Transcription factor involved in iron utilization and homeostasis; binds consensus site PyPuCACCCPu and activates transcription in response to changes in iron availability; in iron-replete conditions localization is regulated by Grx3p, Grx4p, and Fra2p, and promoter binding is negatively regulated via Grx3p-Grx4p binding; AFT1 has a paralog, AFT2, that arose from the whole genome duplication; relative distribution to the nucleus increases upon DNA replication stress
2345678
The S. cerevisiae Reference Genome sequence is derived from laboratory strain
S288C. Download DNA or protein sequence, view genomic context and
coordinates. Click "Sequence Details" to view all sequence information for this locus, including that
for other strains.
Summary
AFT1/YGL071W is located on the left arm of chromosome VII between HSF1 heat shock transcription factor and RPB9 RNA polymerase II subunit; coding sequence is 2073 nucleotides long with 19 SNPs, 12 of which cause amino acid polymorphisms; AFT1 has a paralog, AFT2, that arose from the whole genome duplication
Basic sequence-derived (length, molecular weight, isoelectric point) and experimentally-determined (median abundance, median absolute deviation) protein information. Click "Protein Details" for further information about the protein such as half-life, abundance, domains, domains shared with other proteins, protein sequence retrieval for various strains, physico-chemical properties, protein modification sites, and external identifiers for the protein.
Summary
Aft1p is 690 amino acids long, low in abundance; phosphorylated on 15 residues; relative distribution to the nucleus increases upon DNA replication stress
Length (a.a.)
690
Mol. Weight (Da)
77672.7
Isoelectric Point
6.88
Median Abundance (molecules/cell)
2431 +/- 841
Alleles
Curated mutant alleles for the specified gene, listed alphabetically. Click on the allele name to open the allele page. Click "SGD search" to view all alleles in search results.
GO Annotations consist of four mandatory components: a gene product, a term from one of the three
Gene Ontology (GO) controlled vocabularies
(Molecular Function,
Biological Process, and
Cellular Component), a reference, and an
evidence code. SGD has manually curated and high-throughput GO Annotations, both derived from the
literature, as well as computational, or predicted, annotations. Click "Gene Ontology Details" to view
all GO information and evidence for this locus as well as biological processes it shares with other genes.
Summary
Sequence-specific DNA binding transcription factor that regulates chromatid cohesion, chromosome segregation, and cellular iron homeostasis; localizes to the cytoplasm, nucleus, and kinetochores
Functional Networks display how gene products work together in biological systems. The Shared Annotations
network shows genes with similar GO annotations, suggesting functional relationships. GO-CAMs (Gene
Ontology Causal Activity Models) are manually curated pathway models that illustrate how molecular
activities of multiple gene products connect through causal relationships to carry out biological
processes. GO-CAMs integrate Molecular Function, Biological Process, and Cellular Component information
into unified pathway representations based on published experimental evidence. Click "View GO-CAM at Gene
Ontology" to explore the interactive model at AmiGO.
Click on a gene or Biological Process GO term name to go to its specific page within SGD; drag any of the gene or GO
term name objects around within the visualization for easier viewing; click “Reset” to automatically redraw the
diagram; filter the genes that share GO Biological Process terms with the given gene by the number of terms they
share by clicking anywhere on the slider bar or dragging the tab to the desired filter number.
Phenotype annotations for a gene are curated single mutant phenotypes that require an observable
(e.g., "cell shape"), a qualifier (e.g., "abnormal"), a mutant type (e.g., null), strain background,
and a reference. In addition, annotations are classified as classical genetics or high-throughput
(e.g., large scale survey, systematic mutation set). Whenever possible, allele information and
additional details are provided. Click "Phenotype Details" to view all phenotype annotations and
evidence for this locus as well as phenotypes it shares with other genes.
Summary
Non-essential gene in reference strain S288C; null mutant displays a decreased growth rate, reduced competitive fitness and respiratory growth defects; null mutant is sensitive to metals, alkaline pH, and a variety of chemicals; null mutant displays chromosome instability, has decreased cell size and delayed progression through the G1 phase of the cell cycle; ovexpression and constitutively active alleles also display decreased growth rates
Interaction annotations are curated by BioGRID and include physical
or genetic interactions observed
between at least two genes. An interaction annotation is composed of the interaction type, name of the
interactor, assay type (e.g., Two-Hybrid), annotation type (e.g., manual or high-throughput), and a
reference, as well as other experimental details. Click "Interaction Details" to view all interaction
annotations and evidence for this locus, including an interaction visualization.
Summary
Aft1p interacts physically with proteins involved in transcription; AFT1 interacts genetically with genes involved in transcription; the aft1 null mutant is viable; the null mutant of paralog aft2 is viable; the aft1 aft2 double mutant is inviable or displays a growth defect.
The number of putative Regulators (genes that regulate it) and Targets (genes it regulates) for the
given locus, based on experimental evidence. This evidence includes data generated through
high-throughput techniques. Click "Regulation Details" to view all regulation annotations, shared GO
enrichment among regulation Targets, and a regulator/target diagram for the locus.
Summary
AFT1 and AFT2 encode paralogous low-iron-sensing transcriptional activators that regulate the expression of iron uptake and storage genes. Aft1p and Aft2p activate gene expression under iron-deficient conditions by binding to the same promoter elements, containing 5'-RCACCC-3' motifs. Aft1p is considered the primary regulator of iron homeostasis, but Aft2 can partially compensate for the loss of Aft1. The activities of Aft1p and Aft2p are regulated by monothiol glutaredoxins Grx3p and Grx4p, and exportin Msn5p. Aft1p cycles between the nucleus and cytosol, favoring cytosolic localization under iron-replete conditions, which induce multimerization of Aft1p/2p and favor export from the nucleus via interaction with the exportin Msn5p. Under low-iron conditions, Aft1p and Aft2p accumulates in the nucleus where it binds to and activates genes involved in iron uptake, transport, and storage, known collectively as the iron regulon.
Expression data are derived from records contained in the
Gene Expression Omnibus (GEO), and are first log2
transformed and normalized. Referenced datasets may contain one or more condition(s), and as a result
there may be a greater number of conditions than datasets represented in a single clickable histogram
bar. The histogram division at 0.0 separates the down-regulated (green) conditions and datasets from
those that are up-regulated (red). Click "Expression Details" to view all expression annotations and
details for this locus, including a visualization of genes that share a similar expression pattern.
Summary Paragraph
A summary of the locus, written by SGD Biocurators following a thorough review of the literature. Links
to gene names and curated GO terms are included within the Summary Paragraphs.
All manually curated literature for the specified gene, shown as a count of references by year of
publication followed by the most recent papers. Click "Literature Details" or "See all"
to view all literature information for this locus, organized into topics according to their
relevance to the gene (Primary Literature, Additional Literature, or Review).