Analysis of interphase node proteins in fission yeast by quantitative and superresolution fluorescence microscopy

Mol Biol Cell. 2017 Nov 7;28(23):3203-3214. doi: 10.1091/mbc.E16-07-0522. Epub 2017 May 24.

Abstract

We used quantitative confocal microscopy and FPALM superresolution microscopy of live fission yeast to investigate the structures and assembly of two types of interphase nodes-multiprotein complexes associated with the plasma membrane that merge together and mature into the precursors of the cytokinetic contractile ring. During the long G2 phase of the cell cycle, seven different interphase node proteins maintain constant concentrations as they accumulate in proportion to cell volume. During mitosis, the total numbers of type 1 node proteins (cell cycle kinases Cdr1p, Cdr2p, Wee1p, and anillin Mid1p) are constant even when the nodes disassemble. Quantitative measurements provide strong evidence that both types of nodes have defined sizes and numbers of constituent proteins, as observed for cytokinesis nodes. Type 1 nodes assemble in two phases-a burst at the end of mitosis, followed by steady increase during interphase to double the initial number. Type 2 nodes containing Blt1p, Rho-GEF Gef2p, and kinesin Klp8p remain intact throughout the cell cycle and are constituents of the contractile ring. They are released from the contractile ring as it disassembles and then associate with type 1 nodes around the equator of the cell during interphase.

MeSH terms

  • Cell Cycle / genetics
  • Cell Cycle Proteins / metabolism*
  • Cytokinesis
  • Interphase / genetics
  • Kinesins / metabolism
  • Microscopy, Confocal
  • Microscopy, Fluorescence / methods
  • Mitosis
  • Nodal Protein / genetics
  • Nodal Protein / metabolism*
  • Schizosaccharomyces / genetics
  • Schizosaccharomyces / metabolism
  • Schizosaccharomyces pombe Proteins / metabolism

Substances

  • Cell Cycle Proteins
  • Nodal Protein
  • Schizosaccharomyces pombe Proteins
  • Kinesins