n 2 SET Domain Protein Regulates S. pombe Cytokinesis proteins and has been proposed to recognize unmodified histone tails. Lastly, the LisH domain has been shown to be important in binding to hypoacetylated histone H4 tails. hif2D, set3D and snt1D mutants display cytokinesis defects upon perturbation of the cell division machinery If Hif2p, Set3p, and PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22180813 Snt1p act as part of a protein complex with a common function, then one would expect the respective loss of function mutants to exhibit similar phenotypes. To determine if this were the case, hif2D, set3D, and snt1D strains, as well as the respective double and triple mutant strains, were grown to mid-log phase in liquid 
YES at 30uC and 10-fold serial dilutions were plated onto YES plates containing LatA or DMSO. Interestingly, all mutants buy Taladegib displayed a reduced capacity for growth in the presence of LatA in comparison to wild type. Next, the cells were examined at the microscopic level to determine if the observed sensitivity to LatA was related to defects in cytokinesis. The deletion mutants were treated with LatA or DMSO for 5 hours in liquid YES growth medium, and subsequently fixed and stained with DAPI and aniline blue to visualize the nucleus and cell wall/septum, respectively. The cells were classified into four different phenotypic categories: i) uni-nucleate cells, ii) bi-nucleate cells with a morphologically normal septum, iii) bi-nucleate cells with a fragmented septum, and iv) tetra-nucleate cells. As shown in set3D lsk1D double mutants to exhibit a more severe sensitivity to LatA than either of the respective single mutants. To differentiate between these two possibilities, a wild-type strain, as well as the respective single and double deletion mutants, were treated with LatA or DMSO for 5 hours in liquid YES growth medium. This was followed by fixation and staining with DAPI and aniline blue to visualize the nucleus and cell/wall septum, respectively. Interestingly, both set3D clp1D and set3D lsk1D double mutants showed a significant increase in sensitivity to LatA. At a concentration of 0.1 mM both double mutants displayed a large proportion of tetra-nucleate cells with fragmented septa. In contrast, the phenotypes of single mutants at this dose were far less severe. These results are consistent with a model in which Set3p functions in parallel to both Clp1p and Lsk1p. Thus, set3 defines a novel regulatory pathway governing the successful completion of cytokinesis in fission yeast. Set3p, Hif2p and Snt1p form a nuclear-localized complex Bioinformatics suggested that the hif2, set3, and snt2 gene products exist as part of a conserved histone deacetylase complex. In order to function in chromatin remodeling, one would expect Hif2p, Set3p, and Snt2p to localize to the nucleus. To test this prediction, strains expressing GFP-tagged fusion proteins integrated at their normal genomic loci and under the control of their native promoters were constructed. Consistent with a role in chromatin modification, all three proteins localized to the nucleus. The localization of the fusion proteins was not altered as a function of cell cycle position or as a function of LatA concentration in the growth medium. Next, to determine if Hif2p, Set3p, and Snt1p physically interacted in vivo, co-immunoprecipitation experiments using Myc- or HA-epitope tagged alleles were performed. Interestingly, Set3-HA and Hif2-HA fusion proteins could be detected in antiMyc immuno-precipitates of Snt1-Myc Set3-HA
