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Cited by 379

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Nucleolin and YB-1 are required for JNK-mediated interleukin-2 mRNA stabilization during T-cell activation

Open access
Chen, Ching-Yi, Gherzi, Roberto, Andersen, Jens S., Gaietta, Guido, Jürchott, Karsten, Royer, Hans-Dieter, Mann, Matthias, Karin, Michael·2000·Genes & Development

Abstract

Regulated mRNA turnover is a highly important process, but its mechanism is poorly understood. Using interleukin-2 (IL-2) mRNA as a model, we described a role for the JNK-signaling pathway in stabilization of IL-2 mRNA during T-cell activation, acting via a JNK response element (JRE) in the 5′ untranslated region (UTR). We have now identified two major RNA-binding proteins, nucleolin and YB-1, that specifically bind to the JRE. Binding of both proteins is required for IL-2 mRNA stabilization induced by T-cell activation signals and for JNK-induced stabilization in a cell-free system that duplicates essential features of regulated mRNA decay. Nucleolin and YB-1 are required for formation of an IL-2 mRNP complex that responds to specific mRNA stabilizing signals.

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Metadata

Authors
Chen, C.-Y., Gherzi, R., Andersen, J. S., Gaietta, G., Jürchott, K., Royer, H.-D., Mann, M., & Karin, M.
Venue
Genes & Development
Published
2000-05-15
Volume
14
Issue
10
Pages
1236-1248
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2120764171
Cited by
379
References
4
Type
posted content
Language
en
Open access
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