Seattle Children's Research Institute, Center for Developmental Biology and Regenerative Medicine, Seattle, Washington, United States of America.
Seattle Children's Hospital Craniofacial Center, Seattle, Washington, United States of America.
PLoS One. 2019 Aug 23;14(8):e0221402. doi: 10.1371/journal.pone.0221402. eCollection 2019.
Craniosynostosis is the premature fusion of the sutures of the calvaria and is principally designated as being either syndromic (demonstrating characteristic extracranial malformations) or non-syndromic. While many forms of syndromic craniosynostosis are known to be caused by specific mutations, the genetic etiology of non-syndromic, single-suture craniosynostosis (SSC) is poorly understood. Based on the low recurrence rate (4-7%) and the fact that recurrent mutations have not been identified for most cases of SSC, we propose that some cases of isolated, single suture craniosynostosis may be polygenic. Previous work in our lab identified a disproportionately high number of rare and novel gain-of-function IGF1R variants in patients with SSC as compared to controls. Building upon this result, we used expression array data from calvarial osteoblasts isolated from infants with and without SSC to ascertain correlations between high IGF1 expression and expression of other osteogenic genes of interest. We identified a positive correlation between increased expression of IGF1 and RUNX2, a gene known to cause SSC with increased gene dosage. Subsequent phosphorylation assays revealed that osteoblast cell lines from cases with high IGF1 expression demonstrated inhibition of GSK3β, a serine/threonine kinase known to inhibit RUNX2, thus activating osteogenesis through the IRS1-mediated Akt pathway. With these findings, we have utilized established mouse strains to examine a novel model of polygenic inheritance (a phenotype influenced by more than one gene) of SSC. Compound heterozygous mice with selective disinhibition of RUNX2 and either overexpression of IGF1 or loss of function of GSK3β demonstrated an increase in the frequency and severity of synostosis as compared to mice with the RUNX2 disinhibition alone. These polygenic mouse models reinforce, in-vivo, that the combination of activation of the IGF1 pathway and disinhibition of the RUNX2 pathway leads to an increased risk of developing craniosynostosis and serves as a model of human SSC.
颅缝早闭是颅骨缝线的过早融合,主要分为综合征型(表现出特征性的颅外畸形)或非综合征型。虽然已知许多综合征型颅缝早闭是由特定突变引起的,但非综合征型、单一颅缝早闭(SSC)的遗传病因尚不清楚。基于低复发率(4-7%)以及大多数 SSC 病例未发现反复突变的事实,我们提出一些孤立性、单一颅缝早闭的病例可能是多基因的。我们实验室之前的工作发现,与对照组相比,SSC 患者中 IGF1R 的罕见和新型获得性功能变体数量不成比例地高。在此结果的基础上,我们使用从患有和不患有 SSC 的婴儿中分离的颅骨成骨细胞的表达数组数据,确定高 IGF1 表达与其他感兴趣的成骨基因表达之间的相关性。我们发现 IGF1 表达增加与 RUNX2 呈正相关,RUNX2 是一种已知因基因剂量增加而导致 SSC 的基因。随后的磷酸化测定表明,具有高 IGF1 表达的病例中的成骨细胞系表现出 GSK3β 的抑制,GSK3β 是一种已知抑制 RUNX2 的丝氨酸/苏氨酸激酶,从而通过 IRS1 介导的 Akt 途径激活成骨作用。有了这些发现,我们利用已建立的小鼠品系来研究 SSC 的一种新的多基因遗传模型(一种受多个基因影响的表型)。与仅 RUNX2 抑制的小鼠相比,具有 RUNX2 选择性抑制和 IGF1 过表达或 GSK3β 功能丧失的复合杂合子小鼠的骨融合频率和严重程度增加。这些多基因小鼠模型在体内强化了 IGF1 途径的激活和 RUNX2 途径的抑制的组合导致颅缝早闭风险增加,并作为人类 SSC 的模型。