Transcriptional responses to biologically relevant doses of UV-B radiation in the model archaeon, Halobacterium sp. NRC-1.

Ivan Boubriak, Wooi Loon Ng, Priya DasSarma, Shiladitya DasSarma, David J Crowley, Shirley J McCready
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引用次数: 44

Abstract

Background: Most studies of the transcriptional response to UV radiation in living cells have used UV doses that are much higher than those encountered in the natural environment, and most focus on short-wave UV (UV-C) at 254 nm, a wavelength that never reaches the Earth's surface. We have studied the transcriptional response of the sunlight-tolerant model archaeon, Halobacterium sp. NRC-1, to low doses of mid-wave UV (UV-B) to assess its response to UV radiation that is likely to be more biologically relevant.

Results: Halobacterium NRC-1 cells were irradiated with UV-B at doses equivalent to 30 J/m2 and 5 J/m2 of UV-C. Transcriptional profiling showed that only 11 genes were up-regulated 1.5-fold or more by both UV-B doses. The most strongly up-regulated gene was radA1 (vng2473), the archaeal homologue of RAD51/recA recombinase. The others included arj1 (vng779) (recJ-like exonuclease), top6A (vng884) and top6B (vng885) (coding for Topoisomerase VI subunits), and nrdJ (vng1644) (which encodes a subunit of ribonucleotide reductase). We have found that four of the consistently UV-B up-regulated genes, radA1 (vng2473), vng17, top6B (vng885) and vng280, share a common 11-base pair motif in their promoter region, TTTCACTTTCA. Similar sequences were found in radA promoters in other halophilic archaea, as well as in the radA promoter of Methanospirillum hungatei. We analysed the transcriptional response of a repair-deficient DeltauvrA (vng2636) DeltauvrC (vng2381) double-deletion mutant and found common themes between it and the response in repair proficient cells.

Conclusion: Our results show a core set of genes is consistently up-regulated after exposure to UV-B light at low, biologically relevant doses. Eleven genes were up-regulated, in wild-type cells, after two UV-B doses (comparable to UV-C doses of 30 J/m2 and 5 J/m2), and only four genes were up-regulated by all doses of UV-B and UV-C that we have used in this work and previously. These results suggest that high doses of UV-C radiation do not necessarily provide a good model for the natural response to environmental UV. We have found an 11-base pair motif upstream of the TATA box in four of the UV-B up-regulated genes and suggest that this motif is the binding site for a transcriptional regulator involved in their response to UV damage in this model archaeon.

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模式古菌盐杆菌NRC-1对UV-B辐射生物学相关剂量的转录反应
背景:大多数关于活细胞对紫外线辐射的转录反应的研究都使用了比自然环境中更高的紫外线剂量,而且大多数研究都集中在254 nm的短波紫外线(UV- c)上,这一波长从未到达地球表面。我们研究了耐日光模式古细菌,盐杆菌sp. NRC-1对低剂量中波紫外线(UV- b)的转录反应,以评估其对紫外线辐射的反应,这可能与生物学更相关。结果:用相当于30 J/m2和5 J/m2 UV-C剂量的UV-B照射盐杆菌NRC-1细胞。转录谱分析显示,只有11个基因在两种UV-B剂量下上调1.5倍或更多。上调幅度最大的基因是radA1 (vng2473),这是RAD51/recA重组酶的古细菌同源基因。其他包括arj1 (vng779) (rej样外切酶),top6A (vng884)和top6B (vng885)(编码拓扑异构酶VI亚基)和nrdJ (vng1644)(编码核糖核苷酸还原酶亚基)。我们发现四个持续UV-B上调的基因,radA1 (vng2473), vng17, top6B (vng885)和vng280,在它们的启动子区域TTTCACTTTCA有一个共同的11碱基对基序。在其他嗜盐古菌的radA启动子中也发现了类似的序列,在亨盖特甲烷螺旋菌的radA启动子中也发现了类似的序列。我们分析了修复缺陷DeltauvrA (vng2636)和DeltauvrC (vng2381)双缺失突变体的转录反应,并发现了它与修复熟练细胞中的应答之间的共同主题。结论:我们的研究结果表明,一组核心基因在暴露于低剂量的UV-B光后持续上调。在野生型细胞中,11个基因在两次UV-B剂量(相当于30 J/m2和5 J/m2的UV-C剂量)后上调,只有4个基因在我们在本工作和之前使用的所有剂量的UV-B和UV-C中上调。这些结果表明,高剂量的UV- c辐射不一定能提供对环境紫外线的自然反应的良好模型。我们在四个UV- b上调基因的TATA盒上游发现了一个11碱基对基序,并表明该基序是参与该模型古菌对UV损伤反应的转录调节因子的结合位点。
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