School of Life Sciences, University of Nottingham, NG7 2UH Nottingham, United Kingdom.
Research Centre for Evolutionary Anthropology and Paleoecology, Liverpool John Moores University, L3 3AF Liverpool, United Kingdom.
Proc Natl Acad Sci U S A. 2019 May 21;116(21):10463-10472. doi: 10.1073/pnas.1820556116. Epub 2019 Apr 29.
Paget's disease of bone (PDB) is a chronic skeletal disorder that can affect one or several bones in individuals older than 55 y of age. PDB-like changes have been reported in archaeological remains as old as Roman, although accurate diagnosis and natural history of the disease is lacking. Six skeletons from a collection of 130 excavated at Norton Priory in the North West of England, which dates to medieval times, show atypical and extensive pathological changes resembling contemporary PDB affecting as many as 75% of individual skeletons. Disease prevalence in the remaining collection is high, at least 16% of adults, with age at death estimations as low as 35 y. Despite these atypical features, paleoproteomic analysis identified sequestosome 1 (SQSTM1) or p62, a protein central to the pathological milieu of PDB, as one of the few noncollagenous human sequences preserved in skeletal samples. Targeted proteomic analysis detected >60% of the ancient p62 primary sequence, with Western blotting indicating p62 abnormalities, including in dentition. Direct sequencing of ancient DNA excluded contemporary PDB-associated mutations. Our observations indicate that the ancient p62 protein is likely modified within its C-terminal ubiquitin-associated domain. Ancient miRNAs were remarkably preserved in an osteosarcoma from a skeleton with extensive disease, with miR-16 expression consistent with that reported in contemporary PDB-associated bone tumors. Our work displays the use of proteomics to inform diagnosis of ancient diseases such as atypical PDB, which has unusual features presumably potentiated by yet-unidentified environmental or genetic factors.
佩吉特病(PDB)是一种慢性骨骼疾病,可影响 55 岁以上个体的一个或多个骨骼。考古遗迹中已有类似 PDB 的变化的报告,其年代可追溯到罗马时期,尽管对这种疾病的准确诊断和自然史仍缺乏了解。在英格兰西北部诺顿修道院(Norton Priory)的 130 具挖掘骨骼中,有 6 具骨骼表现出不典型且广泛的病理性变化,类似于当代 PDB,影响多达 75%的个体骨骼。其余骨骼中疾病的患病率很高,至少有 16%的成年人,死亡年龄估计低至 35 岁。尽管存在这些非典型特征,但古蛋白组学分析鉴定出自噬相关蛋白 1(SQSTM1)或 p62,一种在 PDB 病理环境中起核心作用的蛋白质,是保存在骨骼样本中的少数非胶原人类序列之一。靶向蛋白组学分析检测到 >60%的古代 p62 一级序列,Western blot 分析表明 p62 存在异常,包括在牙齿中。古代 DNA 的直接测序排除了当代 PDB 相关突变。我们的观察表明,古代 p62 蛋白可能在其 C 端泛素相关结构域内发生了修饰。在一个骨骼有广泛病变的骨肉瘤中,古代 miRNA 得到了极好的保存,miR-16 的表达与当代 PDB 相关骨肿瘤中的报告一致。我们的工作展示了利用蛋白质组学来诊断古代疾病(如不典型 PDB)的方法,这些疾病具有不寻常的特征,可能是由尚未确定的环境或遗传因素所致。