Cav1.1

Cav1.1
已知的結構
PDB直系同源搜索: PDBe RCSB
PDBID列表

2VAY

識別號
别名CACNA1S;, CACNL1A3, CCHL1A3, Cav1.1, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP, calcium voltage-gated channel subunit alpha1 S, DHPR
外部IDOMIM:114208 MGI:88294 HomoloGene:37257 GeneCards:CACNA1S
相關疾病
低血鉀性週期性麻痺症[1]
為以下藥物的標靶
地尔硫䓬、​维拉帕米、​硝苯地平、​(3RS,4′RS)-benidipine、​拉西地平、​bepridil hydrochloride monohydrate、​diltiazem hydrochloride、​amlodipine besylate[2]
基因位置(人类
1號染色體
染色体1號染色體[3]
1號染色體
Cav1.1的基因位置
Cav1.1的基因位置
基因座1q32.1起始201,039,512 bp[3]
终止201,112,451 bp[3]
基因位置(小鼠
小鼠1号染色体
染色体小鼠1号染色体[4]
小鼠1号染色体
Cav1.1的基因位置
Cav1.1的基因位置
基因座1 E4|1 59.55 cM起始135,980,488 bp[4]
终止136,047,560 bp[4]
RNA表达模式
查阅更多表达数据
基因本體
分子功能 voltage-gated calcium channel activity
calcium channel activity
金屬離子結合
voltage-gated ion channel activity
high voltage-gated calcium channel activity
ion channel activity
血浆蛋白结合
calmodulin binding
細胞組分 細胞質
電壓依賴性鈣通道
integral component of membrane

I band
横小管
L-type voltage-gated calcium channel complex
细胞膜
肌膜
生物學過程 肌肉收缩
membrane depolarization during action potential
regulation of ion transmembrane transport
ion transport
calcium ion transmembrane transport
transmembrane transport
calcium ion transport
cellular response to caffeine
calcium ion import
cardiac conduction
Sources:Amigo / QuickGO
直系同源
物種人類小鼠
Entrez

779

12292

Ensembl

ENSG00000081248

ENSMUSG00000026407

UniProt

Q13698

Q02789

mRNA​序列

​NM_000069

NM_001081023
​NM_014193

蛋白序列

NP_000060

NP_001074492
​NP_055008
​NP_001389878

基因位置​(UCSC)Chr 1: 201.04 – 201.11 MbChr 1: 135.98 – 136.05 Mb
PubMed​查找[5][6]
維基數據
檢視/編輯人類檢視/編輯小鼠

Cav1.1又稱為L型鈣通道α1亞基(calcium channel, voltage-dependent, L type, alpha 1S subunit,CACNA1S),為一種由CACNA1S基因轉譯而成的蛋白質[7]。有時又稱CACNL1A3二氫吡啶英语dihydropyridine受體(dihydropyridine receptor,DHPR)。

功能

該蛋白為骨骼肌L型電性鈣通道的五個次單元中的其中之一。該基因突變可能與低鉀血周期性麻痺英语hypokalemic periodic paralysis甲狀腺毒性週期性麻痺症,和惡性高熱相關[7]

Cav1.1為骨骼肌横小管上的電壓依賴性鈣通道英语voltage-dependent calcium channel。在骨骼肌中會與肌漿網上的蘭諾定受體1(RyR1)相接。當神經衝動發生時,終板電位英语end-plate potential會沿骨骼肌的細胞膜傳入橫小管中,並刺激Cav1.1。先前科學家以為當肌肉去極化時會引發鈣通道開啟,鈣離子流入後活化RyR1,使更多鈣離子從肌漿網釋入細胞質,引發興奮收縮聯合作用,進而使肌肉收縮。最近研究發現在骨骼肌中(並非心肌),鈣離子流入Cav1.1並非必須。Cav1.1活化後構型會改變,並與RyR1相接進行別構調節[8]

臨床意義

在許多低鉀血周期性麻痺英语hypokalemic periodic paralysis(HOKPP)患者身上,Cav1.1的 domains 2 和 domains 4 有突變發生,造成其感測去極化的能力下降,活化蘭諾定受體的能力下降。因此肌肉無法順利收縮,導致患者癱瘓。此類患者會於低血鉀時發生癱瘓,因胞外血鉀降低會使肌肉更快回到静息电位,且會使電位更難達到閾值,使動作電位更難產生,肌肉因此無力。在Cav1.1缺損的患者身上,即使動作電位產生,肌漿網仍難以釋放鈣離子,使肌肉收縮無法完成,因此此類患者必須調整血鉀濃度。相反地,若鈉離子通道突變後功能增強,使肌肉長期維持去極化,則會導致高鉀血周期性麻痺英语hyperkalemic periodic paralysis[9]

歐洲惡性高熱小組(European Malignant Hyperthermia Group)將此 CACNA1S 基因的兩種突變列為惡性高熱的診斷之一[10]

阻斷劑

Cav1.1可由二羥基吡啶英语dihydropyridine阻斷。

參見

參考文獻

  1. ^ 與Cav1.1相關的疾病;在維基數據上查看/編輯參考. 
  2. ^ 對Cav1.1起作用的藥物;在維基數據上查看/編輯參考. 
  3. ^ 3.0 3.1 3.2 GRCh38: Ensembl release 89: ENSG00000081248 - Ensembl, May 2017
  4. ^ 4.0 4.1 4.2 GRCm38: Ensembl release 89: ENSMUSG00000026407 - Ensembl, May 2017
  5. ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  6. ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  7. ^ 7.0 7.1 Entrez Gene: CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit. (原始内容存档于2010-12-05). 
  8. ^ Proenza C, O'Brien J, Nakai J, Mukherjee S, Allen PD, Beam KG. Identification of a region of RyR1 that participates in allosteric coupling with the alpha(1S) (Ca(V)1.1) II-III loop. J. Biol. Chem. February 2002, 277 (8): 6530–5. PMID 11726651. doi:10.1074/jbc.M106471200. 
  9. ^ Jurkat-Rott K, Lehmann-Horn F. Muscle channelopathies and critical points in functional and genetic studies. J. Clin. Invest. August 2005, 115 (8): 2000–9. PMC 1180551可免费查阅. PMID 16075040. doi:10.1172/JCI25525. 
  10. ^ European Malignant Hyperthermia Group: Mutations in RYR1. emhg.org. [2017-07-07]. (原始内容存档于2016-03-21) (英语). 

延伸閱讀

  • Catterall WA, Perez-Reyes E, Snutch TP, Striessnig J. International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels. Pharmacol. Rev. 2005, 57 (4): 411–25. PMID 16382099. doi:10.1124/pr.57.4.5. 
  • Rotman EI, De Jongh KS, Florio V, Lai Y, Catterall WA. Specific phosphorylation of a COOH-terminal site on the full-length form of the alpha 1 subunit of the skeletal muscle calcium channel by cAMP-dependent protein kinase. J. Biol. Chem. 1992, 267 (23): 16100–5. PMID 1322891. 
  • Röhrkasten A, Meyer HE, Nastainczyk W, Sieber M, Hofmann F. cAMP-dependent protein kinase rapidly phosphorylates serine- 687 of the skeletal muscle receptor for calcium channel blockers. J. Biol. Chem. 1988, 263 (30): 15325–9. PMID 2844809. 
  • Tanabe T, Takeshima H, Mikami A, Flockerzi V, Takahashi H, Kangawa K, Kojima M, Matsuo H, Hirose T, Numa S. Primary structure of the receptor for calcium channel blockers from skeletal muscle. Nature. 1987, 328 (6128): 313–8. PMID 3037387. doi:10.1038/328313a0. 
  • Hogan K, Powers PA, Gregg RG. Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3). Genomics. 1994, 24 (3): 608–9. PMID 7713519. doi:10.1006/geno.1994.1677. 
  • Elbaz A, Vale-Santos J, Jurkat-Rott K, Lapie P, Ophoff RA, Bady B, Links TP, Piussan C, Vila A, Monnier N. Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families. Am. J. Hum. Genet. 1995, 56 (2): 374–80. PMC 1801148可免费查阅. PMID 7847370. 
  • Boerman RH, Ophoff RA, Links TP, van Eijk R, Sandkuijl LA, Elbaz A, Vale-Santos JE, Wintzen AR, van Deutekom JC, Isles DE. Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis. J. Med. Genet. 1995, 32 (1): 44–7. PMC 1050178可免费查阅. PMID 7897626. doi:10.1136/jmg.32.1.44. 
  • Gregg RG, Couch F, Hogan K, Powers PA. Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32. Genomics. 1993, 15 (1): 107–12. PMID 7916735. doi:10.1006/geno.1993.1017. 
  • Jurkat-Rott K, Lehmann-Horn F, Elbaz A, Heine R, Gregg RG, Hogan K, Powers PA, Lapie P, Vale-Santos JE, Weissenbach J. A calcium channel mutation causing hypokalemic periodic paralysis. Hum. Mol. Genet. 1994, 3 (8): 1415–9. PMID 7987325. doi:10.1093/hmg/3.8.1415. 
  • Ptácek LJ, Tawil R, Griggs RC, Engel AG, Layzer RB, Kwieciński H, McManis PG, Santiago L, Moore M, Fouad G. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell. 1994, 77 (6): 863–8. PMID 8004673. doi:10.1016/0092-8674(94)90135-X. 
  • Drouet B, Garcia L, Simon-Chazottes D, Mattei MG, Guénet JL, Schwartz A, Varadi G, Pinçon-Raymond M. The gene coding for the alpha 1 subunit of the skeletal dihydropyridine receptor (Cchl1a3 = mdg) maps to mouse chromosome 1 and human 1q32. Mamm. Genome. 1993, 4 (9): 499–503. PMID 8118099. doi:10.1007/BF00364784. 
  • Iles DE, Segers B, Olde Weghuis D, Suijkerbuijk R, Mikala G, Schwartz A, Wieringa B. Refined localization of the alpha 1-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization. Genomics. 1994, 19 (3): 561–3. PMID 8188298. doi:10.1006/geno.1994.1106. 
  • O'Brien RO, Taske NL, Hansbro PM, Matthaei KI, Hogan SP, Denborough MA, Foster PS. Exclusion of defects in the skeletal muscle specific regions of the DHPR alpha 1 subunit as frequent causes of malignant hyperthermia. J. Med. Genet. 1995, 32 (11): 913–4. PMC 1051750可免费查阅. PMID 8592342. doi:10.1136/jmg.32.11.913. 
  • Hogan K, Gregg RG, Powers PA. The structure of the gene encoding the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3). Genomics. 1996, 31 (3): 392–4. PMID 8838325. doi:10.1006/geno.1996.0066. 
  • Robinson RL, Monnier N, Wolz W, Jung M, Reis A, Nuernberg G, Curran JL, Monsieurs K, Stieglitz P, Heytens L, Fricker R, van Broeckhoven C, Deufel T, Hopkins PM, Lunardi J, Mueller CR. A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees. Hum. Mol. Genet. 1997, 6 (6): 953–61. PMID 9175745. doi:10.1093/hmg/6.6.953. 
  • Monnier N, Procaccio V, Stieglitz P, Lunardi J. Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle. Am. J. Hum. Genet. 1997, 60 (6): 1316–25. PMC 1716149可免费查阅. PMID 9199552. doi:10.1086/515454. 
  • Meyers MB, Puri TS, Chien AJ, Gao T, Hsu PH, Hosey MM, Fishman GI. Sorcin associates with the pore-forming subunit of voltage-dependent L-type Ca2+ channels. J. Biol. Chem. 1998, 273 (30): 18930–5. PMID 9668070. doi:10.1074/jbc.273.30.18930. 
  • Morrill JA, Brown RH, Cannon SC. Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H. J. Neurosci. 1998, 18 (24): 10320–34. PMID 9852570. 
  • Protasi F, Paolini C, Nakai J, Beam KG, Franzini-Armstrong C, Allen PD. Multiple regions of RyR1 mediate functional and structural interactions with alpha(1S)-dihydropyridine receptors in skeletal muscle. Biophys. J. 2002, 83 (6): 3230–44. PMC 1302400可免费查阅. PMID 12496092. doi:10.1016/S0006-3495(02)75325-3. 
  • Carsana A, Fortunato G, De Sarno C, Brancadoro V, Salvatore F. Identification of new polymorphisms in the CACNA1S gene. Clin. Chem. Lab. Med. 2003, 41 (1): 20–2. PMID 12636044. doi:10.1515/CCLM.2003.004. 

外部連結


Cav1.1引用了美国国家医学图书馆提供的資料,这些資料属于公共领域

 
Ca2+: 钙通道
电压门控
L型/Cavα(1.1、1.2英语Cav1.21.3英语Cav1.31.4英语Cav1.4 · N型/Cavα2.2 · P型/Cavα2.1英语Cav2.1 · Q型/Cavα2.1 · R型/Cavα2.3 · T型/Cavα3.1英语CACNA1G3.2英语CACNA1H3.3英语CACNA1I
α2δ亚基单元1英语CACNA2D12英语CACNA2D2 · β亚基单元β1英语CACNB1β2英语CACNB2β3英语CACNB3β4英语CACNB4 · γ亚基单元γ1γ2英语CACNG2γ3英语CACNG3γ4英语CACNG4
精子阳离子通道(1英语CatSper12英语CatSper23英语CatSper34英语CatSper4 · 双孔通道(1英语TPCN12英语TPCN2
配体门控
三磷酸肌醇受体(1英语ITPR12英语ITPR23英语ITPR3 · 兰尼碱受体(1、2、3)
 
Navα1.1英语Nav1.11.2英语Nav1.21.3英语SCN3A1.4英语Nav1.41.5英语Nav1.51.6英语SCN8A1.7英语Nav1.71.8英语SCN10A1.9英语Nav1.97A英语SCN7A · Navβ1英语SCN1B2英语SCN2B3英语SCN3B4英语SCN4B
持续活化
上皮钠离子通道(α英语SCNN1Aβ英语SCNN1Bγ英语SCNN1Gδ英语SCNN1D
 
Kvα1-61.1英语Kv1.11.2英语KCNA21.3英语KCNA31.4英语KCNA41.5英语KCNA51.6英语KCNA61.7英语KCNA71.10英语KCNA10 ·2.1英语KCNB12.2英语KCNB2 ·3.1英语KCNC13.2英语KCNC23.3英语KCNC33.4英语KCNC4 ·4.1英语KCND14.2英语KCND24.3英语KCND3 ·5.1英语KCNF1 ·6.1英语KCNG16.2英语KCNG26.3英语KCNG36.4英语KCNG4
Kvα7-127.1英语KvLQT17.2英语KvLQT27.3英语KvLQT37.4英语KCNQ47.5英语KCNQ5 ·8.1英语KCNV18.2英语KCNV2 ·9.1英语KCNS19.2英语KCNS29.3英语KCNS3 ·10.1英语KCNH110.2英语KCNH5 ·11.1/hERG11.2英语KCNH611.3英语KCNH7 ·12.1英语KCNH812.2英语KCNH312.3英语KCNH4
Kvβ1英语KCNAB12英语KCNAB23英语KCNAB3 · KCNIP1英语KCNIP12英语KCNIP23英语Calsenilin4英语KCNIP4 · minK/ISK英语KCNE1 · 类似minK/ISK英语KCNE1L · MiRP1英语KCNE22英语KCNE33英语KCNE4 · 摇摆基因
钙激活
BK通道(α1英语KCNMA1β1英语KCNMB1β2英语KCNMB2β3英语KCNMB3β4英语KCNMB4 · SK通道(SK1英语KCNN1SK2英语KCNN2SK3英语SK3SK4英语KCNN4 · KCa(1.1、2.1英语KCNN12.2英语KCNN22.3英语KCNN33.1英语KCNN44.1英语KCNT14.2英语KCNT25.1英语KCNU1
内向整流
Kir1.1英语ROMK2.1英语Kir2.12.2英语KCNJ122.3英语KCNJ42.4英语KCNJ14 · GIRK/Kir3.1英语KCNJ33.2英语KCNJ63.3英语KCNJ93.4英语KCNJ5 · Kir4.1英语KCNJ104.2英语KCNJ155.1英语KCNJ166.1英语KCNJ86.2英语Kir6.27.1英语KCNJ13
串联孔域
K2P1英语KCNK12英语KCNK23英语KCNK34英语KCNK45英语KCNK56英语KCNK67英语KCNK79英语KCNK910英语KCNK1012英语KCNK1213英语KCNK1315英语KCNK1516英语KCNK1617英语KCNK1718英语KCNK18
 
其它
M+: 瞬時受體電位通道
TRPA(1 · TRPC英语TRPC1英语TRPC12英语TRPC23英语TRPC34英语TRPC44AP英语TRPC4AP56英语TRPC67英语TRPC7 · TRPM英语TRPM1英语TRPM12英语TRPM23英语TRPM34英语TRPM45英语TRPM56英语TRPM67英语TRPM78 · TRPML英语TRPML1英语Mucolipin-12英语MCOLN23英语MCOLN3 · TRPP英语TRPP(1、2) · TRPV英语TRPV12英语TRPV23英语TRPV34英语TRPV45英语TRPV56英语TRPV6
Cl-: 氯离子通道
ANO1英语ANO1 · 斑萎蛋白(1、2) · CFTR · CLCA1英语CLCA12英语CLCA23英语CLCA34英语CLCA4 · CLCN1英语CLCN12英语CLCN23英语CLCN34英语CLCN45英语CLCN56英语CLCN67英语CLCN7KA英语CLCNKAKB英语CLCNKB · CLIC1英语CLIC12英语CLIC23英语CLIC34英语CLIC45英语CLIC56英语CLIC6L1英语CLCC1 · CLNS1A英语CLNS1A1B英语CLNS1B
环核苷酸门控(起搏电流通道)
α(1、2、3、4) · β(1、2、3) · HCN1英语HCN12英语HCN23英语HCN34英语HCN4
水通道蛋白(1、2、3、4、5、7、8、9) · 电压依赖阴离子通道(12英语VDAC23英语VDAC3 · 常见细菌外膜蛋白族
常见
配体门控离子通道 · 电压门控离子通道 · 机械力激活离子通道
参见失调症
細胞模板索引
描述
  • 結構
      • 染色體基因
  • 胞器
    • 過氧小體英语Template:Peroxisomal proteins
    • 細胞骨架
    • 中心體
    • 上皮
    • 纖毛
    • 粒線體
    • 蛋白質
    • 細胞連結
  • 膜運輸
    • 離子通道
    • 囊泡運輸
    • 溶質載體英语Template:Solute carrier family
    • ABC transporters英语Template:ABC transporters
    • ATPase
    • 氧化还原驱动
疾病
  • 結構
    • 過氧小體
    • 細胞骨架英语Template:Cytoskeletal defects
    • 纖毛
    • 粒線體英语Template:Mitochondrial diseases
    • 英语Template:Nucleus diseases
    • 硬蛋白
    • 離子通道
    • 溶質載體
    • ATP酶英语Template:ATPase disorders
    • ABC transporters
    • 其他英语Template:Other cell membrane protein disorders
    • 胞外配體英语Template:Extracellular ligand disorders
    • 細胞表面受體
    • 胞内信号
  • 囊泡運輸英语Template:Vesicular transport protein disorders
  • 成孔毒素