Celis J E, Ratz G P, Celis A
Department of Medical Biochemistry, Aarhus University, Denmark.
FEBS Lett. 1987 Nov 2;223(2):237-42. doi: 10.1016/0014-5793(87)80296-x.
A novel proliferation-sensitive and cell cycle-specific basic protein, termed progressin (Mr = 33,000), has been identified in proliferating human cells of epithelial, fibroblast and lymphoid origin. Progressin is synthesized almost exclusively during the S-phase of transformed human amnion cells (AMA). Increased synthesis of this protein is first detected late in G1, at or near the G1/S transition border, reaches a maximum in mid to late S-phase, and declines thereafter. Contrary to histones, progressin synthesis is not coupled to DNA replication. As expected for an S-phase-specific protein, no detectable synthesis of progressin was observed in non-proliferating human MRC-5 fibroblasts and epidermal basal keratinocytes. Elevated, but variable levels of this protein were observed in proliferating normal fibroblasts and transformed cells of fibroblast, epithelial and lymphoid origin. Taken together the above observations suggest that progressin may be a component of the common pathway leading to DNA replication and cell division.
一种名为进展素(Mr = 33,000)的新型增殖敏感且细胞周期特异性碱性蛋白已在源自上皮、成纤维细胞和淋巴细胞的增殖人细胞中被鉴定出来。进展素几乎仅在转化的人羊膜细胞(AMA)的S期合成。这种蛋白质合成的增加首先在G1晚期、G1/S转换边界处或附近被检测到,在S期中期至晚期达到最大值,此后下降。与组蛋白相反,进展素的合成与DNA复制不相关。正如对S期特异性蛋白的预期,在非增殖的人MRC - 5成纤维细胞和表皮基底角质形成细胞中未观察到进展素的可检测合成。在增殖的正常成纤维细胞以及源自成纤维细胞、上皮细胞和淋巴细胞的转化细胞中观察到该蛋白水平升高但有所变化。综上所述,上述观察结果表明进展素可能是导致DNA复制和细胞分裂的共同途径的一个组成部分。