增强子
软骨发生
软骨细胞
肢体发育
生物
硫氧化物9
基因
遗传学
细胞生物学
计算生物学
基因表达
体外
作者
Fabrice Darbellay,Anna Ramisch,Lucille Lopez-Delisle,Michael Kosicki,Antonella Rauseo,Zahra Jouini,Axel Visel,Guillaume Andrey
标识
DOI:10.1038/s41467-024-49203-2
摘要
Abstract Chondrocyte differentiation controls skeleton development and stature. Here we provide a comprehensive map of chondrocyte-specific enhancers and show that they provide a mechanistic framework through which non-coding genetic variants can influence skeletal development and human stature. Working with fetal chondrocytes isolated from mice bearing a Col2a1 fluorescent regulatory sensor, we identify 780 genes and 2'704 putative enhancers specifically active in chondrocytes using a combination of RNA-seq, ATAC-seq and H3K27ac ChIP-seq. Most of these enhancers (74%) show pan -chondrogenic activity, with smaller populations being restricted to limb (18%) or trunk (8%) chondrocytes only. Notably, genetic variations overlapping these enhancers better explain height differences than those overlapping non-chondrogenic enhancers. Finally, targeted deletions of identified enhancers at the Fgfr3 , Col2a1 , Hhip and, Nkx3-2 loci confirm their role in regulating cognate genes. This enhancer map provides a framework for understanding how genes and non-coding variations influence bone development and diseases.
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