Functional research progress of UBIAD1 and pathogenesis of SCCD / 国际眼科杂志(Guoji Yanke Zazhi)
International Eye Science
;
(12): 981-986, 2020.
Artigo
em Chinês
| WPRIM
| ID: wpr-876795
ABSTRACT
@#The molecular basis of schnyder crystalline corneal dystrophy(SCCD)is UBIAD1 gene mutation. The pathogenesis of SCCD includes conformational change of UBIAD1 protein which leads to loss of combination with GGpp compounds. UBIAD1-HMG CoA reductase complexes can't be separated, and the rate-limiting enzyme can't dissociate from endoplasmic reticulum to cytoplasm, which results in loss of recognition and degradation by the proteasome. The direct consequence is the gradual accumulation and biosynthesis of cholesterol and non-sterol isoprenoids compounds in the cell. This paper reviews the clinical manifestation, molecular basis, pathogenesis of SCCD and the function of UBIAD1 which provide guidance for molecular diagnosis and treatment of SCCD and pave the way for elucidating the function of UBIAD1 <i>in vivo</i>.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo de etiologia
/
Guia de Prática Clínica
Idioma:
Chinês
Revista:
International Eye Science
Ano de publicação:
2020
Tipo de documento:
Artigo
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