Journal of Biomedical Science

, Volume 14, Issue 5, pp 681–694

Apoptotic cleavage of NuMA at the C-terminal end is related to nuclear disruption and death amplification

Article

DOI: 10.1007/s11373-007-9165-3

Cite this article as:
Lin, HH., Hsu, HL. & Yeh, NH. J Biomed Sci (2007) 14: 681. doi:10.1007/s11373-007-9165-3

Abstract

NuMA is a nuclear matrix protein in interphase and distributes to the spindle poles during mitosis. While the essential function of NuMA for mitotic spindle assembly is well established, a structural role of NuMA in interphase nucleus has also been proposed. Several observations suggest that the apoptotic degradation of NuMA may relate to chromatin condensation and micronucleation. Here we demonstrate that four apoptotic cleavage sites are clustered at a junction between the globular tail and the central coiled-coil domains of NuMA. Cleavage of a caspase-6-sensitive site at D1705 produced the R-form, a major tail-less product of NuMA during apoptosis. The other two cleavage sites were defined at D1726 and D1747 that were catalyzed, respectively, by caspase-3 and an unknown aspartase. A NuMA deletion mutant missing the entire cleavage region of residues 1701–1828 resisted degradation and protected cells from nuclear disruption upon apoptotic attack. Under such conditions, cytochrome c was released from mitochondria, but the subsequent apoptotic events such as caspase-3 activation, poly(ADP-ribose) polymerase degradation, and DNA fragmentation were attenuated. Conversely, the tail-less NuMA alone, a mutant mimicking the R-form, induced chromatin condensation and activated the death machinery. It supports that intact NuMA is a structural element in maintaining nuclear integrity.

Keywords

apoptosis caspase chromatin condensation micronucleation nuclear matrix nucleus NuMA 

Copyright information

© National Science Council Taipei 2007

Authors and Affiliations

  • Hsueh-Hsuan Lin
    • 1
  • Hsin-Ling Hsu
    • 1
    • 2
  • Ning-Hsing Yeh
    • 1
  1. 1.Institute of Microbiology and Immunology, School of Life ScienceNational Yang-Ming UniversityTaipeiTaiwan ROC
  2. 2.Division of Molecular and Genomic MedicineNational Health Research InstitutesMiaoli CountyTaiwan ROC