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PIk1-Dependent and -Independent Roles of an ODF2 Splice Variant, hCenexin1, at the Centrosome of Somatic Cells

  1. Author:
    Soung, N. K.
    Park, J. E.
    Yu, L. R.
    Lee, K. H.
    Lee, J. M.
    Bang, J. K.
    Veenstra, T. D.
    Rhee, K.
    Lee, K. S.
  2. Author Address

    Soung, Nak-Kyun, Park, Jung-Eun, Lee, Kyung H.; Lee, Kyung S.] NCI, Lab Metab, NIH, Bethesda, MD 20892 USA. [Yu, Li-Rong] US FDA, Ctr Prote, Div Syst Toxicol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA. [Lee, Jung-Min, Rhee, Kunsoo] Seoul Natl Univ, Sch Biol Sci, Seoul 151742, South Korea. [Bang, Jeong K.] Korea Basic Sci Inst, Pusan 609735, South Korea. [Veenstra, Timothy D.] NCI, Lab Prote & Analyt Technol, Ft Detrick, MD 21702 USA.
    1. Year: 2009
  1. Journal: Developmental Cell
    1. 16
    2. 4
    3. Pages: 539-550
  2. Type of Article: Article
  1. Abstract:

    Outer dense fiber 2 (ODF2) was initially identified as a major component of the sperm tail cytoskeleton, and was later suggested to be localized to somatic centrosomes and required for the formation of primary cilia. Here we show that a splice variant of hODF2 called hCenexin1, but not hODF2 itself, efficiently localizes to somatic centrosomes via a variant-specific C-terminal extension and recruits PIk1 through a Cdc2-dependent phospho-S796 motif within the extension. This interaction and PIk1 activity were important for proper recruitment of pericentrin and gamma-tubulin, and, ultimately, for formation of normal bipolar spindles. Earlier in the cell cycle, hCenexin1, but again not hODF2, also contributed to centrosomal recruitment of ninein and primary cilia formation independent of PIk1 interaction. These findings provide a striking example of how a splice-generated C-terminal extension of a sperm tail-associating protein mediates unanticipated centrosomal events at distinct stages of the somatic cell cycle.

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External Sources

  1. DOI: 10.1016/j.devcel.2009.02.004
  2. PMID: 19386263

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