KIF13A overexpression favors NP distribution to the cell edge and requires KIF13A binding to microtubules. KIF13A overexpressionfavorsNP distribution to.

Slides:



Advertisements
Similar presentations
Rap1 regulates the accumulation of AJ material during ZA morphogenesis
Advertisements

Transient Membrane Localization of SPV-1 Drives Cyclical Actomyosin Contractions in the C. elegans Spermatheca  Pei Yi Tan, Ronen Zaidel-Bar  Current.
Phenotypic analysis of spo73∆ mutant.
Characterization of DPR proteins in primary rat neurons and HEK293 cells. Characterization of DPR proteins in primary rat neurons and HEK293 cells. GFP,
Volume 21, Issue 5, Pages e5 (May 2017)
Fig. 3 BX795 blocks the synthesis of HSV-1 virions.
Disrupted dynamics of early stages of differentiation perturbs neural cell fate specification. Disrupted dynamics of early stages of differentiation perturbs.
Atp1a3 phosphomutants show alterations in subcellular localization.
Leukemia involves the accumulation of ISP CD8+T-cells and blockages in B-cell development. Leukemia involves the accumulation of ISP CD8+T-cells and blockages.
Fig. 1 BX795 suppresses HSV-1 infection.
HURP is an obstacle for KIF18A on K-fibers in metaphase cells.
R1441G‐LRRK2 co‐localizes with Rab10 in the periphery and Rab8 near the nucleus R1441G‐LRRK2 co‐localizes with Rab10 in the periphery and Rab8 near the.
Nuclear DNA signal is altered in Chd5-deficient NSCs.
Tapetal mitochondria in wild-type (WT), drp3b, and elm1 mutants.
Figure 5 Electron microscopy of transfected HeLa cells and Dnm1Ftfl neurons (A) Electron microscopy (EM) of HeLa cells transfected with wild type (WT)
Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
The histidine-rich loop regulates accessibility of the active site and RDEL motif in vivo. The histidine-rich loop regulates accessibility of the active.
Fig. 4. Seeding density modulates cell shape in both cell types
A highly conserved six-amino-acid region in the C-terminal CT domain of MARCH8 is responsible for its ability to downregulate TfR. A highly conserved six-amino-acid.
The C-terminal membrane-proximal region of MARCH8 interacts with TfR.
The effects of a dominant negative mutant of lamin B1 on lamin distribution in HeLa cells. The effects of a dominant negative mutant of lamin B1 on lamin.
Subcellular distribution of TACE-eGFP changes with the coexpression of active ERK2. Subcellular distribution of TACE-eGFP changes with the coexpression.
Fig. 5. Expression of either dFMRP or human FMRP does not induce eIF2α phosphorylation.(A) Analysis of eIF2α phosphorylation upon dFMRP expression. Expression.
Fig. 1. Loss of PC following INT depletion
Indirect fluorescence assay of N. gruberi cells.
The trafficking of VSVG–GFP to pre‐Golgi structures is impaired by depletion of GMAP‐210.The trafficking of VSVG–GFP to pre‐Golgi structures is impaired.
Fig. 3. Mutation of Y520 and Y667 result in increased delivery of prestin to the apical surface of MDCK cells.MDCK cells transiently transfected with wt.
Fig. 3. Genetic interactions between unc-53 and unc-6 and between unc-53 and unc-5 affect intracellular UNC-40::GFP localization.(A–H) Photomicrographs.
Fcp1 CTD phosphatase affects a broad range of transcripts in the +N and -N media. Fcp1 CTD phosphatase affects a broad range of transcripts in the +N and.
The coding potential of GFP-Sec61b is not required for its localization to the ER. (A) COS7 cells were transfected with plasmid encoding various GFP-tagged.
Fig. 6. Comparison of Plk4 with Sas-6 localization
Don1 localization in vps13Δ cells.
Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.
ICAM-1 forms distinct complexes with filamin B, α-actinin-4 and cortactin. ICAM-1 forms distinct complexes with filamin B, α-actinin-4 and cortactin. (A)
The effect of TDP-43A315T expression on dendrite spine development.
FAK/Src activity is required to trap PTP1BDA in adhesions.
Loss of LAR phosphatase activity is associated with decreased adhesion complex formation. Loss of LAR phosphatase activity is associated with decreased.
The effect of TDP-43A315T expression at the synapse.
ArfGAP1 expression alters GBF1 recruitment to Golgi membranes.
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.
Fig. 1. Loss of PC following INT depletion
Facilitated migration of implanted Schwann cells infected with Ad-Cdc2 viral vectors in the injured sciatic nerve. Facilitated migration of implanted Schwann.
Effect of γ-secretase inhibition on the vulnerability of primary neurons to OGD. (A) Experimental design. Effect of γ-secretase inhibition on the vulnerability.
Exo70 is recruited to the plasma membrane at sites of mechanical wounding. Exo70 is recruited to the plasma membrane at sites of mechanical wounding. NRK.
Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells.
Expression of active Rho partially rescues Erk1/2 activation and peripheral FA phenotype in RIAM-knockdown cells. Expression of active Rho partially rescues.
Lysine residues in the cytoplasmic region of TfR are involved in the MARCH8-induced downregulation of TfR. Lysine residues in the cytoplasmic region of.
ALS-CSF induces atrophy of type 2 fibres in EDL muscle of neonatal rats. ALS-CSF induces atrophy of type 2 fibres in EDL muscle of neonatal rats. (A,B)
miR-145 overexpression reduces IGF1-coated bead attachment.
Wrch-1 localizes to focal adhesions.
Volume 26, Issue 12, Pages e5 (March 2019)
KIF13A depletion leads to a drop in virus titers, without affecting viral protein expression. KIF13A depletion leadsto a drop in virus titers, without.
The vps13 mutants are hypersensitive to SDS but cell wall integrity is not compromised. The vps13 mutants are hypersensitive to SDS but cell wall integrity.
The BRCA1 aggregates exclude large nuclear structures.
PtdIns(4,5)P2 dependence of TbEpsinR and TbCALM membrane targeting.
WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates TfR. WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates.
Sensory neurons grow and downregulate UCHL1 expression levels during postnatal maturation. Sensory neurons grow and downregulate UCHL1 expression levels.
Conservation of key sequence features and endocytic localisation in TbCALM. Conservation of key sequence features and endocytic localisation in TbCALM.
The regulatory domain of HSF1 is involved in the pro-apoptotic response to TNF. (A) Upper panel, functional domains and potential DAPK phosphorylation.
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Ubiquitin mediates the interaction between Smo and Vps36.
Subnuclear localization of HA-tagged EBNA1 protein.
GFP-Myo10 overexpression increases TNT numbers in neuronal CAD cells.
Subcellular distribution of Mst4 and aPKCι in in vivo enterocytes.
Vps36 regulates the accumulation of Smo and Hh signaling activity.
FISH with pooled large-insert clones representing chromosome 17 early-replicating (green) and chromosome 5 late-replicating (red) loci to (A) human (schematics.
Taro Ohkawa, Matthew D. Welch  Current Biology 
Autophagy Activation Is Mediated by the Secretion of T3Es.
NBR1 Counteracts P. syringae Infection.
Presentation transcript:

KIF13A overexpression favors NP distribution to the cell edge and requires KIF13A binding to microtubules. KIF13A overexpressionfavorsNP distribution to the cell edge and requires KIF13A binding to microtubules. (A-C) HeLa cells were transfected with GFP (A) GFP-KIF13A-WT (GFP-KIF13A) (B) or GFP-KIF13A-ST (GFP-KIF-ST) (C). At 24 h post transfection cells were infected (or mock-infected) with PR8 at an MOI=3. After 8 hpi cells were fixed and stained for NP (red), endogenous Rab11 (gray) and counterstained with DAPI (scale bars: 10 µm). Boxed areas highlight the proximity between KIF13A and vRNP-Rab11 vesicles and are magnified to the right of these panels. (D) Sketch of KIF13A wild-type (WT) and mutant (KIF13A-ST) forms. (E) The amount of NP at the edge of the cell was quantified in percent by calculating the ratio of NP intensity within 2 μm from the plasma membrane to the NP intensity of the whole cell. Data obtained of 25 cells and three replicates were plotted and analysed statistically by using one-way ANOVA followed by Tukey's multiple comparisons, and were considered significant at **P<0.01 and ***P<0.001. Ana Ramos-Nascimento et al. J Cell Sci 2017;130:4038-4050 © 2017. Published by The Company of Biologists Ltd