Transcription factor; activated by proteolytic processing in response to signals from the SPS sensor system for external amino acids; activates transcription of amino acid permease genes; STP2 has a paralog, STP1, that arose from the whole genome duplication
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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
STP2 has a paralog, STP1, 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.
Length (a.a.)
541
Mol. Weight (Da)
60784.8
Isoelectric Point
6.26
Median Abundance (molecules/cell)
610 +/- 490
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 RNA polymerase II transcription activator
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.
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
The stp2 null mutant is viable; the null mutant of paralog stp1 is viable; the stp2 stp1 double mutant displays growth defects and aberrations in gene expression; the stp1 stp2 gap1 triple mutant is inviable.
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
STP2 and its paralog STP1 encode transcription factors that are members of the C2H2 zinc finger class. Stp1p and Stp2p act independently of each other but have redundant roles in regulation of genes encoding amino acid and peptide permeases, including AGP1, BAP2, BAP3, DIP5, GNP1, MUP1, TAT1 and TAT2, and PTR2. In response to the presence of extracellular amino acids, they bind to UAS-aa elements in the promoters of their target genes and activate transcription. Stp1p and Stp2p are among several transcription factors involved in nitrogen source utilization (including Uga3p, Dal82p, Stp1p, and Stp2p) whose function depends on cooperation with the transcription factor Dal81p. In the case of Stp1p and Stp2p, Dal81p facilitates their promoter binding and contributes to transcription activation, but is not absolutely required for activity. The involvement of Dal81p in pathways for utilization of several different nitrogen sources allows the cell to integrate the disparate nutritional signals and to induce different pathways according to availability of each source. Activity of Stp1p and Stp2p is regulated by the SPS-sensing pathway, so-called because its first step is sensing by a plasma membrane complex composed of Ssy1p, Ptr3, and Ssy5p. In the absence of extracellular amino acids, Stp1p and Stp2p exist as precursor proteins that are largely cytoplasmic. The small amounts of precursor that do enter the nucleus are prevented from binding to target promoters by three nuclear inner membrane proteins, Asi1p, Asi2p, and Asi3p. Under inducing conditions, the proteolytic activity of Ssy5p is activated and it cleaves inhibitory N-terminal domains from Stp1p and Stp2p. The mature forms of Stp1p and Stp2p are able to enter the nucleus and activate transcription.
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.
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).