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首页> 外文期刊>Fish Physiology and Biochemistry >Acyl-coenzyme A oxidases 1 and 3 in brown trout (Salmo trutta f. fario): Can peroxisomal fatty acid beta-oxidation be regulated by estrogen signaling?
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Acyl-coenzyme A oxidases 1 and 3 in brown trout (Salmo trutta f. fario): Can peroxisomal fatty acid beta-oxidation be regulated by estrogen signaling?

机译:褐鳟(Salmo trutta f。fario)中的酰基辅酶A氧化酶1和3:过氧化物酶体脂肪酸β-氧化可以通过雌激素信号传导来调节吗?

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Acyl-coenzyme A oxidases 1 (Acox1) and 3 (Acox3) are key enzymes in the regulation of lipid homeostasis. Endogenous and exogenous factors can disrupt their normal expression/activity. This study presents for the first time the isolation and characterization of Acox1 and Acox3 in brown trout (Salmo trutta f. fario). Additionally, as previous data point to the existence of a cross-talk between two nuclear receptors, namely peroxisome proliferator-activated receptors and estrogen receptors, it was here evaluated after in vitro exposures of trout hepatocytes the interference caused by ethynylestradiol in the mRNA levels of an inducible (by peroxisome proliferators) and a non-inducible oxidase. The isolated Acox1 and Acox3 show high levels of sequence conservation compared to those of other teleosts. Additionally, it was found that Acox1 has two alternative splicing isoforms, corresponding to 3I and 3II isoforms of exon 3 splicing variants. Both isoforms display tissue specificity, with Acox1-3II presenting a more ubiquitous expression in comparison with Acox1-3I. Acox3 was expressed in almost all brown trout tissues. According to real-time PCR data, the highest estrogenic stimulus was able to cause a down-regulation of Acox1 and an up-regulation of Acox3. So, for Acox1 we found a negative association between an estrogenic input and a directly activated PPAR alpha target gene. In conclusion, changes in hormonal estrogenic stimulus may impact the mobilization of hepatic lipids to the gonads, with ultimate consequences in reproduction. Further studies using in vivo assays will be fundamental to clarify these issues.
机译:酰基辅酶A氧化酶1(Acox1)和3(Acox3)是调节脂质体内平衡的关键酶。内源性和外源性因子可破坏其正常表达/活性。这项研究首次提出了褐鳟(Salmo trutta f。fario)中Acox1和Acox3的分离和表征。此外,由于先前的数据表明两个核受体,即过氧化物酶体增殖物激活的受体和雌激素受体之间存在串扰,因此,在鳟鱼肝细胞体外暴露后,本文评估了乙炔雌二醇对mRNA水平的干扰。一种可诱导的(通过过氧化物酶体增殖物)和一种不可诱导的氧化酶。与其他硬骨鱼相比,分离出的Acox1和Acox3具有较高的序列保守性。此外,发现Acox1具有两个替代的剪接异构体,分别对应于外显子3剪接变体的3I和3II异构体。两种同工型均显示组织特异性,与Acox1-3I相比,Acox1-3II的表达更为普遍。 Acox3在几乎所有的褐鳟组织中都有表达。根据实时PCR数据,最高的雌激素刺激能够引起Acox1的下调和Acox3的上调。因此,对于Acox1,我们发现雌激素输入与直接激活的PPARα目标基因之间存在负相关。总之,激素雌激素刺激的变化可能会影响肝脂质向性腺的动员,最终对生殖产生影响。使用体内测定法进行的进一步研究对于阐明这些问题至关重要。

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