation of median fin Anlagen into discrete spiny and soft rayed domains during the ontogeny of the direct-developing cichlid fish Astatotilapia burtoni. Distinct transcription factor signatures characterize these two fin domains, whereby mutually exclusive expression of hoxa13a/b with alx4a/b and tbx2b marks the spine to soft-ray boundary. The soft-ray domain is established by BMP inhibition via gremlin1b, which synergizes in the posterior fin with shh secreted from a zone of polarizing activity. Modulation of BMP signaling by chemical inhibition or gremlin1b CRISPR/Cas9 knockout induces homeotic transformations of spines into soft rays and vice versa. The expression of spine and soft-ray genes in nonacanthomorph fins indicates that a combination of exaptation and posterior expansion of an ancestral developmental program for the anterior fin margin allowed the evolution of robustly individuated spiny and soft-rayed domains. We propose that a repeated exaptation of such pattern might underly the convergent evolution of anterior spiny fin elements across fishes.

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