Aragon Anthony D, Quiñones Gabriel A, Thomas Edward V, Roy Sushmita, Werner-Washburne Margaret
Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.
Genome Biol. 2006;7(2):R9. doi: 10.1186/gb-2006-7-2-r9. Epub 2006 Feb 8.
As carbon sources are exhausted, Saccharomyces cerevisiae cells exhibit reduced metabolic activity and cultures enter the stationary phase. We asked whether cells in stationary phase cultures respond to additional stress at the level of transcript abundance.
Microarrays were used to quantify changes in transcript abundance in cells from stationary phase cultures in response to stress. More than 800 mRNAs increased in abundance by one minute after oxidative stress. A significant number of these mRNAs encode proteins involved in stress responses. We tested whether mRNA increases were due to new transcription, rapid poly-adenylation of message (which would not be detected by microarrays), or potential release of mature mRNA present in the cell but resistant to extraction during RNA isolation. Examination of the response to oxidative stress in an RNA polymerase II mutant, rpb1-1, suggested that new transcription was not required. Quantitative RT-PCR analysis of a subset of these transcripts further suggested that the transcripts present in isolated total RNA from stationary phase cultures were polyadenylated. In contrast, over 2,000 transcripts increased after protease treatment of cell-free lysates from stationary phase but not exponentially growing cultures. Different subsets of transcripts were released by oxidative stress and temperature upshift, suggesting that mRNA release is stress-specific.
Cells in stationary phase cultures contain a large number of extraction-resistant mRNAs in a protease-labile, rapidly releasable form. The transcript release appears to be stress-specific. We hypothesize that these transcripts are associated with P-bodies.
随着碳源耗尽,酿酒酵母细胞的代谢活性降低,培养物进入稳定期。我们探究处于稳定期培养的细胞在转录本丰度水平上是否对额外的应激作出反应。
利用微阵列定量分析处于稳定期培养的细胞在应激反应中转录本丰度的变化。氧化应激一分钟后,800多个mRNA的丰度增加。这些mRNA中有相当一部分编码参与应激反应的蛋白质。我们测试了mRNA增加是由于新转录、信息的快速多聚腺苷酸化(微阵列无法检测到),还是细胞中存在的成熟mRNA在RNA分离过程中难以提取但可能被释放出来。对RNA聚合酶II突变体rpb1-1的氧化应激反应进行检测,结果表明不需要新转录。对这些转录本的一个子集进行定量逆转录-聚合酶链反应分析,进一步表明从稳定期培养物中分离的总RNA中存在的转录本是多聚腺苷酸化的。相比之下,用蛋白酶处理来自稳定期而非指数生长期培养物的无细胞裂解物后,超过2000个转录本增加。氧化应激和温度升高释放出不同的转录本子集,表明mRNA释放具有应激特异性。
处于稳定期培养的细胞含有大量以蛋白酶不稳定、可快速释放形式存在的难以提取的mRNA。转录本释放似乎具有应激特异性。我们推测这些转录本与P小体相关。