期刊
CELL METABOLISM
卷 7, 期 6, 页码 555-564出版社
CELL PRESS
DOI: 10.1016/j.cmet.2008.04.010
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资金
- NIDDK NIH HHS [F31 DK081304] Funding Source: Medline
- NIGMS NIH HHS [R01 GM041840, R01 GM041840-20, GM41840] Funding Source: Medline
- PHS HHS [FDK081304A] Funding Source: Medline
Iron (Fe) is an essential cofactor for a wide range of cellular processes. We have previously demonstrated in yeast that Cth2 is expressed during Fe deficiency and promotes degradation of a battery of mRNAs leading to reprogramming of Fe-dependent metabolism and Fe storage. We report here that the Cth2-homologous protein Cth1 is transiently expressed during Fe deprivation and participates in the response to Fe deficiency through the degradation of mRNAs primarily involved in mitochondrially localized activities including respiration and amino acid biosynthesis. In parallel, wild-type cells, but not cth1 Delta cth2 Delta cells, accumulate mRNAs encoding proteins that function in glucose import and storage and store high levels of glycogen. In addition, Fe deficiency leads to phosphorylation of Snf1, an AMP-activated protein kinase family member required for the cellular response to glucose starvation. These studies demonstrate a metabolic reprogramming as a consequence of Fe starvation that is dependent on the coordinated activities of two mRNA-binding proteins.
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