胱天蛋白酶12

胱天蛋白酶12
識別號
别名	CASP12；, CASP-12, CASP12P1, caspase 12 (gene/pseudogene)
外部ID	OMIM：608633 GeneCards：CASP12
為以下藥物的標靶
	emricasan
基因位置（人类）
染色体	11號染色體
终止	104,898,670 bp
基因本體
分子功能	• cysteine-type endopeptidase activity involved in apoptotic process; • 半胱氨酸型肽酶活性; • cysteine-type endopeptidase activity; • cysteine-type endopeptidase activity involved in apoptotic signaling pathway;
細胞組分	• NLRP3 inflammasome complex; • AIM2 inflammasome complex; • IPAF inflammasome complex; • 内质网; • 細胞質;
生物學過程	• regulation of apoptotic process; • regulation of inflammatory response; • 蛋白酶解; • execution phase of apoptosis; • 细胞凋亡; • activation of cysteine-type endopeptidase activity involved in apoptotic process; • apoptotic signaling pathway;
	Sources:Amigo / QuickGO
直系同源
	100506742
	无数据
	ENSG00000204403
	无数据
	Q6UXS9
	无数据
	NM_001191016
	无数据
	NP_001177945
	无数据
	維基數據
檢視/編輯人類

胱天蛋白酶12（英语：Caspase 12）是人类中由CASP12基因编码的蛋白质。该蛋白质属于胱天蛋白酶家族，可在C端天冬氨酸残基处裂解其底物。它与胱天蛋白酶1和胱天蛋白酶家族的其他成员密切相关。它们被称为炎性胱天蛋白酶，这些酶处理并激活炎性细胞因子，如白细胞介素1和白细胞介素18。

基因[编辑]

该酶位于人类11号染色体上，与其他炎性胱天蛋白酶位于同一位点。^[4]许多可获得完整基因组数据的哺乳动物都已鉴定出CASP12直系同源物。^[5]

临床意义[编辑]

CASP12基因存在多态性，可以生成完整的胱天蛋白酶（Csp12L）或无活性的截短形式（Csp12S）。该功能形式似乎仅存在于非洲人后裔，并且与败血症的易感性有关。携带该功能基因的人对脂多糖（LPS）等细菌分子的反应会减弱。^[6]^[7]

麦吉尔大学健康中心于2009年5月的一项研究表明，雌激素可能会阻止胱天蛋白酶12的产生，从而导致对细菌病原体产生更强的炎症反应。该试验是在植入了人类胱天蛋白酶12基因的实验小鼠身上进行的。^[8]^[9]^[10]

大约60至10万年前开始的正选择，CASP12基因的非活性截短形式（Csp12S）在非非洲人群中传播并几乎是固定的。它的选择性优势被认为是体现为随着人口规模和密度的增加而经历更多传染病的人群对败血症的抵抗力。^[11]^[12]

参考文献[编辑]

^ 對Caspase 12 (gene/pseudogene)起作用的藥物；在維基數據上查看/編輯參考.
^ ^2.0 ^2.1 ^2.2 GRCh38: Ensembl release 89: ENSG00000204403 - Ensembl, May 2017
^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Fischer H, Koenig U, Eckhart L, Tschachler E. Human caspase 12 has acquired deleterious mutations. Biochem. Biophys. Res. Commun. 2002, 293 (2): 722–6. PMID 12054529. doi:10.1016/S0006-291X(02)00289-9.
^ OrthoMaM phylogenetic marker: CASP12 coding sequence. ^{[永久失效連結]}
^ Saleh M, Vaillancourt JP, Graham RK, Huyck M, Srinivasula SM, Alnemri ES, Steinberg MH, Nolan V, Baldwin CT, Hotchkiss RS, Buchman TG, Zehnbauer BA, Hayden MR, Farrer LA, Roy S, Nicholson DW. Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms. Nature. 2004, 429 (6987): 75–9. Bibcode:2004Natur.429...75S. PMID 15129283. doi:10.1038/nature02451 .
^ Saleh, Maya Mathison; John C. Wolinski; Melissa K. Bensinger; Steve J. Fitzgerald; Patrick Droin; Nathalie Ulevitch; Richard J. Green; Douglas R. Nicholson; Donald W. Enhanced bacterial clearance and sepsis resistance in caspase-12-deficient mice. Nature. 2006, 440 (7087): 1064–1068. Bibcode:2006Natur.440.1064S. PMID 16625199. S2CID 4321520. doi:10.1038/nature04656.
^ Yeretssian G, Doiron K, Shao W, Leavitt BR, Hayden MR, Nicholson DW, Saleh M. Gender differences in expression of the human caspase-12 long variant determines susceptibility to Listeria monocytogenes infection. Proc. Natl. Acad. Sci. U.S.A. May 2009, 106 (22): 9016–20. Bibcode:2009PNAS..106.9016Y. PMC 2690057 . PMID 19447924. doi:10.1073/pnas.0813362106 .
^ Man flu: real or myth?. Health. NHS UK. 2009-05-18 [23 May 2009]. （原始内容存档于16 February 2010）.
^ Women 'fight off disease better'. Health. BBC News. 2009-05-13 [2009-05-13]. （原始内容存档于2023-03-08）.
^ Xue, Yali; Daly, Allan; Yngvadottir, Bryndis; Liu, Mengning; Coop, Graham; Kim, Yuseob; Sabeti, Pardis; Chen, Yuan; Stalker, Jim; Huckle, Elizabeth; Burton, John; Leonard, Steven; Rogers, Jane; Tyler-Smith, Chris. Spread of an Inactive Form of Caspase-12 in Humans Is Due to Recent Positive Selection. The American Journal of Human Genetics. 2006, 78 (4): 659–670. PMC 1424700 . PMID 16532395. doi:10.1086/503116.
^ Wang, Xiaoxia; Grus, Wendy E.; Zhang, Jianzhi. Gene Losses during Human Origins. PLOS Biology. 2006, 4 (3): e52. PMC 1361800 . PMID 16464126. doi:10.1371/journal.pbio.0040052 .

外部链接[编辑]

肽酶及其抑制剂的MEROPS在线数据库：C14.013 （页面存档备份，存于互联网档案馆）

[1] 對Caspase 12 (gene/pseudogene)起作用的藥物；在維基數據上查看/編輯參考.

[refGRCh38Ensembl-2] 2.0 ^2.1 ^2.2 GRCh38: Ensembl release 89: ENSG00000204403 - Ensembl, May 2017

[3] Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] Fischer H, Koenig U, Eckhart L, Tschachler E. Human caspase 12 has acquired deleterious mutations. Biochem. Biophys. Res. Commun. 2002, 293 (2): 722–6. PMID 12054529. doi:10.1016/S0006-291X(02)00289-9.

[OrthoMaM-5] OrthoMaM phylogenetic marker: CASP12 coding sequence. ^{[永久失效連結]}

[6] Saleh M, Vaillancourt JP, Graham RK, Huyck M, Srinivasula SM, Alnemri ES, Steinberg MH, Nolan V, Baldwin CT, Hotchkiss RS, Buchman TG, Zehnbauer BA, Hayden MR, Farrer LA, Roy S, Nicholson DW. Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms. Nature. 2004, 429 (6987): 75–9. Bibcode:2004Natur.429...75S. PMID 15129283. doi:10.1038/nature02451 .

[7] Saleh, Maya Mathison; John C. Wolinski; Melissa K. Bensinger; Steve J. Fitzgerald; Patrick Droin; Nathalie Ulevitch; Richard J. Green; Douglas R. Nicholson; Donald W. Enhanced bacterial clearance and sepsis resistance in caspase-12-deficient mice. Nature. 2006, 440 (7087): 1064–1068. Bibcode:2006Natur.440.1064S. PMID 16625199. S2CID 4321520. doi:10.1038/nature04656.

[pmid19447924-8] Yeretssian G, Doiron K, Shao W, Leavitt BR, Hayden MR, Nicholson DW, Saleh M. Gender differences in expression of the human caspase-12 long variant determines susceptibility to Listeria monocytogenes infection. Proc. Natl. Acad. Sci. U.S.A. May 2009, 106 (22): 9016–20. Bibcode:2009PNAS..106.9016Y. PMC 2690057 . PMID 19447924. doi:10.1073/pnas.0813362106 .

[urlNHS-9] Man flu: real or myth?. Health. NHS UK. 2009-05-18 [23 May 2009]. （原始内容存档于16 February 2010）.

[urlBBC-10] Women 'fight off disease better'. Health. BBC News. 2009-05-13 [2009-05-13]. （原始内容存档于2023-03-08）.

[11] Xue, Yali; Daly, Allan; Yngvadottir, Bryndis; Liu, Mengning; Coop, Graham; Kim, Yuseob; Sabeti, Pardis; Chen, Yuan; Stalker, Jim; Huckle, Elizabeth; Burton, John; Leonard, Steven; Rogers, Jane; Tyler-Smith, Chris. Spread of an Inactive Form of Caspase-12 in Humans Is Due to Recent Positive Selection. The American Journal of Human Genetics. 2006, 78 (4): 659–670. PMC 1424700 . PMID 16532395. doi:10.1086/503116.

[12] Wang, Xiaoxia; Grus, Wendy E.; Zhang, Jianzhi. Gene Losses during Human Origins. PLOS Biology. 2006, 4 (3): e52. PMC 1361800 . PMID 16464126. doi:10.1371/journal.pbio.0040052 .

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