Literature DB >> 27872148

Proteomics Screen Identifies Class I Rab11 Family Interacting Proteins as Key Regulators of Cytokinesis.

Carl Laflamme1, Jacob A Galan1, Khaled Ben El Kadhi1, Antoine Méant1, Carlos Zeledon1, Sébastien Carréno1,2, Philippe P Roux3,2, Gregory Emery3,2.   

Abstract

The 14-3-3 protein family orchestrates a complex network of molecular interactions that regulates various biological processes. Owing to their role in regulating the cell cycle and protein trafficking, 14-3-3 proteins are prevalent in human diseases such as cancer, diabetes, and neurodegeneration. 14-3-3 proteins are expressed in all eukaryotic cells, suggesting that they mediate their biological functions through evolutionarily conserved protein interactions. To identify these core 14-3-3 client proteins, we used an affinity-based proteomics approach to characterize and compare the human and Drosophila 14-3-3 interactomes. Using this approach, we identified a group of Rab11 effector proteins, termed class I Rab11 family interacting proteins (Rab11-FIPs), or Rip11 in Drosophila We found that 14-3-3 binds to Rip11 in a phospho-dependent manner to ensure its proper subcellular distribution during cell division. Our results indicate that Rip11 plays an essential role in the regulation of cytokinesis and that this function requires its association with 14-3-3 but not with Rab11. Together, our results suggest an evolutionarily conserved role for 14-3-3 in controlling Rip11-dependent protein transport during cytokinesis.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  14-3-3; cell division; cytokinesis; proteomics; vesicular trafficking

Mesh:

Substances:

Year:  2017        PMID: 27872148      PMCID: PMC5247615          DOI: 10.1128/MCB.00278-16

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  49 in total

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Review 5.  Phospho-Ser/Thr-binding domains: navigating the cell cycle and DNA damage response.

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2.  Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population.

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