{"title":"水痘-带状疱疹病毒感染和生化转化细胞中的脱氧胸腺嘧啶激酶。","authors":"T Ogino, P Lopetegui, K Yamanishi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Deoxythymidine kinase (TK) activity induced in varicella-zoster virus (VZV)-infected human embryonic fibroblast (HEF) cells was immunologically distinguishable from that in non infected HEF cells and also from that in herpes simplex virus type 1 (HSV-1) infected HEF cells. The TKs in VZV-biochemically transformed cells were immunologically the same as that induced in VZV-infected human cells and immunologically different from that in Ltk- cells or in HSV-biochemically transformed cells. One peak of TK activity with an Rm value of 0.8-0.9, corresponding to mitochondrial TK, was observed on polyacrylamide gel electrophoresis of Ltk- cell extracts. VZV infected Ltk- cells had two peaks of TK activity with Rm values of 0.45-0.5 (peak I) and 0.8-0.9 (peak II). Peak I and II were concluded to be virus-specific TK and mitochondrial TK, respectively. VZV-biochemically transformed cells had a peak of activity with an Rm value of 0.4-0.5, corresponding to peak I in VZV-infected Ltk- cells; that is VZV-specific TK activity. The present study indicates that VZV has a gene coding for its own TK.</p>","PeriodicalId":8767,"journal":{"name":"Biken journal","volume":"25 3","pages":"149-56"},"PeriodicalIF":0.0000,"publicationDate":"1982-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Deoxythymidine kinases in varicella-zoster virus infected and biochemically transformed cells.\",\"authors\":\"T Ogino, P Lopetegui, K Yamanishi\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Deoxythymidine kinase (TK) activity induced in varicella-zoster virus (VZV)-infected human embryonic fibroblast (HEF) cells was immunologically distinguishable from that in non infected HEF cells and also from that in herpes simplex virus type 1 (HSV-1) infected HEF cells. The TKs in VZV-biochemically transformed cells were immunologically the same as that induced in VZV-infected human cells and immunologically different from that in Ltk- cells or in HSV-biochemically transformed cells. One peak of TK activity with an Rm value of 0.8-0.9, corresponding to mitochondrial TK, was observed on polyacrylamide gel electrophoresis of Ltk- cell extracts. VZV infected Ltk- cells had two peaks of TK activity with Rm values of 0.45-0.5 (peak I) and 0.8-0.9 (peak II). Peak I and II were concluded to be virus-specific TK and mitochondrial TK, respectively. VZV-biochemically transformed cells had a peak of activity with an Rm value of 0.4-0.5, corresponding to peak I in VZV-infected Ltk- cells; that is VZV-specific TK activity. The present study indicates that VZV has a gene coding for its own TK.</p>\",\"PeriodicalId\":8767,\"journal\":{\"name\":\"Biken journal\",\"volume\":\"25 3\",\"pages\":\"149-56\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1982-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biken journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biken journal","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Deoxythymidine kinases in varicella-zoster virus infected and biochemically transformed cells.
Deoxythymidine kinase (TK) activity induced in varicella-zoster virus (VZV)-infected human embryonic fibroblast (HEF) cells was immunologically distinguishable from that in non infected HEF cells and also from that in herpes simplex virus type 1 (HSV-1) infected HEF cells. The TKs in VZV-biochemically transformed cells were immunologically the same as that induced in VZV-infected human cells and immunologically different from that in Ltk- cells or in HSV-biochemically transformed cells. One peak of TK activity with an Rm value of 0.8-0.9, corresponding to mitochondrial TK, was observed on polyacrylamide gel electrophoresis of Ltk- cell extracts. VZV infected Ltk- cells had two peaks of TK activity with Rm values of 0.45-0.5 (peak I) and 0.8-0.9 (peak II). Peak I and II were concluded to be virus-specific TK and mitochondrial TK, respectively. VZV-biochemically transformed cells had a peak of activity with an Rm value of 0.4-0.5, corresponding to peak I in VZV-infected Ltk- cells; that is VZV-specific TK activity. The present study indicates that VZV has a gene coding for its own TK.