Mus musculus Gene: Casp1 | |||||||||||||||||||||||||||||||||||||||||||
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Summary | |||||||||||||||||||||||||||||||||||||||||||
InnateDB Gene | IDBG-131590.6 | ||||||||||||||||||||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||||||||||||||||||||
Gene Symbol | Casp1 | ||||||||||||||||||||||||||||||||||||||||||
Gene Name | caspase 1 | ||||||||||||||||||||||||||||||||||||||||||
Synonyms | ICE; Il1bc | ||||||||||||||||||||||||||||||||||||||||||
Species | Mus musculus | ||||||||||||||||||||||||||||||||||||||||||
Ensembl Gene | ENSMUSG00000025888 | ||||||||||||||||||||||||||||||||||||||||||
Encoded Proteins |
caspase 1
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||||||||||||||||||||||||||
InnateDB Annotation | |||||||||||||||||||||||||||||||||||||||||||
Summary |
Casp1 is involved in key innate and healing responses to influenza A virus where Casp1(-/-) mice exhibited increased morbidity after infection with a pathogenic influenza A virus correlating with decreased neutrophil and monocyte recruitment and reduced Il1b (IL-1-beta), Il18 (IL-18), Tnf (TNF-alpha), Il6 (IL-6), Cxcl1 (KC), and Cxcl2 (MIP-2) production.
Casp1 is part of the inflammasome complex, along with pathogen-specific nucleotide oligomerization and binding domain (NOD)-like receptors (NLRs) and in some cases the scaffolding protein ASC. Formation of the membrane-associated inflammasome complex in murine macrophages, results in cleavage of cytosolic Casp1 substrates and cell death.
Casp1 is a component of the inflammasome and is required for inflammation in acute pancreatitis.
Casp1-dependent inflammatory cell death, or pyroptosis, is only induced by viable, but not heat-killed, E. coli.
Naturally occurring variants of Casp1 differ considerably in structure and the ability to activate Il1b.
(Demonstrated in human)
Activation of the Nlrp3 inflammasome is detrimental during leishmaniasis. Mice lacking the inflammasome components Nlrp3, Pycard, Casp1 exhibit defective Il1b and Il18 production at the infection site and are resistant to cutaneous Leishmania major infection.
Type 1 regulatory (Tr1) cells suppress Il1b transcription and Casp1 activation via an IL10R â??dependent mechanism
Uropathogenic Escherichia coli protein TcpC attenuates activation of the Nlrp3 inflammasome by binding both Nlrp3 and Casp1.
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InnateDB Annotation from Orthologs | |||||||||||||||||||||||||||||||||||||||||||
Summary |
[Homo sapiens] CASP1 activates NF-kappaB independent of its enzymatic activity and contributes to inflammation by proteolysis of pro-IL1B (IL-1 beta) and RIPK2 activation of NF-kappaB and MAPK1.
[Homo sapiens] CASP1 is part of the inflammasome complex, along with pathogen-specific nucleotide oligomerization and binding domain (NOD)-like receptors (NLRs) and in some cases the scaffolding protein ASC. Formation of the membrane-associated inflammasome complex in murine macrophages, results in cleavage of cytosolic CASP1 substrates and cell death.
[Homo sapiens] CASP1 activity is required for discrimination between translocon-positive and -negative bacteria in bone-marrow derived cells and interleukin-1 receptor signalling. Activation of CASP1 by bacteria expressing Type 3 secretion systems allows for rapid recognition of bacteria expressing conserved functions associated with virulence.
[Homo sapiens] CASP1 clears intracellular bacteria in vivo independently of IL1B (IL-1-beta) and IL18 and establishes pyroptosis as an efficient mechanism of bacterial clearance by the innate immune system. CASP1-induced pyroptotic cell death releases bacteria from macrophages and exposes the bacteria to uptake and killing by reactive oxygen species in neutrophils.
[Homo sapiens] CASP1 is a component of the inflammasome and is required for inflammation in acute pancreatitis. (Demonstrated in murine model)
[Homo sapiens] CASP1-dependent inflammatory cell death, or pyroptosis, is only induced by viable, but not heat-killed, E. coli. (Demonstrated in murine model)
[Homo sapiens] Naturally occurring variants of CASP1 differ considerably in structure and the ability to activate IL1B.
[Homo sapiens] The precursor and mature forms of IL37 are secreted from activated cells upon inflammasome activation and CASP1 processing of IL37 is important for its anti-inflammatory activity.
[Homo sapiens] 20-kDa IL1B generated from CASP1 cleaved pro-IL1B limits the available pro-IL1B for generation of CASP1 cleaved 17-kDa IL1B, thus reducing inflammation.
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Entrez Gene | |||||||||||||||||||||||||||||||||||||||||||
Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000137752:
This gene encodes a protein which is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce 2 subunits, large and small, that dimerize to form the active enzyme. This gene was identified by its ability to proteolytically cleave and activate the inactive precursor of interleukin-1, a cytokine involved in the processes such as inflammation, septic shock, and wound healing. This gene has been shown to induce cell apoptosis and may function in various developmental stages. Studies of a similar gene in mouse suggest a role in the pathogenesis of Huntington disease. Alternative splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Mar 2012] |
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Gene Information | |||||||||||||||||||||||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||||||||||||||||||||||
Genomic Location | Chromosome 9:5298517-5307265 | ||||||||||||||||||||||||||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||||||||||||||||||||||||||
Band | A1 | ||||||||||||||||||||||||||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 20 experimentally validated interaction(s) in this database.
They are also associated with 34 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||||||||||||||||||||||
Species
Homo sapiens
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Gene ID
Gene Order
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Pathways | |||||||||||||||||||||||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||||||||||||||||||||||
REACTOME |
Innate Immune System pathway
Cytokine Signaling in Immune system pathway
Immune System pathway
The NLRP3 inflammasome pathway
Inflammasomes pathway
The AIM2 inflammasome pathway
Signaling by Interleukins pathway
Interleukin-1 processing pathway
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways pathway
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KEGG |
Amyotrophic lateral sclerosis (ALS) pathway
NOD-like receptor signaling pathway pathway
Cytosolic DNA-sensing pathway pathway
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INOH | |||||||||||||||||||||||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||||||||||||||||||||||
Pathway Predictions based on Human Orthology Data | |||||||||||||||||||||||||||||||||||||||||||
NETPATH |
AndrogenReceptor pathway
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REACTOME |
NOD1/2 Signaling Pathway pathway
The AIM2 inflammasome pathway
The IPAF inflammasome pathway
The NLRP3 inflammasome pathway
Inflammasomes pathway
Interleukin-1 processing pathway
Cytokine Signaling in Immune system pathway
Innate Immune System pathway
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways pathway
Immune System pathway
Signaling by Interleukins pathway
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KEGG |
Amyotrophic lateral sclerosis (ALS) pathway
NOD-like receptor signaling pathway pathway
Cytosolic DNA-sensing pathway pathway
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INOH | |||||||||||||||||||||||||||||||||||||||||||
PID NCI |
Cellular roles of Anthrax toxin
Direct p53 effectors
IFN-gamma pathway
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Cross-References | |||||||||||||||||||||||||||||||||||||||||||
SwissProt | P29452 | ||||||||||||||||||||||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||||||||||||||||||||
Entrez Gene | 12362 | ||||||||||||||||||||||||||||||||||||||||||
UniGene | |||||||||||||||||||||||||||||||||||||||||||
RefSeq | NM_009807 | ||||||||||||||||||||||||||||||||||||||||||
OMIM | |||||||||||||||||||||||||||||||||||||||||||
CCDS | CCDS22798 | ||||||||||||||||||||||||||||||||||||||||||
HPRD | |||||||||||||||||||||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||||||||||||||||||||
MGI ID | MGI:96544 | ||||||||||||||||||||||||||||||||||||||||||
MGI Symbol | Casp1 | ||||||||||||||||||||||||||||||||||||||||||
EMBL | BC008152 L03799 L28095 U04269 | ||||||||||||||||||||||||||||||||||||||||||
GenPept | AAA20209 AAA39306 AAA56992 AAH08152 | ||||||||||||||||||||||||||||||||||||||||||
RNA Seq Atlas | 12362 | ||||||||||||||||||||||||||||||||||||||||||