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The epithelial splicing factors ESRP1 and ESRP2 positively and negatively regulate diverse types of alternative splicing events
被引:184
作者:
Warzecha, Claude C.
[1
,2
]
Shen, Shihao
[5
]
Xing, Yi
[3
,4
]
Carstens, Russ P.
[1
,2
,6
]
机构:
[1] Univ Penn, Sch Med, Div Renal, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
[3] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Biomed Engn, Iowa City, IA 52242 USA
[5] Univ Iowa, Dept Biostat, Iowa City, IA 52242 USA
[6] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
来源:
基金:
美国国家卫生研究院;
关键词:
alternative splicing;
exons;
ESRP;
splicing regulatory network;
epithelial to mesenchymal transition;
exon arrays;
POLARITY;
EXPRESSION;
COMPLEX;
CELLS;
RIBONUCLEOPROTEIN;
TRANSCRIPTOME;
PROTEINS;
INSIGHTS;
JUNCTION;
INTEGRIN;
D O I:
10.4161/rna.6.5.9606
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Cell-type and tissue-specific alternative splicing events are regulated by combinatorial control involving both abundant RNA binding proteins as well as those with more discrete expression and specialized functions. Epithelial Splicing Regulatory Proteins 1 and 2 (ESRP1 and ESRP2) are recently discovered epithelial-specific RNA binding proteins that promote splicing of the epithelial variant of the FGFR2, ENAH, CD44 and CTNND1 transcripts. To catalogue a larger set of splicing events under the regulation of the ESRPs we profiled splicing changes induced by RNA interference-mediated knockdown of ESRP1 and ESRP2 expression in a human epithelial cell line using the splicing sensitive Affymetrix Exon ST1.0 Arrays. Analysis of the microarray data resulted in the identification of over a hundred candidate ESRP regulated splicing events. We were able to independently validate 38 of these targets by RT-PCR. The ESRP regulated events encompass all known types of alternative splicing events, most prominent being alternative cassette exons and splicing events leading to alternative 3' terminal exons. Importantly, a number of these regulated splicing events occur in gene transcripts that encode proteins with well-described roles in the regulation of actin cytoskeleton organization, cell-cell adhesion, cell polarity and cell migration. In sum, this work reveals a novel list of transcripts differentially spliced in epithelial and mesenchymal cells, implying that coordinated alternative splicing plays a critical role in determination of cell type identity. These results further establish ESRP1 and ESRP2 as global regulators of an epithelial splicing regulatory network.
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页码:546 / 562
页数:17
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