Literature DB >> 15949538

14-3-3 protein signaling in development and growth factor responses.

Daniel Thomas1, Mark Guthridge, Jo Woodcock, Angel Lopez.   

Abstract

Tyrosine and serine phosphorylation are central to cellular signaling in growth and development. 14-3-3 proteins function as dimeric phosphoserine-binding proteins with documented interactions throughout the eukaryotic proteome and are highly conserved in both the animal and plant kingdoms. Binding of 14-3-3 to a client protein can have a range of context-dependent effects, including conformational change, enzyme inhibition, a shielding effect, re-localization, and bridging between two molecules. Proteome-based strategies utilizing mass spectrometry have revealed an unprecedented central stage for 14-3-3 in signal transduction with interacting partners composing at least 0.6% of the cellular proteome. 14-3-3 has been shown to bind to the human GM-CSF, IL-3, and IL-5 receptors and is required for the transmission of cell survival. 14-3-3 is involved in survival-specific signals, acting not only at the receptor level but also at critical steps downstream of the receptor. This phosphoserine-mediated pathway works independently of tyrosine kinases, highlighting an alternative mechanism of signaling for this receptor family. Other growth factor receptors and their adaptors are also being shown to associate with 14-3-3 and/or have putative 14-3-3 interaction sequences, such as the prolactin receptor, IGF-1 receptor, and some G-protein coupled receptors. 14-3-3 proteins are remarkably conserved through eukaryotic organisms and in Drosophila are required for photoreceptor development, learning, timing of cell cycles, and maintenance of cellular polarity. These findings are elevating our initial description of biochemical interactions to a better understanding of 14-3-3 function at the level of the whole organism. Further study should explore the integration of phosphoserine and phosphotyrosine signaling by 14-3-3 proteins and the role of isoform-specific functions in higher organisms. The prevalence of functional 14-3-3 binding sites throughout the proteome, and especially among growth factor receptors and signaling molecules, reflects a global role for 14-3-3 in multiple cellular decision making.

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Year:  2005        PMID: 15949538     DOI: 10.1016/S0070-2153(05)67009-3

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  16 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-02       Impact factor: 11.205

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Authors:  Liang Zhang; Zhi-Ping Zhang; Xian-En Zhang; Fu-Sen Lin; Feng Ge
Journal:  J Virol       Date:  2010-04-14       Impact factor: 5.103

3.  Tyrosine kinase of insulin-like growth factor receptor as target for novel treatment and prevention strategies of colorectal cancer.

Authors:  Michael Hopfner; Andreas P Sutter; Alexander Huether; Viola Baradari; Hans Scherubl
Journal:  World J Gastroenterol       Date:  2006-09-21       Impact factor: 5.742

4.  The 14-3-3η/GSK-3β/β-catenin complex regulates EndMT induced by 27-hydroxycholesterol in HUVECs and promotes the migration of breast cancer cells.

Authors:  Jing Zhen; Kailin Jiao; Keke Yang; Maoxuan Wu; Qian Zhou; Bingmo Yang; Wei Xiao; Chunyan Hu; Ming Zhou; Zhong Li
Journal:  Cell Biol Toxicol       Date:  2020-11-01       Impact factor: 6.691

5.  14-3-3ζ: A suppressor of inflammatory arthritis.

Authors:  Joshua Kim; Krista Chun; Jenna McGowan; Youjie Zhang; Piotr J Czernik; Blair Mell; Bina Joe; Saurabh Chattopadhyay; Joseph Holoshitz; Ritu Chakravarti
Journal:  Proc Natl Acad Sci U S A       Date:  2021-08-24       Impact factor: 11.205

6.  Proteomic Analysis Reveals Differential Protein Expression Induced by Inhibition of Prolyl Oligopeptidase in Filarial Parasites.

Authors:  Mohit Wadhawan; Faiyaz Ahmad; Smita Yadav; Sushma Rathaur
Journal:  Protein J       Date:  2022-10-22       Impact factor: 4.000

7.  Modulation of 14-3-3 interaction with phosphorylated histone H3 by combinatorial modification patterns.

Authors:  Stefan Winter; Wolfgang Fischle; Christian Seiser
Journal:  Cell Cycle       Date:  2008-03-11       Impact factor: 4.534

8.  14-3-3ζ-TRAF5 axis governs interleukin-17A signaling.

Authors:  Jenna McGowan; Cara Peter; Joshua Kim; Sonam Popli; Brent Veerman; Jessica Saul-McBeth; Heather Conti; Shondra M Pruett-Miller; Saurabh Chattopadhyay; Ritu Chakravarti
Journal:  Proc Natl Acad Sci U S A       Date:  2020-09-23       Impact factor: 11.205

9.  Phosphorylation-dependent 14-3-3 binding to LRRK2 is impaired by common mutations of familial Parkinson's disease.

Authors:  Xianting Li; Qing Jun Wang; Nina Pan; Sangkyu Lee; Yingming Zhao; Brian T Chait; Zhenyu Yue
Journal:  PLoS One       Date:  2011-03-01       Impact factor: 3.240

10.  14-3-3ε mediates the cell fate decision-making pathways in response of hepatocellular carcinoma to Bleomycin-induced DNA damage.

Authors:  Siwei Tang; Huimin Bao; Yang Zhang; Jun Yao; Pengyuan Yang; Xian Chen
Journal:  PLoS One       Date:  2013-03-05       Impact factor: 3.240

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