| Literature DB >> 32220312 |
Daniel Richard1, Zun Liu1, Jiaxue Cao2, Ata M Kiapour3, Jessica Willen1, Siddharth Yarlagadda1, Evelyn Jagoda1, Vijaya B Kolachalama4, Jakob T Sieker5, Gary H Chang6, Pushpanathan Muthuirulan1, Mariel Young1, Anand Masson7, Johannes Konrad3, Shayan Hosseinzadeh3, David E Maridas8, Vicki Rosen8, Roman Krawetz7, Neil Roach1, Terence D Capellini9.
Abstract
During human evolution, the knee adapted to the biomechanical demands of bipedalism by altering chondrocyte developmental programs. This adaptive process was likely not without deleterious consequences to health. Today, osteoarthritis occurs in 250 million people, with risk variants enriched in non-coding sequences near chondrocyte genes, loci that likely became optimized during knee evolution. We explore this relationship by epigenetically profiling joint chondrocytes, revealing ancient selection and recent constraint and drift on knee regulatory elements, which also overlap osteoarthritis variants that contribute to disease heritability by tending to modify constrained functional sequence. We propose a model whereby genetic violations to regulatory constraint, tolerated during knee development, lead to adult pathology. In support, we discover a causal enhancer variant (rs6060369) present in billions of people at a risk locus (GDF5-UQCC1), showing how it impacts mouse knee-shape and osteoarthritis. Overall, our methods link an evolutionarily novel aspect of human anatomy to its pathogenesis.Entities:
Keywords: ATAC-seq; GDF5; chondrocyte; gene regulation; genetic drift; human evolution; knee; mouse model; natural selection; osteoarthritis
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Year: 2020 PMID: 32220312 PMCID: PMC7179902 DOI: 10.1016/j.cell.2020.02.057
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582