Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.cell.2005.10.043
Title: A global map of p53 transcription-factor binding sites in the human genome
Authors: Wei, C.-L.
Wu, Q.
Vega, V.B.
Chiu, K.P.
Ng, P.
Zhang, T.
Shahab, A.
Yong, H.C.
Fu, Y.
Weng, Z.
Liu, J.
Zhao, X.D.
Chew, J.-L.
Lee, Y.L.
Kuznetsov, V.A.
Sung, W.-K.
Miller, L.D.
Lim, B.
Liu, E.T.
Yu, Q.
Ng, H.-H. 
Ruan, Y.
Issue Date: 13-Jan-2006
Citation: Wei, C.-L., Wu, Q., Vega, V.B., Chiu, K.P., Ng, P., Zhang, T., Shahab, A., Yong, H.C., Fu, Y., Weng, Z., Liu, J., Zhao, X.D., Chew, J.-L., Lee, Y.L., Kuznetsov, V.A., Sung, W.-K., Miller, L.D., Lim, B., Liu, E.T., Yu, Q., Ng, H.-H., Ruan, Y. (2006-01-13). A global map of p53 transcription-factor binding sites in the human genome. Cell 124 (1) : 207-219. ScholarBank@NUS Repository. https://doi.org/10.1016/j.cell.2005.10.043
Abstract: The ability to derive a whole-genome map of transcription-factor binding sites (TFBS) is crucial for elucidating gene regulatory networks. Herein, we describe a robust approach that couples chromatin immunoprecipitation (ChIP) with the paired-end ditag (PET) sequencing strategy for unbiased and precise global localization of TFBS. We have applied this strategy to map p53 targets in the human genome. From a saturated sampling of over half a million PET sequences, we characterized 65,572 unique p53 ChIP DNA fragments and established overlapping PET clusters as a readout to define p53 binding loci with remarkable specificity. Based on this information, we refined the consensus p53 binding motif, identified at least 542 binding loci with high confidence, discovered 98 previously unidentified p53 target genes that were implicated in novel aspects of p53 functions, and showed their clinical relevance to p53-dependent tumorigenesis in primary cancer samples. ©2006 Elsevier Inc.
Source Title: Cell
URI: http://scholarbank.nus.edu.sg/handle/10635/99837
ISSN: 00928674
DOI: 10.1016/j.cell.2005.10.043
Appears in Collections:Staff Publications

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