Coupry Isabelle, Monnet Laurence, Attia Azza Abd El Moneim, Taine Laurence, Lacombe Didier, Arveiler Benoît
Laboratoire de Génétique Humaine, Développement et Cancer, Université Victor Segalen Bordeaux 2, Bordeaux, France.
Hum Mutat. 2004 Mar;23(3):278-84. doi: 10.1002/humu.20001.
Rubinstein-Taybi syndrome (RTS) is a well-defined syndrome characterized by facial abnormalities, broad thumbs, broad big toes, and growth and mental retardation as the main clinical features. RTS was shown to be associated with disruption of the CREB-binding protein gene CBP (CREBBP), either by gross chromosomal rearrangements or by point mutations. Translocations and inversions involving chromosome band 16p13.3 form the minority of CBP mutations, whereas microdeletions occur more frequently (about 10%). Most deletion studies in RTS are performed by FISH analysis, and five cosmids must be used to cover the whole of the CBP gene, which spreads over 150 kb. Here we report the design of gene dosage assays by real-time quantitative PCR that are targeted on three exons located respectively at the 5' end (exon 2), in the middle (exon 12), and at the 3' end (exon 30) of the CBP gene. This technique proved to be efficient and powerful in finding deletions and complementary to the other available techniques, since it allowed us to identify deletions at the 3' end of the gene that had been missed by FISH analysis, and to refine some deletion breakpoints. Our results therefore suggest that real-time quantitative PCR is a useful technique to be included in the deletion search in RTS patients.
鲁宾斯坦-泰比综合征(RTS)是一种明确的综合征,其主要临床特征为面部异常、拇指宽大、大脚趾宽大以及生长和智力发育迟缓。研究表明,RTS与CREB结合蛋白基因CBP(CREBBP)的破坏有关,破坏方式包括染色体大片段重排或点突变。涉及染色体带16p13.3的易位和倒位构成了CBP突变的少数情况,而微缺失则更为常见(约10%)。RTS中的大多数缺失研究通过荧光原位杂交(FISH)分析进行,必须使用五个黏粒来覆盖整个CBP基因,该基因跨度超过150 kb。在此,我们报告了通过实时定量PCR设计的基因剂量测定方法,该方法针对分别位于CBP基因5'端(外显子2)、中间(外显子12)和3'端(外显子30)的三个外显子。这项技术在发现缺失方面被证明是高效且强大的,并且是对其他现有技术的补充,因为它使我们能够识别FISH分析遗漏的基因3'端的缺失,并细化一些缺失断点。因此,我们的结果表明,实时定量PCR是RTS患者缺失检测中一项有用的技术。