Mistargeting of B-type lamins at the end of mitosis: implications on cell survival and regulation of lamins A/C expression

J Cell Biol. 2001 Apr 30;153(3):621-6. doi: 10.1083/jcb.153.3.621.

Abstract

We previously showed that targeting of protein phosphatase 1 (PP1) to the nuclear envelope (NE) by the A-kinase anchoring protein, AKAP149, correlates with nuclear assembly of B-type lamins in vitro. We demonstrate here that failure of AKAP149-mediated assembly of B-type lamins into the nuclear lamina at the end of mitosis is followed by apoptosis, and induces expression of the gene encoding A-type lamins in cells that normally do not express lamins A/C. In HeLa cells, inhibition of PP1 association with the NE mediated by a peptide containing the PP1-binding domain of AKAP149 results in failure of B-type lamins to assemble, and in their rapid caspase-dependent proteolysis. However, assembly of lamins A/C is not affected. Nonetheless, apoptosis follows within hours of nuclear reformation after mitosis. In lymphoid KE37 cells, which do not express lamins A/C, inhibition of B-type lamin assembly triggers rapid synthesis and nuclear assembly of both lamins A and C before apoptosis takes place. The results indicate that nuclear assembly of B-type lamins is essential for cell survival. They also suggest that mistargeting of B-type lamins at the end of mitosis elicits a tentative rescue process to assemble a nuclear lamina in lymphoid cells that normally do not express lamins A/C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A Kinase Anchor Proteins
  • Adaptor Proteins, Signal Transducing*
  • Apoptosis
  • Carrier Proteins / metabolism*
  • Cell Compartmentation
  • Gene Expression Regulation
  • HeLa Cells
  • Hematopoietic Stem Cells
  • Humans
  • Lamins
  • Lymphocytes / cytology
  • Membrane Proteins / metabolism*
  • Mitosis*
  • Nocodazole / pharmacology
  • Nuclear Envelope / metabolism*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Phosphoprotein Phosphatases / metabolism*
  • Protein Phosphatase 1
  • Protein Transport*

Substances

  • A Kinase Anchor Proteins
  • AKAP1 protein, human
  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • Lamins
  • Membrane Proteins
  • Nuclear Proteins
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 1
  • Nocodazole