Intermuscular bones (IBs) are critical yet poorly understood evolutionary specializations. These bones exhibit considerable morphological variability, proposed as adaptations to teleost diversification; however, the explicit adaptive and evolutionary mechanisms remain unresolved. By integrating comparative morphological analysis of 360 teleost species and eco-functional performance assays, we demonstrate that IB complexity is associated with ecological niche expansion and enhanced burst swimming capacity, underscoring IBs as versatile adaptations. Single-cell transcriptomic profiling across four ray-finned fish species reveals that the teleost-specific emergence of IBs originated from a tendon-associated ossification pathway. This evolutionary pathway is mechanistically linked to the co-option of existing cell types and gene networks, including the osteogenic program initiated by runx2b and the critical tendon microenvironment maintained by mkxa/b . Furthermore, we provide evidence of repeated IB loss events associated with alterations or losses of these key osteogenic and tendon niche-regulating genes, highlighting the variability of this adaptive trajectory. Our findings reveal a distinct tendon-associated osteogenic system in teleosts, providing a mechanistic framework for IB evolution during teleost adaptive radiation.
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Xiong et al. (2026) studied this question.
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