Steinemann M
Chromosoma. 1981;82(2):289-307. doi: 10.1007/BF00286112.
Using DNA fiber autoradiography, the rate of fork movement in D. virilis salivary glands was determined to be 0.1 micron/ml (25 degrees C). This value is 3.5 times slower than the replication rate determined in the diploid brain cells using the same experimental conditions (Steinemann, 1981). Replicon lengths in the polytene cells span from 5 to 203 micron, with a mean of approximately x = 46.7 micron and a median of approximately x = 39.5 micron. The polytene replicon length is about the same as that for diploid brain cells (31.0 micron). Dividing the haploid genome of D. virilis by the estimated number of 5,000 bands and taking the resulting 13.6 micron as average DNA length per chromomere, the average replicon length covers 3.4 chromomere units. This result does not support the concept that "one-band-plus interband" behaves as a replicating unit (Pelling, 1966). From the positive skew of the replicon length distributions, combined with the results derived from the chromosomal labelling patterns, the following schedule of chromosomal euchromatin doubling is infered: A short initiation period (discontinuous phase I), asynchronous with respect to individual origins, is followed by a phase of common replication activity at all inducible origins (continuous phase). The discontinuous II pattern is formed by few, long replicons which are still replicating while the shorter ones have already finished (weak points are not considered). Replicons, distributed in the main peak of the histogram and smaller than about 100 micron, are then responsible for the replication of the bulk of chromosomal euchromatin, the continuous phase. the interpretation is in conflict with the hypothesis assuming a clustered organization of the replicons to explain spot labelling (reviewed in Hand 1978). The diploid karyotype of D. virilis contains 45% satellite sequences, located in the alpha-heterochromatin (Gall et al., 1971). They do not replicate in the highly polytene salivary gland cells of 3rd instar larvae. Comparison of DNA fiber autoradiograph patterns from salivary glands and brains suggests that these satellite sequences replicate in short (less than 10 micron), to some extent irregularly spaced replicons.
利用DNA纤维放射自显影技术,测定出果蝇唾液腺中复制叉移动速率为0.1微米/分钟(25摄氏度)。该值比在相同实验条件下二倍体脑细胞中测定的复制速率慢3.5倍(施泰内曼,1981年)。多线细胞中的复制子长度范围为5至203微米,平均约为x = 46.7微米,中位数约为x = 39.5微米。多线复制子长度与二倍体脑细胞的复制子长度(31.0微米)大致相同。将果蝇的单倍体基因组除以估计的5000条带数,并将所得的13.6微米作为每个染色粒的平均DNA长度,平均复制子长度覆盖3.4个染色粒单位。这一结果不支持“一条带加带间区”作为复制单位的概念(佩林,196)。从复制子长度分布的正偏态,结合染色体标记模式得出的结果,可以推断出以下染色体常染色质加倍的时间表:一个短暂的起始期(不连续的第一阶段),相对于各个起始点是异步的,随后是所有可诱导起始点共同进行复制活动的阶段(连续阶段)。不连续的第二模式由少数长复制子形成,当较短的复制子已经完成复制时,这些长复制子仍在复制(不考虑弱点)。分布在直方图主峰且小于约100微米的复制子,随后负责大部分染色体常染色质的复制,即连续阶段。这一解释与假设复制子呈簇状组织以解释斑点标记的假说是相互矛盾的(汉德1978年综述)。果蝇的二倍体核型包含45%的卫星序列,位于α-异染色质中(高尔等人,1971年)。它们在三龄幼虫的高度多线唾液腺细胞中不进行复制。唾液腺和大脑的DNA纤维放射自显影片模式的比较表明,这些卫星序列在短(小于10微米)且在一定程度上间隔不规则的复制子中进行复制。