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延伸因子1α启动子和SUMF1对N-乙酰半乳糖胺-6-硫酸酯硫酸酯酶体外表达的影响。

Effect of elongation factor 1alpha promoter and SUMF1 over in vitro expression of N-acetylgalactosamine-6-sulfate sulfatase.

作者信息

Alméciga-Díaz Carlos J, Rueda-Paramo Maria A, Espejo Angela J, Echeverri Olga Y, Montaño Adriana, Tomatsu Shunji, Barrera Luis A

机构信息

Instituto de Errores Innatos del Metabolismo, Pontificia Universidad Javeriana, Bogota, D.C., Colombia.

出版信息

Mol Biol Rep. 2009 Sep;36(7):1863-70. doi: 10.1007/s11033-008-9392-3. Epub 2008 Nov 7.

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.

摘要

黏多糖贮积症IV型A是一种常染色体隐性疾病,由N - 乙酰半乳糖胺 - 6 - 硫酸酯酶(GALNS)缺乏引起,导致硫酸角质素和硫酸软骨素 - 6在溶酶体中蓄积。我们在人胚肾293细胞中评估了巨细胞病毒立即早期增强子/启动子(CMV)或延伸因子1α(EF1α)启动子的作用,以及与硫酸酯酶修饰因子1(SUMF1)共表达对GALNS活性的影响。转染后4天,用CMV - pIRES - GALNS转染的细胞中GALNS活性达到平台期,而用EF1α - pIRES - GALNS转染的细胞中GALNS活性持续增加直至第8天。与pCXN - SUMF1共转染显示GALNS活性增加至2.6倍。最后,转录因子结合位点和CpG岛的计算分析表明,与CMV相比,EF1α启动子具有长的CpG岛和高密度的Sp1结合位点。这些结果显示了SUMF1共表达对GALNS活性的优势,并表明与CMV相比,使用EF1α启动子对表达稳定性有相当大的影响。

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