Tristetraprolin (TTP)-14-3-3 complex formation protects TTP from dephosphorylation by protein phosphatase 2a and stabilizes tumor necrosis factor-alpha mRNA (Q24336740)

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English	Tristetraprolin (TTP)-14-3-3 complex formation protects TTP from dephosphorylation by protein phosphatase 2a and stabilizes tumor necrosis factor-alpha mRNA	scientific article

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Tristetraprolin (TTP)-14-3-3 complex formation protects TTP from dephosphorylation by protein phosphatase 2a and stabilizes tumor necrosis factor-alpha mRNA (English)

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Zinc finger protein 36

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GOA release 2020-03-11

Georg Stoecklin

object named as

Georg Stoecklin

2

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Thomas P Shanley

object named as

Thomas Patrick Shanley

7

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author name string

Lei Sun

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Susan Van Way

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Vania Hinkovska-Galcheva

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Ren-Feng Guo

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Paul Anderson

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language of work or name

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publication date

9 February 2007

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Journal of Biological Chemistry

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282

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3766-77

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6

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Analysis of the function, expression, and subcellular distribution of human tristetraprolin

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A KH domain RNA binding protein, KSRP, promotes ARE-directed mRNA turnover by recruiting the degradation machinery

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Expression and purification of recombinant tristetraprolin that can bind to tumor necrosis factor-alpha mRNA and serve as a substrate for mitogen-activated protein kinases

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Post-transcriptional regulation of gene expression by mitogen-activated protein kinase p38.

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AU binding proteins recruit the exosome to degrade ARE-containing mRNAs

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Phosphatases in apoptosis: to be or not to be, PP2A is in the heart of the question

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AU-rich elements: characterization and importance in mRNA degradation

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MK2-induced tristetraprolin:14-3-3 complexes prevent stress granule association and ARE-mRNA decay

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The ARE-dependent mRNA-destabilizing activity of BRF1 is regulated by protein kinase B

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ARE-mRNA degradation requires the 5'-3' decay pathway.

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Similar but distinct effects of the tristetraprolin/TIS11 immediate-early proteins on cell survival

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Identification of a common nucleotide sequence in the 3'-untranslated region of mRNA molecules specifying inflammatory mediators

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HNS, a nuclear-cytoplasmic shuttling sequence in HuR

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Regulation of protein phosphatase 2A activity by caspase-3 during apoptosis

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Developmental regulation of RNA transcript destabilization by A + U-rich elements is AUF1-dependent

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Identification of AUF1 as a parathyroid hormone mRNA 3'-untranslated region-binding protein that determines parathyroid hormone mRNA stability

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MK2 targets AU-rich elements and regulates biosynthesis of tumor necrosis factor and interleukin-6 independently at different post-transcriptional levels

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Raf-1-associated Protein Phosphatase 2A as a Positive Regulator of Kinase Activation

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Decreased sensitivity of tristetraprolin-deficient cells to p38 inhibitors suggests the involvement of tristetraprolin in the p38 signaling pathway

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Protein phosphatase 2A interacts with and directly dephosphorylates RelA

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Cytoplasmic localization of tristetraprolin involves 14-3-3-dependent and -independent mechanisms

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Translational repression of human matrix metalloproteinases-13 by an alternatively spliced form of T-cell-restricted intracellular antigen-related protein (TIAR)

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Rim, a component of the presynaptic active zone and modulator of exocytosis, binds 14-3-3 through its N terminus

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MAPKAP kinase 2 phosphorylates tristetraprolin on in vivo sites including Ser178, a site required for 14-3-3 binding

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Positive regulation of IkappaB kinase signaling by protein serine/threonine phosphatase 2A

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Kappa B-type enhancers are involved in lipopolysaccharide-mediated transcriptional activation of the tumor necrosis factor alpha gene in primary macrophages

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Overexpression of HuR, a nuclear-cytoplasmic shuttling protein, increases the in vivo stability of ARE-containing mRNAs

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RNA stabilization by the AU-rich element binding protein, HuR, an ELAV protein

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Functional cloning of BRF1, a regulator of ARE-dependent mRNA turnover

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Recruitment and activation of mRNA decay enzymes by two ARE-mediated decay activation domains in the proteins TTP and BRF-1

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Feedback inhibition of macrophage tumor necrosis factor-alpha production by tristetraprolin

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Mitogen-activated protein kinase p38 controls the expression and posttranslational modification of tristetraprolin, a regulator of tumor necrosis factor alpha mRNA stability

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Convergent actions of I kappa B kinase beta and protein kinase C delta modulate mRNA stability through phosphorylation of 14-3-3 beta complexed with tristetraprolin

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Mitogen-activated protein kinase-activated protein kinase 2 regulates tumor necrosis factor mRNA stability and translation mainly by altering tristetraprolin expression, stability, and binding to adenine/uridine-rich element

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Bone marrow transplantation reproduces the tristetraprolin-deficiency syndrome in recombination activating gene-2 (-/-) mice. Evidence that monocyte/macrophage progenitors may be responsible for TNFalpha overproduction

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