Mitochondrial DNA-binding and packaging factor; mtDNA maintenance factor involved in mitochondrial DNA replication and recombination, regulating mtDNA copy number in opposition to DPI34; HMG1 DNA-binding protein family member containing two HMG-boxes; activity may be regulated by protein kinase A phosphorylation; ABF2 has a paralog, IXR1, that arose from the whole genome duplication; human homolog TFAM can complement yeast abf2 mutant, rescuing the loss-of-mitochondrial DNA phenotype
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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
ABF2 has a paralog, IXR1, 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
Abf1p is 183 amino acids long, of average half-life, low-to-moderate in abundance; contains 2 high mobility group box domains
Length (a.a.)
183
Mol. Weight (Da)
21575.0
Isoelectric Point
10.24
Median Abundance (molecules/cell)
14668 +/- 6733
Half-life (hr)
9.6
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
DNA binding and DNA bending protein involved in mitochondrion inheritance and mitochondrial chromosome packaging; localizes to mitochondrial nucleoid
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
ABF2/YMR072W is a non-essential gene in reference strain S288C; null mutant is incapable of respiratory growth, sensitive to hyperosmotic stress, and shows defects in mitochondrial genome maintenance; overexpression causes abnormal budding and cell cycle progression through G2 phase
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 abf2 null mutant is viable; the null mutant of paralog ixr1 is viable; the abf2 ixr1 double mutant has not been annotated for phenotype.
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
ABF2 encodes a mitochondrial DNA (mtDNA)-binding histone-like protein that is a member of HMG1 DNA-binding protein family and has two HMG1-Box domains, HMG1-Box A and B. Abf2p functions in mitochondrial genome maintenance and packaging by introducing sharp bends and superhelical turns into the mtDNA, and associates with mitochondrial nucleoids under conditions of low respiration. Glucose repression activates the phosphorylation of the N-terminal segment of HMG1-Box A by cAMP-dependent protein kinase (PKA), which inhibits the binding of Abf2p to DNA. Mutant cells carrying the abf2-T47A/S48A unphosphorylatable allele have a severe defect in the regulation of mtDNA content during glucose repression. This suggests that the phosphorylation of Abf2p via PKA may regulate its functions for the control of mtDNA content during the shift from gluconeogenic to fermentative growth. ABF2 is up-regulated in cells overexpressing the HCM1 winged helix-turn-helix/forkhead transcription factor, which regulates the late S-phase specific expression of genes involved in chromosome segregation, spindle dynamics, and budding. Moderate increases in ABF2 expression lead to comparable increases in mtDNA copy number, and deletion of ABF2 results in ~50% reduction in mtDNA copy number. ABF2 has paralog IXR1, and ABF2 expression is decreased in ixr1 null mutants. Caloric restriction represses the synthesis of Abf2p. ABF2 is the ortholog of mammalian mitochondrial Transcription Factor A (TFAM).
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).