Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells. / Bro, Christoffer; Regenberg, Birgitte; Lagniel, Gilles; Labarre, Jean; Montero-Lomelí, Mónica; Nielsen, Jens.

In: Journal of Biological Chemistry, Vol. 278, No. 34, 22.08.2003, p. 32141-32149.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bro, C, Regenberg, B, Lagniel, G, Labarre, J, Montero-Lomelí, M & Nielsen, J 2003, 'Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells', Journal of Biological Chemistry, vol. 278, no. 34, pp. 32141-32149. https://doi.org/10.1074/jbc.M304478200

APA

Bro, C., Regenberg, B., Lagniel, G., Labarre, J., Montero-Lomelí, M., & Nielsen, J. (2003). Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells. Journal of Biological Chemistry, 278(34), 32141-32149. https://doi.org/10.1074/jbc.M304478200

Vancouver

Bro C, Regenberg B, Lagniel G, Labarre J, Montero-Lomelí M, Nielsen J. Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells. Journal of Biological Chemistry. 2003 Aug 22;278(34):32141-32149. https://doi.org/10.1074/jbc.M304478200

Author

Bro, Christoffer ; Regenberg, Birgitte ; Lagniel, Gilles ; Labarre, Jean ; Montero-Lomelí, Mónica ; Nielsen, Jens. / Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells. In: Journal of Biological Chemistry. 2003 ; Vol. 278, No. 34. pp. 32141-32149.

Bibtex

@article{02fa2f87b3e344ccb4ceaadbc514e040,
title = "Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells",
abstract = "Lithium is highly toxic to yeast when grown in galactose medium mainly because phosphoglucomutase, a key enzyme of galactose metabolism, is inhibited. We studied the global protein and gene expression profiles of Saccharomyces cerevisiae grown in galactose in different time intervals after addition of lithium. These results were related to physiological studies where both secreted and intracellular metabolites were determined. Microarray analysis showed that 664 open reading frames were down-regulated and 725 up-regulated in response to addition of lithium. Genes involved in transcription, translation, and nucleotide metabolism were down-regulated at the transcriptional level, whereas genes responsive to different stresses as well as genes from energy reserve metabolism and monosaccharide metabolism were up-regulated. Compared with the proteomic data, 26% of the down-regulated and 48% of the up-regulated proteins were also identified as being changed on the mRNA level. Functional clusters obtained from proteome data were coincident with transcriptional clusters. Physiological studies showed that acetate, glycerol, and glycogen accumulate in response to lithium, as reflected in expression data, whereas a change from respiro-fermentative to respiratory growth could not be predicted from the expression analyses.",
author = "Christoffer Bro and Birgitte Regenberg and Gilles Lagniel and Jean Labarre and M{\'o}nica Montero-Lomel{\'i} and Jens Nielsen",
year = "2003",
month = aug,
day = "22",
doi = "10.1074/jbc.M304478200",
language = "English",
volume = "278",
pages = "32141--32149",
journal = "Journal of Biological Chemistry",
issn = "0021-9258",
publisher = "American Society for Biochemistry and Molecular Biology, Inc.",
number = "34",

}

RIS

TY - JOUR

T1 - Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells

AU - Bro, Christoffer

AU - Regenberg, Birgitte

AU - Lagniel, Gilles

AU - Labarre, Jean

AU - Montero-Lomelí, Mónica

AU - Nielsen, Jens

PY - 2003/8/22

Y1 - 2003/8/22

N2 - Lithium is highly toxic to yeast when grown in galactose medium mainly because phosphoglucomutase, a key enzyme of galactose metabolism, is inhibited. We studied the global protein and gene expression profiles of Saccharomyces cerevisiae grown in galactose in different time intervals after addition of lithium. These results were related to physiological studies where both secreted and intracellular metabolites were determined. Microarray analysis showed that 664 open reading frames were down-regulated and 725 up-regulated in response to addition of lithium. Genes involved in transcription, translation, and nucleotide metabolism were down-regulated at the transcriptional level, whereas genes responsive to different stresses as well as genes from energy reserve metabolism and monosaccharide metabolism were up-regulated. Compared with the proteomic data, 26% of the down-regulated and 48% of the up-regulated proteins were also identified as being changed on the mRNA level. Functional clusters obtained from proteome data were coincident with transcriptional clusters. Physiological studies showed that acetate, glycerol, and glycogen accumulate in response to lithium, as reflected in expression data, whereas a change from respiro-fermentative to respiratory growth could not be predicted from the expression analyses.

AB - Lithium is highly toxic to yeast when grown in galactose medium mainly because phosphoglucomutase, a key enzyme of galactose metabolism, is inhibited. We studied the global protein and gene expression profiles of Saccharomyces cerevisiae grown in galactose in different time intervals after addition of lithium. These results were related to physiological studies where both secreted and intracellular metabolites were determined. Microarray analysis showed that 664 open reading frames were down-regulated and 725 up-regulated in response to addition of lithium. Genes involved in transcription, translation, and nucleotide metabolism were down-regulated at the transcriptional level, whereas genes responsive to different stresses as well as genes from energy reserve metabolism and monosaccharide metabolism were up-regulated. Compared with the proteomic data, 26% of the down-regulated and 48% of the up-regulated proteins were also identified as being changed on the mRNA level. Functional clusters obtained from proteome data were coincident with transcriptional clusters. Physiological studies showed that acetate, glycerol, and glycogen accumulate in response to lithium, as reflected in expression data, whereas a change from respiro-fermentative to respiratory growth could not be predicted from the expression analyses.

UR - http://www.scopus.com/inward/record.url?scp=0042357079&partnerID=8YFLogxK

U2 - 10.1074/jbc.M304478200

DO - 10.1074/jbc.M304478200

M3 - Journal article

C2 - 12791685

AN - SCOPUS:0042357079

VL - 278

SP - 32141

EP - 32149

JO - Journal of Biological Chemistry

JF - Journal of Biological Chemistry

SN - 0021-9258

IS - 34

ER -

ID: 239905767