Late rDNA Condensation Ensures Timely Cdc14 Release and Coordination of Mitotic Exit Signaling with Nucleolar Segregation

Curr Biol. 2017 Nov 6;27(21):3248-3263.e5. doi: 10.1016/j.cub.2017.09.028. Epub 2017 Oct 19.

Abstract

The nucleolus plays a pivotal role in multiple key cellular processes. An illustrative example is the regulation of mitotic exit in Saccharomyces cerevisiae through the nucleolar sequestration of the Cdc14 phosphatase. The peculiar structure of the nucleolus, however, has also its drawbacks. The repetitive nature of the rDNA gives rise to cohesion-independent linkages whose resolution in budding yeast requires the Cdc14-dependent inhibition of rRNA transcription, which facilitates condensin accessibility to this locus. Thus, the rDNA condenses and segregates later than most other yeast genomic regions. Here, we show that defective function of a small nucleolar ribonucleoprotein particle (snoRNP) assembly factor facilitates condensin accessibility to the rDNA and induces nucleolar hyper-condensation. Interestingly, this increased compaction of the nucleolus interferes with the proper release of Cdc14 from this organelle. This observation provides an explanation for the delayed rDNA condensation in budding yeast, which is necessary to efficiently coordinate timely Cdc14 release and mitotic exit with nucleolar compaction and segregation.

Keywords: Cdc14; FEAR; MEN; condensin; mitotic exit; nucleolus; snoRNPs.

MeSH terms

  • Cell Cycle Proteins / metabolism*
  • Cytoskeletal Proteins / metabolism
  • DNA, Fungal / genetics
  • DNA, Ribosomal / genetics*
  • DNA-Directed RNA Polymerases / metabolism
  • Gene Deletion
  • Guanine Nucleotide Exchange Factors / genetics
  • Mitosis / physiology
  • Nucleolus Organizer Region / physiology*
  • Protein Tyrosine Phosphatases / metabolism*
  • Ribonucleoproteins, Small Nucleolar / genetics
  • Ribonucleoproteins, Small Nucleolar / metabolism*
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • BFA1 protein, S cerevisiae
  • CDC14 protein, S cerevisiae
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • DNA, Fungal
  • DNA, Ribosomal
  • Guanine Nucleotide Exchange Factors
  • Hit1 protein, S cerevisiae
  • LTE1 protein, S cerevisiae
  • Ribonucleoproteins, Small Nucleolar
  • Saccharomyces cerevisiae Proteins
  • DNA-Directed RNA Polymerases
  • Protein Tyrosine Phosphatases