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Mol Biol Rep ; 36(7): 1863-70, 2009 Sep.
Article in English | MEDLINE | ID: mdl-18989752

ABSTRACT

Morquio A is an autosomal recessive disease caused by the deficiency of N-acetylgalactosamine-6-sulfate sulfatase (GALNS), leading to the lysosomal accumulation of keratan-sulfate and chondroitin-6-sulfate. We evaluated in HEK293 cells the effect of the cytomegalovirus immediate early enhancer/promoter (CMV) or the elongation factor 1alpha (EF1alpha) promoters, and the coexpression with the sulfatase modifying factor 1 (SUMF1) on GALNS activity. Four days postransfection GALNS activity in transfected cells with CMV-pIRES-GALNS reached a plateau, whereas in cells transfected with EF1alpha-pIRES-GALNS continued to increase until day 8. Co-transfection with pCXN-SUMF1 showed an increment up to 2.6-fold in GALNS activity. Finally, computational analysis of transcription factor binding-sites and CpG islands showed that EF1alpha promoter has long CpG islands and high-density binding-sites for Sp1 compared to CMV. These results show the advantage of the SUMF1 coexpression on GALNS activity and indicate a considerable effect on the expression stability using EF1alpha promoter compared to CMV.


Subject(s)
Chondroitinsulfatases/metabolism , Gene Expression , Peptide Elongation Factor 1/genetics , Promoter Regions, Genetic/genetics , Sulfatases/metabolism , Binding Sites , Cell Line , Chondroitinsulfatases/genetics , Computational Biology , CpG Islands/genetics , Cytomegalovirus/genetics , Humans , Oxidoreductases Acting on Sulfur Group Donors , Plasmids/genetics , Sp1 Transcription Factor/metabolism , Transfection
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