Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression.
Hum Mol Genet
; 21(11): 2572-87, 2012 Jun 01.
Article
en En
| MEDLINE
| ID: mdl-22378147
ABSTRACT
Biallelic mutations of the DNA annealing helicase SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like 1) cause Schimke immuno-osseous dysplasia (SIOD, MIM 242900), an incompletely penetrant autosomal recessive disorder. Using human, Drosophila and mouse models, we show that the proteins encoded by SMARCAL1 orthologs localize to transcriptionally active chromatin and modulate gene expression. We also show that, as found in SIOD patients, deficiency of the SMARCAL1 orthologs alone is insufficient to cause disease in fruit flies and mice, although such deficiency causes modest diffuse alterations in gene expression. Rather, disease manifests when SMARCAL1 deficiency interacts with genetic and environmental factors that further alter gene expression. We conclude that the SMARCAL1 annealing helicase buffers fluctuations in gene expression and that alterations in gene expression contribute to the penetrance of SIOD.
Texto completo:
1
Colección:
01-internacional
Asunto principal:
Osteocondrodisplasias
/
Arteriosclerosis
/
Embolia Pulmonar
/
Expresión Génica
/
ADN Helicasas
/
Alelos
/
Síndromes de Inmunodeficiencia
/
Mutación
/
Síndrome Nefrótico
Tipo de estudio:
Prognostic_studies
/
Risk_factors_studies
Límite:
Animals
/
Humans
Idioma:
En
Revista:
Hum Mol Genet
Asunto de la revista:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Año:
2012
Tipo del documento:
Article
País de afiliación:
Canadá