Division of Molecular Medicine, Leeds Institute of Medical Research, Faculty of Medicine and Health, St James's University Hospital, University of Leeds, Leeds LS9 7TF, UK.
School of Dentistry, Faculty of Medicine and Health, University of Leeds, Leeds LS2 9LU, UK.
Hum Mol Genet. 2020 Jun 3;29(9):1417-1425. doi: 10.1093/hmg/ddaa041.
Amelogenesis is the process of enamel formation. For amelogenesis to proceed, the cells of the inner enamel epithelium (IEE) must first proliferate and then differentiate into the enamel-producing ameloblasts. Amelogenesis imperfecta (AI) is a heterogeneous group of genetic conditions that result in defective or absent tooth enamel. We identified a 2 bp variant c.817_818GC>AA in SP6, the gene encoding the SP6 transcription factor, in a Caucasian family with autosomal dominant hypoplastic AI. The resulting missense protein change, p.(Ala273Lys), is predicted to alter a DNA-binding residue in the first of three zinc fingers. SP6 has been shown to be crucial to both proliferation of the IEE and to its differentiation into ameloblasts. SP6 has also been implicated as an AI candidate gene through its study in rodent models. We investigated the effect of the missense variant in SP6 (p.(Ala273Lys)) using surface plasmon resonance protein-DNA binding studies. We identified a potential SP6 binding motif in the AMBN proximal promoter sequence and showed that wild-type (WT) SP6 binds more strongly to it than the mutant protein. We hypothesize that SP6 variants may be a very rare cause of AI due to the critical roles of SP6 in development and that the relatively mild effect of the missense variant identified in this study is sufficient to affect amelogenesis causing AI, but not so severe as to be incompatible with life. We suggest that current AI cohorts, both with autosomal recessive and dominant disease, be screened for SP6 variants.
成釉作用是釉质形成的过程。为了使成釉作用进行,内釉上皮细胞(IEE)的细胞必须首先增殖,然后分化为产生釉质的成釉细胞。釉质不全(AI)是一组遗传条件,导致牙釉质缺陷或缺失。我们在一个常染色体显性遗传性发育不全 AI 的白种人家系中发现了 SP6 基因中的 2 个碱基变异 c.817_818GC>AA,该基因编码 SP6 转录因子。由此产生的错义蛋白变化,p.(Ala273Lys),预计会改变三个锌指中的第一个中的一个 DNA 结合残基。已经表明 SP6 对于 IEE 的增殖及其分化为成釉细胞至关重要。通过在啮齿动物模型中的研究,SP6 也被认为是 AI 候选基因之一。我们使用表面等离子体共振蛋白-DNA 结合研究来研究 SP6(p.(Ala273Lys))中的错义变体的影响。我们在 AMBN 近端启动子序列中确定了一个潜在的 SP6 结合基序,并表明野生型(WT)SP6 比突变蛋白更强烈地结合它。我们假设 SP6 变体可能是 AI 的一个非常罕见的原因,因为 SP6 在发育中的关键作用,并且在这项研究中鉴定的错义变体的相对温和的影响足以影响导致 AI 的成釉作用,但不足以使其与生命不相容。我们建议对常染色体隐性和显性疾病的当前 AI 队列进行 SP6 变体筛查。