125I-UdR掺入位点对中国仓鼠细胞的染色体损伤。

W L Hughes, A C Weinblatt, W Prensky
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引用次数: 0

摘要

125i标记的碘脱氧尿苷(125I-UdR)在细胞周期s期结束时掺入中国仓鼠Don细胞,产生中期染色体畸变。记录全细胞、4号和5号染色体对以及X和Y染色体的染色体损伤和放射自显影银粒数。X染色体和Y染色体在S染色体后期被标记,其标记程度至少是4号和5号染色体的两倍,这两个染色体的大小相似,很容易识别。染色体损伤的发生率至少是同等剂量x射线预期的六倍,而损伤的发生率与每条染色体上的银颗粒数量直接相关。我们估计需要四到十次分裂才能产生可见的染色体畸变。染色体损伤局限于125I衰变的位置,这一发现最容易解释为在合并的125I原子衰变的位置出现了高能量的俄歇电子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chromosome damage in Chinese hamster cells produced by 125I-UdR at the site of its incorporation.

Metaphase chromosomal aberrations were produced by 125I-labeled iododeoxyuridine (125I-UdR) incorporated into Chinese hamster Don cells at the end of the S-period of the cell cycle. Chromosome damage and the number of autoradiographic silver grains were recorded for whole cells, for chromosome pairs No. 4 and No. 5, and for the X and the Y chromosomes. The X and the Y chromosomes, which label late in S, were at least twice as heavily labeled as chromosome pairs No. 4 and No. 5--two readily recognizable autosomes of similar size. The incidence of chromosome damage was at least six times that which would have been expected from equivalent doses of X-rays and the incidence of damage was directly related to the number of silver grains over each chromosome. We estimate that it takes four to ten disintegrations to produce a visible chromosome aberration. The finding that chromosome damage is localized at the site of the 125I decay is most readily explained by the high flux of low energy Auger electrons occurring at the site of the decay of the incorporated 125I atom.

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