TY - JOUR
T1 - An ESRP-regulated splicing programme is abrogated during the epithelial-mesenchymal transition
AU - Warzecha, Claude C.
AU - Jiang, P.
AU - Amirikian, Karine
AU - Dittmar, Kimberly A.
AU - Lu, Hezhe
AU - Shen, Shihao
AU - Guo, Wei
AU - Xing, Yi
AU - Carstens, Russ P.
PY - 2010/10/6
Y1 - 2010/10/6
N2 - Alternative splicing achieves coordinated changes in post-transcriptional gene expression programmes through the activities of diverse RNA-binding proteins. Epithelial splicing regulatory proteins 1 and 2 (ESRP1 and ESRP2) are cell-type-specific regulators of transcripts that switch splicing during the epithelial-mesenchymal transition (EMT). To define a comprehensive programme of alternative splicing that is regulated during the EMT, we identified an extensive ESRP-regulated splicing network of hundreds of alternative splicing events within numerous genes with functions in cell-cell adhesion, polarity, and migration. Loss of this global ESRP-regulated epithelial splicing programme induces the phenotypic changes in cell morphology that are observed during the EMT. Components of this splicing signature provide novel molecular markers that can be used to characterize the EMT. Bioinformatics and experimental approaches revealed a high-affinity ESRP-binding motif and a predictive RNA map that governs their activity. This work establishes the ESRPs as coordinators of a complex alternative splicing network that adds an important post-transcriptional layer to the changes in gene expression that underlie epithelial-mesenchymal transitions during development and disease. © 2010 European Molecular Biology Organization | All Rights Reserved.
AB - Alternative splicing achieves coordinated changes in post-transcriptional gene expression programmes through the activities of diverse RNA-binding proteins. Epithelial splicing regulatory proteins 1 and 2 (ESRP1 and ESRP2) are cell-type-specific regulators of transcripts that switch splicing during the epithelial-mesenchymal transition (EMT). To define a comprehensive programme of alternative splicing that is regulated during the EMT, we identified an extensive ESRP-regulated splicing network of hundreds of alternative splicing events within numerous genes with functions in cell-cell adhesion, polarity, and migration. Loss of this global ESRP-regulated epithelial splicing programme induces the phenotypic changes in cell morphology that are observed during the EMT. Components of this splicing signature provide novel molecular markers that can be used to characterize the EMT. Bioinformatics and experimental approaches revealed a high-affinity ESRP-binding motif and a predictive RNA map that governs their activity. This work establishes the ESRPs as coordinators of a complex alternative splicing network that adds an important post-transcriptional layer to the changes in gene expression that underlie epithelial-mesenchymal transitions during development and disease. © 2010 European Molecular Biology Organization | All Rights Reserved.
KW - alternative splicing
KW - epithelial splicing regulatory proteins
KW - epithelial-mesenchymal transition
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U2 - 10.1038/emboj.2010.195
DO - 10.1038/emboj.2010.195
M3 - Article
C2 - 20711167
SN - 0261-4189
VL - 29
SP - 3286
EP - 3300
JO - EMBO Journal
JF - EMBO Journal
IS - 19
ER -