Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH

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Mitochondria localize to both the front and the rear of neutrophils.

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Sec1p requires Boi1/2p for proper localization.

Exposure to stress and SGs formation.

Scanning electron microscopy analysis of EGK-I to -V chick embryos.

Juxtapositioning of ARF5 with IRES-luc mRNA.

Juxtaposition of GFP-Rab1b with IRES-containing RNA.

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. 8. In vitro effect of CMPs on adult DSS-treated stomach explants.

Fig. 8. CCA and ChQ treatment induce accumulation of F-actin rings.

Fig. 3. Hts and Dlg are in a complex at the postsynaptic membrane of larval NMJs.(A–B″) PLA with HtsM and Dlg antibodies (green) performed on third instar.

Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.

Fig. 2. Spectral sensitivity of smolt melanophores and candidate photopigments involved in melanophore photosensitive processes.(A,B) Incident light triggered.

Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.

Fig. 5. Differentiated cells sort to the outer layer, regardless of E- or N-cadherin status.Wildtype and mutant ES cells were distinguished by GFP expression.

Fig. 4. Seeding density modulates cell shape in both cell types

Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle

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

Fig. 2. Mapping of the interaction domain on coilin for association with the dyskerin complex. Mapping of the interaction domain on coilin for association.

Fig. 1. Exogenous folic acid and Folr1 rescues the function of a Rho-kinase binding mutation in Shroom3. Exogenous folic acid and Folr1 rescues thefunction.

Fig. 1. Mitochondrial internalization in cardiomyocytes.

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

Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.

Fig. 1. E-cadherin localizes in nano-scale clusters.

PfSec13 does not co-localize with P. falciparum heterochromatin.

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

The initial targeting of Sec61b mRNA to the ER is partially dependent on ribosomes and translation. The initial targeting of Sec61b mRNA to the ER is partially.

Formation of papilloma lesions in the UroIICre+Fgfr3+/K644EK-RasG12D/+ model. Formation of papilloma lesions in theUroIICre+Fgfr3+/K644EK-RasG12D/+model.

Fig. 7. The sma gene is necessary for ampA mRNA accumulation and its loss phenocopies some ampA effects.(A) RT-PCR showing levels of ampA transcripts in.

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. 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. 2. The localisation of integrins β1 and α6 in the hES cells grown in a colony and as a single-cell culture. hES cells were harvested manually as small.

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. 5. UV reflections from the eye cup.

In 6CFSMEo- cells, UPF1 protein is concentrated partially or totally in P-bodies after cytoskeleton inhibitor treatment. In 6CFSMEo- cells, UPF1 protein.

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.

G418 causes UPF1 to localize to cytoplasmic foci containing NMD substrates but not the P-body marker DCP1a. 6CFSMEo- cells were transfected with constructs.

Detection of nuclear foci by FISH on frozen sections of diaphragm muscle prepared from 2-month-old DMSXL mice. Detection of nuclear foci by FISH on frozen.

GFP–Sec61b mRNA competes with t-ftz mRNA for the ribosome-binding sites on the ER. (A,B) COS7 cells were transfected with plasmid containing a test gene.

HSP90β interacts with HNF4A to regulate protein half-life.

Fig. 6. STK35 KO mice show ovary defects.

Fig. 6. Meis1 protein is present in CR4. 2-GFP+ and Foxn4+ cells

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)

Effect of the plastid translation inhibitor Spec on LR development

Transbilayer distribution of cholesterol in the plasma membrane is defective in staurosporine-treated cells. Transbilayer distribution of cholesterol in.

Fig. 5. Upregulation of N. vectensis thrombospondin during regeneration.(A,B) Juvenile polyps were fixed 48 hours following transection and processed.

Fig. 1. Loss of PC following INT depletion

Analysis of Cdc7p at the end of meiosis.

Tau–RFP–RBPs colocalize with mRNA on microtubules and lead to the wetting of stress granules on microtubules. Tau–RFP–RBPs colocalize with mRNA on microtubules.

Z-stack compressions showing triple labelling of different cell types in the gills of bowfin with antibodies for serotonin (5-HT, green) and HNK-1 (magenta),

Fig. 4. CR4.2 may be active in amacrine cells but not in ganglion cells.Chick retinas were electroporated with either the control CAG-GFP construct or.

BRG1 interacts with RAD52 and regulates its accumulation at DSB sites during homologous recombination repair. BRG1 interacts with RAD52 and regulates its.

Fig. 2. Acetylation stiffens primary cilia.

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.

Expression of smc3 in whole-mount and cryosectioned regenerating fins

Fig. 7. Eye defects in STK35 KO mouse.

Nanoscale adhesive geometry modulates integrin–FN clustering.

The BRCA1 aggregates exclude large nuclear structures.

The lmpA kd strain shows severe defects in phagocytosis.

EPLIN also plays a crucial role in the apical extrusion of RasV12-transformed cells. EPLIN also plays a crucial role in the apical extrusion of RasV12-transformed.

WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates TfR. WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates.

Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP

Effective TcdB cell interactions correlate with endocytosis.

Ribosomal RNA and β-catenin mRNA localize to newly formed presynaptic terminals. Ribosomal RNA and β-catenin mRNA localize to newly formed presynaptic.

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Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH.(A) Schneider cells were transfected with GFP-dFMRP. Detection of dFMR1 mRNA in dFMRP granules by FISH.(A) Schneider cells were transfected with GFP-dFMRP. Cells were then fixed, permeabilized, and incubated with 3 nM of Alexa Fluor 488-labeled antisense RNA probe to detect dFMR1 mRNA (panels 6 and 8) or with Alexa Fluor 488-labeled sense probe (panels 2 and 4) as control. dFMRP granules were visualized as green fluorescence. Scale bar: 10 µm. (B) Densitometry quantification of FISH poly(A)+ mRNA signal was done with Photoshop software as above. Cristina Gareau et al. Biology Open 2013;2:68-81 © 2012. Published by The Company of Biologists Ltd