Literature DB >> 12095998

Combinatorial control of yeast FET4 gene expression by iron, zinc, and oxygen.

Brian M Waters1, David J Eide.   

Abstract

Acquisition of metals such as iron, copper, and zinc by the yeast Saccharomyces cerevisiae is tightly regulated. High affinity uptake systems are induced under metal-limiting conditions to maintain an adequate supply of these essential nutrients. Low affinity uptake systems function when their substrates are in greater supply. The FET4 gene encodes a low affinity iron and copper uptake transporter. FET4 expression is regulated by several environmental factors. In this report, we describe the molecular mechanisms underlying this regulation. First, we found that FET4 expression is induced in iron-limited cells by the Aft1 iron-responsive transcriptional activator. Second, FET4 is regulated by zinc status via the Zap1 transcription factor. We present evidence that FET4 is a physiologically relevant zinc transporter and this provides a rationale for its regulation by Zap1. Finally, FET4 expression is regulated in response to oxygen by the Rox1 repressor. Rox1 attenuates activation by Aft1 and Zap1 in aerobic cells. Derepression of FET4 may allow the Fet4 transporter to play an even greater role in metal acquisition under anaerobic conditions. Thus, Fet4 is a multisubstrate metal ion transporter under combinatorial control by iron, zinc, and oxygen.

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Year:  2002        PMID: 12095998     DOI: 10.1074/jbc.M206214200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  60 in total

1.  Zinc fingers can act as Zn2+ sensors to regulate transcriptional activation domain function.

Authors:  Amanda J Bird; Keith McCall; Michelle Kramer; Elizabeth Blankman; Dennis R Winge; David J Eide
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

2.  The Zap1 transcriptional activator also acts as a repressor by binding downstream of the TATA box in ZRT2.

Authors:  Amanda J Bird; Elizabeth Blankman; David J Stillman; David J Eide; Dennis R Winge
Journal:  EMBO J       Date:  2004-02-19       Impact factor: 11.598

Review 3.  Metal-responsive transcription factors that regulate iron, zinc, and copper homeostasis in eukaryotic cells.

Authors:  Julian C Rutherford; Amanda J Bird
Journal:  Eukaryot Cell       Date:  2004-02

4.  The effect of phosphate accumulation on metal ion homeostasis in Saccharomyces cerevisiae.

Authors:  Leah Rosenfeld; Amit R Reddi; Edison Leung; Kimberly Aranda; Laran T Jensen; Valeria C Culotta
Journal:  J Biol Inorg Chem       Date:  2010-04-29       Impact factor: 3.358

5.  Repression of ADH1 and ADH3 during zinc deficiency by Zap1-induced intergenic RNA transcripts.

Authors:  Amanda J Bird; Mat Gordon; David J Eide; Dennis R Winge
Journal:  EMBO J       Date:  2006-11-30       Impact factor: 11.598

6.  Recruitment of Tup1p and Cti6p regulates heme-deficient expression of Aft1p target genes.

Authors:  Robert J Crisp; Erika M Adkins; Emily Kimmel; Jerry Kaplan
Journal:  EMBO J       Date:  2006-01-26       Impact factor: 11.598

7.  Probing the mechanism of FET3 repression by Izh2p overexpression.

Authors:  Brian R Kupchak; Ibon Garitaonandia; Nancy Y Villa; Matthew B Mullen; Marilee G Weaver; Lisa M Regalla; Elizabeth A Kendall; Thomas J Lyons
Journal:  Biochim Biophys Acta       Date:  2007-04-13

Review 8.  Siderophore-based iron acquisition and pathogen control.

Authors:  Marcus Miethke; Mohamed A Marahiel
Journal:  Microbiol Mol Biol Rev       Date:  2007-09       Impact factor: 11.056

9.  Activator and repressor functions of the Mot3 transcription factor in the osmostress response of Saccharomyces cerevisiae.

Authors:  Fernando Martínez-Montañés; Alessandro Rienzo; Daniel Poveda-Huertes; Amparo Pascual-Ahuir; Markus Proft
Journal:  Eukaryot Cell       Date:  2013-02-22

10.  A novel negative Fe-deficiency-responsive element and a TGGCA-type-like FeRE control the expression of FTR1 in Chlamydomonas reinhardtii.

Authors:  Xiaowen Fei; Mats Eriksson; Yajun Li; Xiaodong Deng
Journal:  J Biomed Biotechnol       Date:  2010-02-22
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