4.8 Article

Systematic Analysis of Human Protein Complexes Identifies Chromosome Segregation Proteins

期刊

SCIENCE
卷 328, 期 5978, 页码 593-599

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1181348

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资金

  1. European Commission [LSHG-CT-2004-503464]
  2. Boehringer Ingelheim
  3. Vienna Spots of Excellence Programme
  4. Austrian Science Fund Special Research Programme Chromosome Dynamics
  5. Genome Research in Austria Programme
  6. Max Planck Society
  7. Bundesministerium fur Bildung und Forschung [NGFN-2 SMP-RNAi (01GR0402), NGFN-Plus (01GS0859)]
  8. Natural Science and Engineering Research Council of Canada [RGPIN-355644-2008]
  9. National Cancer Institute of Canada [019562]
  10. Human Frontier Science Program [CDA0044/200]
  11. Japan Society for the Promotion of Science

向作者/读者索取更多资源

Chromosome segregation and cell division are essential, highly ordered processes that depend on numerous protein complexes. Results from recent RNA interference screens indicate that the identity and composition of these protein complexes is incompletely understood. Using gene tagging on bacterial artificial chromosomes, protein localization, and tandem-affinity purification-mass spectrometry, the MitoCheck consortium has analyzed about 100 human protein complexes, many of which had not or had only incompletely been characterized. This work has led to the discovery of previously unknown, evolutionarily conserved subunits of the anaphase-promoting complex and the g-tubulin ring complex-large complexes that are essential for spindle assembly and chromosome segregation. The approaches we describe here are generally applicable to high-throughput follow-up analyses of phenotypic screens in mammalian cells.

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