{"title":"5-Azadeoxycytidine诱导了3种哺乳动物(Pipistrellus abramus, Millardia meltada和Apodemus argentteus) X染色体c区异型低凝聚","authors":"Michitada Okada, Y. Obara, K. Tsuchiya","doi":"10.11352/SCR.17.3","DOIUrl":null,"url":null,"abstract":"5-azadeoxycytidine (5-aza-dC)-induced undercondensation (UC) was described with cultured lung fibroblasts from three mammalian species, Pipistrellus abramus , Millardia meltada , and Apodemus argenteus , all of which carry a large amount of C-heterochromatin (C-block) on their X chromosomes. The C-blocks were GC-rich in P. abramus , AT/GC-balanced in M. meltada , and AT-rich in A. argenteus , as revealed by fluorescent staining with quinacrine mustard (QM) and chromomycin A 3 (CMA). P. abramus conspicuously undercondensed, irrespective of autosomes or gonosomes, in all C-band regions including C-blocks. The extent of UC was most prominent in P. abramus , rather weak in M. meltada , and weakest in A. argenteus , suggesting a close relation to the amount of GC base pairs contained in C-heterochromatin. Thus 5-aza-dC treatment may be an easy method for detect-ing GC-rich heterochromatin. The appropriate conditions for inducing UC in the C-blocks were 10 -5 –10 -6 M and 2–3 hours. The decondensing effect of 5-aza-dC on the C-blocks was time- and concentration-dependent in all species examined, asynchronously acting with certain time lag between the early-replicating X and late-repli-cating X. The heteromorphic UC between the C-blocks of the XX homologue was observed with a frequency of 8% at maximum, reflecting the allocyclic behavior of the C-blocks.","PeriodicalId":10221,"journal":{"name":"Chromosome science","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"5-Azadeoxycytidine induced heteromorphic undercondensation in the C-blocks of X chromosomes of three mammalian species, Pipistrellus abramus, Millardia meltada, and Apodemus argenteus\",\"authors\":\"Michitada Okada, Y. Obara, K. Tsuchiya\",\"doi\":\"10.11352/SCR.17.3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"5-azadeoxycytidine (5-aza-dC)-induced undercondensation (UC) was described with cultured lung fibroblasts from three mammalian species, Pipistrellus abramus , Millardia meltada , and Apodemus argenteus , all of which carry a large amount of C-heterochromatin (C-block) on their X chromosomes. The C-blocks were GC-rich in P. abramus , AT/GC-balanced in M. meltada , and AT-rich in A. argenteus , as revealed by fluorescent staining with quinacrine mustard (QM) and chromomycin A 3 (CMA). P. abramus conspicuously undercondensed, irrespective of autosomes or gonosomes, in all C-band regions including C-blocks. The extent of UC was most prominent in P. abramus , rather weak in M. meltada , and weakest in A. argenteus , suggesting a close relation to the amount of GC base pairs contained in C-heterochromatin. Thus 5-aza-dC treatment may be an easy method for detect-ing GC-rich heterochromatin. The appropriate conditions for inducing UC in the C-blocks were 10 -5 –10 -6 M and 2–3 hours. The decondensing effect of 5-aza-dC on the C-blocks was time- and concentration-dependent in all species examined, asynchronously acting with certain time lag between the early-replicating X and late-repli-cating X. The heteromorphic UC between the C-blocks of the XX homologue was observed with a frequency of 8% at maximum, reflecting the allocyclic behavior of the C-blocks.\",\"PeriodicalId\":10221,\"journal\":{\"name\":\"Chromosome science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chromosome science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11352/SCR.17.3\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chromosome science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11352/SCR.17.3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
5-Azadeoxycytidine induced heteromorphic undercondensation in the C-blocks of X chromosomes of three mammalian species, Pipistrellus abramus, Millardia meltada, and Apodemus argenteus
5-azadeoxycytidine (5-aza-dC)-induced undercondensation (UC) was described with cultured lung fibroblasts from three mammalian species, Pipistrellus abramus , Millardia meltada , and Apodemus argenteus , all of which carry a large amount of C-heterochromatin (C-block) on their X chromosomes. The C-blocks were GC-rich in P. abramus , AT/GC-balanced in M. meltada , and AT-rich in A. argenteus , as revealed by fluorescent staining with quinacrine mustard (QM) and chromomycin A 3 (CMA). P. abramus conspicuously undercondensed, irrespective of autosomes or gonosomes, in all C-band regions including C-blocks. The extent of UC was most prominent in P. abramus , rather weak in M. meltada , and weakest in A. argenteus , suggesting a close relation to the amount of GC base pairs contained in C-heterochromatin. Thus 5-aza-dC treatment may be an easy method for detect-ing GC-rich heterochromatin. The appropriate conditions for inducing UC in the C-blocks were 10 -5 –10 -6 M and 2–3 hours. The decondensing effect of 5-aza-dC on the C-blocks was time- and concentration-dependent in all species examined, asynchronously acting with certain time lag between the early-replicating X and late-repli-cating X. The heteromorphic UC between the C-blocks of the XX homologue was observed with a frequency of 8% at maximum, reflecting the allocyclic behavior of the C-blocks.