Smith P A, Jackson V, Chalkley R
Biochemistry. 1984 Mar 27;23(7):1576-81. doi: 10.1021/bi00302a036.
HTC cells have been labeled by short exposures to [3H]thymidine in order to identify newly synthesized DNA. By either isolating nuclei directly or isolating them after an extensive fixation with formaldehyde, we have been able to identify two phases in the maturation process of newly replicated chromatin. The first phase which is relatively brief (less than 5 min) is reflected in a diffuse, irregular organization of nucleosomes on new DNA immediately postreplicatively . The second phase which lasts from 5 to 30 min postreplication is characterized by a normal repeat length for the nucleosomes which are nonetheless more weakly bound than bulk nucleosomes. This is reflected in increased sliding during nuclease digestion as well as increased nuclease sensitivity and the presence of easily dissociated histones which has been described by other workers.
通过短时间暴露于[3H]胸腺嘧啶核苷对HTC细胞进行标记,以鉴定新合成的DNA。通过直接分离细胞核或在用甲醛进行广泛固定后再分离细胞核,我们能够在新复制染色质的成熟过程中识别出两个阶段。第一个阶段相对较短(少于5分钟),表现为复制后立即在新DNA上核小体呈弥散、不规则的组织形式。第二个阶段在复制后持续5至30分钟,其特征是核小体的正常重复长度,但其结合比整体核小体更弱。这表现为核酸酶消化过程中滑动增加、核酸酶敏感性增加以及存在易于解离的组蛋白,其他研究人员也对此进行过描述。