Phospho-regulation of DDA3 function in mitosis

Biochem Biophys Res Commun. 2010 Mar 5;393(2):259-63. doi: 10.1016/j.bbrc.2010.01.115. Epub 2010 Feb 1.

Abstract

DDA3 is a microtubule-associated protein that controls chromosome congression and segregation by regulating the mitotic spindle. Depletion of DDA3 alters spindle structure, generates unaligned chromosomes at metaphase, and delays the mitotic progression. Through a mass spectrometry analysis, we found that DDA3 is phosphorylated on Ser225 during mitosis. Phosphorylation of this residue is important for the mitotic function of DDA3, as the phospho-mimicking DDA3-S225D variant, but not the nonphosphorable DDA3-S225A mutant, rescues the DDA3-knockdown phenotype. We conclude that the mitotic function of DDA3 is regulated by phosphorylation on the Ser225 residue.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Chromosome Pairing
  • HeLa Cells
  • Humans
  • Mitosis*
  • Molecular Sequence Data
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Phosphorylation / genetics
  • Serine / genetics
  • Serine / metabolism

Substances

  • PSRC1 protein, human
  • Phosphoproteins
  • Serine