Clinic for Special Children, Strasburg, Pennsylvania, United States of America.
PLoS One. 2012;7(1):e28936. doi: 10.1371/journal.pone.0028936. Epub 2012 Jan 17.
The Clinic for Special Children (CSC) has integrated biochemical and molecular methods into a rural pediatric practice serving Old Order Amish and Mennonite (Plain) children. Among the Plain people, we have used single nucleotide polymorphism (SNP) microarrays to genetically map recessive disorders to large autozygous haplotype blocks (mean = 4.4 Mb) that contain many genes (mean = 79). For some, uninformative mapping or large gene lists preclude disease-gene identification by Sanger sequencing. Seven such conditions were selected for exome sequencing at the Broad Institute; all had been previously mapped at the CSC using low density SNP microarrays coupled with autozygosity and linkage analyses. Using between 1 and 5 patient samples per disorder, we identified sequence variants in the known disease-causing genes SLC6A3 and FLVCR1, and present evidence to strongly support the pathogenicity of variants identified in TUBGCP6, BRAT1, SNIP1, CRADD, and HARS. Our results reveal the power of coupling new genotyping technologies to population-specific genetic knowledge and robust clinical data.
特殊儿童诊所(CSC)已将生化和分子方法整合到农村儿科实践中,为老派阿米什人和门诺派(平原)儿童提供服务。在平原人中,我们使用单核苷酸多态性(SNP)微阵列将隐性疾病遗传图谱绘制到包含许多基因(平均 79 个)的大型纯合子单倍型块上(平均值为 4.4Mb)。对于某些疾病,无信息映射或大型基因列表排除了通过 Sanger 测序鉴定疾病基因。这七种情况已在 Broad Institute 进行了外显子组测序选择;所有这些疾病都曾在 CSC 使用低密度 SNP 微阵列与纯合子和连锁分析相结合进行过映射。我们使用每个疾病 1 到 5 个患者样本,在已知的致病基因 SLC6A3 和 FLVCR1 中鉴定出了序列变异,并提供了有力证据支持在 TUBGCP6、BRAT1、SNIP1、CRADD 和 HARS 中鉴定出的变异的致病性。我们的研究结果显示了将新型基因分型技术与特定人群的遗传知识和强大的临床数据相结合的强大功能。