{"title":"人间期细胞中X和Y染色质的荧光。","authors":"A. B. Mukherjee, G. Moser, H. Nitowsky","doi":"10.1097/00006254-197303000-00014","DOIUrl":null,"url":null,"abstract":"The fluorescent characteristics of X (sex) and Y chromatin of human interphase nuclei stained with quinacrine mustard (QM) were studied in fibroblast-like cell cultures derived from several different tissues. X chromatin in female cells was clearly distinguishable from Y chromatin in male cells on the basis of size and fluorescent intensity. The frequency of X chromatin was dependent on cell density in vitro, whereas the frequency of Y chromatin was independent of cell density. The fluorescent intensity of X chromatin in cultured cells was much stronger than that in uncultured cells, such as those of the oral mucosa. The intensity of Y-chromatin fluorescence, however, was nearly the same in both cultured and uncultured cells. Nuclei first stained with QM, photographed, and then restained with thionin and rephotographed showed identical X- and Y-chromatin morphology.","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"11 3 1","pages":"216-27"},"PeriodicalIF":0.0000,"publicationDate":"1973-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1097/00006254-197303000-00014","citationCount":"21","resultStr":"{\"title\":\"Fluorescence of X and Y chromatin in human interphase cells.\",\"authors\":\"A. B. Mukherjee, G. Moser, H. Nitowsky\",\"doi\":\"10.1097/00006254-197303000-00014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The fluorescent characteristics of X (sex) and Y chromatin of human interphase nuclei stained with quinacrine mustard (QM) were studied in fibroblast-like cell cultures derived from several different tissues. X chromatin in female cells was clearly distinguishable from Y chromatin in male cells on the basis of size and fluorescent intensity. The frequency of X chromatin was dependent on cell density in vitro, whereas the frequency of Y chromatin was independent of cell density. The fluorescent intensity of X chromatin in cultured cells was much stronger than that in uncultured cells, such as those of the oral mucosa. The intensity of Y-chromatin fluorescence, however, was nearly the same in both cultured and uncultured cells. Nuclei first stained with QM, photographed, and then restained with thionin and rephotographed showed identical X- and Y-chromatin morphology.\",\"PeriodicalId\":78202,\"journal\":{\"name\":\"Cytogenetics\",\"volume\":\"11 3 1\",\"pages\":\"216-27\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1973-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1097/00006254-197303000-00014\",\"citationCount\":\"21\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cytogenetics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1097/00006254-197303000-00014\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytogenetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/00006254-197303000-00014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fluorescence of X and Y chromatin in human interphase cells.
The fluorescent characteristics of X (sex) and Y chromatin of human interphase nuclei stained with quinacrine mustard (QM) were studied in fibroblast-like cell cultures derived from several different tissues. X chromatin in female cells was clearly distinguishable from Y chromatin in male cells on the basis of size and fluorescent intensity. The frequency of X chromatin was dependent on cell density in vitro, whereas the frequency of Y chromatin was independent of cell density. The fluorescent intensity of X chromatin in cultured cells was much stronger than that in uncultured cells, such as those of the oral mucosa. The intensity of Y-chromatin fluorescence, however, was nearly the same in both cultured and uncultured cells. Nuclei first stained with QM, photographed, and then restained with thionin and rephotographed showed identical X- and Y-chromatin morphology.