Transcriptional repressor; recruits the Cyc8p-Tup1p complex to promoters; mediates glucose repression and negatively regulates a variety of processes including filamentous growth and alkaline pH response; activated in stochastic pulses of nuclear localization in response to low glucose
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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
NRG1/YDR043C is located on the right arm of chromosome IV; coding sequence is 696 nucleotides long with 2 nonsynonymous SNPs
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.)
231
Mol. Weight (Da)
26750.3
Isoelectric Point
8.97
Median Abundance (molecules/cell)
1323 +/- 767
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 that regulates transcription by RNA polymerase II; involved in regulation of pseudohyphal growth, biofilm formation, hyperosmotic response, and glucose sensing
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, are auxotrophic for myo-inositol, sensitive to acids and cations, and are resistant to antifungal miconazole; overexpression slows growth, decreases resistance to TOR inhibitor rapamycin
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 nrg1 null mutant is viable; the null mutant of paralog nrg2 is viable; the nrg1nrg2 double mutant displays a phenotypic enhancement.
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
NRG1 encodes a transcriptional repressor that is a member of the C2H2 zinc finger class. Nrg1p, along with its paralog Nrg2p, responds to glucose signals received via Snf1p kinase, and to stress signals received via the Rim101p transcriptional repressor. Nrg1p and Nrg2p regulate a variety of processes, including response to glucose levels; response to alkaline pH and to salt, osmotic, and oxidative stress; filamentous growth; and biofilm formation. Some major targets of Nrg1p and Nrg2p include FLO11, encoding a cell surface adhesin, ENA1, encoding a plasma membrane salt efflux pump, and SUC2, encoding extracellular invertase. The set of genes regulated by Nrg1p overlaps with, but is not identical to, the set regulated by Nrg2p. Some targets repressed by Nrg1p but apparently not by Nrg2p include RSB1, encoding a lipid translocase that regulates plasma membrane lipid composition, and DIT1, encoding an enzyme required for spore wall maturation. Nrg1p represses transcription by recruiting the Cyc8p-Tup1p complex to promoters. NRG1 expression and Nrg1p activity are regulated on multiple levels. NRG1 transcription is glucose-repressed and is up-regulated at acidic pH, in contrast to NRG2 transcription which does not respond to glucose levels and is up-regulated at alkaline pH. Stability of the NRG1 mRNA is negatively regulated via mRNA decay, and activity of Nrg1p is regulated via phosphorylation by protein kinase CK2 in response to salt, osmotic, and other stresses.
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.
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).