Mitogen-activated protein kinase Hog1 is activated in response to curcumin exposure in the budding yeast Saccharomyces cerevisiae

被引:21
作者
Azad, Gajendra Kumar [1 ]
Singh, Vikash [1 ]
Thakare, Mayur Jankiram [1 ]
Baranwal, Shivani [1 ]
Tomar, Raghuvir Singh [1 ]
机构
[1] Indian Inst Sci Educ & Res, Dept Biol Sci, Lab Chromatin Biol, Bhopal 462023, India
关键词
Yeast drug response; Curcumin; HOG pathway; Hog1; phosphorylation; Glycerol-3-phosphate dehydrogenase 1 (GPD1); Mitogen-activated protein kinases; DNA-DAMAGE RESPONSE; 2-COMPONENT SYSTEM; OSMOTIC-STRESS; PATHWAY; MAPK; PHOSPHORYLATION; DEHYDROGENASE; INDUCTION; REQUIRES; CASCADE;
D O I
10.1186/s12866-014-0317-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Curcumin (CUR), an active polyphenol derived from the spice turmeric, has been traditionally used for centuries in ancient Indian medicine to treat a number of diseases. The physiological effects of CUR have been shown to be diverse; however, the target molecules and pathways that CUR affects have yet to be fully described. Results: Here, we demonstrate for the first time that the budding yeast mitogen-activated protein kinase (MAPK) Hog1 is essential for the response to CUR. Moreover, CUR-induced Hog1 phosphorylation was rescued by supplementation of iron to the growth medium. Hog1 was rapidly phosphorylated upon CUR treatment, but unlike the response to hyperosmotic shock (0.8 M NaCl), it remains activated for an extended period of time. A detailed analysis of HOG pathway mutants revealed that Pbs2p, Ptc2p, and Ssk2p are required for optimal CUR-induced Hog1 phosphorylation. We also observed a Hog1 dependent transcriptional response to CUR treatment that involved the up-regulation of glycerol-3-phosphate dehydrogenase 1 (GPD1), a factor that is essential for the hyperosmotic stress response. Conclusions: Our present finding revealed the role of Hog1 MAPK in regulation of CUR-induced transcriptional response. We anticipate that our finding will enhance the understanding on the molecular mode of action of CUR on S. cerevisiae.
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页数:11
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