Department of Pediatrics, The University of Michigan Medical School, Ann Arbor, USA.
Am J Med Genet A. 2011 Jan;155A(1):154-63. doi: 10.1002/ajmg.a.33751. Epub 2010 Dec 10.
Genomic rearrangements are increasingly recognized as important contributors to human disease. Here we report on an 11½-year-old child with myopia, Duane retraction syndrome, bilateral mixed hearing loss, skeletal anomalies including multiple epiphyseal dysplasia, and global developmental delay, and a complex 6p25 genomic rearrangement. We have employed oligonucleotide-based comparative genomic hybridization arrays (aCGH) of different resolutions (44 and 244K) as well as a 1 M single nucleotide polymorphism (SNP) array to analyze this complex rearrangement. Our analyses reveal a complex rearrangement involving a ∼2.21 Mb interstitial deletion, a ∼240 kb terminal deletion, and a 70-80 kb region in between these two deletions that shows maintenance of genomic copy number. The interstitial deletion contains eight known genes, including three Forkhead box containing (FOX) transcription factors (FOXQ1, FOXF2, and FOXC1). The region maintaining genomic copy number partly overlaps the dual specificity protein phosphatase 22 (DUSP22) gene. Array analyses suggest a homozygous loss of genomic material at the 5' end of DUSP22, which was corroborated using TaqMan® copy number analysis. It is possible that this homozygous genomic loss may render both copies of DUSP22 or its products non-functional. Our analysis suggests a rearrangement mechanism distinct from a previously reported replication-based error-prone mechanism without template switching for a specific 6p25 rearrangement with a 1.22 Mb interstitial deletion. Our study demonstrates the utility and limitations of using oligonucleotide-based aCGH and SNP array technologies of increasing resolutions in order to identify complex DNA rearrangements and gene disruptions.
基因组重排越来越被认为是人类疾病的重要原因。在这里,我们报道了一例 11 岁半的儿童,其患有近视、Duane 退缩综合征、双侧混合性听力损失、骨骼异常包括多发性骨骺发育不良和全面发育迟缓,以及复杂的 6p25 基因组重排。我们采用了不同分辨率的寡核苷酸比较基因组杂交阵列(aCGH)(44 和 244K)以及 1M 单核苷酸多态性(SNP)阵列来分析这个复杂的重排。我们的分析揭示了一个涉及约 2.21Mb 间质缺失、约 240kb 末端缺失以及这两个缺失之间的 70-80kb 区域的复杂重排,该区域保持了基因组拷贝数。间质缺失包含 8 个已知基因,包括三个 Forkhead box containing(FOX)转录因子(FOXQ1、FOXF2 和 FOXC1)。保持基因组拷贝数的区域部分重叠双特异性蛋白磷酸酶 22(DUSP22)基因。阵列分析表明 DUSP22 5'端存在基因组物质的纯合缺失,这一点通过 TaqMan®拷贝数分析得到了证实。这种纯合性基因组缺失可能使 DUSP22 或其产物的两个拷贝都失去功能。我们的分析表明,与之前报道的基于复制的易错机制不同,该机制不存在模板切换,是一种特定的 6p25 重排,具有 1.22Mb 间质缺失。我们的研究表明,采用不同分辨率的寡核苷酸 aCGH 和 SNP 阵列技术来识别复杂的 DNA 重排和基因缺失是非常有用的,但也存在一定的局限性。