Coactivator, regulates transcription of ribosomal protein (RP) genes; recruited to RP gene promoters during optimal growth conditions via Fhl1p; subunit of CURI, a complex that coordinates RP production and pre-rRNA processing; regulated by acetylation and phosphorylation at different growth states via TORC1 signaling; IFH1 has a paralog, CRF1, that arose from the whole genome duplication
123456
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
IFH1/YLR223C is located near the middle of chromosome XII between UTP13 nucleolar protein and UCC1 F-box protein; coding sequence is 3258 nucleotides long with 24 SNPs and variable 5' end; IFH1 has a paralog, CRF1, that arose from the whole genome duplication
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
Ifh1p is 1085 amino acids long, very low in abundance, extremely short-lived; contains disordered regions throughout; acetylated on 4 lysines, ubiquitinylated on 5 lysines, phosphorylated on 41 residues
Length (a.a.)
1085
Mol. Weight (Da)
122378.2
Isoelectric Point
4.27
Median Abundance (molecules/cell)
1958 +/- 528
Half-life (min)
38.8
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
Transcription regulator involved in the positive regulation of ribosomal protein gene transcription and also telomeric silencing; subunit of CURI complex
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.
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 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
IFH1/YLR223C is an essential gene in reference strain S288C; overexpression slows growth, interferes with silencing, and increases production of ribosomal protein mRNAs; reduced function alleles increase lifespan, hamper growth and rRNA processing, reduce resistance to DNA damaging agents and TOR inhibitor rapamycin; heterozygous diploids are haploinsufficient
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
Ifh1p interacts physically with proteins involved in transcription; IFH1 interacts genetically with genes involved in transcription; the ifh1 null mutant is inviable, the null mutant of paralog crf1 is viable, the ifh1 crf1 double mutant is viable.
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
IFH1/YLR223C encodes a transcription coactivator that regulates genes involved in growth and metabolism. The complex of Ifh1p with the forkhead domain transcription factor Fhl1p activates transcription of nearly every ribosomal protein-encoding gene, as well as genes encoding a transcription factor (GCN4), translation factors, and metabolic enzymes (ADH2, ALD4, GDH1, MET6). Fhl1p is bound to target promoters at a relatively constant level, and recruitment of Ifh1p in response to growth conditions activates transcription. Modification of Ifh1p by various nutritional pathways serves to integrate nutritional signals. Stability of Ifh1p is regulated by acetylation in response to cellular levels of acetyl-CoA, mediated by the Gcn5p-containing SAGA complex. Ifh1p is deacetylated by the sirtuin family deacetylases Hst1p and Sir2p. Ifh1p is also phosphorylated by protein kinase A (PKA), and an ifh1 mutation that blocks phosphorylation confers an extended replicative lifespan. Both acetylation and phosphorylation levels of Ifh1p are regulated by the TORC1 complex. Ifh1p binding to Fhl1p is mutually exclusive with binding of the Ifh1p paralog Crf1p, which acts as a transcriptional corepressor for Fhl1p. In addition to binding Fhl1p, Ifh1p also forms a complex, termed CURI, that includes casein kinase Ckb2p and the rRNA processing factors Utp22p and Rrp7p. The CURI complex may help to couple regulation of ribosomal protein gene expression with regulation of rRNA production.
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).