Transcriptional and antioxidative responses to endogenous polyunsaturated fatty acid accumulation in yeast

被引:0
|
作者
Luka Andrisic
Emma J. Collinson
Oksana Tehlivets
Eleonora Perak
Tomislav Zarkovic
Ian W. Dawes
Neven Zarkovic
Ana Cipak Gasparovic
机构
[1] Rudjer Boskovic Institute,Discipline of Anatomy and Histology, School of Medical Sciences
[2] University of Sydney,Institute of Molecular Biosciences, Lipidomics Research Center Graz
[3] University of Graz,School of Biotechnology and Biomolecular Sciences
[4] Veterinary Institute,undefined
[5] Molecular Biosciences Study Program on Bioinformatics/Zagrebacka banka,undefined
[6] University of New South Wales,undefined
来源
Molecular and Cellular Biochemistry | 2015年 / 399卷
关键词
PUFA; Desaturase; ROS; Fatty acid β-oxidation; Catalase;
D O I
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中图分类号
学科分类号
摘要
Pathophysiology of polyunsaturated fatty acids (PUFAs) is associated with aberrant lipid and oxygen metabolism. In particular, under oxidative stress, PUFAs are prone to autocatalytic degradation via peroxidation, leading to formation of reactive aldehydes with numerous potentially harmful effects. However, the pathological and compensatory mechanisms induced by lipid peroxidation are very complex and not sufficiently understood. In our study, we have used yeast capable of endogenous PUFA synthesis in order to understand the effects triggered by PUFA accumulation on cellular physiology of a eukaryotic organism. The mechanisms induced by PUFA accumulation in S. cerevisiae expressing Hevea brasiliensis Δ12-fatty acid desaturase include down-regulation of components of electron transport chain in mitochondria as well as up-regulation of pentose-phosphate pathway and fatty acid β-oxidation at the transcriptional level. Interestingly, while no changes were observed at the transcriptional level, activities of two important enzymatic antioxidants, catalase and glutathione-S-transferase, were altered in response to PUFA accumulation. Increased intracellular glutathione levels further suggest an endogenous oxidative stress and activation of antioxidative defense mechanisms under conditions of PUFA accumulation. Finally, our data suggest that PUFA in cell membrane causes metabolic changes which in turn lead to adaptation to endogenous oxidative stress.
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页码:27 / 37
页数:10
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