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渐进性缺氧对心脏脂肪酸氧化酶编码基因转录的对抗调节作用。

Counter-regulatory effects of incremental hypoxia on the transcription of a cardiac fatty acid oxidation enzyme-encoding gene.

作者信息

Ngumbela Kholiswa C, Sack Michael N, Essop M Faadiel

机构信息

Hatter Institute for Cardiology Research, University of Cape Town Medical School, Cape Town, South Africa.

出版信息

Mol Cell Biochem. 2003 Aug;250(1-2):151-8. doi: 10.1023/a:1024921329885.

Abstract

Cardiac fatty acid oxidation (FAO) enzyme gene expression is known to be downregulated during hypoxia in concordance with reduced FAO rates. To evaluate this metabolic switch, the transcriptional control of a cardiac FAO enzyme-encoding gene (medium-chain acyl-CoA dehydrogenase, MCAD) was characterized in response to hypobaric hypoxia. Transgenic mice harboring 560-bp of the human MCAD gene promoter fused to the bacterial chloramphenicol acetyl transferase (CAT) reporter gene were exposed to moderate (14% O2) or severe (8% O2) hypoxia for 2 or 7 days. MCAD-CAT activity and gene expression were significantly downregulated following 7 days of moderate hypoxia versus normoxic controls (p < 0.05). In parallel two known transcriptional regulators of MCAD expression, PPARalpha and Sp3, were concordantly downregulated at 7 days hypoxia. In contrast, severe hypoxia increased MCAD-CAT activity by 31 +/- 1.4% after 2 days hypoxia, returning to base +/- 4% after 2 days (p < 0.001) and returned to control levels after 7 days of hypoxia. These data demonstrate that MCAD gene expression is downregulated after 7 days of moderate hypoxia and inversely regulated with severe hypoxia. The known MCAD transcriptional regulators PPARalpha and Sp3 mirror MCAD expression. These data indicate that the transcriptional regulatory circuits involved in the control of MCAD gene expression under hypoxic conditions are modulated by upstream factors that are sensitive to the levels of oxygen.

摘要

已知在缺氧期间,心脏脂肪酸氧化(FAO)酶基因表达会随着FAO速率降低而下调。为了评估这种代谢转换,对一种心脏FAO酶编码基因(中链酰基辅酶A脱氢酶,MCAD)在低压缺氧反应中的转录调控进行了表征。将携带与细菌氯霉素乙酰转移酶(CAT)报告基因融合的560 bp人MCAD基因启动子的转基因小鼠暴露于中度(14% O₂)或重度(8% O₂)缺氧环境中2天或7天。与常氧对照组相比,中度缺氧7天后,MCAD-CAT活性和基因表达显著下调(p < 0.05)。同时,在缺氧7天时,两个已知的MCAD表达转录调节因子PPARα和Sp3也一致下调。相比之下,重度缺氧2天后,MCAD-CAT活性增加31±1.4%,2天后恢复到基线水平±4%(p < 0.001),缺氧7天后恢复到对照水平。这些数据表明,中度缺氧7天后MCAD基因表达下调,且与重度缺氧呈反向调节。已知的MCAD转录调节因子PPARα和Sp3反映了MCAD的表达。这些数据表明,缺氧条件下控制MCAD基因表达的转录调节回路受到对氧水平敏感的上游因子的调节。

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