Mitsis P G
Department of Biochemistry, Beckman Center, Stanford University School of Medicine, California 94305, USA.
Dev Biol. 1995 Aug;170(2):445-56. doi: 10.1006/dbio.1995.1228.
The phosphorylation and localization of Drosophila melanogaster Replication Protein A (DRP-A) was examined during oogenesis and in single embryos during the syncytial nuclear divisions of embryogenesis. DRP-A from ovaries was separated by two-dimensional electrophoresis into multiple phosphorylated species that include a previously unresolved form of RP-A. These forms are developmentally regulated with a major phosphorylated form appearing at stage 11 of oogenesis and persisting into mature eggs. Actively cycling early embryos were examined to investigate DNA replication in the absence of repair synthesis due to perturbation by drugs or mutation. An oscillation of the two major forms of DPR-A was observed over multiple cell cycles. The phosphorylated form was most abundant at mitosis and the nonphosphorylated form at interphase. In contrast to other systems where a phosphorylated form of RP-A has been correlated with S phase, only the nonphosphorylated form of Drosophila RP-A is observed in early Drosophila embryos during DNA replication. Consistent with this role in DNA metabolism, DRP-A was localized to the nucleus. Subsequently at mitosis, DRP-A becomes delocalized. Strikingly, in ovaries a relatively large amount of DRP-A was observed during the early mitotic stages of oogenesis.
在卵子发生过程中以及胚胎发育的合胞体核分裂期间的单个胚胎中,对果蝇复制蛋白A(DRP-A)的磷酸化和定位进行了检测。通过二维电泳将来自卵巢的DRP-A分离为多种磷酸化形式,其中包括一种先前未解析的RP-A形式。这些形式受到发育调控,一种主要的磷酸化形式出现在卵子发生的第11阶段,并持续到成熟卵子中。对活跃循环的早期胚胎进行检测,以研究在由于药物干扰或突变而不存在修复合成的情况下的DNA复制。在多个细胞周期中观察到DPR-A的两种主要形式的振荡。磷酸化形式在有丝分裂时最为丰富,而非磷酸化形式在间期最为丰富。与其他系统中RP-A的磷酸化形式与S期相关不同,在果蝇早期胚胎的DNA复制过程中,仅观察到果蝇RP-A的非磷酸化形式。与在DNA代谢中的这一作用一致,DRP-A定位于细胞核。随后在有丝分裂时,DRP-A变得不再定位。引人注目的是,在卵子发生的早期有丝分裂阶段,在卵巢中观察到相对大量的DRP-A。