ATM1/YMR301C Literature Guide Help

Other names published for ATM1: ATP-binding cassette Fe/S cluster precursor transporter ATM1, YMR301C

ATM1 - Mutants/Phenotypes (24)

ReferenceOther Genes Addressed
Alhebshi A, et al.  (2012) The essential iron-sulfur protein Rli1 is an important target accounting for inhibition of cell growth by reactive oxygen species. Mol Biol Cell 23(18):3582-90
Ueta R, et al.  (2012) Iron-induced dissociation of the Aft1p transcriptional regulator from target gene promoters is an initial event in iron-dependent gene suppression. Mol Cell Biol 32(24):4998-5008
Lindahl PA and Holmes-Hampton GP  (2011) Biophysical probes of iron metabolism in cells and organelles. Curr Opin Chem Biol 15(2):342-6
Ihrig J, et al.  (2010) Iron Regulation through the Back Door: Iron-Dependent Metabolite Levels Contribute to Transcriptional Adaptation to Iron Deprivation in Saccharomyces cerevisiae. Eukaryot Cell 9(3):460-71
Bernard DG, et al.  (2009) An Allelic Mutant Series of ATM3 Reveals Its Key Role in the Biogenesis of Cytosolic Iron-Sulfur Proteins in Arabidopsis. Plant Physiol 151(2):590-602
Miao R, et al.  (2009) Biophysical characterization of the iron in mitochondria from Atm1p-depleted Saccharomyces cerevisiae. Biochemistry 48(40):9556-68
Naranuntarat A, et al.  (2009) The interaction of mitochondrial iron with manganese superoxide dismutase. J Biol Chem 284(34):22633-40
Breslow DK, et al.  (2008) A comprehensive strategy enabling high-resolution functional analysis of the yeast genome. Nat Methods 5(8):711-8
Hausmann A, et al.  (2008) Cellular and Mitochondrial Remodeling upon Defects in Iron-Sulfur Protein Biogenesis. J Biol Chem 283(13):8318-30
Lain S, et al.  (2008) Discovery, in vivo activity, and mechanism of action of a small-molecule p53 activator. Cancer Cell 13(5):454-63
Gompf S, et al.  (2007) Switching of the homooligomeric ATP-binding cassette transport complex MDL1 from post-translational mitochondrial import to endoplasmic reticulum insertion. FEBS J 274(20):5298-310
Snoek IS and Steensma HY  (2006) Why does Kluyveromyces lactis not grow under anaerobic conditions? Comparison of essential anaerobic genes of Saccharomyces cerevisiae with the Kluyveromyces lactis genome. FEMS Yeast Res 6(3):393-403
Rutherford JC, et al.  (2005) Activation of the iron regulon by the yeast Aft1/Aft2 transcription factors depends on mitochondrial but not cytosolic iron-sulfur protein biogenesis. J Biol Chem 280(11):10135-40
Chloupkova M, et al.  (2004) The mitochondrial ABC transporter Atm1p functions as a homodimer. FEBS Lett 569(1-3):65-9
Chloupkova M, et al.  (2003) MDL1 is a high copy suppressor of ATM1: evidence for a role in resistance to oxidative stress. J Mol Biol 331(1):155-65
Sipos K, et al.  (2002) Maturation of cytosolic iron-sulfur proteins requires glutathione. J Biol Chem 277(30):26944-9
Kushnir S, et al.  (2001) A mutation of the mitochondrial ABC transporter Sta1 leads to dwarfism and chlorosis in the Arabidopsis mutant starik. Plant Cell 13(1):89-100
Schueck ND, et al.  (2001) The role of the mitochondrion in cellular iron homeostasis. Mitochondrion 1(1):51-60
Adamec J, et al.  (2000) Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia. Am J Hum Genet 67(3):549-62
Li J, et al.  (1999) Yeast mitochondrial protein, Nfs1p, coordinately regulates iron-sulfur cluster proteins, cellular iron uptake, and iron distribution. J Biol Chem 274(46):33025-34
Senbongi H, et al.  (1999) A mutation in a mitochondrial ABC transporter results in mitochondrial dysfunction through oxidative damage of mitochondrial DNA. Mol Gen Genet 262(3):426-36
Kispal G, et al.  (1997) The ABC transporter Atm1p is required for mitochondrial iron homeostasis. FEBS Lett 418(3):346-50
Kispal G, et al.  (1996) Mitochondrial and cytosolic branched-chain amino acid transaminases from yeast, homologs of the myc oncogene-regulated Eca39 protein. J Biol Chem 271(40):24458-64
Leighton J and Schatz G  (1995) An ABC transporter in the mitochondrial inner membrane is required for normal growth of yeast. EMBO J 14(1):188-95