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sod 基因过表达和缺失突变对秀丽隐杆线虫主要解毒途径报告基因表达谱的影响。

Effects of sod gene overexpression and deletion mutation on the expression profiles of reporter genes of major detoxification pathways in Caenorhabditis elegans.

机构信息

Laboratory for Aging Physiology and Molecular Evolution, Department of Biology, Ghent University, K.L. Ledeganckstraat 35, Ghent, Belgium.

出版信息

Exp Gerontol. 2010 Aug;45(7-8):603-10. doi: 10.1016/j.exger.2010.01.014. Epub 2010 Jan 22.

DOI:10.1016/j.exger.2010.01.014
PMID:20096764
Abstract

Reactive oxygen species have long been considered a major cause of aging. However, previous work showed that loss of superoxide dismutase (SOD) only weakly affects lifespan of Caenorhabditis elegans. Here, we examined the impact of sod gene deletion and overexpression on the mRNA levels of the remaining sod genes and other detoxification genes. We detected no compensatory upregulation of other sod genes in any of the sod deletion mutants in both wild-type and daf-2(m577) genetic backgrounds when L4 larvae were shifted from 17 to 24 degrees C, and harvested as young adults. Elimination of MnSOD increased transcription of SKN-1 regulated genes and reduced transcription of multiple DAF-16 targets. Loss of the major Cu/ZnSOD isoform SOD-1 caused enhanced expression of subsets of both SKN-1 and DAF-16 targets when the animals were grown continuously at 24 degrees C, and strong overexpression of sod-1 induced a compensatory decrease in all tested SKN-1 regulated gst genes. When combined, these results suggest that low cytosolic SOD may activate SKN-1 signaling, whereas high levels may be repressive. Overall, our results suggest that sod gene manipulation causes complex, combinatorial regulation of expression of individual targets of stress sensitive transcription factors.

摘要

活性氧一直被认为是衰老的主要原因。然而,先前的工作表明,超氧化物歧化酶(SOD)的缺失仅微弱地影响秀丽隐杆线虫的寿命。在这里,我们研究了 sod 基因缺失和过表达对其余 sod 基因和其他解毒基因的 mRNA 水平的影响。我们在野生型和 daf-2(m577)遗传背景下,当 L4 幼虫从 17°C 转移到 24°C 并作为幼体收获时,没有检测到任何 sod 缺失突变体中其他 sod 基因的代偿性上调。MnSOD 的消除增加了 SKN-1 调控基因的转录,并降低了多个 DAF-16 靶基因的转录。当动物在 24°C 下连续生长时,主要的 Cu/ZnSOD 同工型 SOD-1 的缺失导致 SKN-1 和 DAF-16 靶基因的亚组表达增强,而 sod-1 的过表达强烈诱导所有测试的 SKN-1 调控的 gst 基因的代偿性下降。综合这些结果表明,低细胞溶质 SOD 可能激活 SKN-1 信号通路,而高浓度 SOD 可能具有抑制作用。总的来说,我们的结果表明,sod 基因操作导致应激敏感转录因子的个别靶基因的复杂组合调控。

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