Prediction and Experimental Validation of Novel STAT3 Target Genes in Human Cancer Cells 英文参考文献.docVIP
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Prediction and Experimental Validation of Novel STAT3 Target Genes in Human Cancer Cells 英文参考文献
PredictionandExperimentalValidationofNovelSTAT3
TargetGenesinHumanCancerCells
YoungMinOh1.,JongKyoungKim2.,YongwookChoi1,SeungjinChoi2*,Joo-YeonYoo1*
1Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea, 2Department of Computer Science, Pohang University of
ScienceandTechnology,Pohang,RepublicofKorea
Abstract
The comprehensive identification of functional transcription factor binding sites (TFBSs) is an important step in
understanding complex transcriptional regulatory networks. This study presents a motif-based comparative approach,
STAT-Finder,foridentifyingfunctionalDNAbindingsitesofSTAT3transcriptionfactor.STAT-FindercombinesSTAT-Scanner,
whichwasdesignedtopredictfunctionalSTATTFBSswithimprovedsensitivity,andamotif-basedalignmenttominimize
false positive prediction rates. Using two reference sets containing promoter sequences of known STAT3 target genes,
STAT-Finder identified functional STAT3 TFBSs with enhanced prediction efficiency and sensitivity relative to other
conventionalTFBSpredictiontools.Inaddition,STAT-FinderidentifiednovelSTAT3targetgenesamongagroupofgenes
that are over-expressed in human cancer cells. The binding of STAT3 to the predicted TFBSs was also experimentally
confirmed through chromatin immunoprecipitation. Our proposed method provides a systematic approach to the
predictionoffunctionalTFBSsthatcanbeappliedtootherTFs.
Citation: Oh YM, Kim JK, Choi Y, Choi S, Yoo J-Y (2009) Prediction and Experimental Validation of Novel STAT3 Target Genes in Human Cancer Cells. PLoS
ONE4(9):e6911.doi:10.1371/journal.pone.0006911
Editor:SridharHannenhalli,UniversityofPennsylvaniaSchoolofMedicine,UnitedStatesofAmerica
ReceivedApril2,2009;AcceptedAugust3,2009;PublishedSeptember4,2009
Copyright:?2009Ohetal.Thisisanopen-accessarticledistributedunderthetermsoftheCreativeCommonsAttributionLicense,whichpermitsunrestricted
use,distribution,andreproductioninanymedium,providedtheoriginalauthorandsourcearecredited.
F
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