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X 染色体拷贝数变异和插入缺失导致智力障碍的精细尺度调查。

Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability.

机构信息

Department of Medical Genetics, Cambridge Institute for Medical Research, Cambridge CB2 0XY, UK.

出版信息

Am J Hum Genet. 2010 Aug 13;87(2):173-88. doi: 10.1016/j.ajhg.2010.06.017. Epub 2010 Jul 22.

Abstract

Copy number variants and indels in 251 families with evidence of X-linked intellectual disability (XLID) were investigated by array comparative genomic hybridization on a high-density oligonucleotide X chromosome array platform. We identified pathogenic copy number variants in 10% of families, with mutations ranging from 2 kb to 11 Mb in size. The challenge of assessing causality was facilitated by prior knowledge of XLID-associated genes and the ability to test for cosegregation of variants with disease through extended pedigrees. Fine-scale analysis of rare variants in XLID families leads us to propose four additional genes, PTCHD1, WDR13, FAAH2, and GSPT2, as candidates for XLID causation and the identification of further deletions and duplications affecting X chromosome genes but without apparent disease consequences. Breakpoints of pathogenic variants were characterized to provide insight into the underlying mutational mechanisms and indicated a predominance of mitotic rather than meiotic events. By effectively bridging the gap between karyotype-level investigations and X chromosome exon resequencing, this study informs discussion of alternative mutational mechanisms, such as noncoding variants and non-X-linked disease, which might explain the shortfall of mutation yield in the well-characterized International Genetics of Learning Disability (IGOLD) cohort, where currently disease remains unexplained in two-thirds of families.

摘要

通过在高密度寡核苷酸 X 染色体阵列平台上进行阵列比较基因组杂交,对 251 个具有 X 连锁智力障碍(XLID)证据的家族进行了拷贝数变异和插入缺失的研究。我们在 10%的家族中发现了致病性拷贝数变异,突变大小从 2kb 到 11Mb 不等。通过对 XLID 相关基因的先验知识和通过扩展家系测试变体与疾病的共分离的能力,评估因果关系的挑战得到了简化。对 XLID 家族中罕见变体的精细分析使我们提出了另外四个基因,即 PTCHD1、WDR13、FAAH2 和 GSPT2,作为 XLID 致病的候选基因,并鉴定了进一步影响 X 染色体基因但没有明显疾病后果的缺失和重复。对致病性变体的断点进行了特征分析,为深入了解潜在的突变机制提供了线索,并表明有丝分裂而非减数分裂事件占主导地位。通过有效地弥合染色体水平研究和 X 染色体外显子重测序之间的差距,本研究为讨论替代突变机制提供了信息,例如非编码变体和非 X 连锁疾病,这可能解释了在 well-characterized International Genetics of Learning Disability (IGOLD) 队列中突变产量不足的情况,目前三分之二的家族的疾病仍然无法解释。

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