BIR1 / YJR089W Overview
- Standard Name
- BIR1 1
- Systematic Name
- YJR089W
- SGD ID
- SGD:S000003849
- Feature Type
- ORF , Verified
- Description
- Subunit of chromosomal passenger complex (CPC); CPC is comprised of Ipl1p-Sli15p-Bir1p-Nbl1p and regulates chromosome segregation; required for chromosome bi-orientation and for spindle assembly checkpoint activation upon reduced sister kinetochore tension; relative distribution to shortened microtubules increases upon DNA replication stress; sumoylated in an Mms21p-dependent manner; human survivin homolog 2 3 4 5 6 7
- Name Description
- Baculoviral IAP Repeat-containing protein 1 3
- 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.
- Summary
- Relative distribution to shortened microtubules increases upon DNA replication stress; sumoylated in an Mms21p-dependent manner
- Length (a.a.)
- 954
- Mol. Weight (Da)
- 108657.6
- Isoelectric Point
- 6.41
- Median Abundance (molecules/cell)
- 1518 +/- 890
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 BIR1 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 involved in mitotic spindle assembly checkpoint signaling and septin cytoskeleton organization; localizes to cytoplasm, nucleus and mitochondria
View computational annotations
Molecular Function
- Manually Curated
- enables zinc ion binding (RCA)
Biological Process
- Manually Curated
- involved in apoptotic process (IMP)
- involved in chromosome segregation (IMP)
- involved in mitotic spindle assembly checkpoint signaling (IMP)
- involved in mitotic spindle elongation (IMP)
- involved in sister chromatid biorientation (IMP)
Cellular Component
- Manually Curated
- part of chromosome passenger complex (IDA)
- located in cytoplasm (IDA)
- located in kinetochore (IGI)
- located in microtubule (HDA)
- located in mitochondrion (HDA)
- located in nucleus (IDA)
- located in spindle (IDA)
- located in spindle midzone (IDA)
Complex
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
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
- Essential gene in some strain backgrounds and non-essential in others; deletion and overexpression result in elevated rates of chromosome loss and missegregation; conditional mutant has a chromosome biorientation defect; heterozygous null mutant has a growth defect, displays elevated polyploidy and grossly altered morphology; CDK phosphorylation site mutant has short anaphase spindles and is unable to properly localize Cbf2p/Ndc10p to the anaphase spindle and midzone; conditional mutant mislocalizes both Bub1p and Ipl1p, and has decreased levels of Pds1p; conditional mutant displays increased oxidative stress-induced apoptosis, while overexpression reduces apoptosis; overexpression results in a growth advantage; diploid null mutant has delayed and inefficient sporulation while the haploid null mutant has a severe spore germination defect; homozygous diploid null mutant forms pseudohyphal structures in sporulation media
Classical Genetics
- overexpression
- null
- apoptosis: increased
- cellular morphology: abnormal
- colony sectoring: increased
- growth in exponential phase: decreased rate
- inviable
- oxidative stress resistance: decreased
- polyploidy: increased
- pseudohyphal growth: abnormal
- spore germination: decreased
- sporulation efficiency: decreased
- sporulation: delayed
- viable
- conditional
- unspecified
- reduction of function
- overexpression
Large-scale Survey
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.
1058 total interactions for 989 unique genes
Physical Interactions
- Affinity Capture-MS: 26
- Affinity Capture-RNA: 5
- Affinity Capture-Western: 10
- Biochemical Activity: 6
- Co-fractionation: 2
- Co-localization: 2
- Reconstituted Complex: 2
- Two-hybrid: 17
Genetic Interactions
- Dosage Growth Defect: 1
- Dosage Rescue: 6
- Negative Genetic: 518
- Phenotypic Suppression: 2
- Positive Genetic: 428
- Synthetic Growth Defect: 7
- Synthetic Lethality: 11
- Synthetic Rescue: 15
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.
- Regulators
- 9
- Targets
- 0
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: 2011-04-19
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.