14-3-3 proteins regulate Tctp–Rheb interaction for organ growth in Drosophila

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14-3-3 proteins regulate Tctp-Rheb interaction for organ growth in Drosophila.

14-3-3 family proteins regulate multiple signalling pathways. Understanding biological functions of 14-3-3 proteins has been limited by the functional redundancy of conserved isotypes. Here we provide evidence that 14-3-3 proteins regulate two interacting components of Tor signalling in Drosophila, translationally controlled tumour protein (Tctp) and Rheb GTPase. Single knockdown of 14-3-3ɛ or ...

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The 14-3-3 proteins positively regulate rapamycin-sensitive signaling

BACKGROUND The kinase Tor is the target of the immunosuppressive drug rapamycin and is a member of the phosphatidylinositol kinase (PIK)-related kinase family. It plays an essential role in progression through the G1 phase of the cell cycle. The molecular details of Tor signaling remain obscure, however. RESULTS We isolated two Saccharomyces cerevisiae genes, BMH1 and BMH2, as multicopy suppr...

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14-3-3 proteins regulate protein kinase a activity to modulate growth cone turning responses.

Growth cones regulate the speed and direction of neuronal outgrowth during development and regeneration. How the growth cone spatially and temporally regulates signals from guidance cues is poorly understood. Through a proteomic analysis of purified growth cones we identified isoforms of the 14-3-3 family of adaptor proteins as major constituents of the growth cone. Disruption of 14-3-3 via the...

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Interaction between Rho GTPases and 14-3-3 Proteins

The Rho GTPase family accounts for as many as 20 members. Among them, the archetypes RhoA, Rac1, and Cdc42 have been the most well-characterized. Like all members of the small GTPases superfamily, Rho proteins act as molecular switches to control cellular processes by cycling between active, GTP-bound and inactive, GDP-bound states. The 14-3-3 family proteins comprise seven isoforms. They exist...

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Interaction of phosphorylated tryptophan hydroxylase with 14-3-3 proteins.

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ژورنال

عنوان ژورنال: Nature Communications

سال: 2016

ISSN: 2041-1723

DOI: 10.1038/ncomms11501