Nitrogen catabolite repression transcriptional regulator; inhibits GLN3 transcription in rich nitrogen; sequesters Gln3p and Gat1p in the cytoplasm; contains glutathione peroxidase activity and can mutate to acquire GST activity; involved in resistance to heavy metal ions and oxidants; catabolite repression, induced by limiting nitrogen, does not occur if Ure2p has polymerized to form the [URE3] prion; translated by cap-dependent and -independent mechanisms; contains homology to human GST
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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
URE2/YNL229C is located on the left arm of chromosome XIV between ELA1 elongin A and JJJ1 co-chaperone; coding sequence is 1065 nucleotides long with one synonymous SNP
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
Ure2p is 354 amino acids long, shorter-lived, low in abundance; contains disordered region at N-terminus; ubiquitinylated on K104, phosphorylated on 6 residues
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
Cytosolic glutathione peroxidase involved in regulating cellular nitrogen utilization via cytoplasmic sequestering of Gln3p
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
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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
URE2/YNL229C is a non-essential gene; null mutants are viable but exhibit a range of phenotypic changes including abnormal autophagy, altered chemical compound accumulation and excretion, increased fermentative metabolism rate, altered metal resistance, decreased oxidative stress resistance, abnormal protein/peptide distribution, absent or decreased pseudohyphal growth, increased replicative lifespan, decreased vegetative growth rate, decreased acid and alkaline pH resistance, auxotrophy, decreased biofilm formation, delayed cell cycle progression in the G1 phase, increased cell size, altered competitive fitness, decreased desiccation resistance, decreased fermentative growth rate, increased heat sensitivity, decreased killer toxin resistance, increased stress resistance, decreased telomere length, altered toxin resistance, decreased utilization rates of nitrogen and phosphorus sources, and abnormal vacuolar morphology. Overexpression of URE2 results in increased filamentous growth, altered metal resistance, altered resistance to chemicals, increased toxin resistance, and decreased UV resistance.
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
Ure2p interacts physically with proteins involved in transcription; URE2 interacts genetically with genes involved in transcription
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
URE2 encodes a protein involved in regulation of nitrogen catabolite repression (NCR). Constitutively produced, cytoplasmic Ure2p acts as a transcriptional repressor by controlling localization of the GATA transcription factor Gln3p, which is a key activator of NCR. During growth in the presence of easily assimilated nitrogen sources, such as ammonium or glutamine, Ure2p binds and sequesters Gln3p in the cytoplasm, thus preventing expression of genes involved in poor nitrogen catabolism. In the presence of only poor nitrogen sources, such as urea or proline, or under nitrogen starvation, Ure2p dissociates from Gln3p, which allows Gln3p to enter the nucleus and, along with Gat1p, activate transcription of multiple genes required for utilization of those alternative nitrogen sources. Seemingly unrelated to its role in NCR, Ure2p has the ability to form self-propagating aggregates known as [URE3] prion. Formation of [URE3] does have an effect on NCR: by sequestering free Ure2p from the cytoplasm, [URE3] derepresses nitrogen catabolism regardless of nitrogen source.
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).