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表达T4内切核酸酶V的烟草植株对紫外线和DNA烷化剂表现出增强的敏感性。

Tobacco plants expressing T4 endonuclease V show enhanced sensitivity to ultraviolet light and DNA alkylating agents.

作者信息

Lapointe G, Mori T, Evans D H

机构信息

Department of Molecular Biology & Genetics, University of Guelph, Ontario, Canada.

出版信息

Mutat Res. 1996 Mar 26;351(1):19-31. doi: 10.1016/0027-5107(95)00193-x.

Abstract

DNA repair processes and UV-filtering pigments protect organisms from the cytotoxicity of UV light and endow plants with a high degree of natural UV resistance. In an attempt to further enhance this UV resistance we have constructed transgenic tobacco lines that express a DNA repair enzyme encoded by the bacteriophage T4 denV gene. The denV gene encodes endonuclease V, an enzyme which initiates base excision repair of cyclobutane pyrimidine dimers. Its presence is expected to provide transgenotes with a repair pathway complementary to, but likely distinct from, the repair pathways found in tobacco. The denV gene, flanked by a CaMV 35S promoter and poly(A) addition site, was introduced into tobacco and mature plants regenerated. The transgenotes expressed high levels of a UV-specific endonuclease and no such activity was found in control plants. Curiously, assays which detected several different biological endpoints showed that the denV+ transgenotes were also hypersensitive to UV-C light. This hypersensitivity segregated with the denV gene and was not caused by altered concentrations of UV-filtering pigments. Moreover, the denV+ transgenotes were also hypersensitive to high levels of baseless lesions that would be generated by a transgenically expressed beta-eliminating lyase such as endonuclease V.

摘要

DNA修复过程和紫外线过滤色素可保护生物体免受紫外线的细胞毒性,并赋予植物高度的天然抗紫外线能力。为了进一步增强这种抗紫外线能力,我们构建了转基因烟草品系,这些品系表达由噬菌体T4 denV基因编码的一种DNA修复酶。denV基因编码核酸内切酶V,该酶启动环丁烷嘧啶二聚体的碱基切除修复。预计它的存在将为转基因植株提供一条与烟草中发现的修复途径互补但可能不同的修复途径。将两侧带有CaMV 35S启动子和聚腺苷酸添加位点的denV基因导入烟草,并再生出成熟植株。转基因植株表达高水平的紫外线特异性核酸内切酶,而对照植株中未发现此类活性。奇怪的是,检测几种不同生物学终点的试验表明,denV+转基因植株对UV-C光也高度敏感。这种超敏反应与denV基因分离,并非由紫外线过滤色素浓度的改变引起。此外,denV+转基因植株对高水平的无碱基损伤也高度敏感,这些损伤可由转基因表达的β-消除裂解酶(如核酸内切酶V)产生。

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