Anoctamin 6
Anoctamin 6 is a protein that in humans is encoded by the ANO6 gene.[5]
Function
[edit]This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Research
[edit]The protein may play a role in syncytia formation during COVID-19 infection.[6]
See also
[edit]References
[edit]- ^ a b c GRCh38: Ensembl release 89: ENSG00000177119 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000064210 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Anoctamin 6". Retrieved 2017-09-28.
- ^ Braga L, Ali H, Secco I, Chiavacci E, Neves G, Goldhill D, et al. (June 2021). "Drugs that inhibit TMEM16 proteins block SARS-CoV-2 spike-induced syncytia". Nature. 594 (7861): 88–93. Bibcode:2021Natur.594...88B. doi:10.1038/s41586-021-03491-6. PMC 7611055. PMID 33827113.
Further reading
[edit]- Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Molecular Medicine. 16 (7–8): 247–253. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.
- Suzuki J, Umeda M, Sims PJ, Nagata S (December 2010). "Calcium-dependent phospholipid scrambling by TMEM16F". Nature. 468 (7325): 834–838. Bibcode:2010Natur.468..834S. doi:10.1038/nature09583. hdl:2433/131831. PMID 21107324. S2CID 205223048.
- Castoldi E, Collins PW, Williamson PL, Bevers EM (April 2011). "Compound heterozygosity for 2 novel TMEM16F mutations in a patient with Scott syndrome". Blood. 117 (16): 4399–4400. doi:10.1182/blood-2011-01-332502. PMID 21511967.
- Suzuki J, Nagata S (November 2011). "[Phospholipid scrambling by TMEM16F]". Seikagaku. The Journal of Japanese Biochemical Society (in Japanese). 83 (11): 1050–1054. PMID 22256604.
- Wei JC, Hsu YW, Hung KS, Wong RH, Huang CH, Liu YT, et al. (2013). "Association study of polymorphisms rs4552569 and rs17095830 and the risk of ankylosing spondylitis in a Taiwanese population". PLOS ONE. 8 (1): e52801. Bibcode:2013PLoSO...852801W. doi:10.1371/journal.pone.0052801. PMC 3537770. PMID 23308121.
- Shimizu T, Iehara T, Sato K, Fujii T, Sakai H, Okada Y (April 2013). "TMEM16F is a component of a Ca2+-activated Cl- channel but not a volume-sensitive outwardly rectifying Cl- channel". American Journal of Physiology. Cell Physiology. 304 (8): C748–C759. doi:10.1152/ajpcell.00228.2012. PMID 23426967.
- Kmit A, van Kruchten R, Ousingsawat J, Mattheij NJ, Senden-Gijsbers B, Heemskerk JW, et al. (April 2013). "Calcium-activated and apoptotic phospholipid scrambling induced by Ano6 can occur independently of Ano6 ion currents". Cell Death & Disease. 4 (4): e611. doi:10.1038/cddis.2013.135. PMC 3668637. PMID 23618909.
- Suzuki T, Suzuki J, Nagata S (March 2014). "Functional swapping between transmembrane proteins TMEM16A and TMEM16F". The Journal of Biological Chemistry. 289 (11): 7438–7447. doi:10.1074/jbc.M113.542324. PMC 3953258. PMID 24478309.
- Ousingsawat J, Wanitchakool P, Schreiber R, Wuelling M, Vortkamp A, Kunzelmann K (March 2015). "Anoctamin-6 controls bone mineralization by activating the calcium transporter NCX1". The Journal of Biological Chemistry. 290 (10): 6270–6280. doi:10.1074/jbc.M114.602979. PMC 4358264. PMID 25589784.
External links
[edit]- Overview of all the structural information available in the PDB for UniProt: Q6P9J9 (Mouse Anoctamin-6) at the PDBe-KB.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.