Dathe Katarina, Kjaer Klaus W, Brehm Anja, Meinecke Peter, Nürnberg Peter, Neto Jordao C, Brunoni Decio, Tommerup Nils, Ott Claus E, Klopocki Eva, Seemann Petra, Mundlos Stefan
Institut für Medizinische Genetik, Charité Universitätsmedizin Berlin, 13353 Berlin, Germany.
Am J Hum Genet. 2009 Apr;84(4):483-92. doi: 10.1016/j.ajhg.2009.03.001. Epub 2009 Mar 26.
Autosomal-dominant brachydactyly type A2 (BDA2), a limb malformation characterized by hypoplastic middle phalanges of the second and fifth fingers, has been shown to be due to mutations in the Bone morphogenetic protein receptor 1B (BMPR1B) or in its ligand Growth and differentiation factor 5 (GDF5). A linkage analysis performed in a mutation-negative family identified a novel locus for BDA2 on chromosome 20p12.3 that incorporates the gene for Bone morphogenetic protein 2 (BMP2). No point mutation was identified in BMP2, so a high-density array CGH analysis covering the critical interval of approximately 1.3 Mb was performed. A microduplication of approximately 5.5 kb in a noncoding sequence approximately 110 kb downstream of BMP2 was detected. Screening of other patients by qPCR revealed a similar duplication in a second family. The duplicated region contains evolutionary highly conserved sequences suggestive of a long-range regulator. By using a transgenic mouse model we can show that this sequence is able to drive expression of a X-Gal reporter construct in the limbs. The almost complete overlap with endogenous Bmp2 expression indicates that a limb-specific enhancer of Bmp2 is located within the identified duplication. Our results reveal an additional functional mechanism for the pathogenesis of BDA2, which is duplication of a regulatory element that affects the expression of BMP2 in the developing limb.
常染色体显性A2型短指症(BDA2)是一种肢体畸形疾病,其特征为第二和第五指中节指骨发育不全,研究表明该病是由骨形态发生蛋白受体1B(BMPR1B)或其配体生长分化因子5(GDF5)的突变所致。在一个无突变的家系中进行的连锁分析在20号染色体p12.3区域确定了一个新的BDA2基因座,该区域包含骨形态发生蛋白2(BMP2)基因。未在BMP2中发现点突变,因此对覆盖约1.3 Mb关键区间的高密度阵列比较基因组杂交(CGH)分析。在BMP2下游约110 kb的非编码序列中检测到一个约5.5 kb的微重复。通过定量聚合酶链反应(qPCR)对其他患者进行筛查,在另一个家系中发现了类似的重复。重复区域包含进化上高度保守的序列,提示存在一个远距离调控因子。通过使用转基因小鼠模型,我们发现该序列能够驱动X - Gal报告基因构建体在肢体中表达。其与内源性Bmp2表达几乎完全重叠,表明Bmp2的一个肢体特异性增强子位于所鉴定的重复序列内。我们的研究结果揭示了BDA2发病机制的另一种功能机制,即一个影响发育中肢体BMP2表达的调控元件发生重复。