CRF1 / YDR223W Overview


Standard Name
CRF1 1
Systematic Name
YDR223W
SGD ID
SGD:S000002631
Feature Type
ORF , Verified
Description
Transcriptional corepressor; involved in repression of ribosomal protein (RP) gene transcription via the TOR signaling pathway which promotes accumulation of Crf1p in the nucleus; role in repression of RP genes varies by strain; CRF1 has a paralog, IFH1, that arose from the whole genome duplication 1 2 3
Name Description
Co-Repressor with FHL1 1
Paralog
IFH1 3
Comparative Info
Sequence Details

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.


Summary
CRF1 has a paralog, IFH1, that arose from the whole genome duplication
Protein Details

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.)
467
Mol. Weight (Da)
51668.8
Isoelectric Point
4.58

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 CRF1 alleles in SGD search

Gene Ontology Details

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
Transcription corepressor that negative regulates transcription of ribosomal protein genes; localizes to both cytoplasm and nucleus

View computational annotations

Molecular Function

Manually Curated

Cellular Component

Manually Curated
Phenotype Details

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 exhibits decreased sensitivity to rapamycin and reduced repression of ribosomal protein genes in response to rapamycin treatment; overexpression causes slow growth
Interaction Details

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.


Summary
The crf1 null mutant is viable; the null mutant of paralog ifh1 is inviable; the crf1 ifh1 double mutant has not been annotated for phenotype.

42 total interactions for 30 unique genes

Physical Interactions

  • Affinity Capture-RNA: 2
  • Affinity Capture-Western: 1
  • Biochemical Activity: 3
  • PCA: 1
  • Reconstituted Complex: 1
  • Two-hybrid: 1

Genetic Interactions

  • Dosage Lethality: 1
  • Dosage Rescue: 2
  • Negative Genetic: 20
  • Phenotypic Suppression: 1
  • Positive Genetic: 2
  • Synthetic Growth Defect: 4
  • Synthetic Lethality: 2
  • Synthetic Rescue: 1
Regulation Details

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.


Summary
CRF1 encodes a transcription corepressor that regulates genes involved in growth and metabolism. The complex of Crf1p with the forkhead domain transcription factor Fhl1p represses transcription of ribosomal protein-encoding genes under conditions of nutrient deficiency. Crf1p binding to Fhl1p is mutually exclusive with binding of the Crf1p paralog Ifh1p, which acts as a transcriptional coactivator for Fhl1p. Crl1p activity is regulated via its localization to the nucleus or cytoplasm. When nutrients are abundant, TORC1 inhibits the Yak1p kinase via regulation of protein kinase A (PKA). Inhibition of Yak1p activity causes Crf1p to become dephosphorylated and exit the nucleus, relieving repression of the ribosomal protein genes and allowing Ifh1p to bind Fhl1p and activate transcription. When nutrients are scarce, or when TORC1 is inhibited with rapamycin, TORC1 does not inhibit Yak1p and Crf1p becomes phosphorylated. The phosphorylated form is able to accumulate in the nucleus, where it binds to Fhl1p and represses ribosomal protein gene transcription. Interestingly, this mechanism appears not to occur in the common lab strain background W303: the crf1 null mutation in W303 has no phenotype, and Crf1p cannot be detected at promoters. Since rapamycin treatment does repress ribosomal protein gene transcription in W303, this suggests that TORC1 regulation can occur through additional mechanisms.
Regulators
5
Targets
0
Expression Details

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.


Literature Details

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.


Primary
10
Additional
10
Reviews
17

Resources