Stevens A R, Pachler P F
J Cell Biol. 1973 May;57(2):525-37. doi: 10.1083/jcb.57.2.525.
Alterations in transcription that precede and accompany encystment (E) of suspension grown A. castellanii have been investigated. Comparative studies were performed on cells undergoing spontaneous E in high density stationary phase cultures or after experimental induction of E at low cell densities by deprivation of nutrients in exponential growth. Onset of growth deceleration at high cell densities was accompanied by an increase in the cellular RNA. The maximum RNA content occurred in cells at stationary phase and subsequently declined with the appearance of cysts in the cultures. On the contrary, the RNA content in cells whose growth was immediately terminated by experimental E induction remained at a constant exponential level through 5 h postinduction and then began to decline shortly before the appearance of cysts. The mature cyst formed in stationary phase cultures and after experimental E induction contained an equivalent amount of RNA ( approximately 50% of the exponential value). Comparison of the kinetics of [(3)H]uridine incorporation demonstrated that there was an abrupt reduction in the rate of uridine incorporation into RNA with onset of growth deceleration or after growth termination in experimental E induction. The reduced incorporation of uridine into RNA could not be attributed to to a reduced uptake of the isotope by the cells or an altered capacity of the cells to phosphorylate uridine. Uridine continued to be incorporated into RNA at a reduced rate in cells throughout growth deceleration, in stationary phase, and up to 12 h postexperimental induction. Considered together, these results indicate that a buildup in RNA is not necessary for induction of encystment in acanthamoeba. The accumulated RNA in stationary phase cells appears to be due to the greater reduction in the growth rate than in transcription and the absence of RNA turnover in cells during growth deceleration. Initiation of RNA turnover appears to accompany growth termination and induction of E. The results further demonstrate that the regulation of the rate of transcription is closely coordinated with the control of growth and encystment in acanthamoeba.
对悬浮培养的卡氏棘阿米巴在包囊形成(E)之前及伴随过程中的转录变化进行了研究。对在高密度稳定期培养物中经历自发包囊形成的细胞,或在指数生长期通过剥夺营养在低细胞密度下实验诱导包囊形成后的细胞进行了比较研究。在高细胞密度下生长减速开始时,细胞RNA含量增加。RNA含量在稳定期细胞中达到最大值,随后随着培养物中囊肿的出现而下降。相反,通过实验诱导包囊形成而立即终止生长的细胞中的RNA含量在诱导后5小时内保持在恒定的指数水平,然后在囊肿出现前不久开始下降。在稳定期培养物和实验诱导包囊形成后形成的成熟囊肿含有等量的RNA(约为指数期值的50%)。对[³H]尿苷掺入动力学的比较表明,随着生长减速开始或在实验诱导包囊形成后生长终止,尿苷掺入RNA的速率急剧降低。尿苷掺入RNA减少不能归因于细胞对同位素摄取减少或细胞磷酸化尿苷能力改变。在整个生长减速、稳定期以及实验诱导后长达12小时内,尿苷继续以降低的速率掺入细胞中的RNA。综合考虑,这些结果表明RNA积累对于棘阿米巴包囊形成诱导并非必要。稳定期细胞中积累的RNA似乎是由于生长速率的降低幅度大于转录速率,以及在生长减速期间细胞中不存在RNA周转。RNA周转的启动似乎伴随着生长终止和包囊形成诱导。结果进一步表明,转录速率的调节与棘阿米巴生长和包囊形成的控制密切协调。