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PMID: 12196168 Published · ppublish English Journal Article Review

The response to iron deprivation in Saccharomyces cerevisiae: expression of siderophore-based systems of iron uptake.

Biochemical Society transactions ·Vol. 30 ·No. 4 ·2002-08-00 ·Pages 698-702

Philpott CC, Protchenko O, Kim YW, Boretsky Y, Shakoury-Elizeh M

Abstract

The budding yeast Saccharomyces cerevisiae responds to growth in limiting amounts of iron by activating the transcription factor Aft1p and expressing a set of genes that ameliorate the effects of iron deprivation. Analysis of iron-regulated gene expression using cDNA microarrays has revealed the set of genes controlled by iron and Aft1p. Many of these genes are involved in the uptake of siderophore-bound iron from the environment. One family of genes, FIT1, FIT2 and FIT3, codes for mannoproteins that are incorporated into the cell wall via glycosylphosphatidylinositol anchors. These genes are involved in the retention of siderophore-iron in the cell wall. Siderophore-bound iron can be taken up into the cell via two genetically separable systems. One system requires the reduction and release of the iron from the siderophore prior to uptake by members of the Fre family of plasma-membrane metalloreductases. Following reduction and release from the siderophore, the iron is then taken up via the high-affinity ferrous transport system. A set of transporters that specifically recognizes siderophore-iron chelates is also expressed under conditions of iron deprivation. These transporters, encoded by ARN1, ARN2/TAF1, ARN3/SIT1 and ARN4/ENB1, facilitate the uptake of both hydroxamate- and catecholate-type siderophores. The Arn transporters are expressed in intracellular vesicles that correspond to the endosomal compartment, which suggests that intracellular trafficking of the siderophore and/or its transporter may be important for uptake.

MeSH Terms
Biological Transport Iron/metabolism Membrane Proteins/metabolism Models, Biological Saccharomyces cerevisiae/genetics,metabolism Saccharomyces cerevisiae Proteins/metabolism Siderophores/biosynthesis
Chemicals
Membrane Proteins Saccharomyces cerevisiae Proteins Siderophores Iron
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Philpott C C
Liver Diseases Section, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institutes of Health, Building 10, Room 9B-16, 10 Center Drive, Bethesda, MD 20892-1800, USA. carolinep@intra.niddk.nih.gov
Protchenko O
Kim Y W
Boretsky Y
Shakoury-Elizeh M
Article Info
Journal
Biochemical Society transactions
Abbr.
Biochem Soc Trans
ISSN
0300-5127
Published
2002-08-00
Pages
698-702
Language
English
Region
England
NLM ID
7506897
Subset
IM
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