Maszewski J, Kwiatkowska M
Folia Histochem Cytobiol. 1984;22(1):9-19.
In antheridial filaments of Chara vulgaris the number of nucleoli within a single cell nucleus ranges from 3 to 12. The sizes of nucleoli vary from 0.2 to 3.5 micron in diameter. Mean number of micronucleoli, i.e. the smallest nucleoli of 0.2-0.5 micron in diameter which are distinguished after silver staining is higher than that estimated with the use of toluidine blue method according to Smetana et al. [34], the latter procedure resulting in a less contrasting visualization. Throughout the course of the whole period of interphase the mean number of nucleoli was found unchanged in successive phases and it equals some 6.5 per nucleus. Concurrently, the total volume of nucleoli increases progressively reaching maximum value by the end of the G2 phase which is attributed to the increase in number of largest nucleoli. On the basis of the analysis of 3H uridine incorporation and an in situ determination of RNA polymerase activity using the method adopted by Moore and Ringertz [25] it was evidenced that the mean transcriptional activity of nucleoli larger than 0.5 micron in diameter is not dependent upon nucleolar number within a single nucleus. It is concluded that the diverse appearance of nucleoli in cells being located precisely at the same stage of interphase reflects temporal changes of their sizes consisting in an asynchronous pulsation of individual nucleoli.
在普通轮藻的雄器丝中,单个细胞核内核仁的数量在3到12个之间。核仁直径大小在0.2到3.5微米之间变化。微核仁的平均数量,即直径为0.2 - 0.5微米的最小核仁(经银染后可区分)高于根据斯梅塔纳等人[34]使用甲苯胺蓝法估计的数量,后一种方法导致的可视化对比度较低。在整个间期过程中,连续各阶段核仁的平均数量保持不变,每个细胞核约为6.5个。同时,核仁的总体积逐渐增加,在G2期结束时达到最大值,这归因于最大核仁数量的增加。基于对3H尿苷掺入的分析以及使用摩尔和林格茨[25]采用的方法对RNA聚合酶活性进行原位测定,结果表明直径大于0.5微米的核仁的平均转录活性不依赖于单个细胞核内核仁的数量。得出的结论是,处于精确相同间期阶段的细胞中核仁的不同外观反映了它们大小的时间变化,即单个核仁的异步脉动。