MRVI1
Murine retrovirus integration site 1 homolog | |||||||||||||
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Identifiers | |||||||||||||
Symbols | MRVI1 ; IRAG; JAW1L | ||||||||||||
External IDs | OMIM: 604673 MGI: 1338023 HomoloGene: 4425 GeneCards: MRVI1 Gene | ||||||||||||
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RNA expression pattern | |||||||||||||
More reference expression data | |||||||||||||
Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 10335 | 17540 | |||||||||||
Ensembl | ENSG00000072952 | ENSMUSG00000005611 | |||||||||||
UniProt | Q9Y6F6 | Q9WUX5 | |||||||||||
RefSeq (mRNA) | NM_001098579 | NM_010826 | |||||||||||
RefSeq (protein) | NP_001092049 | NP_034956 | |||||||||||
Location (UCSC) | Chr 11: 10.59 – 10.72 Mb | Chr 7: 110.87 – 110.98 Mb | |||||||||||
PubMed search | |||||||||||||
Protein MRVI1 is a protein that in humans is encoded by the MRVI1 gene.[1][2]
Function
This gene is similar to a mouse putative tumor suppressor gene that is frequently disrupted by mouse AIDS-related virus (MRV). The encoded protein, which is found in the membrane of the endoplasmic reticulum, is similar to Jaw1, a lymphoid-restricted protein whose expression is downregulated during myeloid differentiation. Therefore, this gene may be a myeloid leukemia tumor suppressor gene. Several alternatively spliced transcripts have been found for this gene, however, the full-length nature of some variants has not been determined. Of the two characterized variants which encode different isoforms, one initiates translation at a non-AUG start site.[2]
Interactions
MRVI1 has been shown to interact with ITPR1[3] and PRKG1.[3][4]
References
- ↑ Shaughnessy JD, Largaespada DA, Tian E, Fletcher CF, Cho BC, Vyas P et al. (June 1999). "Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1". Oncogene 18 (12): 2069–84. doi:10.1038/sj.onc.1202419. PMID 10321731.
- ↑ 2.0 2.1 "Entrez Gene: MRVI1 murine retrovirus integration site 1 homolog".
- ↑ 3.0 3.1 Schlossmann J, Ammendola A, Ashman K, Zong X, Huber A, Neubauer G et al. (March 2000). "Regulation of intracellular calcium by a signalling complex of IRAG, IP3 receptor and cGMP kinase Ibeta". Nature 404 (6774): 197–201. doi:10.1038/35004606. PMID 10724174.
- ↑ Ammendola A, Geiselhöringer A, Hofmann F, Schlossmann J (June 2001). "Molecular determinants of the interaction between the inositol 1,4,5-trisphosphate receptor-associated cGMP kinase substrate (IRAG) and cGMP kinase Ibeta". J. Biol. Chem. 276 (26): 24153–9. doi:10.1074/jbc.M101530200. PMID 11309393. Vancouver style error (help)
Further reading
- Adams MD, Dubnick M, Kerlavage AR, Moreno R, Kelley JM, Utterback TR et al. (1992). "Sequence identification of 2,375 human brain genes". Nature 355 (6361): 632–4. doi:10.1038/355632a0. PMID 1538749.
- Baltensperger K, Chiesi M, Carafoli E (1990). "Substrates of cGMP kinase in vascular smooth muscle and their role in the relaxation process". Biochemistry 29 (41): 9753–60. doi:10.1021/bi00493a035. PMID 2271613.
- Schlossmann J, Ammendola A, Ashman K, Zong X, Huber A, Neubauer G et al. (2000). "Regulation of intracellular calcium by a signalling complex of IRAG, IP3 receptor and cGMP kinase Ibeta". Nature 404 (6774): 197–201. doi:10.1038/35004606. PMID 10724174.
- Ammendola A, Geiselhöringer A, Hofmann F, Schlossmann J (2001). "Molecular determinants of the interaction between the inositol 1,4,5-trisphosphate receptor-associated cGMP kinase substrate (IRAG) and cGMP kinase Ibeta". J. Biol. Chem. 276 (26): 24153–9. doi:10.1074/jbc.M101530200. PMID 11309393. Vancouver style error (help)
- Koller A, Schlossmann J, Ashman K, Uttenweiler-Joseph S, Ruth P, Hofmann F (2003). "Association of phospholamban with a cGMP kinase signaling complex". Biochem. Biophys. Res. Commun. 300 (1): 155–60. doi:10.1016/S0006-291X(02)02799-7. PMID 12480535.
- Fritsch RM, Saur D, Kurjak M, Oesterle D, Schlossmann J, Geiselhöringer A et al. (2004). "InsP3R-associated cGMP kinase substrate (IRAG) is essential for nitric oxide-induced inhibition of calcium signaling in human colonic smooth muscle". J. Biol. Chem. 279 (13): 12551–9. doi:10.1074/jbc.M313365200. PMID 14729908. Vancouver style error (help)
- Casteel DE, Boss GR, Pilz RB (2005). "Identification of the interface between cGMP-dependent protein kinase Ibeta and its interaction partners TFII-I and IRAG reveals a common interaction motif". J. Biol. Chem. 280 (46): 38211–8. doi:10.1074/jbc.M507021200. PMID 16166082.
- Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
- Antl M, von Brühl ML, Eiglsperger C, Werner M, Konrad I, Kocher T et al. (2007). "IRAG mediates NO/cGMP-dependent inhibition of platelet aggregation and thrombus formation". Blood 109 (2): 552–9. doi:10.1182/blood-2005-10-026294. PMID 16990611. Vancouver style error (help)
External links
- MRVI1 human gene location in the UCSC Genome Browser.
- MRVI1 human gene details in the UCSC Genome Browser.