Transcriptional Response to Deletion of the Phosphatidylserine Decarboxylase Psd1p in the Yeast Saccharomyces cerevisiae

被引:9
作者
Gsell, Martina [1 ]
Mascher, Gerald [1 ]
Schuiki, Irmgard [1 ]
Ploier, Birgit [1 ]
Hrastnik, Claudia [1 ]
Daum, Guenther [1 ]
机构
[1] Graz Univ Technol, Inst Biochem, A-8010 Graz, Austria
基金
奥地利科学基金会;
关键词
SYNTHETIC LETHAL INTERACTION; PLASMA-MEMBRANE; MITOCHONDRIAL PHOSPHATIDYLETHANOLAMINE; BIOSYNTHETIC PATHWAYS; GENE; IDENTIFICATION; PROTEINS; PHOSPHATIDYLCHOLINE; LOCALIZATION; CASSETTE;
D O I
10.1371/journal.pone.0077380
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the yeast, Saccharomyces cerevisiae, the synthesis of the essential phospholipid phosphatidylethanolamine (PE) is accomplished by a network of reactions which comprises four different pathways. The enzyme contributing most to PE formation is the mitochondrial phosphatidylserine decarboxylase 1 (Psd1p) which catalyzes conversion of phosphatidylserine (PS) to PE. To study the genome wide effect of an unbalanced cellular and mitochondrial PE level and in particular the contribution of Psd1p to this depletion we performed a DNA microarray analysis with Delta psd1 deletion mutant. This approach revealed that 54 yeast genes were significantly up-regulated in the absence of PSD1 compared to wild type. Surprisingly, marked down-regulation of genes was not observed. A number of different cellular processes in different subcellular compartments were affected in Delta psd1 mutant. Deletion mutants bearing defects in all 54 candidate genes, respectively, were analyzed for their growth phenotype and their phospholipid profile. Only three mutants, namely Delta pm2, Delta gph1 and Delta rsb1, were affected in one of these parameters. The possible link of these mutations to PE deficiency and PSD1 deletion is discussed.
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页数:11
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