Characterization of Cep135, a novel coiled-coil centrosomal protein involved in microtubule organization in mammalian cells

J Cell Biol. 2002 Jan 7;156(1):87-99. doi: 10.1083/jcb.200108088. Epub 2002 Jan 7.

Abstract

By using monoclonal antibodies raised against isolated clam centrosomes, we have identified a novel 135-kD centrosomal protein (Cep135), present in a wide range of organisms. Cep135 is located at the centrosome throughout the cell cycle, and localization is independent of the microtubule network. It distributes throughout the centrosomal area in association with the electron-dense material surrounding centrioles. Sequence analysis of cDNA isolated from CHO cells predicted a protein of 1,145-amino acid residues with extensive alpha-helical domains. Expression of a series of deletion constructs revealed the presence of three independent centrosome-targeting domains. Overexpression of Cep135 resulted in the accumulation of unique whorl-like particles in both the centrosome and the cytoplasm. Although their size, shape, and number varied according to the level of protein expression, these whorls were composed of parallel dense lines arranged in a 6-nm space. Altered levels of Cep135 by protein overexpression and/or suppression of endogenous Cep135 by RNA interference caused disorganization of interphase and mitotic spindle microtubules. Thus, Cep135 may play an important role in the centrosomal function of organizing microtubules in mammalian cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • CHO Cells
  • Centrosome / chemistry*
  • Centrosome / immunology
  • Centrosome / metabolism*
  • Centrosome / ultrastructure
  • Cloning, Molecular
  • Cricetinae
  • Cytoplasm / metabolism
  • Cytoplasm / ultrastructure
  • Fibroblasts
  • Interphase / drug effects
  • Mice
  • Microscopy, Immunoelectron
  • Microtubule-Associated Proteins / chemistry*
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / immunology
  • Microtubule-Associated Proteins / metabolism*
  • Microtubules / drug effects
  • Microtubules / metabolism*
  • Microtubules / ultrastructure
  • Molecular Weight
  • Nocodazole / pharmacology
  • Peptides / chemistry
  • Peptides / genetics
  • Peptides / metabolism
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • RNA, Double-Stranded / genetics
  • RNA, Double-Stranded / metabolism
  • RNA, Double-Stranded / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sequence Deletion
  • Spindle Apparatus / chemistry
  • Spindle Apparatus / drug effects
  • Spindle Apparatus / metabolism
  • Spindle Apparatus / ultrastructure
  • Transfection
  • Xenopus

Substances

  • Antibodies, Monoclonal
  • Microtubule-Associated Proteins
  • Peptides
  • RNA, Double-Stranded
  • RNA, Messenger
  • Nocodazole