SCNN1B
Podjedinica beta-1natrijevog kanalajestproteinkoji je kodljudikodirangenomSCN1Bsahromosoma 19.[5][6]
Aminokiselinska sekvenca
[uredi|uredi izvor]Dužinapolipeptidnoglanca je 218aminokiselina,amolekulska težina24.707Da.[6]
10 | 20 | 30 | 40 | 50 | ||||
---|---|---|---|---|---|---|---|---|
MGRLLALVVG | AALVSSACGG | CVEVDSETEA | VYGMTFKILC | ISCKRRSETN | ||||
AETFTEWTFR | QKGTEEFVKI | LRYENEVLQL | EEDERFEGRV | VWNGSRGTKD | ||||
LQDLSIFITN | VTYNHSGDYE | CHVYRLLFFE | NYEHNTSVVK | KIHIEVVDKA | ||||
NRDMASIVSE | IMMYVLIVVL | TIWLVAEMIY | CYKKIAAATE | TAAQENASEY | ||||
LAITSESKEN | CTGVQVAE |
Funkcija
[uredi|uredi izvor]Naponski vođeni natrijski kanali su neophodni za stvaranje i širenjeakcijskih potencijalau poprečno-prugastim mišićima ineuronskimtkivima. Biohemijski, sastoje se od velike podjedinice alfa i 1 ili 2 manje beta podjedinice, kao što je SCN1B. Sama alfa podjedinica može pokazati sve funkcionalne atribute naponsko vođenogNa+ kanala,ali joj je potrebna podjedinica beta-1 za normalnu kinetiku inaktivacije (premaOMIM][6]
Klinički značaj
[uredi|uredi izvor]Mutacije u genu SCN1B povezane su s poremećajima kao što suBrugadaov sindrom,Dravetov sindromiGEFS.
Također pogledajte
[uredi|uredi izvor]Reference
[uredi|uredi izvor]- ^abcGRCh38: Ensembl release 89: ENSG00000168447-Ensembl,maj 2017
- ^abcGRCm38: Ensembl release 89: ENSMUSG00000030873-Ensembl,maj 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.
- ^McClatchey AI, Cannon SC, Slaugenhaupt SA, Gusella JF (Sep 1993). "The cloning and expression of a sodium channel beta 1-subunit cDNA from human brain".Hum Mol Genet.2(6): 745–9.doi:10.1093/hmg/2.6.745.PMID8394762.
- ^abc"Entrez Gene: SCN1B sodium channel, voltage-gated, type I, beta".
Dopunska literatura
[uredi|uredi izvor]- Hartshorne RP, Catterall WA (1984)."The sodium channel from rat brain. Purification and subunit composition".J. Biol. Chem.259(3): 1667–75.doi:10.1016/S0021-9258(17)43460-0.PMID6319405.
- Makita N, Sloan-Brown K, Weghuis DO, et al. (1995). "Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B)".Genomics.23(3): 628–34.doi:10.1006/geno.1994.1551.PMID7851891.
- Makita N, Bennett PB, George AL (1994)."Voltage-gated Na+ channel beta 1 subunit mRNA expressed in adult human skeletal muscle, heart, and brain is encoded by a single gene".J. Biol. Chem.269(10): 7571–8.doi:10.1016/S0021-9258(17)37325-8.PMID8125980.
- Wallace RH, Wang DW, Singh R, et al. (1998). "Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B".Nat. Genet.19(4): 366–70.doi:10.1038/1252.PMID9697698.S2CID20962841.
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- Strausberg RL, Feingold EA, Grouse LH, et al. (2003)."Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences".Proc. Natl. Acad. Sci. U.S.A.99(26): 16899–903.Bibcode:2002PNAS...9916899M.doi:10.1073/pnas.242603899.PMC139241.PMID12477932.
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- Aronica E, Troost D, Rozemuller AJ, et al. (2003). "Expression and regulation of voltage-gated sodium channel beta1 subunit protein in human gliosis-associated pathologies".Acta Neuropathol.105(5): 515–23.doi:10.1007/s00401-003-0677-2.hdl:2027.42/42208.PMID12677453.S2CID30847819.
- Audenaert D, Claes L, Ceulemans B, et al. (2004)."A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy".Neurology.61(6): 854–6.doi:10.1212/01.wnl.0000080362.55784.1c.PMID14504340.S2CID20308172.
- Qin N, D'Andrea MR, Lubin ML, et al. (2004). "Molecular cloning and functional expression of the human sodium channel beta1B subunit, a novel splicing variant of the beta1 subunit".Eur. J. Biochem.270(23): 4762–70.doi:10.1046/j.1432-1033.2003.03878.x.PMID14622265.
- McEwen DP, Meadows LS, Chen C, et al. (2004)."Sodium channel beta1 subunit-mediated modulation of Nav1.2 currents and cell surface density is dependent on interactions with contactin and ankyrin".J. Biol. Chem.279(16): 16044–9.doi:10.1074/jbc.M400856200.PMID14761957.
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Vanjski linkovi
[uredi|uredi izvor]- GeneReviews/NIH/NCBI/UW entry on Brugada syndrome
- SCN1B protein, humannaUS National Library of MedicineMedical Subject Headings(MeSH)
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