knockdowns of APC1, CDC27 and AP2 were each found to arrest the procyclic form T. brucei cells in metaphase, suggesting that the APC/C function is required for metaphase-anaphase transition. The APC/C function is also needed for degradation of the mitotic cyclin CycB2/cyc6 during mitosis in T. brucei. The degradation, essential for mitotic exit among the other eukaryotes, is mediated by the 26S proteasome in T. brucei, which recognizes poly-ubiquitinated CycB2/cyc6 as substrate. This ubiquitination-dependent degradation is likely provided by the poly-ubiquitinating action of APC/ C on CycB2/cyc6, a function that apparently remains conserved in T. brucei. We have thus characterized an APC/C in T. brucei that performs apparently both of the well-known functions during mitosis. But its unusually simple composition and the apparent BMS-345541 functional redundancy among the 10 subunits distinguish it from the other APC/C’s. The lack of an MCC mediated regulatory mechanism and the apparent absence of securin/Pds1 and CDC20 in T. brucei further demonstrates a significant discrepancy between T. brucei APC/C and the others. The APC/C in T. brucei could be thus easily classified as a potential target for antitrypanosomiasis chemotherapy. Supporting Information The APC/C of Trypanosoma brucei signals. Approximately 200 cells from each sample were counted and data are presented as localization pattern of S-phase, metaphase and anaphase from two independent experiments. hydroxyurea for 16 hours, washed twice in fresh medium and allowed to progress synchronously for 8 hours. The hourly cell samples were stained with propidium iodide, processed for flow cytometry and the FL2-A DNA peaks are presented. DNA contents were shown at the bottom. The RNAi knockdown of AP1/APC4. qPCR assay of the level of AP1/APC4 mRNA 72 hrs after the induction of AP1/APC4 RNAi. The rate of cell growth was monitored for 7 days after the RNAi induction. N/K tabulations of the AP1/APC4-depleted cells on days 0, 1, 3 and 5 after RNAi induction. Flow cytometric analysis of DNA contents in AP1/ APC4-depleted cells. Little distinction was observed in the results from RNAi-induced and un-induced cells. Acknowledgments We thank Drs D. Toczyski, P. Walter and D. Morgan at the University of California San Francisco for their generous gift of yeast wild type and APC/C mutant strains. Mass spectrometry analysis was performed in the Bio-Organic Biomedical Mass Spectrometry Resource at the University of California San Francisco. We would also like to thank Chris Adams and the Stanford University Mass Spectrometry Core, for data acquisition and analysis of one of the MS data sets. types; hydrocephalus and abnormal ossification in one case and defects in hippocampal development, neural stem cell differentiation, and weight-loss in the other. Thus, other members 16483784 of the family do not compensate for the functions of individual NFI genes. There are very few reports on the mechanisms of action of 18772318 human NFI proteins. NFI protein 
overexpression results in resistance of chicken cells to transformation by qin, jun and fos oncogenes. NFIC interacts with histone H1, PIRIN and TAFII55 proteins and activates transcription at specific loci, such as glucocorticoidresponsive MMTV promoter. NFIX is important for activation of GFAP transcription in astrocytes and provides resistance against TGFB-induced apoptosis in mink epithelial cells. At the CDKN1A promoter, all different NFI members exhibit different levels of tr
