Steinmann Katharina, Cooper David N, Kluwe Lan, Chuzhanova Nadia A, Senger Cornelia, Serra Eduard, Lazaro Conxi, Gilaberte Montserrat, Wimmer Katharina, Mautner Viktor-Felix, Kehrer-Sawatzki Hildegard
Institute of Human Genetics, University of Ulm, Ulm, Germany.
Am J Hum Genet. 2007 Dec;81(6):1201-20. doi: 10.1086/522089. Epub 2007 Oct 31.
Approximately 5% of patients with neurofibromatosis type 1 (NF1) exhibit gross deletions that encompass the NF1 gene and its flanking regions. The breakpoints of the common 1.4-Mb (type 1) deletions are located within low-copy repeats (NF1-REPs) and cluster within a 3.4-kb hotspot of nonallelic homologous recombination (NAHR). Here, we present the first comprehensive breakpoint analysis of type 2 deletions, which are a second type of recurring NF1 gene deletion. Type 2 deletions span 1.2 Mb and are characterized by breakpoints located within the SUZ12 gene and its pseudogene, which closely flank the NF1-REPs. Breakpoint analysis of 13 independent type 2 deletions did not reveal any obvious hotspots of NAHR. However, an overrepresentation of polypyrimidine/polypurine tracts and triplex-forming sequences was noted in the breakpoint regions that could have facilitated NAHR. Intriguingly, all 13 type 2 deletions identified so far are characterized by somatic mosaicism, which indicates a positional preference for mitotic NAHR within the NF1 gene region. Indeed, whereas interchromosomal meiotic NAHR occurs between the NF1-REPs giving rise to type 1 deletions, NAHR during mitosis appears to occur intrachromosomally between the SUZ12 gene and its pseudogene, thereby generating type 2 deletions. Such a clear distinction between the preferred sites of mitotic versus meiotic NAHR is unprecedented in any other genomic disorder induced by the local genomic architecture. Additionally, 12 of the 13 mosaic type 2 deletions were found in females. The marked female preponderance among mosaic type 2 deletions contrasts with the equal sex distribution noted for type 1 and/or atypical NF1 deletions. Although an influence of chromatin structure was strongly suspected, no sex-specific differences in the methylation pattern exhibited by the SUZ12 gene were apparent that could explain the higher rate of mitotic recombination in females.
约5%的1型神经纤维瘤病(NF1)患者存在包含NF1基因及其侧翼区域的大片段缺失。常见的1.4兆碱基(1型)缺失的断点位于低拷贝重复序列(NF1-REPs)内,并聚集在一个3.4千碱基的非等位基因同源重组(NAHR)热点区域内。在此,我们展示了对2型缺失的首次全面断点分析,2型缺失是另一种反复出现的NF1基因缺失类型。2型缺失跨度为1.2兆碱基,其特征是断点位于紧密侧翼于NF1-REPs的SUZ12基因及其假基因内。对13个独立的2型缺失进行断点分析未发现任何明显的NAHR热点区域。然而,在可能促进NAHR的断点区域中发现了多嘧啶/多嘌呤序列和三链形成序列的过度富集。有趣的是,到目前为止鉴定出的所有13个2型缺失均具有体细胞镶嵌性,这表明在NF1基因区域内有丝分裂NAHR存在位置偏好。实际上,1型缺失是由NF1-REPs之间发生染色体间减数分裂NAHR导致的,而有丝分裂期间的NAHR似乎发生在SUZ12基因及其假基因之间的染色体内,从而产生2型缺失。在由局部基因组结构引发的任何其他基因组疾病中,有丝分裂与减数分裂NAHR的偏好位点之间如此明显的区别是前所未有的。此外,13个镶嵌型2型缺失中有12个在女性中被发现。镶嵌型2型缺失中明显的女性优势与1型和/或非典型NF1缺失中观察到的性别均等分布形成对比。尽管强烈怀疑染色质结构有影响,但未发现SUZ12基因表现出的甲基化模式存在性别特异性差异,而这种差异本可解释女性中有丝分裂重组率较高的现象。