Fig. 8. Compared mobilities of passenger proteins in G2/M-prophase, metaphase and anaphase.FRAP experiments were performed on HeLa cells stably expressing.

Slides:



Advertisements
Similar presentations
Mitochondria localize to both the front and the rear of neutrophils.
Advertisements

Localization of H2B-GFP protein in HeLa cells.
María Dolores Vázquez-Novelle, Mark Petronczki  Current Biology 
KIN-3 depletion leads to increased levels of centrosomal ZYG-1
Cortical NuMA enrichment upon Plk1 inhibition is dynein independent.
MMAP is required for spindle dynamics regulation.
Recruitment of PH-Akt-GFP to the leading edge of the cell during chemotaxis. Recruitment of PH-Akt-GFP to the leading edge of the cell during chemotaxis.
Fig. 4. Clinically defined SMN mutants show alterations in the association with telomerase complex proteins. Clinically defined SMN mutants show alterations.
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 4. Expression of oxt is undetectable in the med12 mutant but is unaffected by treatment with Wnt inhibitors. Expression of oxt is undetectable in.
Fig. 1. Chlamydia infection causes elevated levels of sortilin.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
Fig. 2. Proportion of motile objects and track length
Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle
Fig. 4. A primary screen based on scrape closure
A Drosophila cell culture model to study VAP(P58S) aggregation.
Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.
Fig. 2. Histone H3 phosphorylation appears at prometaphase upon C4 treatment.(A) Western blots were realized on cells synchronized at mitotic entry in.
Fig. 1. Mitochondrial internalization in cardiomyocytes.
Fig. 5. Onecut transcription factors are important for the correct generation of the mdDA neuronal population.(A) Schematic representation of the region.
Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.
Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.
Fig. 2. Salivary glands from RasV12-expressing larvae produce MMP1, release tissue fragments into the hemolymph and express apoptotic markers.Salivary.
Table 2. Cell surface abundance of β1 integrin measured by flow cytometry.DDR wild type and DDR over-expressing cells were treated with deoxymannojirimycin.
Fig. 1. E-cadherin localizes in nano-scale clusters.
Fig. 4. Acentriolar mitotic spindle assembly
Fig. 1. γ-Tubulin localizes in close proximity to centriole walls in interphase but within an extended PCM meshwork in mitosis.U2OS cells were fixed and.
Fig. 2. DDR1 over-expression enhances collagen fibril reorganization
Fig. 1. Ovarian cancer spheroids can bud from a monolayer
Fig. 6. Comparison of Plk4 with Sas-6 localization
Fig. 3. The checkpoint proteins Mad2 and BubR1 remain associated with the kinetochores of unaligned chromosomes in cenp-metaΔ mutant cells entering anaphase.(A–C)
Fig. 5. GFP fluorescence colocalization of Gcn5.
Fig. 6. Effect of SAHA and ML on histone acetylation, BAX, and p21CDKN1A expression.PANC-1 and BxPC-3 cells were incubated for 48 hours with 5 µM.
Fig. 7. Lhx1-RNAi reduces the eye size
The TER94-p47 complex isinvolved in Notch signaling regulation
Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.
Fig. 7. Ror-GFP binds to Myc-tagged Wnts and Wnt receptors.
Fig. 6. STK35 KO mice show ovary defects.
Fig. 2. Sorting in chimeric embryoid bodies of wildtype with E- or N-cadherin null ES cells.Wildtype, E-cadherin null (9J), and N-cadherin null (Ncad95)
Fig. 4. SMXL6 is degraded in response to SL treatment.
Fig. 8. The morphology of the ventral nerve cord in Ror-Myc overexpressing embryos is normal. The morphology of the ventral nerve cord in Ror-Myc overexpressing.
Statistical chart of significantly differentially expressed genes
Fig. 4. Quantitative mRNA expression of two membrane-bound trehalase genes in Harmonia axyridis in response to starvation (0–72 h). Quantitative mRNA expression.
Fig. 2. Kinetics of OptoEphB2 activation.
Effect of the plastid translation inhibitor Spec on LR development
The FRAP mobility of EGFP-UAP56, but not its K95N mutant, is ATP-dependent. The FRAP mobility of EGFP-UAP56, but not its K95N mutant, is ATP-dependent.
EpiDEG efficiently degrades GFP-tagged proteins that localize to different subcellular localizations. epiDEG efficiently degrades GFP-tagged proteins that.
dcn1-deletion results in attenuated cohesin cleavage at anaphase
Lysine residues in the cytoplasmic region of TfR are involved in the MARCH8-induced downregulation of TfR. Lysine residues in the cytoplasmic region of.
Regulation of lipid droplet formation by PI3-kinase activity.
FRAP and FLIP analysis of GFP-ADAR2 and GFP-ADAR1C-Term.
Fig. 2. Acetylation stiffens primary cilia.
Fig. 1. Cell adhesion molecule expression and the aggregation of wildtype and mutant ES cells.(A) Wildtype (WT), E-cadherin null (9J), and N-cadherin null.
Fig. 5. Testis defects in STK35 KO mice.
Fig. 1. Rnd2 and Rnd3 induce stress fibres whereas Rnd1 reduces stress fibres in endothelial cells.(A) Rnd mRNAs are expressed in HUVECs. Total RNA was.
Fig. 3. Mean force and velocity during jumping
Fig. 5. EGL-20 inhibits anterior and posterior orientation of UNC-40 asymmetric localization and the formation of axons from these sites.(A–D) HSN neurons.
The BRCA1 aggregates exclude large nuclear structures.
Fig. 1. Expression of a Ror-eGFP fusion protein under control of the endogenous Ror promoter in Drosophila embryos. Expression of a Ror-eGFP fusion protein.
Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.
Fig. 5. Co-expression analyses of disease mutations in YFP-RPGRIP1α1 with wild-type RFP-RPGR1–19 or RFP-RPGRORF15 in COS7 cells.YFP-RPGRIP1α1 with disease-associated.
Ectopic expression of caveolin-1 in ZR75 human breast cancer cells downregulated survivin and decreased cell proliferation. Ectopic expression of caveolin-1.
Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.
WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates TfR. WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates.
Fig. 3. Inclusion of E-cadherin into stationary clusters requires cis-, trans-, and cytoplasmic interactions. Inclusion of E-cadherin into stationary clusters.
Fig. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Dynamics of actin-binding proteins in the ICAM-1 complex.
Cdk1 Negatively Regulates Midzone Localization of the Mitotic Kinesin Mklp2 and the Chromosomal Passenger Complex  Stefan Hümmer, Thomas U. Mayer  Current.
Melina Schuh, Christian F. Lehner, Stefan Heidmann  Current Biology 
Presentation transcript:

Fig. 8. Compared mobilities of passenger proteins in G2/M-prophase, metaphase and anaphase.FRAP experiments were performed on HeLa cells stably expressing GFP-INCENP or survivin-GFP or aurora kinase B-GFP. Compared mobilities of passenger proteins in G2/M-prophase, metaphase and anaphase.FRAP experiments were performed on HeLa cells stably expressing GFP-INCENP or survivin-GFP or aurora kinase B-GFP. The bleached zone is indicated by the dotted line. The recovery of fluorescence was registered at the times indicated and expressed as relative intensities. The kinetics of recovery are shown on the right side of the cell images. Time is in seconds. Survivin and aurora recovering are already published (Delacour-Larose et al., 2004; Delacour-Larose et al., 2007) and recalled in the figure for comparison. The localization of passenger proteins during mitosis progression is indicated as well as the timing of efficiency of C4 (from G2/M to prometaphase and at anaphase onset). The proposed variations of aurora kinase B affinity for ATP are visualized with arrows. Ly-Thuy-Tram Le et al. Biology Open 2013;bio.20133079 © 2013. Published by The Company of Biologists Ltd