Lu Peng, Nakorchevskiy Aleksey, Marcotte Edward M
Department of Chemistry and Biochemistry, Center for Computational Biology and Bioinformatics, 1 University Station, A4800, University of Texas, Austin, TX 78712-0159, USA.
Proc Natl Acad Sci U S A. 2003 Sep 2;100(18):10370-5. doi: 10.1073/pnas.1832361100. Epub 2003 Aug 21.
Cells grow in dynamically evolving populations, yet this aspect of experiments often goes unmeasured. A method is proposed for measuring the population dynamics of cells on the basis of their mRNA expression patterns. The population's expression pattern is modeled as the linear combination of mRNA expression from pure samples of cells, allowing reconstruction of the relative proportions of pure cell types in the population. Application of the method, termed expression deconvolution, to yeast grown under varying conditions reveals the population dynamics of the cells during the cell cycle, during the arrest of cells induced by DNA damage and the release of arrest in a cell cycle checkpoint mutant, during sporulation, and following environmental stress. Using expression deconvolution, cell cycle defects are detected and temporally ordered in 146 yeast deletion mutants; six of these defects are independently experimentally validated. Expression deconvolution allows a reinterpretation of the cell cycle dynamics underlying all previous microarray experiments and can be more generally applied to study most forms of cell population dynamics.
细胞在动态演化的群体中生长,但实验的这一方面往往未被测量。本文提出了一种基于细胞mRNA表达模式来测量细胞群体动态的方法。群体的表达模式被建模为细胞纯样本mRNA表达的线性组合,从而能够重建群体中纯细胞类型的相对比例。将这种称为表达反卷积的方法应用于在不同条件下生长的酵母,揭示了细胞在细胞周期、DNA损伤诱导的细胞停滞以及细胞周期检查点突变体中停滞解除过程、孢子形成过程和环境应激后的群体动态。使用表达反卷积,在146个酵母缺失突变体中检测到细胞周期缺陷并按时间顺序排列;其中六个缺陷得到了独立的实验验证。表达反卷积能够重新解读此前所有微阵列实验背后的细胞周期动态,并且更广泛地应用于研究大多数形式的细胞群体动态。