Dipartimento di Scienze della Vita e Sanità Pubblica, Università Cattolica del Sacro Cuore, Rome, Italy.
Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Sci Rep. 2021 Oct 29;11(1):21316. doi: 10.1038/s41598-021-00511-3.
RUNX2 encodes the master bone transcription factor driving skeletal development in vertebrates, and playing a specific role in craniofacial and skull morphogenesis. The anatomically modern human (AMH) features sequence changes in the RUNX2 locus compared with archaic hominins' species. We aimed to understand how these changes may have contributed to human skull globularization occurred in recent evolution. We compared in silico AMH and archaic hominins' genomes, and used mesenchymal stromal cells isolated from skull sutures of craniosynostosis patients for in vitro functional assays. We detected 459 and 470 nucleotide changes in noncoding regions of the AMH RUNX2 locus, compared with the Neandertal and Denisovan genomes, respectively. Three nucleotide changes in the proximal promoter were predicted to alter the binding of the zinc finger protein Znf263 and long-distance interactions with other cis-regulatory regions. By surface plasmon resonance, we selected nucleotide substitutions in the 3'UTRs able to affect miRNA binding affinity. Specifically, miR-3150a-3p and miR-6785-5p expression inversely correlated with RUNX2 expression during in vitro osteogenic differentiation. The expression of two long non-coding RNAs, AL096865.1 and RUNX2-AS1, within the same locus, was modulated during in vitro osteogenic differentiation and correlated with the expression of specific RUNX2 isoforms. Our data suggest that RUNX2 may have undergone adaptive phenotypic evolution caused by epigenetic and post-transcriptional regulatory mechanisms, which may explain the delayed suture fusion leading to the present-day globular skull shape.
RUNX2 编码的主骨骼转录因子驱动脊椎动物骨骼发育,并在颅面和颅骨形态发生中发挥特定作用。与古人类物种相比,解剖学上的现代人类(AMH)在 RUNX2 基因座具有序列变化。我们旨在了解这些变化如何促成了最近进化中人类颅骨球形化的发生。我们比较了 AMH 和古人类的基因组,并使用颅缝早闭患者颅骨缝分离的间充质基质细胞进行体外功能测定。与尼安德特人和丹尼索瓦人基因组相比,我们在 AMH RUNX2 基因座的非编码区检测到 459 和 470 个核苷酸变化。近端启动子中的三个核苷酸变化预计会改变锌指蛋白 Znf263 的结合,并与其他顺式调控区进行长距离相互作用。通过表面等离子体共振,我们选择了能够影响 miRNA 结合亲和力的 3'UTR 核苷酸取代。具体而言,miR-3150a-3p 和 miR-6785-5p 的表达在体外成骨分化过程中与 RUNX2 表达呈负相关。同一基因座内的两个长非编码 RNA,AL096865.1 和 RUNX2-AS1 的表达在体外成骨分化过程中受到调节,并与特定 RUNX2 异构体的表达相关。我们的数据表明,RUNX2 可能经历了由表观遗传和转录后调控机制引起的适应性表型进化,这可能解释了导致现今球形颅骨形状的延迟缝融合。