Analysis ofS. pombeSIN protein SPB-association reveals two genetically separable states of the SIN
Author(s) -
Paulina Wachowicz,
Anastasia Chasapi,
Andrea Krapp,
Elena Cano del Rosario,
Daniel Schmitter,
Daniel Sage,
Michaël Unser,
Ioannis Xénarios,
Jacques Rougemont,
Viesturs Simanis
Publication year - 2014
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.160150
Subject(s) - biology , cytokinesis , anaphase , schizosaccharomyces pombe , mitosis , microbiology and biotechnology , spindle pole body , spindle apparatus , mitotic exit , spindle checkpoint , genetics , mutant , cell division , cell cycle , cell , gene
The Schizosaccharomyces pombe septation initiation network (SIN) regulates cytokinesis, and asymmetric association of SIN proteins with the mitotic spindle pole bodies (SPBs) is important for its regulation. Here, we have used semi-automated image analysis to study SIN proteins in large numbers of wild-type and mutant cells. Our principal conclusions are: first, that the association of Cdc7p with the SPBs in early mitosis is frequently asymmetric, with a bias in favour of the new SPB; second, that the early association of Cdc7p-GFP to the SPB depends on Plo1p but not Spg1p, and is unaffected by mutations that influence its asymmetry in anaphase; third, that Cdc7p asymmetry in anaphase B is delayed by Pom1p and by activation of the spindle assembly checkpoint, and is promoted by Rad24p; and fourth, that the length of the spindle, expressed as a fraction of the length of the cell, at which Cdc7p becomes asymmetric is similar in cells dividing at different sizes. These data reveal that multiple regulatory mechanisms control the SIN in mitosis and lead us to propose a two-state model to describe the SIN.
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