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基因表达谱的基本模式:从复杂中提炼简单

Fundamental patterns underlying gene expression profiles: simplicity from complexity.

作者信息

Holter N S, Mitra M, Maritan A, Cieplak M, Banavar J R, Fedoroff N V

机构信息

Department of Physics and Center for Materials Physics, 104 Davey Laboratory, Consortium, 519 Wartik Laboratory, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.

出版信息

Proc Natl Acad Sci U S A. 2000 Jul 18;97(15):8409-14. doi: 10.1073/pnas.150242097.

DOI:10.1073/pnas.150242097
PMID:10890920
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC26961/
Abstract

Analysis of previously published sets of DNA microarray gene expression data by singular value decomposition has uncovered underlying patterns or "characteristic modes" in their temporal profiles. These patterns contribute unequally to the structure of the expression profiles. Moreover, the essential features of a given set of expression profiles are captured using just a small number of characteristic modes. This leads to the striking conclusion that the transcriptional response of a genome is orchestrated in a few fundamental patterns of gene expression change. These patterns are both simple and robust, dominating the alterations in expression of genes throughout the genome. Moreover, the characteristic modes of gene expression change in response to environmental perturbations are similar in such distant organisms as yeast and human cells. This analysis reveals simple regularities in the seemingly complex transcriptional transitions of diverse cells to new states, and these provide insights into the operation of the underlying genetic networks.

摘要

通过奇异值分解对先前发表的DNA微阵列基因表达数据集进行分析,揭示了其时间分布中的潜在模式或“特征模式”。这些模式对表达谱结构的贡献并不均等。此外,仅使用少数特征模式就能捕捉到给定表达谱集的基本特征。这得出了一个惊人的结论,即基因组的转录反应是按照基因表达变化的一些基本模式精心编排的。这些模式既简单又稳健,主导着整个基因组中基因表达的变化。此外,在酵母和人类细胞等如此遥远的生物体中,基因表达响应环境扰动而变化的特征模式是相似的。该分析揭示了不同细胞向新状态看似复杂的转录转变中的简单规律,这些规律为潜在遗传网络的运作提供了见解。

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本文引用的文献

1
Sum1 and Hst1 repress middle sporulation-specific gene expression during mitosis in Saccharomyces cerevisiae.Sum1和Hst1在酿酒酵母有丝分裂过程中抑制中期孢子形成特异性基因的表达。
EMBO J. 1999 Nov 15;18(22):6448-54. doi: 10.1093/emboj/18.22.6448.
2
The transcriptional program in the response of human fibroblasts to serum.人类成纤维细胞对血清反应中的转录程序。
Science. 1999 Jan 1;283(5398):83-7. doi: 10.1126/science.283.5398.83.
3
Cluster analysis and display of genome-wide expression patterns.全基因组表达模式的聚类分析与展示
Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14863-8. doi: 10.1073/pnas.95.25.14863.
4
Comprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization.通过微阵列杂交全面鉴定酿酒酵母细胞周期调控基因。
Mol Biol Cell. 1998 Dec;9(12):3273-97. doi: 10.1091/mbc.9.12.3273.
5
The transcriptional program of sporulation in budding yeast.芽殖酵母中孢子形成的转录程序。
Science. 1998 Oct 23;282(5389):699-705. doi: 10.1126/science.282.5389.699.
6
Induction of meiosis in Saccharomyces cerevisiae depends on conversion of the transcriptional represssor Ume6 to a positive regulator by its regulated association with the transcriptional activator Ime1.酿酒酵母减数分裂的诱导取决于转录抑制因子Ume6通过与转录激活因子Ime1的调控结合而转变为正调控因子。
Mol Cell Biol. 1996 May;16(5):2518-26. doi: 10.1128/MCB.16.5.2518.
7
Light-generated oligonucleotide arrays for rapid DNA sequence analysis.用于快速DNA序列分析的光生成寡核苷酸阵列。
Proc Natl Acad Sci U S A. 1994 May 24;91(11):5022-6. doi: 10.1073/pnas.91.11.5022.
8
Quantitative monitoring of gene expression patterns with a complementary DNA microarray.利用互补DNA微阵列对基因表达模式进行定量监测。
Science. 1995 Oct 20;270(5235):467-70. doi: 10.1126/science.270.5235.467.