Martelli A M, Gilmour R S, Bareggi R, Cocco L
Istituto di Anatomia Umana Normale, Bologna, Italy.
Exp Cell Res. 1992 Aug;201(2):470-6. doi: 10.1016/0014-4827(92)90296-k.
HeLa S3 cells were synchronized by a double thymidine block or aphidicolin treatment and the levels of nuclear matrix-bound DNA polymerase alpha activity were then measured using activated calf thymus DNA as template. The nuclear matrix was obtained by 2 M NaCl extraction and DNase I digestion of isolated nuclei incubated at 37 degrees C for 45 min prior to subfractionation. In all phases of the cell cycle 25-30% of nuclear DNA polymerase alpha activity remained matrix-bound, even when cells were in the G1 phase. No dynamic association of DNA polymerase alpha activity with the matrix was seen, at variance with previous results obtained in regenerating rat liver. The variations measured in matrix-bound activity closely followed those detected in isolated nuclei throughout the cell cycle. If nuclei were not heat-stabilized very low levels of DNA polymerase alpha activity were measured in the matrix (1-2% of total nuclear activity). Heat incubation of nuclei failed to produce any enrichment in matrix-associated newly replicated DNA, whereas the sulfhydryl cross-linking chemical sodium tetrathionate did. Therefore the results obtained after the heat stabilization procedure do not completely fit with the model that envisions the nuclear matrix as the active site where eucaryotic DNA replication takes place.
采用双胸腺嘧啶核苷阻断法或阿非迪霉素处理使HeLa S3细胞同步化,然后以活化的小牛胸腺DNA为模板,测定与核基质结合的DNA聚合酶α活性水平。核基质通过2M NaCl抽提并对在37℃温育45分钟后的分离细胞核进行DNase I消化获得,之后再进行亚分级分离。在细胞周期的所有阶段,即便细胞处于G1期,仍有25% - 30%的核DNA聚合酶α活性与基质结合。未观察到DNA聚合酶α活性与基质的动态关联,这与先前在再生大鼠肝脏中获得的结果不同。在整个细胞周期中,与基质结合的活性变化与在分离细胞核中检测到的变化密切相关。如果细胞核未进行热稳定处理,则在基质中测得的DNA聚合酶α活性水平非常低(占总核活性的1% - 2%)。细胞核的热孵育未能使与基质相关的新复制DNA产生任何富集,而巯基交联化学试剂连四硫酸钠则可以。因此,热稳定处理后获得的结果并不完全符合将核基质设想为真核生物DNA复制发生的活性位点的模型。