Sahasrabuddhe C G, Pathak S, Hsu T C
Chromosoma. 1978 Dec 6;69(3):331-8. doi: 10.1007/BF00332136.
Digestion of fixed metaphase chromosomes by endonucleases (micrococcal nuclease and DNase II) under optimal digestion conditions followed by Giemsa staining produces sharp banding patterns identical to G-bands. In 3H-thymidine labeled, synchronized metaphase cells of the chinese hamster (CHO line), the band induction is accompanied by the removal of DNA. The single strand specific nuclease S1 and DNase I do not produce such banding patterns.
在最佳消化条件下,用核酸内切酶(微球菌核酸酶和脱氧核糖核酸酶II)消化固定的中期染色体,随后进行吉姆萨染色,可产生与G带相同的清晰条带模式。在3H-胸腺嘧啶核苷标记的、同步化的中国仓鼠中期细胞(CHO系)中,条带的诱导伴随着DNA的去除。单链特异性核酸酶S1和脱氧核糖核酸酶I不会产生这种条带模式。