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2
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本文引用的文献

1
THE GENETIC BASIS OF SOMATIC DAMAGE PRODUCED BY RADIATION IN THIRD INSTAR LARVAE OF DROSOPHILA MELANOGASTER. I. DEATH BEFORE MATURITY.黑腹果蝇三龄幼虫辐射产生的体细胞损伤的遗传基础。I. 成熟前死亡
Z Vererbungsl. 1963 Aug 13;94:143-62. doi: 10.1007/BF00895892.
2
Cytogenetic analysis of major heterochromatic elements (especially Xh and Y) in Drosophila melanogaster, and the theory of "heterochromatin".黑腹果蝇主要异染色质成分(尤其是Xh和Y)的细胞遗传学分析以及“异染色质”理论
Chromosoma. 1959;10:535-88. doi: 10.1007/BF00396588.
3
X-ray-induced chromosomal aberrations in vicia faba: changes in response during the cell cycle.X射线诱导的蚕豆染色体畸变:细胞周期中反应的变化
Mutat Res. 1967 Sep-Oct;4(5):579-99. doi: 10.1016/0027-5107(67)90044-9.
4
X-ray sensitivity during the cell generation cycle of cultured Chinese hamster cells.培养的中国仓鼠细胞在细胞生成周期中的X射线敏感性。
Radiat Res. 1966 Nov;29(3):450-74.
5
Radiosensitivity and repair time: the repair time of chromosome breaks produced during the different stages of the cell cycle.放射敏感性与修复时间:细胞周期不同阶段产生的染色体断裂的修复时间。
Mutat Res. 1969 May-Jun;7(3):441-51. doi: 10.1016/0027-5107(69)90115-8.
6
Studies on a recombination-deficient mutant of Drosophila. I. Dominant lethals.果蝇重组缺陷型突变体的研究。I. 显性致死
Mutat Res. 1969 Jul-Aug;8(1):91-100. doi: 10.1016/0027-5107(69)90144-4.
7
A study of the causes underlying the differences in radiosensitivity between mature spermatozoa and late spermatids in Drosophila.一项关于果蝇中成熟精子与晚期精细胞放射敏感性差异潜在原因的研究。
Mutat Res. 1969 Jul-Aug;8(1):111-25. doi: 10.1016/0027-5107(69)90146-8.
8
Repair of radiation-induced damage to chromosomes. Independence of known DNA dark repair mechanisms.辐射诱导的染色体损伤修复。已知DNA暗修复机制的独立性。
Exp Cell Res. 1969 Apr;55(1):9-16. doi: 10.1016/0014-4827(69)90447-9.
9
Chromosome aberrations and the cell cycle.染色体畸变与细胞周期
Radiat Res. 1968 Mar;33(3):609-19.
10
The effects of x-rays on the chromosomes of locust embryos. IV. Dose-response and variation in sensitivity of the cell cycle for the induction of chromatid aberrations.X射线对蝗虫胚胎染色体的影响。IV. 诱导染色单体畸变的剂量反应及细胞周期敏感性的变化
Chromosoma. 1967;20(4):413-41.

对X射线诱导的黑腹果蝇体细胞染色体畸变的分析。

Analysis of the chromosome aberrations induced by x-rays in somatic cells of Drosophila melanogaster.

作者信息

Gatti M, Tanzarella C, Olivieri G

出版信息

Genetics. 1974 Aug;77(4):701-19. doi: 10.1093/genetics/77.4.701.

DOI:10.1093/genetics/77.4.701
PMID:4214530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1213162/
Abstract

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.

摘要

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。