National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Herts, UK.
Eur J Hum Genet. 2011 Aug;19(8):857-64. doi: 10.1038/ejhg.2011.59. Epub 2011 May 18.
Prader Willi and Angelman syndromes are clinically distinct genetic disorders both mapping to chromosome region 15q11-q13, which are caused by a loss of function of paternally or maternally inherited genes in the region, respectively. With clinical diagnosis often being difficult, particularly in infancy, confirmatory genetic diagnosis is essential to enable clinical intervention. However, the latter is challenged by the complex genetics behind both disorders and the unmet need for characterised reference materials to aid accurate molecular diagnosis. With this in mind, a panel of six genotyping reference materials for Prader Willi and Angelman syndromes was developed, which should be stable for many years and available to all diagnostic laboratories. The panel comprises three Prader Willi syndrome materials (two with different paternal deletions, and one with maternal uniparental disomy (UPD)) and three Angelman syndrome materials (one with a maternal deletion, one with paternal UPD or an epigenetic imprinting centre defect, and one with a UBE3A point mutation). Genomic DNA was bulk-extracted from Epstein-Barr virus-transformed lymphoblastoid cell lines established from consenting patients, and freeze-dried as aliquots in glass ampoules. In total, 37 laboratories from 26 countries participated in a collaborative study to assess the suitability of the panel. Participants evaluated the blinded, triplicate materials using their routine diagnostic methods against in-house controls or externally sourced uncertified reference materials. The panel was established by the Expert Committee on Biological Standardization of the World Health Organization as the first International Genetic Reference Panel for Prader Willi and Angelman syndromes.
普拉德-威利和安格曼综合征是两种临床特征明显的遗传性疾病,均定位于染色体 15q11-q13 区域,分别由该区域内父源或母源遗传基因的功能丧失引起。由于临床诊断通常较为困难,尤其是在婴儿期,因此明确的遗传诊断对于进行临床干预至关重要。然而,由于这两种疾病的遗传背景复杂,且缺乏特征明确的参考材料来辅助准确的分子诊断,因此后者具有挑战性。有鉴于此,开发了用于普拉德-威利和安格曼综合征的六种基因分型参考材料面板,该面板应该具有多年的稳定性,并可供所有诊断实验室使用。该面板包括三种普拉德-威利综合征材料(两种具有不同的父源缺失,一种具有母源单亲二倍体 (UPD))和三种安格曼综合征材料(一种具有母源缺失,一种具有父源 UPD 或表观遗传印记中心缺陷,一种具有UBE3A 点突变)。从同意参与的患者建立的 Epstein-Barr 病毒转化的淋巴母细胞系中批量提取基因组 DNA,并在玻璃安瓿中作为等分冷冻干燥。总共有来自 26 个国家的 37 个实验室参与了一项合作研究,以评估该面板的适用性。参与者使用常规诊断方法,根据内部对照或外部来源的未经认证的参考材料,对盲法、重复的材料进行评估。该面板已被世界卫生组织生物标准化专家委员会确认为普拉德-威利和安格曼综合征的首个国际遗传参考面板。