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1.
Cells Tissues Organs ; 201(5): 380-9, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27193493

RESUMO

Foxc1 and Foxc2 play key roles in mouse development. Foxc1 mutant mice develop duplex kidneys with double ureters, and lack calvarial and sternal bones. Foxc2 null mice have been reported to have glomerular abnormalities in the kidney and axial skeletal anomalies. Expression patterns of Foxc1 and Foxc2 overlap extensively and are believed to have interactive roles. However, cooperative roles of these factors in glomerular and skeletal development are unknown. Therefore, we examined the kidneys and skeleton of mice that were double heterozygous for Foxc1 and Foxc2. Double heterozygotes were generated by mating single heterozygotes for Foxc1 and Foxc2. Newborn double heterozygous mice showed many anomalies in the kidney and urinary tract resembling Foxc1 phenotypes, including duplex kidneys, double ureters, hydronephrosis and mega-ureter. Some mice had hydronephrosis alone. In addition to these macroscopic anomalies, some mice had abnormal glomeruli and disorganized glomerular capillaries observed in Foxc2 phenotypes. Interestingly, these mice also showed glomerular cysts not observed in the single-gene knockout of either Foxc1 or Foxc2 but observed in conditional knockout of Foxc2 in the kidney. Serial section analysis revealed that all cystic glomeruli were connected to proximal tubules, precluding the possibility of atubular glomeruli resulting in cyst formation. Dorsally opened vertebral arches and malformations of sternal bones in the double heterozygotes were phenotypes similar to Foxc1 null mice. Absent or split vertebral bodies in the double heterozygotes were phenotypes similar to Foxc2 null mice, whilst hydrocephalus noted in the Foxc1 phenotype was not observed. Thus, Foxc1 and Foxc2 have a role in kidney and axial skeleton development. These transcription factors might interact in the regulation of the embryogenesis of these organs.


Assuntos
Osso e Ossos/patologia , Fatores de Transcrição Forkhead/metabolismo , Rim/patologia , Animais , Osso e Ossos/anormalidades , Osso e Ossos/metabolismo , Coristoma/patologia , Heterozigoto , Rim/anormalidades , Rim/metabolismo , Doenças Renais Císticas/patologia , Glomérulos Renais/patologia , Túbulos Renais/patologia , Células Mesangiais/patologia , Camundongos Knockout , Fenótipo
3.
PLoS One ; 10(6): e0130231, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26090680

RESUMO

Congenital vertebral malformations caused by embryonic segmentation defects are relatively common in humans and domestic animals. Although reverse genetics approaches in mice have provided information on the molecular mechanisms of embryonic somite segmentation, hypothesis-driven approaches cannot adequately reflect human dysmorphology within the population. In a N-ethyl-N-nitrosourea (ENU) mutagenesis project in Kyoto, the Oune mutant rat strain was isolated due to a short and kinked caudal vertebra phenotype. Skeletal staining of heterozygous rats showed partial loss of the cervical vertebrae as well as hemivertebrae and fused vertebral blocks in lumbar and sacral vertebrae. In homozygous embryos, severe displacement of the whole vertebrae was observed. The Oune locus was genetically mapped to rat chromosome 1 using 202 backcross animals and 50 genome-wide microsatellite markers. Subsequently, a miss-sense mutation in the Tbx6 gene was identified in the critical region. Although the mutation is located within the T-box domain near a predicted dimmer-interface, in vitro experiments revealed that the Tbx6 variant retains normal DNA binding ability and translational efficiency. However, the variant has decreased transcriptional activation potential in response to Notch-mediated signaling. Recently, it was reported that a dominant type of familial spondylocostal dysostosis is caused by a stoploss mutation in TBX6. Thus, we propose that partial dysfunction of Tbx6 leads to similar congenital vertebral malformations in both humans and rats. The Oune strain could be a unique animal model for dominant spondylocostal dysostosis and is useful for molecular dissection of the pathology of congenital vertebral malformations in humans.


Assuntos
Anormalidades Múltiplas/genética , Anormalidades Múltiplas/patologia , Genes Dominantes , Hérnia Diafragmática/genética , Hérnia Diafragmática/patologia , Mutação , Fenótipo , Coluna Vertebral/anormalidades , Animais , Sequência de Bases , Mapeamento Cromossômico , Análise Mutacional de DNA , Modelos Animais de Doenças , Etilnitrosoureia/efeitos adversos , Feminino , Regulação da Expressão Gênica , Ordem dos Genes , Loci Gênicos , Genótipo , Masculino , Mutação/efeitos dos fármacos , Ratos , Alinhamento de Sequência
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