Sequence-specific damage induced by the impact of 3-30 eV electrons on oligonucleotides

被引:0
|
作者
Abdoul-Carime, H [1 ]
Sanche, L [1 ]
机构
[1] Univ Sherbrooke, Fac Med, Dept Med Nucl & Radiobiol, Grp Inst Canadiens Rech Sante Sci Radiat, Sherbrooke, PQ J1H 5N4, Canada
关键词
D O I
10.1667/0033-7587(2001)156[0151:SSDIBT]2.0.CO;2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability of low-energy electrons to induce single- and double-strand breaks in DNA has recently been demonstrated. Here we show the propensity of 3-30 eV electrons to initiate base sequence-dependent damage to a short single DNA strand. Solid monolayer films of homogeneous thymidine (T-9) and deoxycytidine (dCy(9)) and heterogeneous oligomers (T(6)dCy(3)) are bombarded with 1-30 eV electrons in an ultrahigh-vacuum system. CN, OCN and/or H2NCN are detected by a mass spectrometer as the most intense neutral fragments desorbing in vacuum. A weaker signal of CH3CCO is also detected, but only from oligonucleotides containing thymine. Below 17 eV, the energy dependence of the yields of CN, OCN and CH3CCO exhibits resonance-like structures, attributed to dissociative electron attachment (DEA). Above 17 eV, the monotonic increase in the fragment yields indicates that nonresonant processes (i.e. dipolar dissociation) control the fragmentation of these molecules. Within the energy range investigated, comparison of the magnitude of the total fragment yields produced by electron attack on dCy(9), T-6-dCy(3) and T-9 suggests the following order in the sensitivity of single-strand DNA: dCy(9) > T-6-dCy(3) > T-9. At 12 eV, the total fragment yields are found to be 5.8, 5.0 and 3.9 x 10(-3) fragment/electron, respectively. From the yields obtained with the two homo-oligonucleotides, we differentiate between contributions arising from the chemical nature of the base and the effect of environment (i.e. the sequence) when a thymidine unit in T-9 is replaced by dCy. The base sequence-dependent damage is found to vary with incident electron energy. These results reinforce the idea that genomic sensitivity to ionizing radiation depends on local genetic information. Furthermore, they underscore the possible role of low-energy electrons in the pathways responsible for the induction of specific genomic lesions. (C) 2001 by Radiation Research Society.
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页码:151 / 157
页数:7
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