Gatti M, Tanzarella C, Olivieri G
Genetics. 1974 Aug;77(4):701-19. doi: 10.1093/genetics/77.4.701.
A technique has been perfected for enabling good microscope preparations to be obtained from the larval ganglia of Drosophila melanogaster. This system was then tested with X-rays and an extensive series of data was obtained on the chromosome aberrations induced in the various stages of the cell cycle.-The analysis of the results obtained offers the following points of interest: (1) There exists a difference in radio-sensitivity between the two sexes. The females constantly display a greater frequency of both chromosome and chromatid aberrations. They also display a greater frequency of spontaneous aberrations. (2) In both sexes the overall chromosome damage is greater in cells irradiated in stages G(2) and G(1). These two peaks of greater radiosensitivity are produced by a high frequency of terminal deletions and chromatid exchanges and by a high frequency of dicentrics, respectively. (3) The aberrations are not distributed at random among the various chromosomes. On the average, the Y chromosome is found to be more resistant and the breaks are preferentially localized in the pericentromeric heterochromatin of the X chromosome and of the autosomes. (4) Somatic pairing influences the frequency and type of the chromosome aberrations induced. In this system, such an arrangement of the chromosomes results in a high frequency of exchanges and dicentrics between homologous chromosomes and a low frequency of scorable translocations. Moreover, somatic pairing, probably by preventing the formation of looped regions in the interphase chromosomes, results in the almost total absence of intrachanges at both chromosome and chromatid level.
一种从黑腹果蝇幼虫神经节获取优质显微镜标本的技术已臻完善。然后用X射线对该系统进行测试,并获得了一系列关于细胞周期各阶段诱导产生的染色体畸变的广泛数据。对所得结果的分析有以下几点值得关注:(1)两性之间存在放射敏感性差异。雌性染色体和染色单体畸变的频率始终更高。它们的自发畸变频率也更高。(2)在两性中,处于G(2)期和G(1)期的细胞受到辐射时,整体染色体损伤更大。这两个更高放射敏感性的峰值分别是由高频的末端缺失和染色单体交换以及高频的双着丝粒产生的。(3)畸变并非随机分布在不同染色体之间。平均而言,Y染色体更具抗性,断裂优先定位在X染色体和常染色体的着丝粒周围异染色质中。(4)体细胞配对会影响诱导产生的染色体畸变的频率和类型。在这个系统中,染色体的这种排列导致同源染色体之间高频的交换和双着丝粒以及低频的可计分易位。此外,体细胞配对可能通过阻止间期染色体中环状区域的形成,导致在染色体和染色单体水平上几乎完全没有内部交换。