Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2

• Autor(a) principal: Dathe, Katarina
• Data de Publicação: 2009
• Outros Autores: Kjaer, Klaus W., Brehm, Anja, Meinecke, Peter, Nuernberg, Peter, Corrêa Neto, Jordão [UNIFESP], Brunoni, Decio [UNIFESP], Tommerup, Nils, Ott, Claus E., Klopocki, Eva, Seemann, Petra, Mundlos, Stefan
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• dARK ID: ark:/48912/0013000008r73
• DOI: 10.1016/j.ajhg.2009.03.001
• Texto Completo: http://dx.doi.org/10.1016/j.ajhg.2009.03.001; http://repositorio.unifesp.br/handle/11600/31453

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 similar to 1.3 Mb was performed. A microduplication of: similar to 5.5 kb in a noncoding sequence similar to 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.