Vermeulen Stefan, Menten Björn, Van Roy Nadine, Van Limbergen Heidi, De Paepe Anne, Mortier Geert, Speleman Frank
Center for Medical Genetics, Ghent University Hospital 0K5, De Pintelaan 185, 9000 Ghent, Belgium.
Am J Med Genet A. 2004 Jan 1;124A(1):10-8. doi: 10.1002/ajmg.a.20378.
Constitutional de novo complex chromosomal rearrangements (CCRs) are a rare finding in patients with mild to severe mental retardation. CCRs pose a challenge to the clinical cytogeneticist: generally CCRs are assumed to be the cause of the observed phenotypic abnormalities, but the complex nature of these chromosomal changes often hamper the accurate delineation of the chromosomal breakpoints and the identification of possible imbalances. In a first step towards a more detailed molecular cytogenetic characterization of CCRs, we studied four de novo CCRs using multicolor fluorescent in situ hybridization (M-FISH), comparative genomic hybridization (CGH), and FISH with region specific probes. These methods allowed a more refined characterization of the breakpoints in three of the four CCRs. The occurrence of 7q breakpoints in three out of these four CCRs and in 30% of reported CCRs suggested preferential involvement of this chromosomal region in the formation of CCRs. Further analysis of these 7q breakpoints revealed a 2 Mb deletion at 7q21.11 in one patient and involvement of the same region in a cryptic insertion in a second patient. This particular region contains at least 5 candidate genes for mental retardation. The other patient had a breakpoint more proximal to this region. The present data together with these from the literature provide evidence that a region within 7q21.11 may be prone to breakage and formation of CCRs.
先天性新发复杂染色体重排(CCRs)在轻至重度智力发育迟缓患者中是一种罕见的发现。CCRs给临床细胞遗传学家带来了挑战:一般认为CCRs是观察到的表型异常的原因,但这些染色体变化的复杂性常常妨碍对染色体断点的准确界定以及对可能的失衡情况的识别。作为迈向对CCRs进行更详细分子细胞遗传学特征分析的第一步,我们使用多色荧光原位杂交(M-FISH)、比较基因组杂交(CGH)以及使用区域特异性探针的FISH技术研究了四个新发CCRs。这些方法使得能够对四个CCRs中的三个的断点进行更精细的特征分析。这四个CCRs中有三个以及30%已报道的CCRs中出现了7q断点,这表明该染色体区域在CCRs形成过程中优先受累。对这些7q断点的进一步分析显示,一名患者在7q21.11处有一个2 Mb的缺失,另一名患者的一个隐匿插入涉及同一区域。这个特定区域至少包含5个智力发育迟缓候选基因。另一名患者的断点更靠近该区域。目前的数据以及文献中的数据共同提供了证据,表明7q21.11内的一个区域可能易于发生断裂并形成CCRs。