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如荧光原位杂交所示,1.5千电子伏特的超软铝K X射线是复杂染色体交换畸变的有效产生源。

Ultrasoft 1.5 keV aluminum K X rays are efficient producers of complex chromosome exchange aberrations as revealed by fluorescence in situ hybridization.

作者信息

Griffin C S, Stevens D L, Savage J R

机构信息

MRC Radiation and Genome Stability Unit, Harwell, Didcot, United Kingdom.

出版信息

Radiat Res. 1996 Aug;146(2):144-50.

PMID:8693064
Abstract

The electron pairs generated by ultrasoft 1.5 keV aluminum K X-ray photons deposit their energy in tracks of length < 70 nm and provide an ideal tool for analyzing the spatial distribution of breaks and misrepair processes. We have undertaken the analysis of changes in chromosome structure produced by aluminum K X rays in untransformed HF12 human fibroblasts in G1 phase using fluorescence in situ hybridization (FISH). Multicolored chromosome-specific DNA probes for chromosomes 1 and 2 and an alpha-satellite pan-centromeric probe were used to examine in vitro radiation-induced chromosome-type exchange aberrations. After mean doses of 0.37-2.93 Gy the relative frequencies of complex exchanges, derived from three or more breaks in two or more chromosomes, ranged from 15-35%. For the classic break-age-and-rejoining theory to hold, very large interaction distances are needed to account for this high frequency of multibreak interactions, unless many sites pre-exist where several different chromosomes come very close together. Alternatively, damaged DNA may be able to interact with adjacent undamaged DNA, obviating the need for large rejoining distances.

摘要

由1.5 keV超软铝K X射线光子产生的电子对,将其能量沉积在长度小于70纳米的径迹中,为分析断裂和错配修复过程的空间分布提供了理想工具。我们利用荧光原位杂交(FISH)技术,对处于G1期的未转化HF12人成纤维细胞中铝K X射线产生的染色体结构变化进行了分析。使用针对1号和2号染色体的多色染色体特异性DNA探针以及一个α卫星全着丝粒探针,来检测体外辐射诱导的染色体类型交换畸变。平均剂量为0.37 - 2.93 Gy后,源自两条或更多条染色体上三个或更多断裂的复杂交换的相对频率在15% - 35%之间。要使经典的断裂 - 重接理论成立,需要非常大的相互作用距离来解释这种高频率的多断裂相互作用,除非预先存在许多不同染色体非常靠近的位点。或者,受损的DNA可能能够与相邻的未受损DNA相互作用,从而无需大的重接距离。

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