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The RNA-Binding Protein KSRP Promotes Decay of  -Catenin mRNA and Is Inactivated by PI3K-AKT Signaling Roberto Gherzi et al. PLoS Biol. (2006)

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Presentation on theme: "The RNA-Binding Protein KSRP Promotes Decay of  -Catenin mRNA and Is Inactivated by PI3K-AKT Signaling Roberto Gherzi et al. PLoS Biol. (2006)"— Presentation transcript:

1 The RNA-Binding Protein KSRP Promotes Decay of  -Catenin mRNA and Is Inactivated by PI3K-AKT Signaling Roberto Gherzi et al. PLoS Biol. (2006)

2 Carol J. Wilusz and Jeffrey Wilusz. Trends Genet. (2004) Decay of ARE-containing mRNA The process of mRNA decay is integral to the posttranscriptional control of gene expression. AU-rich element (AREs), located in the 3’untranslated region (3’UTR) of many short-lived transcripts, promote mRNA degradation.

3 FBP2 is also known as KH-type splicing regulatory protein (KSRP). FBP2 was identified as an ARE-BP in Jurkat cell extracts that could be UV cross-linked to the IL-2 3’UTR. What is KSRP? Dean JL. et al. Cell Signal. (2004 )

4 Barreau C. et al. Nucleic Acids Res. (2006) p38-dependent phosphorylation of the mRNA decay-promoting factor KSRP controls the stability of select myogenic transcripts Briata P. et al. Mol Cell. (2005) KSRP targets c-fos, NOSII, TNF- , IL-2 mRNA for rapid degradation by binding to an AU-rich element (ARE). KSRP, a KH domain-containing ARE-BP, is an essential factor for ARE-directed mRNA decay. Gherzi R. et al. Mol Cell. (2004) Hall MP. et al. Mol Biol Cell. (2004) Function of KSRP

5 http://www.cellsignal.com/reference/pathway/pdfs/Akt_PKB.pdf Scheme of PI3K-AKT signaling

6 Cross-talks between Wnt and PI3K-AKT pathway Akt phosphorylates  -catenin, which results in 14-3-3  binding and stabilization of  -catenin. Tian Q. et al. Proc Natl Acad Sci U S A. (2004) Activated Akt by Wnt bound to the Axin-GSK3  complex in the presence of Dvl, phosphorylated GSK3  and increased free  -catenin levels. Fukumoto S. et al. J Biol Chem. (2001) Insulin and IGF-1 to activate the  -catenin pathway through GSK-3  inhibition by PI3K-AKT pathway. Desbois-Mouthon C. et al. Oncogene. (2001) Wnt proteins prolong the survival of osteoblasts and uncommitted osteoblast progenitors via activation of the Src/ERK and PI3K/Akt signaling cascades. Almeida M. et al. J Biol Chem. (2005) The phosphatidyl inositol 3 kinases (PI3K)-Akt pathway is also involved in the Wnt3a-induced proliferation. Kim SE. et al. Cell Signal. (2006)

7 mRNA Encoding  -Catenin Is Labile and Is Stabilized by LiCl and Wnt-3A

8 PI3K-AKT Signaling Stabilizes  -Catenin mRNA and Increases Its Expression

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10 Insulin Stabilizes  -Catenin mRNA and Increases Its Expression

11 KSRP Is Phosphorylated by AKT in Serine 193

12 KSRP Is Required for  -Catenin mRNA Degradation

13 KSRP Phosphorylation by AKT Promotes Its Interaction with 14-3-3 and Affects Its mRNA-Destabilizing Function

14 AKT Activation Affects KSRP-Exosome Interaction GST-KH1-4

15 KSRP P 14-3-3 P KSRP 14-3-3 P KSRP 14-3-3 P PARN KSRP 14-3-3 P AAAAAAAAAAAA ARE AKT Summary AKT phosphorylates KSRP, induces its interaction with 14-3-3, and prevents KSRP interaction with the exosome. Decay of  -catenin mRNA by KSRP is inactivated.


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