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开发一种基于新型寡核苷酸阵列的转录因子分析平台,用于在酿酒酵母中进行全基因组活性转录因子分析。

Development of a novel oligonucleotide array-based transcription factor assay platform for genome-wide active transcription factor profiling in Saccharomyces cerevisiae.

作者信息

Zhao Yongchao, Shao Wei, Wei Huajiang, Qiao Jiying, Lu Ying, Sun Yimin, Mitchelson Keith, Cheng Jing, Zhou Yuxiang

机构信息

Medical Systems Biology Research Center, Tsinghua University, Beijing 100084, China.

出版信息

J Proteome Res. 2008 Mar;7(3):1315-25. doi: 10.1021/pr700642g. Epub 2008 Jan 26.

Abstract

Transcription factors (TFs) play a central role in regulating gene expression and in providing interconnecting regulatory networks between related pathway elements. Although single TF assays provide some insights into pathway regulation, a method that allows the parallel investigation of all active TFs is highly desired to elucidate the complex inter-regulated cellular mechanisms. We have developed a novel oligonucleotide array-based transcription factor assay platform for genome-wide active TF profiling of Saccharomyces cerevisiae, which can simultaneously analyze the activities of 93 different TFs. The platform has been validated using 28 purified TFs produced in Escherichia coli, cell extracts from yeast strains overexpressing particular TFs, and by detailed control experiments. We then used the platform to examine the activity changes of all yeast TFs during diauxic shift, and results showed, in good agreement with previous studies, that the Sip4 was induced specifically. Other individual TFs required for growth in synthetic complete medium were also identified. Genome-wide analysis of TF activity is extremely useful in investigating complex gene regulatory networks and for the development of systematic understanding of the complexity of genomic functions. These results obtained in this report demonstrate the validity, and for the first time the utility, of this technology for genome-wide investigation of TF activities.

摘要

转录因子(TFs)在调节基因表达以及在相关信号通路元件之间提供相互连接的调控网络方面发挥着核心作用。尽管单个转录因子分析能为信号通路调控提供一些见解,但人们迫切需要一种能够同时研究所有活性转录因子的方法,以阐明复杂的相互调控的细胞机制。我们开发了一种基于新型寡核苷酸阵列的转录因子分析平台,用于酿酒酵母全基因组活性转录因子分析,该平台可同时分析93种不同转录因子的活性。该平台已通过使用在大肠杆菌中产生的28种纯化转录因子、过表达特定转录因子的酵母菌株的细胞提取物以及详细的对照实验进行了验证。然后,我们使用该平台研究了酵母在二次生长转换期间所有转录因子的活性变化,结果与先前的研究结果高度一致,即Sip4被特异性诱导。还鉴定了在合成完全培养基中生长所需的其他单个转录因子。转录因子活性的全基因组分析在研究复杂的基因调控网络以及系统理解基因组功能的复杂性方面极其有用。本报告中获得的这些结果证明了该技术用于全基因组转录因子活性研究的有效性,并且首次证明了其实用性。

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