Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion


Autoria(s): Klopocki, Eva; Lohan, Silke; Doelken, Sandra C.; Stricker, Sigmar; Ockeloen, Charlotte W.; Thiele de Aguiar, Renata Soares; Lezirovitz, Karina; Netto, Regina Celia Mingroni; Jamsheer, Aleksander; Shah, Hitesh; Kurth, Ingo; Habenicht, Rolf; Warman, Matthew; Devriendt, Koenraad; Kordass, Ulrike; Hempel, Maja; Rajab, Anna; Maekitie, Outi; Naveed, Mohammed; Radhakrishna, Uppala; Antonarakis, Stylianos E.; Horn, Denise; Mundlos, Stefan
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Background Split-hand/foot malformation (SHFM)-also known as ectrodactyly-is a congenital disorder characterised by severe malformations of the distal limbs affecting the central rays of hands and/or feet. A distinct entity termed SHFLD presents with SHFM and long bone deficiency. Mouse models suggest that a defect of the central apical ectodermal ridge leads to the phenotype. Although six different loci/mutations (SHFM1-6) have been associated with SHFM, the underlying cause in a large number of cases is still unresolved. Methods High resolution array comparative genomic hybridisation (CGH) was performed in patients with SHFLD to detect copy number changes. Candidate genes were further evaluated for expression and function during limb development by whole mount in situ hybridisation and morpholino knock-down experiments. Results Array CGH showed microduplications on chromosome 17p13.3, a locus previously associated with SHFLD. Detailed analysis of 17 families revealed that this copy number variation serves as a susceptibility factor for a highly variable phenotype with reduced penetrance, particularly in females. Compared to other known causes for SHFLD 17p duplications appear to be the most frequent cause of SHFLD. A similar to 11.8 kb minimal critical region was identified encompassing a single gene, BHLHA9, a putative basic loop helix transcription factor. Whole mount in situ hybridisation showed expression restricted to the limb bud mesenchyme underlying the apical ectodermal ridge in mouse and zebrafish embryos. Knock down of bhlha9 in zebrafish resulted in shortening of the pectoral fins. Conclusions Genomic duplications encompassing BHLHA9 are associated with SHFLD and non-Mendelian inheritance characterised by a high degree of non-penetrance with sex bias. Knock-down of bhlha9 in zebrafish causes severe reduction defects of the pectoral fin, indicating a role for this gene in limb development.

Deutsche Forschungsgemeinschaft

Deutsche Forschungsgemeinschaft [KL 2158/2-1]

Polish Ministry of Science and Higher Education

Polish Ministry of Science and Higher Education [495/N-NIEMCY/2009/0]

Identificador

JOURNAL OF MEDICAL GENETICS, LONDON, v. 49, n. 2, supl. 1, Part 6, pp. 119-125, FEB, 2012

0022-2593

http://www.producao.usp.br/handle/BDPI/42667

10.1136/jmedgenet-2011-100409

http://dx.doi.org/10.1136/jmedgenet-2011-100409

Idioma(s)

eng

Publicador

B M J PUBLISHING GROUP

LONDON

Relação

JOURNAL OF MEDICAL GENETICS

Direitos

closedAccess

Copyright B M J PUBLISHING GROUP

Palavras-Chave #SPLIT-HAND/FOOT MALFORMATION #APICAL ECTODERMAL RIDGE #LONG-BONE DEFICIENCY #FOOT MALFORMATION #EEC-SYNDROME #LOCUS #MICRODUPLICATIONS #SUSCEPTIBILITY #DACTYLAPLASIA #MUTATIONS #GENETICS & HEREDITY
Tipo

article

original article

publishedVersion