Fry Rebecca C, DeMott Michael S, Cosgrove Joseph P, Begley Thomas J, Samson Leona D, Dedon Peter C
Department of Biological Engineering, Massachusetts Institute of Technology, NE47-277, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
BMC Genomics. 2006 Dec 12;7:313. doi: 10.1186/1471-2164-7-313.
Upon exposure to agents that damage DNA, Saccharomyces cerevisiae undergo widespread reprogramming of gene expression. Such a vast response may be due not only to damage to DNA but also damage to proteins, RNA, and lipids. Here the transcriptional response of S. cerevisiae specifically induced by DNA damage was discerned by exposing S. cerevisiae to a panel of three "radiomimetic" enediyne antibiotics (calicheamicin gamma1I, esperamicin A1 and neocarzinostatin) that bind specifically to DNA and generate varying proportions of single- and double-strand DNA breaks. The genome-wide responses were compared to those induced by the non-selective oxidant gamma-radiation.
Given well-controlled exposures that resulted in similar and minimal cell death (~20-25%) across all conditions, the extent of gene expression modulation was markedly different depending on treatment with the enediynes or gamma-radiation. Exposure to gamma-radiation resulted in more extensive transcriptional changes classified both by the number of genes modulated and the magnitude of change. Common biological responses were identified between the enediynes and gamma-radiation, with the induction of DNA repair and stress response genes, and the repression of ribosomal biogenesis genes. Despite these common responses, a fraction of the response induced by gamma radiation was repressed by the enediynes and vise versa, suggesting that the enediyne response is not entirely "radiomimetic." Regression analysis identified 55 transcripts with gene expression induction associated both with double- or single-strand break formation. The S. cerevisiae "DNA damage signature" genes as defined by Gasch et al. 1 were enriched among regulated transcripts associated with single-strand breaks, while genes involved in cell cycle regulation were associated with double-strand breaks.
Dissection of the transcriptional response in yeast that is specifically signaled by DNA strand breaks has identified that single-strand breaks provide the signal for activation of transcripts encoding proteins involved in the DNA damage signature in S. cerevisiae, and double-strand breaks signal changes in cell cycle regulation genes.
酿酒酵母在接触破坏DNA的因子后,会经历广泛的基因表达重编程。如此大规模的反应可能不仅是由于DNA受损,还可能是由于蛋白质、RNA和脂质受损。在此,通过将酿酒酵母暴露于一组三种“放射模拟”烯二炔抗生素(加利车霉素γ1I、埃斯帕霉素A1和新制癌菌素)来辨别由DNA损伤特异性诱导的酿酒酵母转录反应,这些抗生素特异性结合DNA并产生不同比例的单链和双链DNA断裂。将全基因组反应与由非选择性氧化剂γ射线诱导的反应进行比较。
在所有条件下进行了控制良好的暴露,导致相似且最小程度的细胞死亡(约20 - 25%),基因表达调节的程度根据烯二炔或γ射线处理而有显著差异。暴露于γ射线导致更广泛的转录变化,这可通过调节基因的数量和变化幅度来分类。在烯二炔和γ射线之间鉴定出共同的生物学反应,包括DNA修复和应激反应基因的诱导以及核糖体生物发生基因的抑制。尽管有这些共同反应,但γ射线诱导的一部分反应被烯二炔抑制,反之亦然,这表明烯二炔反应并非完全“放射模拟”。回归分析确定了55个转录本,其基因表达诱导与双链或单链断裂形成相关。Gasch等人定义的酿酒酵母“DNA损伤特征”基因在与单链断裂相关的调节转录本中富集,而参与细胞周期调节的基因与双链断裂相关。
对酵母中由DNA链断裂特异性发出信号的转录反应的剖析表明,单链断裂为酿酒酵母中参与DNA损伤特征的蛋白质编码转录本的激活提供信号,而双链断裂则为细胞周期调节基因的变化发出信号。