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
FKH1/YIL131C is located on the left arm of chromosome IX between CSM2 and ASG1 zinc cluster protein; coding sequence is 1455 nucleotides long with 21 SNPs, 4 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
Fkh1p is 484 amino acids long, short-lived, low in abundance; contains 3 forkhead domains; acetylated and ubiquitinylated on K13, sumoylated on K9, phosphorylated on 5 residues
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.
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
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.
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 in reference strain S288C; 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 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
Fkh1p interacts physically with proteins involved in DNA replication; FKH1 interacts genetically with genes involved in mitotic cell cycle; the fkh1 null mutant is viable, the null mutant of paralog fkh2 is viable, the fkh1 fkh2 double mutant is inviable
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.
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.
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).