Stage- and cluster-specific regulation of chondrogenic gene programs by Sox9 in mouse embryonic limb buds

Cartilage formation in the limb is initiated and sustained by Sox9, though how its regulatory outputs evolve across developmental time and cell states remains unclear. Here, we integrate single-cell RNA sequencing of mouse forelimb buds across five stages (E9.5-E13.5) with CUT&RUN profiling of Ty1-tagged Sox9 at E11.5 and E13.5. We identify four Sox9-high populations-three chondroprogenitor clusters and mature chondrocytes-with distinct dynamics, and RNA-velocity infers independent trajectories from each progenitor cluster to maturation. Sox9 chromatin occupancy shows a conserved motif signature but undergoes stage- and cluster-dependent reconfiguration, aligning with shifts in extracellular matrix, cell-cycle, and patterning programs. Integrative analysis links these binding differences with coordinated transcriptional changes, suggesting that Sox9 operates through context-associated regulatory modes rather than a single uniform program. Our study provides a stage-resolved regulatory map of Sox9-associated regulation during chondrogenesis and a resource for limb mesenchyme.

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Publication Details

Journal
iScience
Published
2026-02-18
DOI
https://doi.org/10.1016/j.isci.2026.115074
Primary Topic
Developmental Biology and Gene Regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Stage- and cluster-specific regulation of chondrogenic gene programs by Sox9 in mouse embryonic limb buds

Hiroshi Asahara, Tomoki Chiba, Takahide Matsushima, Masayasu SEGA et al.
iScience
Developmental Biology and Gene Regulation
article

Stage- and cluster-specific regulation of chondrogenic gene programs by Sox9 in mouse embryonic limb buds

Hiroshi Asahara, Tomoki Chiba, Takahide Matsushima, Masayasu SEGA, Kohei Kita, Naoyuki Miyasaka, Yutaro Uchida
article en

Abstract

Cartilage formation in the limb is initiated and sustained by Sox9, though how its regulatory outputs evolve across developmental time and cell states remains unclear. Here, we integrate single-cell RNA sequencing of mouse forelimb buds across five stages (E9.5-E13.5) with CUT&RUN profiling of Ty1-tagged Sox9 at E11.5 and E13.5. We identify four Sox9-high populations-three chondroprogenitor clusters and mature chondrocytes-with distinct dynamics, and RNA-velocity infers independent trajectories from each progenitor cluster to maturation. Sox9 chromatin occupancy shows a conserved motif signature but undergoes stage- and cluster-dependent reconfiguration, aligning with shifts in extracellular matrix, cell-cycle, and patterning programs. Integrative analysis links these binding differences with coordinated transcriptional changes, suggesting that Sox9 operates through context-associated regulatory modes rather than a single uniform program. Our study provides a stage-resolved regulatory map of Sox9-associated regulation during chondrogenesis and a resource for limb mesenchyme.

iScienceVol. 29(3)
Scripps Research Institute (US), Tokyo Medical and Dental University (JP)
Japan Agency for Medical Research and Development, National Institutes of Health, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 52%
Developmental Biology and Gene Regulation
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