Rasmussen C D, Berger J D
J Cell Sci. 1982 Oct;57:315-29. doi: 10.1242/jcs.57.1.315.
Two temperature-sensitive cell-cycle mutants were used to generate abnormally large cells (size estimated by protein content) with either normal or increased DNA contents. The first mutant, cc1, blocks DNA synthesis, but allows cell growth at the restrictive temperature. The cells do not progress through the cell cycle while at the restrictive temperature, but do recover and complete the cell cycle when returned to permissive conditions. The progeny have increased cell size and normal DNA content. Downward regulation of cell size occurs during the ensuing cell cycle at permissive temperature. Two processes are involved. First, the G1 period is reduced or eliminated. As initial cell size increases there is a progressive shortening of the cell cycle to 75% of normal. This limit cell-cycle duration is reached when the initial mass of the cell is equal to or greater than that of normal cells at the time of DNA synthesis initiation (0.25 of a cell cycle). Cells with the limit cell cycle begin macronuclear DNA synthesis immediately after fission. The durations of the S period and fission are normal. Second, the rate of cell growth is unaffected by the increase in cell size, and results in the partitioning of excess cell mass between the daughter cells at the next fission. The second mutant, cc2, blocks cell division, but allows DNA synthesis to occur at a reduced rate so that cells with up to about 140% of the normal initial DNA content and twice the normal cell mass can be produced. The pattern of cell-cycle shortening is the same as in ccl. The rates of growth and both the rate and amount of DNA synthesis are proportional to the initial DNA content. This suggests that the rates of growth and DNA synthesis are limited by the transcriptional activity of the macronucleus in both cc1 and cc2 cells when they begin the cell cycle with experimentally increased cell mass. Increases in both cell size and initial DNA content are required to bring about increases in the rates of growth and DNA accumulation.
利用两个温度敏感型细胞周期突变体来产生异常大的细胞(通过蛋白质含量估算细胞大小),这些细胞的DNA含量正常或增加。第一个突变体cc1会阻断DNA合成,但在限制温度下允许细胞生长。在限制温度下,细胞不会进入细胞周期,但回到允许条件时会恢复并完成细胞周期。其后代细胞大小增加而DNA含量正常。在允许温度下的后续细胞周期中,细胞大小会发生下调。这涉及两个过程。首先,G1期缩短或消除。随着初始细胞大小增加,细胞周期会逐渐缩短至正常的75%。当细胞的初始质量等于或大于DNA合成起始时正常细胞的质量(一个细胞周期的0.25)时,就会达到这个细胞周期持续时间的极限。具有极限细胞周期的细胞在分裂后立即开始大核DNA合成。S期和分裂期的持续时间正常。其次,细胞生长速率不受细胞大小增加的影响,这导致在下一次分裂时多余的细胞质量在子细胞之间分配。第二个突变体cc2会阻断细胞分裂,但允许以降低的速率进行DNA合成,从而可以产生初始DNA含量高达正常水平约140%且细胞质量为正常两倍的细胞。细胞周期缩短的模式与cc1相同。生长速率以及DNA合成的速率和量均与初始DNA含量成比例。这表明,当cc1和cc2细胞以实验性增加的细胞质量开始细胞周期时,它们的生长速率和DNA合成速率受到大核转录活性的限制。细胞大小和初始DNA含量的增加都需要才能实现生长速率和DNA积累的增加。