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体外人淋巴细胞中X射线诱导畸变的染色体涂染分析

Chromosome painting analysis of X-ray-induced aberrations in human lymphocytes in vitro.

作者信息

Matsuoka A, Tucker J D, Hayashi M, Yamazaki N, Sofuni T

机构信息

Division of Genetics and Mutagenesis, National Institute of Hygienic Sciences, Tokyo, Japan.

出版信息

Mutagenesis. 1994 Mar;9(2):151-5. doi: 10.1093/mutage/9.2.151.

Abstract

Chromosomal rearrangements in human lymphocytes induced by X-rays (0, 0.5, 1.0 and 2.0 Gray) were analyzed using chromosome painting. DNA probes for human chromosomes 1, 3 or 4 alone, and a combination of 1 and 4, were used for analysis. The frequency of cells with rearrangements, i.e. reciprocal translocations, dicentrics, insertions, tricentrics and fragments, involving chromosome 4 increased with dose in both 48 and 72 h cultures. The number of translocations per cell also increased with dose at 48 and 72 h. Dicentrics increased with dose in 48 h but not in 72 h cultures. The estimated genomic frequency of aberrations per cell was comparable with results in banded cells. No difference was shown on the detection efficiency of chromosome rearrangements among the various DNA probes used. Since this technique does not necessarily require well-spread metaphases for analysis, it is possible to increase the number of analyzable metaphases compared with the banding technique. Chromosome painting is a simpler, more objective and more practical method for detecting chromosome rearrangements than conventional banding analyses.

摘要

使用染色体描绘技术分析了X射线(0、0.5、1.0和2.0戈瑞)诱导的人类淋巴细胞中的染色体重排。单独使用针对人类1号、3号或4号染色体的DNA探针,以及1号和4号染色体探针的组合进行分析。在48小时和72小时培养中,涉及4号染色体的重排细胞频率,即相互易位、双着丝粒、插入、三着丝粒和片段,随剂量增加而增加。在48小时和72小时时,每个细胞的易位数量也随剂量增加。双着丝粒在48小时培养中随剂量增加,但在72小时培养中并非如此。估计的每个细胞基因组畸变频率与带型细胞的结果相当。所使用的各种DNA探针在染色体重排检测效率上没有差异。由于该技术不一定需要分析分散良好的中期相,因此与带型技术相比,有可能增加可分析中期相的数量。与传统的带型分析相比,染色体描绘是一种更简单、更客观、更实用的检测染色体重排的方法。

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