FKH1 / YIL131C Overview


Standard Name
FKH1 1
Systematic Name
YIL131C
SGD ID
SGD:S000001393
Feature Type
ORF , Verified
Description
Forkhead family transcription factor; rate-limiting replication origin activator; evolutionarily conserved lifespan regulator; binds multiple chromosomal elements with distinct specificities, cell cycle dynamics; regulates transcription elongation, chromatin silencing at mating loci, expression of G2/M phase genes; facilitates clustering, activation of early-firing replication origins; binds HML recombination enhancer, regulates donor preference during mating-type switching 1 2 3 4 5 6 7 8 9 10 11 12 13
Name Description
ForK head Homolog 1
Paralog
FKH2
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.


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.)
484
Mol. Weight (Da)
53493.7
Isoelectric Point
8.53
Median Abundance (molecules/cell)
1771 +/- 891
Half-life (hr)
4.1

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. Click "YeastMine" to view all alleles in YeastMine.


View all FKH1 alleles in SGD search | YeastMine

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
Sequence-specific DNA binding transcription factor involved in chromatin remodeling, mitotic transcription regulation, transcription termination, mating-type switching, and pseudohyphal growth; binds DNA replication origins and positively regulates replication initiation; also binds centromeres

View computational annotations

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 mutants have abnormal vacuolar morphology, reduced silencing at mating-type loci and abnormal mating-type switching; nulls are also sensitive to heat, and exhibit altered rates of cell cycle progression through the S and G2/M phases; overexpression slows 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 fkh1 null mutant is viable; the null mutant of paralog fkh2 is viable; the fkh1 fkh2 double mutant is inviable.

203 total interactions for 138 unique genes

Physical Interactions

  • Affinity Capture-MS: 35
  • Affinity Capture-RNA: 4
  • Affinity Capture-Western: 20
  • Co-localization: 1
  • Co-purification: 1
  • PCA: 2
  • Reconstituted Complex: 7
  • Two-hybrid: 9

Genetic Interactions

  • Dosage Growth Defect: 4
  • Dosage Rescue: 4
  • Negative Genetic: 51
  • Phenotypic Enhancement: 21
  • Phenotypic Suppression: 11
  • Positive Genetic: 25
  • Synthetic Growth Defect: 5
  • Synthetic Lethality: 1
  • Synthetic Rescue: 2
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
FKH1 encodes a transcription factor that is a member of the widely conserved eukaryotic forkhead family of proteins, which contain the characteristic forkhead (FH), or winged helix, DNA-binding domain. Many forkhead proteins also have a second domain referred to as the forkhead-associated (FHA) domain which binds phosphorylated threonine residues within proteins. Fkh1p has both FH and FHA domains, and is involved in regulation of expression of the CLB2 cluster of genes during the G2/M phase of the mitotic cell cycle. The CLB2 cluster of genes includes mitotic regulators such as CLB1, CLB2, CDC5 and CDC20, as well as SWI5 and ACE2, transcription factors required for the subsequent temporal wave of cell cycle regulated gene expression in the M/G1 phase interval. Fkh1p cooperates with Isw1p to remodel chromatin and repress transcription of CLB2 during G2/M. Fkh1p associates with coding regions of active genes to regulate transcription by affecting the phosphorylation status of the C-terminal repeat domain (CTD) of RNA Polymerase II. The Fkh1p binding site 5'-GTAAACAAA-3' is present in over 1400 locations throughout the genome. FKH1 has additional roles in the establishment of chromatin silencing at the silent mating-type cassette and in the regulation of donor preference during mating type switching. FKH1 and the Swi4p/Swi6p-containing SCB-binding factor (SBF) independently regulate donor preference through direct interactions with a cis-acting sequence called the recombination enhancer, with Fkh1p binding in the G2 phase and SBF binding in the G1 phase of the cell cycle.
Regulators
2
Targets
2991
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.


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: 2016-03-23

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
52
Additional
95
Reviews
32

Resources