Dissection of a complex transcriptional response using genome-wide transcriptional modelling.
Dissection of a complex transcriptional response using genome-wide transcriptional modelling.
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DOI：
10.1038/msb.2009.84
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发表时间：
2009
影响因子：
9.9
通讯作者：
中科院分区：
文献类型：
--
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Modern genomics technologies generate huge data sets creating a demand for systems level, experimentally verified, analysis techniques. We examined the transcriptional response to DNA damage in a human T cell line (MOLT4) using microarrays. By measuring both mRNA accumulation and degradation over a short time course, we were able to construct a mechanistic model of the transcriptional response. The model predicted three dominant transcriptional activity profiles—an early response controlled by NFκB and c-Jun, a delayed response controlled by p53, and a late response related to cell cycle re-entry. The method also identified, with defined confidence limits, the transcriptional targets associated with each activity. Experimental inhibition of NFκB, c-Jun and p53 confirmed that target predictions were accurate. Model predictions directly explained 70% of the 200 most significantly upregulated genes in the DNA-damage response. Genome-wide transcriptional modelling (GWTM) requires no prior knowledge of either transcription factors or their targets. GWTM is an economical and effective method for identifying the main transcriptional activators in a complex response and confidently predicting their targets.
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影响因子：
12.3
作者：
Gentleman RC;Carey VJ;Bates DM;Bolstad B;Dettling M;Dudoit S;Ellis B;Gautier L;Ge Y;Gentry J;Hornik K;Hothorn T;Huber W;Iacus S;Irizarry R;Leisch F;Li C;Maechler M;Rossini AJ;Sawitzki G;Smith C;Smyth G;Tierney L;Yang JY;Zhang J
通讯作者：
Zhang J
影响因子：
5.8
作者：
Husmeier, D
通讯作者：
Husmeier, D
影响因子：
64.8
作者：
LEE, MG;NORBURY, CJ;NURSE, P
通讯作者：
NURSE, P
DOI：
10.1073/pnas.2136632100
发表时间：
2003-12-23
影响因子：
11.1
作者：
Liao, JC;Boscolo, R;Roychowdhury, VP
通讯作者：
Roychowdhury, VP
影响因子：
4.3
作者：
Carter GW;Galas DJ;Galitski T
通讯作者：
Galitski T