Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Banco de datos
Tipo de estudio
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
N Engl J Med ; 379(11): 1042-1049, 2018 09 13.
Artículo en Inglés | MEDLINE | ID: mdl-30207912

RESUMEN

The causes of ovarian dysgenesis remain incompletely understood. Two sisters with XX ovarian dysgenesis carried compound heterozygous truncating mutations in the BRCA2 gene that led to reduced BRCA2 protein levels and an impaired response to DNA damage, which resulted in chromosomal breakage and the failure of RAD51 to be recruited to double-stranded DNA breaks. The sisters also had microcephaly, and one sister was in long-term remission from leukemia, which had been diagnosed when she was 5 years old. Drosophila mutants that were null for an orthologue of BRCA2 were sterile, and gonadal dysgenesis was present in both sexes. These results revealed a new role for BRCA2 and highlight the importance to ovarian development of genes that are critical for recombination during meiosis. (Funded by the Israel Science Foundation and others.).


Asunto(s)
Proteína BRCA2/deficiencia , Rotura Cromosómica , Reparación del ADN , Genes BRCA2 , Disgenesia Gonadal/genética , Ovario/crecimiento & desarrollo , Adolescente , Animales , Proteína BRCA2/fisiología , Rotura Cromosómica/efectos de los fármacos , Análisis Mutacional de ADN , Drosophila melanogaster , Femenino , Humanos , Hipogonadismo/genética , Masculino , Microcefalia/genética , Mitomicina/farmacología , Modelos Animales , Ovario/fisiología , Linaje , Hermanos , Adulto Joven
2.
Elife ; 112022 03 21.
Artículo en Inglés | MEDLINE | ID: mdl-35311642

RESUMEN

We recently identified a missense mutation in Nucleoporin107 (Nup107; D447N) underlying XX-ovarian-dysgenesis, a rare disorder characterized by underdeveloped and dysfunctional ovaries. Modeling of the human mutation in Drosophila or specific knockdown of Nup107 in the gonadal soma resulted in ovarian-dysgenesis-like phenotypes. Transcriptomic analysis identified the somatic sex-determination gene doublesex (dsx) as a target of Nup107. Establishing Dsx as a primary relevant target of Nup107, either loss or gain of Dsx in the gonadal soma is sufficient to mimic or rescue the phenotypes induced by Nup107 loss. Importantly, the aberrant phenotypes induced by compromising either Nup107 or dsx are reminiscent of bone morphogenetic protein (BMP signaling hyperactivation). Remarkably, in this context, the metalloprotease AdamTS-A, a transcriptional target of both Dsx and Nup107, is necessary for the calibration of BMP signaling. As modulation of BMP signaling is a conserved critical determinant of soma-germline interaction, the sex- and tissue-specific deployment of Dsx-F by Nup107 seems crucial for the maintenance of the homeostatic balance between the germ cells and somatic gonadal cells.


Asunto(s)
Acuaporinas , Proteínas de Drosophila , Animales , Proteínas de Unión al ADN/metabolismo , Drosophila/genética , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/genética , Drosophila melanogaster/metabolismo , Femenino , Diferenciación Sexual/genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA