[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki5\/spastin-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki5\/spastin-wikipedia\/","headline":"Spastin – Wikipedia","name":"Spastin – Wikipedia","description":"From Wikipedia, the free encyclopedia Protein The human gene SPAST codes for the microtubule-severing protein of the same name, commonly","datePublished":"2020-11-25","dateModified":"2020-11-25","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki5\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki5\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/en.wikipedia.org\/wiki\/Special:CentralAutoLogin\/start?type=1x1","url":"https:\/\/en.wikipedia.org\/wiki\/Special:CentralAutoLogin\/start?type=1x1","height":"1","width":"1"},"url":"https:\/\/wiki.edu.vn\/en\/wiki5\/spastin-wikipedia\/","wordCount":4576,"articleBody":"From Wikipedia, the free encyclopediaProteinThe human gene SPAST codes for the microtubule-severing protein of the same name, commonly known as spastin.[5]This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The encoded ATPase may be involved in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full length sequences have not been determined. Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.[6]Table of ContentsSee also[edit]References[edit]Further reading[edit]External links[edit]See also[edit]Spastic paraplegiaReferences[edit]Further reading[edit]Kikuno R, Nagase T, Ishikawa K,  et\u00a0al. (1999). “Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro”. DNA Res. 6 (3): 197\u2013205. doi:10.1093\/dnares\/6.3.197. PMID\u00a010470851.Hazan J, Davoine CS, Mavel D,  et\u00a0al. (1999). “A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia”. Genomics. 60 (3): 309\u201319. doi:10.1006\/geno.1999.5932. PMID\u00a010493830.Hazan J, Fonknechten N, Mavel D,  et\u00a0al. (1999). “Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia”. Nat. Genet. 23 (3): 296\u2013303. doi:10.1038\/15472. PMID\u00a010610178. S2CID\u00a023167276.Fonknechten N, Mavel D, Byrne P,  et\u00a0al. (2000). “Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia”. Hum. Mol. Genet. 9 (4): 637\u201344. doi:10.1093\/hmg\/9.4.637. PMID\u00a010699187.Santorelli FM, Patrono C, Fortini D,  et\u00a0al. (2000). “Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation”. Neurology. 55 (5): 702\u20135. doi:10.1212\/wnl.55.5.702. PMID\u00a010980739. S2CID\u00a038129619.Lindsey JC, Lusher ME, McDermott CJ,  et\u00a0al. (2001). “Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis”. J. Med. Genet. 37 (10): 759\u201365. doi:10.1136\/jmg.37.10.759. PMC\u00a01757167. PMID\u00a011015453.B\u00fcrger J, Fonknechten N, Hoeltzenbein M,  et\u00a0al. (2001). “Hereditary spastic paraplegia caused by mutations in the SPG4 gene”. Eur. J. Hum. Genet. 8 (10): 771\u20136. doi:10.1038\/sj.ejhg.5200528. PMID\u00a011039577.Hentati A, Deng HX, Zhai H,  et\u00a0al. (2000). “Novel mutations in spastin gene and absence of correlation with age at onset of symptoms”. Neurology. 55 (9): 1388\u201390. doi:10.1212\/wnl.55.9.1388. PMID\u00a011087788. S2CID\u00a041471774.Svenson IK, Ashley-Koch AE, Gaskell PC,  et\u00a0al. (2001). “Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia”. Am. J. Hum. Genet. 68 (5): 1077\u201385. doi:10.1086\/320111. PMC\u00a01226088. PMID\u00a011309678.Svenson IK, Ashley-Koch AE, Pericak-Vance MA, Marchuk DA (2002). “A second leaky splice-site mutation in the spastin gene”. Am. J. Hum. Genet. 69 (6): 1407\u20139. doi:10.1086\/324593. PMC\u00a01235553. PMID\u00a011704932.Errico A, Ballabio A, Rugarli EI (2002). “Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics”. Hum. Mol. Genet. 11 (2): 153\u201363. doi:10.1093\/hmg\/11.2.153. PMID\u00a011809724.Meijer IA, Hand CK, Cossette P,  et\u00a0al. (2002). “Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia”. Arch. Neurol. 59 (2): 281\u20136. doi:10.1001\/archneur.59.2.281. PMID\u00a011843700.Patrono C, Casali C, Tessa A,  et\u00a0al. (2002). “Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegia”. J. Neurol. 249 (2): 200\u20135. doi:10.1007\/PL00007865. PMID\u00a011985387. S2CID\u00a022503829.Morita M, Ho M, Hosler BA,  et\u00a0al. (2002). “A novel mutation in the spastin gene in a family with spastic paraplegia”. Neurosci. Lett. 325 (1): 57\u201361. doi:10.1016\/S0304-3940(02)00239-2. PMID\u00a012023066. S2CID\u00a026359975.Sauter S, Miterski B, Klimpe S,  et\u00a0al. (2002). “Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia”. Hum. Mutat. 20 (2): 127\u201332. doi:10.1002\/humu.10105. PMID\u00a012124993. S2CID\u00a028344764.Yabe I, Sasaki H, Tashiro K,  et\u00a0al. (2002). “Spastin gene mutation in Japanese with hereditary spastic paraplegia”. J. Med. Genet. 39 (8): 46e\u201346. doi:10.1136\/jmg.39.8.e46. PMC\u00a01735214. PMID\u00a012161613.Proukakis C, Hart PE, Cornish A,  et\u00a0al. (2002). “Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia”. J. Neurol. Sci. 201 (1\u20132): 65\u20139. doi:10.1016\/S0022-510X(02)00192-2. PMID\u00a012163196. S2CID\u00a044994475.Ki CS, Lee WY, Han DH,  et\u00a0al. (2002). “A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal-dominant hereditary spastic paraplegia”. J. Hum. Genet. 47 (9): 473\u20137. doi:10.1007\/s100380200068. PMID\u00a012202986.Namekawa M, Takiyama Y, Sakoe K,  et\u00a0al. (2003). “A Japanese SPG4 family with a novel missense mutation of the SPG4 gene: intrafamilial variability in age at onset and clinical severity”. Acta Neurol. Scand. 106 (6): 387\u201391. doi:10.1034\/j.1600-0404.2002.01254.x. PMID\u00a012460147. S2CID\u00a043161611.Starling A, Rocco P, Passos-Bueno MR,  et\u00a0al. (2003). “Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree”. J. Med. Genet. 39 (12): 77e\u201377. doi:10.1136\/jmg.39.12.e77. PMC\u00a01757223. PMID\u00a012471215.External links[edit]"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki5\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki5\/spastin-wikipedia\/#breadcrumbitem","name":"Spastin – Wikipedia"}}]}]