Transcription factor targeting filamentation genes and Ty1 expression; Ste12p activation of most filamentation gene promoters depends on Tec1p and Tec1p transcriptional activity is dependent on its association with Ste12p; binds to TCS elements upstream of filamentation genes, which are regulated by Tec1p/Ste12p/Dig1p complex; competes with Dig2p for binding to Ste12p/Dig1p; positive regulator of chronological life span; TEA/ATTS DNA-binding domain family member
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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
TEC1/YBR083W is located on the right arm of chromosome II between replication of origin ARS214 and MIS1 mitochondrial C1-tetrahydrofolate synthase; coding sequence is 1461 nucleotides long with 10 SNPs, 5 of which cause amino acid polymorphisms
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
Tec1p is 486 amino acids long, very low in abundance; contains a TEA/ATTS DNA-binding domain
Length (a.a.)
486
Mol. Weight (Da)
55158.0
Isoelectric Point
7.75
Median Abundance (molecules/cell)
1151 +/- 621
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
DNA-binding RNA polymerase II transcription factor involved in the regulation of pseudohyphal growth, and transposition; subunit of a complex with Ste12p and Dig1p that regulates transcription of mating genes
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.
Macromolecular complex annotations are imported from the Complex Portal. These annotations have been derived from physical molecular interaction evidence extracted from the literature and cross-referenced in the entry, or by curator inference from information on homologs in closely related species or by inference from scientific background.
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
TEC1/YBR083W is a non-essential gene in reference strain S288C; null mutants are viable and show decreased competitive fitness, decreased chronological lifespan, reduced utilization of glucose, ammonium, and allantoin, abnormal subcellular morphology, decreased transposable element transposition, and decreased resistance to rapamycin. In Sigma1278b, the null abolishes invasive growth, decreases filamentous growth and biofilm formation, delays budding, and causes abnormal colony appearance. Overexpression in S288C causes abnormal nuclear morphology, abnormal cell cycle progression, and reduced competitive fitness; in Sigma1278b it increases invasive and filamentous growth.
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
Tec1p interacts physically with proteins involved in transcription and invasive growth; TEC1 interacts genetically with genes involved in stimulus response and 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
TEC1 encodes a helix-turn-helix transcription factor of the homeodomain family involved in the regulation of genes involved in the invasive/pseudohyphal growth cascade. Tec1p belongs to the TEA domain (TEAD) family of regulators that control cellular development in many eukaryotes, and recognizes a motif called the TEA/ATTS consensus sequence (TCS), 5'-RCATTCCY-3'. Tec1p and Ste12p can physically interact and are a model for studying the mechanisms of combinatorial and promoter-specific target gene control. The association of a pheromone-responsive element (PRE), containing the consensus sequence 5'-TGAAACA-3' which is recognized by Ste12p, and a TCS has been designated a filamentous responsive element (FRE) and allows binding of a Tec1p-Ste12p heterodimer to activate gene expression. However, Tec1p-Ste12p heterodimers can also regulate target genes via single TCS elements, with Tec1p providing the DNA binding and Ste12p the transcriptional activation. Tec1p can also activate target genes independently of Ste12p. Tec1p is required for FLO11 expression and for vegetative adhesion. The FLO11 promoter contains both FREs and TCS elements and is bound by Tec1p and Ste12p, though Tec1p is also able to activate FLO11 expression by without Ste12p. During vegetative growth, Dig1p and Dig2p directly inhibit the transcriptional activity of the Tec1p-Ste12p heterodimer. In response to pheromone, the inhibitory functions of Dig1p and Dig2p are relieved by phosphorylation through the mating-specific MAPKs Fus3p and Kss1p. Fus3p also phosphorylates Tec1p, which induces its degradation by the proteasome and abrogating FLO11 expression, thereby maintaining signaling specificity during the pheromone response.
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).