Celis J E, Nielsen S
Proc Natl Acad Sci U S A. 1986 Nov;83(21):8187-90. doi: 10.1073/pnas.83.21.8187.
Studies of the polypeptides synthesized by normal and transformed human cultured cells under a variety of physiological conditions have revealed a basic 54-kDa protein NEPHGE 10a, whose rate of synthesis is sensitive to changes in the rate of cell proliferation. This nuclear phosphoprotein, which we have termed "dividin" (present only in populations of cells committed to divide), is synthesized almost exclusively during the S phase of the cell cycle of transformed human amnion cells (AMA). Dividin synthesis is first detected late in G1 near the G1/S transition border, reaches a maximum late in S phase, and declines thereafter. As expected for an S phase-specific protein, no detectable synthesis of dividin was observed in growth-arrested normal human cultured cells of epithelial and fibroblast origin. These findings suggest a role for this protein in events leading to DNA replication and cell division.
对正常和转化的人类培养细胞在各种生理条件下合成的多肽进行的研究揭示了一种基本的54 kDa蛋白NEPHGE 10a,其合成速率对细胞增殖速率的变化敏感。这种核磷蛋白,我们称之为“分裂素”(仅存在于致力于分裂的细胞群体中),几乎只在转化的人类羊膜细胞(AMA)细胞周期的S期合成。分裂素的合成首先在G1晚期靠近G1/S转换边界处被检测到,在S期晚期达到最大值,然后下降。正如对S期特异性蛋白所预期的那样,在生长停滞的上皮和成纤维细胞来源的正常人类培养细胞中未观察到分裂素的可检测合成。这些发现表明该蛋白在导致DNA复制和细胞分裂的事件中发挥作用。