Literature DB >> 28104305

CP39, CP75 and CP91 are major structural components of the Dictyostelium centrosome's core structure.

Irene Meyer1, Tatjana Peter2, Petros Batsios2, Oliver Kuhnert2, Anne Krüger-Genge2, Carl Camurça2, Ralph Gräf3.   

Abstract

The acentriolar Dictyostelium centrosome is a nucleus-associated body consisting of a core structure with three plaque-like layers, which are surrounded by a microtubule-nucleating corona. The core duplicates once per cell cycle at the G2/M transition, whereby its central layer disappears and the two outer layers form the mitotic spindle poles. Through proteomic analysis of isolated centrosomes, we have identified CP39 and CP75, two essential components of the core structure. Both proteins can be assigned to the central core layer as their centrosomal presence is correlated to the disappearance and reappearance of the central core layer in the course of centrosome duplication. Both proteins contain domains with centrosome-binding activity in their N- and C-terminal halves, whereby the respective N-terminal half is required for cell cycle-dependent regulation. CP39 is capable of self-interaction and GFP-CP39 overexpression elicited supernumerary microtubule-organizing centers and pre-centrosomal cytosolic clusters. Underexpression stopped cell growth and reversed the MTOC amplification phenotype. In contrast, in case of CP75 underexpression of the protein by RNAi treatment elicited supernumerary MTOCs. In addition, CP75RNAi affects correct chromosome segregation and causes co-depletion of CP39 and CP91, another central core layer component. CP39 and CP75 interact with each other directly in a yeast two-hybrid assay. Furthermore, CP39, CP75 and CP91 mutually interact in a proximity-dependent biotin identification (BioID) assay. Our data indicate that these three proteins are all required for proper centrosome biogenesis and make up the major structural components of core structure's central layer.
Copyright © 2017 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Centrosome; Dictyostelium; Microtubules; Mitosis; Nucleus

Mesh:

Substances:

Year:  2017        PMID: 28104305     DOI: 10.1016/j.ejcb.2017.01.004

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  7 in total

1.  BioID: A Method to Generate a History of Protein Associations.

Authors:  Danielle G May; Kyle J Roux
Journal:  Methods Mol Biol       Date:  2019-05-24

2.  Comparative Biology of Centrosomal Structures in Eukaryotes.

Authors:  Ralph Gräf
Journal:  Cells       Date:  2018-11-08       Impact factor: 6.600

3.  Efficient proximity labeling in living cells and organisms with TurboID.

Authors:  Tess C Branon; Justin A Bosch; Ariana D Sanchez; Namrata D Udeshi; Tanya Svinkina; Steven A Carr; Jessica L Feldman; Norbert Perrimon; Alice Y Ting
Journal:  Nat Biotechnol       Date:  2018-08-20       Impact factor: 54.908

4.  Partial Disassembly of the Nuclear Pore Complex Proteins during Semi-Closed Mitosis in Dictyostelium discoideum.

Authors:  Kristina Mitic; Marianne Grafe; Petros Batsios; Irene Meyer
Journal:  Cells       Date:  2022-01-25       Impact factor: 6.600

Review 5.  The Dictyostelium Centrosome.

Authors:  Ralph Gräf; Marianne Grafe; Irene Meyer; Kristina Mitic; Valentin Pitzen
Journal:  Cells       Date:  2021-10-05       Impact factor: 6.600

6.  Dictyostelium spastin is involved in nuclear envelope dynamics during semi-closed mitosis.

Authors:  Ulrike Schweigel; Petros Batsios; Annette Müller-Taubenberger; Ralph Gräf; Marianne Grafe
Journal:  Nucleus       Date:  2022-12       Impact factor: 4.197

7.  CDK5RAP2 Is an Essential Scaffolding Protein of the Corona of the Dictyostelium Centrosome.

Authors:  Valentin Pitzen; Sophie Askarzada; Ralph Gräf; Irene Meyer
Journal:  Cells       Date:  2018-04-23       Impact factor: 6.600

  7 in total

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