ORAI1

ORAI1
Identifiers
AliasesORAI1, CRACM1, IMD9, ORAT1, TAM2, TMEM142A, ORAI calcium release-activated calcium modulator 1
External IDsOMIM: 610277; MGI: 1925542; GeneCards: ORAI1
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez

84876

109305

Ensembl

ENSG00000276045

ENSMUSG00000049686

UniProt

Q96D31

Q8BWG9

RefSeq (mRNA)

NM_032790

NM_175423

RefSeq (protein)

NP_116179

NP_780632

Location (UCSC)Chr 12: 121.63 – 121.64 MbChr 5: 123.15 – 123.17 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Calcium release-activated calcium channel protein 1 is a calcium selective ion channel that in humans is encoded by the ORAI1 gene.[5][6][7] Orai channels play an important role in the activation of T-lymphocytes. The loss of function mutation of Orai1 causes severe combined immunodeficiency (SCID) in humans[5] The mammalian orai family has two additional homologs, Orai2 and Orai3. Orai proteins share no homology with any other ion channel family of any other known proteins. They have 4 transmembrane domains and form hexamers.

Structure and function

ORAI channels are activated upon the depletion of internal calcium stores, which is called the "store-operated" or the "capacitative" mechanism.[8] They are molecular constituents of the "calcium release activated calcium currents" (ICRAC). Upon activation of phospholipase C by various cell surface receptors, inositol trisphosphate is formed that releases calcium from the endoplasmic reticulum. The decreased calcium concentration in the endoplasmic reticulum is sensed by the STIM1 protein. STIM1 clusters upon the depletion of the calcium stores and forms "puncta", and relocates near the plasma membrane, where it activates ORAI1 via protein-protein interaction.[9][10][11][12]

In 2012, a 3.35-angstrom (Å) crystal structure of the Drosophila Orai channel, which shares 73% sequence identity with human Orai1 within its transmembrane region, was published.[13] The structure, thought to show the closed state of the channel, revealed that a single channel is composed of six Orai subunits, with the transmembrane domains arranged in concentric rings around a central aqueous pore formed exclusively by the first transmembrane helix of each subunit. Transmembrane helices 2 and 3 surround TM1 and are hypothesized to shield it from the surrounding lipid bilayer and provide structural support. The fourth transmembrane helix forms the outermost layer.

Clinical relevance

ORAI1 mutations are associated with Immunodeficiency 9 and Tubular aggregate myopathy type 2 (TAM2).[14]

Ligands

Inhibitors

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000276045 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049686 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b Feske S, Gwack Y, Prakriya M, Srikanth S, Puppel SH, Tanasa B, Hogan PG, Lewis RS, Daly M, Rao A (May 2006). "A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function". Nature. 441 (7090): 179–85. Bibcode:2006Natur.441..179F. doi:10.1038/nature04702. PMID 16582901. S2CID 1605392.
  6. ^ Vig M, Peinelt C, Beck A, Koomoa DL, Rabah D, Koblan-Huberson M, Kraft S, Turner H, Fleig A, Penner R, Kinet JP (May 2006). "CRACM1 is a plasma membrane protein essential for store-operated Ca2+ entry". Science. 312 (5777): 1220–3. Bibcode:2006Sci...312.1220V. doi:10.1126/science.1127883. PMC 5685805. PMID 16645049.
  7. ^ Zhang SL, Yeromin AV, Zhang XH, Yu Y, Safrina O, Penna A, Roos J, Stauderman KA, Cahalan MD (June 2006). "Genome-wide RNAi screen of Ca(2+) influx identifies genes that regulate Ca(2+) release-activated Ca(2+) channel activity". Proceedings of the National Academy of Sciences of the United States of America. 103 (24): 9357–62. doi:10.1073/pnas.0603161103. PMC 1482614. PMID 16751269.
  8. ^ Putney JW (September 2009). "Capacitative calcium entry: from concept to molecules". Immunological Reviews. 231 (1): 10–22. doi:10.1111/j.1600-065X.2009.00810.x. PMID 19754887. S2CID 32303982.
  9. ^ Park CY, Hoover PJ, Mullins FM, Bachhawat P, Covington ED, Raunser S, Walz T, Garcia KC, Dolmetsch RE, Lewis RS (March 2009). "STIM1 clusters and activates CRAC channels via direct binding of a cytosolic domain to Orai1". Cell. 136 (5): 876–90. doi:10.1016/j.cell.2009.02.014. PMC 2670439. PMID 19249086.
  10. ^ Zhou Y, Meraner P, Kwon HT, Machnes D, Oh-hora M, Zimmer J, Huang Y, Stura A, Rao A, Hogan PG (January 2010). "STIM1 gates the store-operated calcium channel ORAI1 in vitro". Nature Structural & Molecular Biology. 17 (1): 112–6. doi:10.1038/nsmb.1724. PMC 2902271. PMID 20037597.
  11. ^ Gudlur A, Zhou Y, Hogan PG (2013-01-01). "STIM-ORAI interactions that control the CRAC channel". Current Topics in Membranes. 71: 33–58. doi:10.1016/b978-0-12-407870-3.00002-0. ISBN 9780124078703. PMID 23890110.{{cite journal}}: CS1 maint: periodical has ISBN (link)
  12. ^ Zhou Y, Srinivasan P, Razavi S, Seymour S, Meraner P, Gudlur A, Stathopulos PB, Ikura M, Rao A, Hogan PG (August 2013). "Initial activation of STIM1, the regulator of store-operated calcium entry". Nature Structural & Molecular Biology. 20 (8): 973–81. doi:10.1038/nsmb.2625. PMC 3784406. PMID 23851458.
  13. ^ Hou X, Pedi L, Diver MM, Long SB (December 2012). "Crystal structure of the calcium release-activated calcium channel Orai". Science. 338 (6112): 1308–13. Bibcode:2012Sci...338.1308H. doi:10.1126/science.1228757. PMC 3695727. PMID 23180775.
  14. ^ "ORAI CALCIUM RELEASE-ACTIVATED CALCIUM MODULATOR 1; ORAI1". www.omim.org. Retrieved 2023-11-13.
Stub icon

This article on a gene on human chromosome 12 is a stub. You can help Wikipedia by adding missing information.

Content Disclaimer

Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.

  1. The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
  2. There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
  3. It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
  4. Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
  5. Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.