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Updated: Sep 25, 2026

Engineering Tendon Assembloids to Probe Cellular Crosstalk in Disease and Repair
Published on: March 22, 2024
Co-option of a tendon-associated osteogenic program drives the evolutionary plasticity of intermuscular bones in
Xuemei Xiong1,2, Mingliang Hu3, Jiajia Zhou1,2
1Department of Genetics and Breeding of Aquatic Animals, College of Fisheries, Key Lab of Freshwater Animal Breeding, Ministry of Agriculture and Rural Affairs/Key Lab of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education/Engineering Research Center of Green development for Conventional Aquatic Biological Industry in the Yangtze River Economic Belt, Ministry of Education, Huazhong Agricultural University, Wuhan 430070, China.
Abstract:
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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