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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >DNA DAMAGE CAN ALTER THE STABILITY OF NUCLEOSOMES - EFFECTS ARE DEPENDENT ON DAMAGE TYPE
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DNA DAMAGE CAN ALTER THE STABILITY OF NUCLEOSOMES - EFFECTS ARE DEPENDENT ON DAMAGE TYPE

机译:DNA损伤可以改变核糖体的稳定性-损伤类型的影响取决于

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We have investigated the effects of DNA damage by (+/-)-anti-benzo[a] pyrene diol epoxide (BPDE) and UV light on the formation of a positioned nucleosome in the Xenopus borealis 5S rRNA gene. Gel-shift analysis of the reconstituted products indicates that BPDE damage facilitates the formation of a nucleosome onto this sequence, Competitive reconstitution experiments show that average levels of 0.5, 0.9, and 2.1 BPDE adducts/146 bp of 5S DNA (i.e., the size of DNA associated with a nucleosome core particle) yield changes of -220, -290, and -540 cal/mol, respectively, in the free energy (Delta G) of nucleosome formation, These values yield increases of core histone binding to 5S DNA (K-a) of 1.4-, 1.6-, and 2.5-fold, compared with undamaged DNA, Conversely, irradiation with UV light decreases nucleosome formation, Irradiation at either 500 or 2500 J/m(2) of UV light [0.6 and 0.8 cyclobutane pyrimidine dimer/146 bp (on average), respectively] results in respective changes of +130 and +250 cal/mol, This translates to decreases In core histone binding to irradiated 5S DNA (K-a) of 1.2- and 1.5-fold compared with undamaged DNA, These results indicate that nucleosome stability can be markedly affected by the formation of certain DNA lesions, Such changes could have major effects on the kinetics of DNA processing events. [References: 58]
机译:我们已经研究了(+/-)-抗-苯并[a]二醇环氧化物(BPDE)和紫外线对DNA的影响,对非洲爪蟾5S rRNA基因中定位核小体的形成。重构产物的凝胶位移分析表明BPDE损伤促进了该序列上核小体的形成。竞争性重构实验表明,平均水平为0.5、0.9和2.1 BPDE加合物/ 146 bp的5S DNA(即与核小体核心颗粒相关的DNA)在核小体形成的自由能(ΔG)中分别产生-220,-290和-540 cal / mol的变化。这些值使核心组蛋白与5S DNA的结合增加( Ka)是未损坏DNA的1.4倍,1.6倍和2.5倍,反之,用紫外线照射会减少核小体的形成,以500或2500 J / m(2)的紫外线照射[0.6和0.8环丁烷嘧啶二聚体/ 146 bp(平均),分别导致+130和+250 cal / mol的变化,与未受损伤的5S DNA(Ka)相比,核心组蛋白的结合降低了1.2到1.5倍DNA,这些结果表明核小体稳定性可以受到某些DNA损伤形成的明显影响,这种变化可能会对DNA加工过程的动力学产生重大影响。 [参考:58]

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