Functional rescue of elastin insufficiency in mice by the human elastin gene: implications for mouse models of human disease.
Circ Res
; 101(5): 523-31, 2007 Aug 31.
Article
en En
| MEDLINE
| ID: mdl-17626896
ABSTRACT
Diseases linked to the elastin gene arise from loss-of-function mutations leading to protein insufficiency (supravalvular aortic stenosis) or from missense mutations that alter the properties of the elastin protein (dominant cutis laxa). Modeling these diseases in mice is problematic because of structural differences between the human and mouse genes. To address this problem, we developed a humanized elastin mouse with elastin production being controlled by the human elastin gene in a bacterial artificial chromosome. The temporal and spatial expression pattern of the human transgene mirrors the endogenous murine gene, and the human gene accurately recapitulates the alternative-splicing pattern found in humans. Human elastin protein interacts with mouse elastin to form functional elastic fibers and when expressed in the elastin haploinsufficient background reverses the hypertension and cardiovascular changes associated with that phenotype. Elastin from the human transgene also rescues the perinatal lethality associated with the null phenotype. The results of this study confirm that reestablishing normal elastin levels is a logical objective for treating diseases of elastin insufficiency such as supravalvular aortic stenosis. This study also illustrates how differences in gene structure and alternative splicing present unique problems for modeling human diseases in mice.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Estenosis Aórtica Subvalvular
/
Elastina
/
Cutis Laxo
Tipo de estudio:
Etiology_studies
Límite:
Animals
/
Female
/
Humans
Idioma:
En
Revista:
Circ Res
Año:
2007
Tipo del documento:
Article
País de afiliación:
Estados Unidos