RNA Binding Properties of the AU-rich Element-binding Recombinant Nup475/TIS11/Tristetraprolin Protein
Regulation of messenger RNA stability by AU-rich elements is an important means of regulating genes induced by growth factors and cytokines. Nup475 (also known as tristetraprolin, or TIS11) is the prototype for a family of zinc-binding Cys 3 His motif proteins required for proper regulation of tumor...
Gespeichert in:
Veröffentlicht in: | The Journal of biological chemistry 2002-12, Vol.277 (50), p.48558-48564 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Regulation of messenger RNA stability by AU-rich elements is an important means of regulating genes induced by growth factors
and cytokines. Nup475 (also known as tristetraprolin, or TIS11) is the prototype for a family of zinc-binding Cys 3 His motif proteins required for proper regulation of tumor necrosis factor mRNA stability in macrophages. We developed an
Escherichia coli expression system to produce soluble Nup475 protein in quantity to study its RNA binding properties. Nup475 protein bound
a tumor necrosis factor AU-rich element over a broad range of pH and salt concentrations by RNA gel shift. This binding was
inhibited by excess zinc metal, providing a potential mechanism for previous reports of zinc stabilization of AU-rich element
(ARE) containing messenger RNAs. Immobilized Nup475 protein was used to select its optimal binding site by RNA SELEX and revealed
a strong preference for the extended sequence UUAUUUAUU, rather than a simple AUUUA motif. These findings were confirmed by
site-directed mutagenesis of the tumor necrosis factor ARE and RNA gel shifts on c- fos , interferon-γ, and interferon-β ARE fragments. A weaker binding activity toward adenine-rich sites, such as a poly(A) tail
RNA fragment, can partially disrupt the Nup475-tumor necrosis factor AU-rich element complex. |
---|---|
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M206505200 |