A role for Caenorhabditis elegans importin IMA-2 in germ line and embryonic mitosis

Mol Biol Cell. 2002 Sep;13(9):3138-47. doi: 10.1091/mbc.e02-02-0069.

Abstract

The importin alpha family of nuclear-cytoplasmic transport factors mediates the nuclear localization of proteins containing classical nuclear localization signals. Metazoan animals express multiple importin alpha proteins, suggesting their possible roles in cell differentiation and development. Adult Caenorhabditis elegans hermaphrodites express three importin alpha proteins, IMA-1, IMA-2, and IMA-3, each with a distinct expression and localization pattern. IMA-2 was expressed exclusively in germ line cells from the early embryonic through adult stages. The protein has a dynamic pattern of localization dependent on the stage of the cell cycle. In interphase germ cells and embryonic cells, IMA-2 is cytoplasmic and nuclear envelope associated, whereas in developing oocytes, the protein is cytoplasmic and intranuclear. During mitosis in germ line cells and embryos, IMA-2 surrounded the condensed chromosomes but was not directly associated with the mitotic spindle. The timing of IMA-2 nuclear localization suggested that the protein surrounded the chromosomes after fenestration of the nuclear envelope in prometaphase. Depletion of IMA-2 by RNA-mediated gene interference (RNAi) resulted in embryonic lethality and a terminal aneuploid phenotype. ima-2(RNAi) embryos have severe defects in nuclear envelope formation, accumulating nucleoporins and lamin in the cytoplasm. We conclude that IMA-2 is required for proper chromosome dynamics in germ line and early embryonic mitosis and is involved in nuclear envelope assembly at the conclusion of mitosis.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / metabolism*
  • Caenorhabditis elegans Proteins / physiology*
  • Cell Nucleus / metabolism
  • Crosses, Genetic
  • Cytoplasm / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Karyopherins / metabolism*
  • Karyopherins / physiology*
  • Mitosis*
  • Nuclear Envelope / metabolism
  • Phenotype
  • RNA Interference
  • Time Factors
  • alpha Karyopherins / metabolism*
  • alpha Karyopherins / physiology*

Substances

  • Caenorhabditis elegans Proteins
  • IMA-2 protein, C elegans
  • Karyopherins
  • alpha Karyopherins