4.5 Article

NuMA is a major acceptor of poly(ADP-ribosyl)ation by tankyrase 1 in mitosis

Journal

BIOCHEMICAL JOURNAL
Volume 391, Issue -, Pages 177-184

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BJ20050885

Keywords

mitosis; nuclear mitotic apparatus protein (NuMA); poly(ADP-ribose) polymerase (PARP); spindle pole; tankyrase 1

Funding

  1. NCI NIH HHS [R01 CA95099, R01 CA095099] Funding Source: Medline
  2. NIGMS NIH HHS [T32 GM007238, GM07238] Funding Source: Medline

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Tankyrase 1 is a PARP [poly(ADP-ribose) polymerase] that localizes to multiple subcellular sites, including telomeres and mitotic centrosomes. Previous studies demonstrated that cells deficient in tankyrase 1 suffered a block in resolution of sister telomeres and arrested in early anaphase [Dynek and Smith (2004) Science 304, 97-100]. This phenotype was dependent on the catalytic PARP activity of tankyrase 1. To identify critical acceptors of PARsylation [poly(ADP-ribosyl)ation] by tankyrase 1 in mitosis, tankyrase Iimmunoprecipitates were analysed for associated PARsylated proteins. We identified NuMA (nuclear mitotic apparatus protein) as a major acceptor of poly(ADP-ribose) from tankyrase 1 in mitosis. We showed by immunofluorescence and immunoprecipitation that association between tankyrase 1 and NuMA increases dramatically at the onset of mitosis, concomitant with PARsylation of NuMA. Knockdown of tankyrase 1 by siRNA (small interfering RNA) eliminates PARsylation of NuMA in mitosis, confirming tankyrase 1 as the PARP responsible for this modification. However, even in the absence of tankyrase 1 and PARsylation, NuMA localizes to spindle poles. By contrast, siRNA knockdown of NuMA results in complete loss of tankyrase 1 from spindle poles. We discuss our result in terms of a model where PARsylation of NuMA by tankyrase 1 in mitosis could play a role in sister telomere separation and/or mitotic progression.

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