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Schaub, A. ; Glasmacher, E.

Splicing in immune cells - mechanistic insights and emerging topics.

Int. Immunol. 29, 173-181 (2017)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Differential splicing of mRNAs not only enables regulation of gene expression levels, but also ensures a high degree of gene-product diversity. The extent to which splicing of mRNAs is utilized as a mechanism in immune cells has become evident within the last few years. Still, only a few of these mechanisms have been well studied. In this review we discuss some of the best-understood mechanisms, for instance the differential splicing of CD45 in T cells, as well as immunoglobulin genes in B cells. Beyond that we provide general mechanistic insights on how, when and where this process takes place and discuss the current knowledge regarding these topics in immune cells. We also highlight some of the reported links to immune-related diseases, genome-wide sequencing studies that revealed thousands of differentially spliced transcripts, as well as splicing studies on immune cells that remain mechanistically not fully understood. We thereby display potential emerging topics for future studies centered on splicing mechanisms in immune cells.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter B Cells ; T Cells ; Alternative Splicing ; Nuclear Bodies ; Sequencing; Rna-polymerase-ii; Speckle-related Protein; Secretory Poly(a) Site; Acute Myeloid-leukemia; Messenger-rna; T-cell; Dna Rearrangement; Sequence-analysis; Mammalian-cells; Molecular-basis
Sprache
Veröffentlichungsjahr 2017
HGF-Berichtsjahr 2017
ISSN (print) / ISBN 0953-8178
e-ISSN 1460-2377
Zeitschrift International Immunology
Quellenangaben Band: 29, Heft: 4, Seiten: 173-181 Artikelnummer: , Supplement: ,
Verlag Oxford University Press
Verlagsort Oxford
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Obesity (IDO)
POF Topic(s) 90000 - German Center for Diabetes Research
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-501900-226
DOI 10.1093/intimm/dxx026
WOS ID WOS:000404457800005
Scopus ID 85021355924
PubMed ID 28498981
Erfassungsdatum 2017-07-10
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