The long term goal of this project is to understand how cytokinesis is regulated, how cytokinesis is coordinated with other mitotic events, and how cells delay further cell cycle progression if cytokinesis is delayed. A conserved signaling network called the SIN in the fission yeast S. pombe functions to trigger initiation of cytokinesis at the end of anaphase. Proper regulation of this network is crucial for coordinating cell and nuclear division to maintain genomic stability. The SIN must be activated only once chromosomes have been segregated, its activity must be maintained until cytokinesis is complete, and the pathway must be inactivated once cytokinesis is finished. In the studies proposed here, we will try to define at a molecular level how each of these steps in SIN regulation is accomplished. In addition, we will attempt to identify targets of the SIN crucial for its role in promoting cytokinesis. High cyclin dependent kinase (Cdk) activity in early mitosis inhibits premature SIN activation until chromosomes have segregated in anaphase.
In Specific Aim 1, we will test whether this inhibition works through direct Cdk phosphorylation of SIN components, in particular Sid2p, Cdc7p, and Cdc11 p. Targets of the SIN required for cell division are not known. We will address this in Specific Aim 2 by using a candidate based approach to identify Sid2p substrates required for cell division in vivo. We have shown that during cytokinesis, the SIN acts not just to promote cytokinesis, but also to inhibit interphase cytoskeletal rearrangements, thereby coordinating completion of cytokinesis with initiation of the next cell cycle.
In Specific Aim 3, we will determine the molecular mechanism by which the SIN inhibits interphase polarity, and the functional significance this inhibition has on successful completion of cytokinesis. Once the SIN is activated, its activity is maintained until cytokinesis is complete, and the SIN is inactivated once cytokinesis is completed. In Specifc Aim 4, we will examine how the Etd1p protein promotes SIN signaling, and whether destruction of Etd1p is the signal to inactivate the SIN upon completion of cytokinesis. Homologs of several SIN proteins in animal cells function as tumor suppressors. Because the basic mechanisms of cell division are highly conserved between yeast and humans, we expect characterization of the precise molecular interactions between SIN proteins will help elucidate how their mammalian homologs act to inhibit tumor formation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM058406-12
Application #
7666765
Study Section
Cell Structure and Function (CSF)
Program Officer
Deatherage, James F
Project Start
1998-03-01
Project End
2011-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
12
Fiscal Year
2009
Total Cost
$368,269
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Genetics
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Dutta, Shubham; Mana-Capelli, Sebastian; Paramasivam, Murugan et al. (2018) TRIP6 inhibits Hippo signaling in response to tension at adherens junctions. EMBO Rep 19:337-350
Mana-Capelli, Sebastian; McCollum, Dannel (2018) Angiomotins stimulate LATS kinase autophosphorylation and act as scaffolds that promote Hippo signaling. J Biol Chem 293:18230-18241
Gupta, Sneha; Govindaraghavan, Meera; McCollum, Dannel (2014) Cross talk between NDR kinase pathways coordinates cytokinesis with cell separation in Schizosaccharomyces pombe. Eukaryot Cell 13:1104-12
Li, Qi; Li, Shuangxi; Mana-Capelli, Sebastian et al. (2014) The conserved misshapen-warts-Yorkie pathway acts in enteroblasts to regulate intestinal stem cells in Drosophila. Dev Cell 31:291-304
Mana-Capelli, Sebastian; Paramasivam, Murugan; Dutta, Shubham et al. (2014) Angiomotins link F-actin architecture to Hippo pathway signaling. Mol Biol Cell 25:1676-85
Gupta, Sneha; Mana-Capelli, Sebastian; McLean, Janel R et al. (2013) Identification of SIN pathway targets reveals mechanisms of crosstalk between NDR kinase pathways. Curr Biol 23:333-8
Bajpai, Archana; Feoktistova, Anna; Chen, Jun-Song et al. (2013) Dynamics of SIN asymmetry establishment. PLoS Comput Biol 9:e1003147
Cipak, Lubos; Gupta, Sneha; Rajovic, Iva et al. (2013) Crosstalk between casein kinase II and Ste20-related kinase Nak1. Cell Cycle 12:884-8
Johnson, Alyssa E; McCollum, Dannel; Gould, Kathleen L (2012) Polar opposites: Fine-tuning cytokinesis through SIN asymmetry. Cytoskeleton (Hoboken) 69:686-99
Mana-Capelli, Sebastian; McLean, Janel R; Chen, Chun-Ti et al. (2012) The kinesin-14 Klp2 is negatively regulated by the SIN for proper spindle elongation and telophase nuclear positioning. Mol Biol Cell 23:4592-600

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