LtsAzole Resistant A. fumigatus from Indiaof these analyses 
were used to infer the potential source(s) of the triazole-resistant clinical and environmental A. fumigatus strains in India.AcknowledgmentsWe thank Daniel Diekema (University of Iowa Carver College of Medicine, Iowa City, USA) for Chinese isolates, Andre Paugam (Universite ?Paris Descartes and Hopital Cochin, AP-HP, Paris, France) for French ^ isolates and Jorg Steinmann and Peter-Michael Rath (Institute of Medical Microbiology, University Hospital Essen, Essen, Germany) for the German isolate which were used as controls. We are grateful to Paul Verweij(Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands) for providing us several fungicides (bromuconazole, cyproconazole, difenoconazole, epoxiconazole, penconazole, tebuconazole, triadimefon, metconazole). We acknowledge Rallis India, India and Cheminova India, India for kindly providing us hexaconazole and tricyclazole fungicides.Author ContributionsConceived and designed the experiments: AC JPX JFM. Performed the experiments: AC SK CS GS PKS FH CHK. Analyzed the data: AC SK JPX FH CHK JFM. Contributed reagents/materials/analysis tools: AC SNG JPX FH. Wrote the paper: AC SK JPX CHK JFM.
15-LOX-1 is a peroxidase which catalyzes the oxygenation of free or membrane-bound polyunsaturated fatty acids containing at least one bis-allylic methylene [1]. It is implicated in various physiological processes including membrane remodelling, cell differentiation, inflammation and apoptosis [2,3]. Deregulation of 15-LOX-1 expression is suggested to be involved in the pathogenesis of diverse malignancies, including prostate and colorectal cancer [4,5], asthma [6,7], atherosclerosis [8], orbital fibrosis [9] and K162 web nephritis [10]. Moreover, introduction of 15-LOX1 into cells could result in Lixisenatide oxidative stress and membrane degradation [11,12]. Therefore, the expression and activity of the enzyme are strictly controlled. In most 15-LOX-1 inducible cell types, the enzyme is predominantly activated through the IL4/13-signal transducer and activator of transcription 6 (STAT6) cascade [13,14,15]. 15-LOX1 mRNA transcription is also associated with CpG island methylation status and histone acetylation status at the promoterlevel [16]. Different experimental evidences suggest that histone acetylation is 23727046 positively correlated with 15-LOX-1 transcriptional activation [13,16,17,18,19]. In a previous study of HL cell lines we showed that DNA hyper-methylation is associated with silenced 15-LOX-1 transcription and that demethylation is required for 15LOX-1 transactivation [16]. However, it was recently reported that hypermethylation of specific CpG di-nucleotides in the 15LOX-1 promoter leads to the upregulation of 15-LOX-1 expression and enzyme activity in prostate cancer cells [20]. Moreover, recent work on colorectal cancer showed that 15-LOX1 promoter methylation levels did not significantly correlate with 15-LOX-1 mRNA expression levels in neither cancer cell lines nor in the patients’ tumor specimens [21]. Therefore, additional epigenetic mechanism(s) could be involved in the transcriptional regulation of 15-LOX-1, controlling the tissue- and cell-type specific 15-LOX-1 gene expression. Lysine is the key substrate residue in histone methylation, which can occur one, two or three times (mono-, di- or trimethylation), leading to different biological outcomes. Histone methylationHistone Methylation Regulates 15-LOX-1 Expressioncould have vari.LtsAzole Resistant A. fumigatus from Indiaof these analyses were used to infer the potential source(s) of the triazole-resistant clinical and environmental A. fumigatus strains in India.AcknowledgmentsWe thank Daniel Diekema (University of Iowa Carver College of Medicine, Iowa City, USA) for Chinese isolates, Andre Paugam (Universite ?Paris Descartes and Hopital Cochin, AP-HP, Paris, France) for French ^ isolates and Jorg Steinmann and Peter-Michael Rath (Institute of Medical Microbiology, University Hospital Essen, Essen, Germany) for the German isolate which were used as controls. We are grateful to Paul Verweij(Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands) for providing us several fungicides (bromuconazole, cyproconazole, difenoconazole, epoxiconazole, penconazole, tebuconazole, 
triadimefon, metconazole). We acknowledge Rallis India, India and Cheminova India, India for kindly providing us hexaconazole and tricyclazole fungicides.Author ContributionsConceived and designed the experiments: AC JPX JFM. Performed the experiments: AC SK CS GS PKS FH CHK. Analyzed the data: AC SK JPX FH CHK JFM. Contributed reagents/materials/analysis tools: AC SNG JPX FH. Wrote the paper: AC SK JPX CHK JFM.
15-LOX-1 is a peroxidase which catalyzes the oxygenation of free or membrane-bound polyunsaturated fatty acids containing at least one bis-allylic methylene [1]. It is implicated in various physiological processes including membrane remodelling, cell differentiation, inflammation and apoptosis [2,3]. Deregulation of 15-LOX-1 expression is suggested to be involved in the pathogenesis of diverse malignancies, including prostate and colorectal cancer [4,5], asthma [6,7], atherosclerosis [8], orbital fibrosis [9] and nephritis [10]. Moreover, introduction of 15-LOX1 into cells could result in oxidative stress and membrane degradation [11,12]. Therefore, the expression and activity of the enzyme are strictly controlled. In most 15-LOX-1 inducible cell types, the enzyme is predominantly activated through the IL4/13-signal transducer and activator of transcription 6 (STAT6) cascade [13,14,15]. 15-LOX1 mRNA transcription is also associated with CpG island methylation status and histone acetylation status at the promoterlevel [16]. Different experimental evidences suggest that histone acetylation is 23727046 positively correlated with 15-LOX-1 transcriptional activation [13,16,17,18,19]. In a previous study of HL cell lines we showed that DNA hyper-methylation is associated with silenced 15-LOX-1 transcription and that demethylation is required for 15LOX-1 transactivation [16]. However, it was recently reported that hypermethylation of specific CpG di-nucleotides in the 15LOX-1 promoter leads to the upregulation of 15-LOX-1 expression and enzyme activity in prostate cancer cells [20]. Moreover, recent work on colorectal cancer showed that 15-LOX1 promoter methylation levels did not significantly correlate with 15-LOX-1 mRNA expression levels in neither cancer cell lines nor in the patients’ tumor specimens [21]. Therefore, additional epigenetic mechanism(s) could be involved in the transcriptional regulation of 15-LOX-1, controlling the tissue- and cell-type specific 15-LOX-1 gene expression. Lysine is the key substrate residue in histone methylation, which can occur one, two or three times (mono-, di- or trimethylation), leading to different biological outcomes. Histone methylationHistone Methylation Regulates 15-LOX-1 Expressioncould have vari.
