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Modic, M. ; Grosch, M. ; Rot, G.* ; Schirge, S. ; Lepko, T. ; Yamazaki, T.* ; Lee, F.C.Y.* ; Rusha, E. ; Shaposhnikov, D. ; Palo, M.* ; Merl-Pham, J. ; Cacchiarelli, D.* ; Rogelj, B.* ; Hauck, S.M. ; von Mering, C.* ; Meissner, A.* ; Lickert, H. ; Hirose, T.* ; Ule, J.* ; Drukker, M.

Cross-regulation between TDP-43 and paraspeckles promotes pluripotency-differentiation transition.

Mol. Cell 74, 951-965.e13 (2019)
Verlagsversion Forschungsdaten DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
RNA-binding proteins (RBPs) and long non-coding RNAs (lncRNAs) are key regulators of gene expression, but their joint functions in coordinating cell fate decisions are poorly understood. Here we show that the expression and activity of the RBP TDP-43 and the long isoform of the lncRNA Neat1, the scaffold of the nuclear compartment "paraspeckles," are reciprocal in pluripotent and differentiated cells because of their cross-regulation. In pluripotent cells, TDP-43 represses the formation of paraspeckles by enhancing the polyadenylated short isoform of Neat1. TDP-43 also promotes pluripotency by regulating alternative polyadenylation of transcripts encoding pluripotency factors, including Sox2, which partially protects its 3' UTR from miR-21-mediated degradation. Conversely, paraspeckles sequester TDP-43 and other RBPs from mRNAs and promote exit from pluripotency and embryonic patterning in the mouse. We demonstrate that cross-regulation between TDP-43 and Neat1 is essential for their efficient regulation of a broad network of genes and, therefore, of pluripotency and differentiation.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Long Noncoding Rna; Embryonic Stem-cells; Binding Proteins; Alternative Polyadenylation; Gene-expression; Nuclear-bodies; Neat1; Proteome; Body; Subpopulation
Sprache englisch
Veröffentlichungsjahr 2019
HGF-Berichtsjahr 2019
ISSN (print) / ISBN 1097-2765
e-ISSN 1097-4164
Zeitschrift Molecular Cell
Quellenangaben Band: 74, Heft: 5, Seiten: 951-965.e13 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort 50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Stem Cell Research (ISF)
CF Metabolomics & Proteomics (CF-MPC)
Institute of Diabetes and Regeneration Research (IDR)
Institute of Lung Health and Immunity (LHI)
POF Topic(s) 30204 - Cell Programming and Repair
30203 - Molecular Targets and Therapies
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
90000 - German Center for Diabetes Research

30201 - Metabolic Health
30202 - Environmental Health
Forschungsfeld(er) Stem Cell and Neuroscience
Enabling and Novel Technologies
Helmholtz Diabetes Center

Lung Research
PSP-Element(e) G-500800-001
G-505700-001
G-552400-001
G-501900-231
G-508200-014
G-502300-001
G-501600-001
DOI 10.1016/j.molcel.2019.03.041
WOS ID WOS:000470249100010
Scopus ID 85066440477
PubMed ID 31047794
Erfassungsdatum 2019-05-07
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