Importance of the CEP215-pericentrin interaction for centrosome maturation during mitosis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 24466316.
- Also identified by DOI 10.1371/journal.pone.0087016 and PMC identifier 3899370.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
At the onset of mitosis, the centrosome undergoes maturation, which is characterized by a drastic expansion of the pericentriolar material (PCM) and a robust increase in microtubule-organizing activity. CEP215 is one of the major PCM components which accumulates at the centrosome during mitosis. The depletion phenotypes indicate that CEP215 is essential for centrosome maturation and bipolar spindle formation. Here, we performed a series of knockdown-rescue experiments to link the protein-protein interaction properties of CEP215 to its biological functions. The results showed that CEP215 and pericentrin, another major PCM component, is interdependent for their accumulation at the spindle poles during mitosis. As a result, The CEP215-pericentrin interaction is required for centrosome maturation and subsequent bipolar spindle formation during mitosis. On the other hand, CEP215 interaction with γ-tubulin is dispensable for centrosome maturation. Our results provide an insight how PCM components are assembled to form a spindle pole during mitosis.
Medical subject headings
- Antigens
- Centrosome
- Intracellular Signaling Peptides and Proteins
- Mitosis
- Models, Molecular
- Nerve Tissue Proteins