Fig. 1. Loss of PC following INT depletion

Slides:



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

Knockdown of DAO inhibits DNA damage–induced senescence.
KIN-3 depletion leads to increased levels of centrosomal ZYG-1
CK2 is required for early cell divisions in C. elegans embryos
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. Overview of the nervous system of the adult S. roscoffensis.
Fig. 7. Vinculin recruitment enhances the efficiency of barrier formation.(A) TER measurements after a calcium switch in α-catenin-depleted MDCK cells.
Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 4. E-cadherin expression level affects monomer dynamics.
Fig. 4. smc3 regulates the expression of cx43 in regenerating fins.
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
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. 3. Knockdown of cited3 results in increased cell death but it does not affect proliferation.Embryos that are injected with the control MO (A–C), cited3.
Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.
Fig. 7. Knockdown of Meis1 abolishes CR4. 2-GFP expression
Inflammation is associated with increased basal-cell plasticity in the Nkx3.1 mutant prostate. Inflammation is associated with increased basal-cell plasticity.
Fig. 1. Mitochondrial internalization in cardiomyocytes.
Fig. 3. Read-outs of mTORC1 (P-S6(S235/236)) and mTORC2 (P-Akt(S473)) in wtPC12 and PC12-27 cells.(A,B) wtPC12 and PC12-27 cells were treated for 48 hr.
Fig. 4. Expression of p75NTR and time-course of TrkA autophosphorylation at the Y751 and Y490 sites in PC12-27 cells transfected with the vector, empty.
Neutralization and knockdown of TGFβ2 results in fewer nephrons ex vivo. Neutralization and knockdown of TGFβ2 results in fewer nephrons ex vivo. (A,B)
Fig. 1. Morphological and growth characterization of hBMCs and hPDCs
Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.
Fig. 8. p85β regulates active Cdc42 and Rac localization to deep adhesions.(A) NIH3T3 cell lines expressing p85α or p85β were incubated without serum (2 h),
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. 5. Recovery steps of mitotic acentriolar cells after cold MT depolymerisation.(A,B) Time-lapse sequences of mitotic spindle re-formation at 18°C.
Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.
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. 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. 1. Ovarian cancer spheroids can bud from a monolayer
Fig. 8. Knockdown of Meis1 reduces the expression of Foxn4 and Lim1+2
Fig. 6. LR phenotype of plastid translation-defective mutants with/without Spec. LR phenotype of plastid translation-defective mutants with/without Spec.
Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH
Fig. 1. Co-immunostaining of yeast spheroplasts with anti-hASNS and anti-alpha tubulin revealed that yeast asparagine synthetases formed filaments/foci.
Fig. 3. Coilin levels correlate with altered nascent U2 snRNA, hTR and rRNA levels.RNA isolated from HeLa or WI-38 cells following RNAi targeting coilin.
Fig. 2. Ex vivo inducible knockout of PDCD2 in ESCs results in loss of S phase entry and increased p53.(A) Growth curve of inducible knockout and WT ESCs.
Fig. 5. Morphological changes of the N
Fig. 6. Comparison of Plk4 with Sas-6 localization
Fig. 2. Morphological analysis of acentriolar mitotic spindles
Fig. 7. Lhx1-RNAi reduces the eye size
Fig. 2. Centrosomal proteins display distinct localizations and radial distances from centriole walls.U2OS cells were fixed and stained with the indicated.
Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.
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. 4. Co-immunostaining of nocodazole or ASNase treated RPE-1 cells with anti-hASNS and anti-alpha tubulin showed defect in both mitotic spindle formation.
Fig. 6. STK35 KO mice show ovary defects.
Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.
Loss of LAR phosphatase activity is associated with decreased adhesion complex formation. Loss of LAR phosphatase activity is associated with decreased.
Reb does not play a significant role in regulating TGF-β signaling
Fig. 3. Overexpression of wild-type GFP-CPAP, but not GFP-CPAP-377EE (GFP-377EE), induces cilia formation and promotes the growth of cilia.CAD cells (A,B)
Fig. 4. Perinuclear dynein regulators are not required for primary ciliogenesis.RPE cells were transfected with siRNA and either nocodazole-treated, fixed,
Fig. 1. Loss of PC following INT depletion
Depleting CK2 restores centrosomal ZYG-1 levels in zyg-1(it25) embryos
Loss of ezrin and MISP leads to the formation of cysts containing multiple lumens and spindle orientation defects. Loss of ezrin and MISP leads to the.
Fig. 2. iPSCs produce functional osteoblasts.
Ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis. ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis.
KIF13A overexpression favors NP distribution to the cell edge and requires KIF13A binding to microtubules. KIF13A overexpressionfavorsNP distribution to.
CENP-F staining in prometaphase and metaphase spermatocytes from B6 and Rb/+ mice. CENP-F staining in prometaphase and metaphase spermatocytes from B6.
Fig. 2. Expression of Cx43 mutant T154A resulted in non-radial spreading and formation of protrusions in J558µm3 cells spreading in response to BCR signaling.(A)
Fig. 2. Acetylation stiffens primary cilia.
Depletion of EB1 with small interfering RNA reduces MT minus-end anchoring at the centrosome. Depletion of EB1 with small interfering RNA reduces MT minus-end.
Fig. 6. RhoB is required for Rnd3-induced stress fibre formation
Fig. 3. MO-mediated smc3 knockdown results in reduced regenerate length, segment length and cell proliferation. MO-mediated smc3 knockdown results in reduced.
Fig. 1. p85β localizes at adhesion plaques and associates with FAK
Fig. 3. Mean force and velocity during jumping
mip120 null egg chambers have a condensed nurse cell DNA phenotype
FAK is required for LPA-mediated induction of trailing-edge retraction and the restoration of normal morphology. FAK is required for LPA-mediated induction.
Telomere cohesion is established in S phase in cohesin-ring-depleted cells. Telomere cohesion is established in S phase in cohesin-ring-depleted cells.
Knockdown of ZBP1 in hippocampal neurons decreases dendritic branching
Presentation transcript:

Fig. 1. Loss of PC following INT depletion Fig. 1. Loss of PC following INT depletion.RPE cells were transfected with siRNA, serum-starved, fixed, and stained for acetylated tubulin, γ-tubulin, and DNA. (A–J) Representative images show decreased PC formation after knockdown of most INT subunits tested. Loss of PC following INT depletion.RPE cells were transfected with siRNA, serum-starved, fixed, and stained for acetylated tubulin, γ-tubulin, and DNA. (A–J) Representative images show decreased PC formation after knockdown of most INT subunits tested. Scale bars, 10 (A,B) or 5 (C–J) µm. (K) Quantification of PC formation (normalized to NT-siRNA) in INT-depleted cells. Gray, P<0.0001; black, not significant (both relative to CETN2-siRNA, red). (L) Comparison of INT subunit requirements in snRNA processing (Chen et al., 2012), dynein localization, and ciliogenesis (presented herein). (+), required; (−), not required; (N.D.), not determined. Jeanne N. Jodoin et al. Biology Open 2013;bio.20136981 © 2013. Published by The Company of Biologists Ltd