TCF3 alternative splicing controlled by hnRNP H/F regulates E-cadherin expression and hESC pluripotency Journal Article


Authors: Yamazaki, T.; Liu, L.; Lazarev, D.; Al-Zain, A.; Fomin, V.; Yeung, P. L.; Chambers, S. M.; Lu, C. W.; Studer, L.; Manley, J. L.
Article Title: TCF3 alternative splicing controlled by hnRNP H/F regulates E-cadherin expression and hESC pluripotency
Abstract: Alternative splicing (AS) plays important roles in embryonic stem cell (ESC) differentiation. In this study, we first identified transcripts that display specific AS patterns in pluripotent human ESCs (hESCs) relative to differentiated cells. One of these encodes T-cell factor 3 (TCF3), a transcription factor that plays important roles in ESC differentiation. AS creates two TCF3 isoforms, E12 and E47, and we identified two related splicing factors, heterogeneous nuclear ribonucleoproteins (hnRNPs) H1 and F (hnRNP H/F), that regulate TCF3 splicing. We found that hnRNP H/F levels are high in hESCs, leading to high E12 expression, but decrease during differentiation, switching splicing to produce elevated E47 levels. Importantly, hnRNP H/F knockdown not only recapitulated the switch in TCF3 AS but also destabilized hESC colonies and induced differentiation. Providing an explanation for this, we show that expression of known TCF3 target E-cadherin, critical for maintaining ESC pluripotency, is repressed by E47 but not by E12. © 2018 Yamazaki et al.
Keywords: alternative splicing; heterogeneous nuclear ribonucleoprotein; e2a; human embryonic stem cell; t-cell factor 3
Journal Title: Genes and Development
Volume: 32
Issue: 17-18
ISSN: 0890-9369
Publisher: Cold Spring Harbor Laboratory Press  
Date Published: 2018-09-01
Start Page: 1161
End Page: 1174
Language: English
DOI: 10.1101/gad.316984.118
PROVIDER: scopus
PMCID: PMC6120717
PUBMED: 30115631
DOI/URL:
Notes: Article -- Export Date: 1 October 2018 -- Source: Scopus
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  1. Lorenz Studer
    220 Studer