Filter By:

Journal Check one or more journals to show results from those journals only.

Choose more journals

Article type Check one or more article types to show results from those article types only.
Subject Check one or more subjects to show results from those subjects only.
Date Choose a date option to show results from those dates only.

Custom date range

Clear all filters
Sort by:
Showing 1–6 of 6 results
Advanced filters: Author: Giuliano Callaini Clear advanced filters
  • The midbody is an organelle present at the bridge connecting two cells at the end of cell division. Here, the authors use mass spectrometry to define the midbody interactome and uncover a role for PP1 phosphatases in microtubule dynamics and regulation of cytokinesis.

    • Luisa Capalbo
    • Zuni I. Bassi
    • Pier Paolo D’Avino
    ResearchOpen Access
    Nature Communications
    Volume: 10, P: 1-17
  • Centrioles and cilia are microtubule-based structures of defined architecture, but what regulates this architecture is not clear. Here the authors discover that centrosomal-P4.1-associated-protein (CPAP) binds the α/β-tubulin dimer and licenses it for tubulin delivery contributing to centriolar/ciliary length and architecture control.

    • Xiangdong Zheng
    • Anand Ramani
    • Haitao Li
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-13
  • Centriole duplication requires the loading of centriolar proteins to the daughter centriole during mitosis. Fu and colleagues analyse by 3D-structural illumination microscopy the sequential recruitment of centriolar proteins Cep135, Cep295 and Cep152.

    • Jingyan Fu
    • Zoltan Lipinszki
    • David M. Glover
    Research
    Nature Cell Biology
    Volume: 18, P: 87-99
  • Centrioles are essential for the formation of centrosomes, cilia and flagella. The centriolar protein Polo-like-kinase 4 (Plk4) is a key regulator of centriole biogenesis and for maintaining constant centriole number in cells. These authors show that the centriolar protein Asterless (CEP152 in humans) interacts with Plk4 and Sas-4. They find that Asl functions as a scaffold for Plk4 and Sas-4 that facilitates self-assembly and duplication of the centriole, and organization of pericentriolar material.

    • Nikola S. Dzhindzhev
    • Quan D. Yu
    • David M. Glover
    Research
    Nature
    Volume: 467, P: 714-718