TEL1 / YBL088C Overview
- Standard Name
- TEL1 1
- Systematic Name
- YBL088C
- SGD ID
- SGD:S000000184
- Feature Type
- ORF , Verified
- Description
- Protein kinase primarily involved in telomere length regulation; contributes to cell cycle checkpoint control in response to DNA damage; binds to phosphatidylinositol-4-phosphate; acts with Red1p and Mec1p to promote interhomolog recombination by phosphorylation of Hop1; functionally redundant with Mec1p; regulates P-body formation induced by replication stress; homolog of human ataxia-telangiectasia mutated (ATM) gene 2 3 4 5 6 7 8
- Name Description
- TELomere maintenance 1
- Comparative Info
-
Sequence
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.
Analyze Sequence
S288C only
BLASTN | BLASTP | Design Primers | Restriction Fragment Map | Restriction Fragment Sizes | Six-Frame Translation
S288C vs. other species
BLASTN vs. fungi | BLASTP at NCBI | BLASTP vs. fungi
S288C vs. other strains
Protein
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.)
- 2787
- Mol. Weight (Da)
- 321515.1
- Isoelectric Point
- 6.92
- Median Abundance (molecules/cell)
- 1137 +/- 1097
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.
View all TEL1 alleles in SGD search
Gene Ontology
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
- Protein serine/threonine kinase that binds telomeric DNA; involved in telomere maintenance and DNA repair
View computational annotations
Molecular Function
- Manually Curated
- enables phosphatidylinositol-4-phosphate binding (IDA)
- enables protein kinase activity (IDA)
- enables protein serine/threonine kinase activity (IMP)
- enables telomeric DNA binding (IDA)
Biological Process
- Manually Curated
- involved in DNA damage response (IMP)
- involved in DNA repair (IGI)
- involved in double-strand break repair (IMP, IGI)
- involved in signal transduction in response to DNA damage (IMP)
- involved in telomere maintenance (IGI, IMP)
Cellular Component
- Manually Curated
- located in mitochondrion (HDA)
- located in nucleus (IDA)
Phenotype
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; null mutant displays decreased telomere length, while conditional mutant contains excess C1-3A repeats without telomere lengthening at the non-permissive temperature; null mutant has defective telomeric localization to the nuclear periphery in G1 phase, and improperly localized Rap1p; null mutant has a decreased rate of gross chromosomal rearrangements; null mutant displays decreased mitochondrial stress-induced chronological lifespan extension; null mutant has reduced phosphorylation of Cdc13p at G2/M phase; overexpression results in a G2/M phase delay, decreased resistance to DNA damaging agents and UV radiation, and decreased colony size
Classical Genetics
- overexpression
- null
- acid pH resistance: decreased
- chromosome/plasmid maintenance: abnormal
- chromosome/plasmid maintenance: decreased
- chromosome/plasmid maintenance: decreased rate
- chronological lifespan: decreased
- mitotic recombination: increased rate
- mutation frequency: decreased
- oxidative stress resistance: decreased
- protein/peptide distribution: abnormal
- protein/peptide modification: absent
- protein/peptide modification: decreased
- resistance to chemicals: decreased
- resistance to chemicals: increased
- telomere length: decreased
- transposable element transposition: increased
- conditional
- reduction of function
Disease
Disease Annotations consist of three mandatory components: a gene product, a term from the Disease Ontology (DO) controlled vocabulary and an evidence code. SGD provides manually curated DO Annotations derived from the literature. Click "Disease Details" to view all Disease information and evidence for this locus as well as diseases it shares with other genes.
Interaction
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.
465 total interactions for 196 unique genes
Physical Interactions
- Affinity Capture-MS: 5
- Affinity Capture-RNA: 2
- Affinity Capture-Western: 14
- Biochemical Activity: 9
- Co-crystal Structure: 2
- Protein-peptide: 1
- Reconstituted Complex: 6
- Two-hybrid: 4
Genetic Interactions
- Dosage Growth Defect: 10
- Dosage Lethality: 3
- Dosage Rescue: 7
- Negative Genetic: 79
- Phenotypic Enhancement: 111
- Phenotypic Suppression: 57
- Positive Genetic: 12
- Synthetic Growth Defect: 107
- Synthetic Lethality: 7
- Synthetic Rescue: 29
Regulation
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.
Expression
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.
Last Updated: 1999-04-30
Literature
All manually curated literature for the specified gene, organized into topics according to their relevance to the gene (Primary Literature, Additional Literature, or Review). Click "Literature Details" to view all literature information for this locus, including shared literature between genes.