Nucleolar poly-GR/PR alter nucleolar organization and inhibit translation. Nucleolar poly-GR/PR alter nucleolar organization and inhibit translation. GFP,

Slides:



Advertisements
Similar presentations
Figure 7. Interaction between C9orf72 dipeptides and ribonucleotides in vivo. The concentration of RNA extracted from immunoprecipitated samples from NSC34.
Advertisements

Validating Cdk‐dependent chromatin association changes of selected outliers A–EValidation of changes in chromatin affinity following Cdk inhibition of.
ORL1 inhibits axon regeneration.
Poly-GR and poly-PR interact with overlapping proteins in primary neurons and in HEK293 cells. Poly-GR and poly-PR interact with overlapping proteins in.
Modeling human tumor angiogenesis in a three-dimensional culture system by Giorgio Seano, Giulia Chiaverina, Paolo Armando Gagliardi, Laura di Blasio,
STAU1/2 and YBX1 recruit poly-GR/PR into large cytoplasmic granules.
Overexpression of RNase H1 decreases the induction of phosphorylated H2AX in post‐mitotic cells in response to topoisomerase 1 cleavage complexes. Overexpression.
NPM1 drives poly-GR into the nucleolus of primary neurons.
Poly-GR and poly-PR co-aggregate with ribosomal proteins in C9orf72 patients. Poly-GR and poly-PR co-aggregate with ribosomal proteins in C9orf72 patients.
PPARγ signaling correlates with LATS2 in human and mouse tumors and promotes cell death in a LATS2-dependent manner. PPARγ signaling correlates with LATS2.
Cytoplasmic poly-GR/PR inclusions resemble stress granules in vitro.
Characterization of DPR proteins in primary rat neurons and HEK293 cells. Characterization of DPR proteins in primary rat neurons and HEK293 cells. GFP,
Poly-GR mainly co-localizes with nucleolar ribosomes.
CaMKII inhibition in human primary and pluripotent stem cell-derived chondrocytes modulates effects of TGFβ and BMP through SMAD signaling  B. Saitta,
Dynamics and variability of SMAD2 signaling in single cells
Poly-GR and poly-PR interact with similar low-complexity proteins in neurons. Poly-GR and poly-PR interact with similar low-complexity proteins in neurons.
Volume 10, Issue 4, Pages (April 2018)
Widespread Inhibition of Posttranscriptional Splicing Shapes the Cellular Transcriptome following Heat Shock  Reut Shalgi, Jessica A. Hurt, Susan Lindquist,
The β-tubulin C-terminal tail modulates the coordination of microtubule assembly in an isotype-dependent manner. The β-tubulin C-terminal tail modulates.
Disrupted dynamics of early stages of differentiation perturbs neural cell fate specification. Disrupted dynamics of early stages of differentiation perturbs.
Andreia F.R. Batista, José C. Martínez, Ulrich Hengst  Cell Reports 
Poly-PR inhibits translation in neurons.
Fig. 5 Hypoxic tumors from obese mice associate with increased production of IL-6 by adipocytes and myeloid cells. Hypoxic tumors from obese mice associate.
Arc expression increases H4K12Ac levels.
Nec‐1 inhibits the phosphorylation and aggregation of tau
Fig. 5 Local gel scaffold for T cell memory response.
Plk1 inhibition or depletion causes robust cortical NuMA localization in mitosis. Plk1 inhibition or depletion causes robust cortical NuMA localization.
The ER is the main source of cholesterol accumulated by STARD3 in endosomes The ER is the main source of cholesterol accumulated by STARD3 in endosomes.
VAP silencing restores a normal plasma membrane cholesterol level in STARD3‐expressing cells VAP silencing restores a normal plasma membrane cholesterol.
Volume 25, Issue 10, Pages (October 2017)
Juxtaposition of GFP-Rab1b with IRES-containing RNA.
Pharmacological inhibition of DAO impairs DNA damage– and oncogene-induced senescence. Pharmacological inhibition of DAO impairs DNA damage– and oncogene-induced.
Activin Signals through SMAD2/3 to Increase Photoreceptor Precursor Yield during Embryonic Stem Cell Differentiation  Amy Q. Lu, Evgenya Y. Popova, Colin.
Modification of the βIII-tubulin C-terminal tail does not affect the incorporation of the protein into the microtubule network, the microtubule architecture,
Cortical NuMA enrichment upon Plk1 inhibition is dynein independent.
Nox1 as a potential therapeutic target to inhibit matricellular-mediated endothelial senescence. Nox1 as a potential therapeutic target to inhibit matricellular-mediated.
Nuclear DNA signal is altered in Chd5-deficient NSCs.
V-SVZ cultures express transcription factors expected for region of origin. V-SVZ cultures express transcription factors expected for region of origin.
Endogenous SMN1 is not recruited to stress granules in HeLa cells after diverse stresses. Endogenous SMN1 is not recruited to stress granules in HeLa cells.
The effects of KY19382 on chondrocyte proliferation and differentiation. The effects of KY19382 on chondrocyte proliferation and differentiation. (A) ATDC5.
W. Y. Lee, C. J. Park, T. J. Shin, K. W. Yum, T. G. Yoon, K. S. Seo, H
Fig. 2. Proportion of motile objects and track length
Mammary cell proliferation is inhibited when LAD1 is depleted.
FGF/ERK inhibition accelerates neural fate conversion of EpiSCs.
The effect of TDP-43A315T expression on dendrite spine development.
MET/β-catenin complexes during synapse development.
Chd5 deficiency leads to compromised expression of the repressive histone mark H3K27me3 and up-regulation of ribosomal protein genes. Chd5 deficiency leads.
Socs1 KD tumors exhibit a more T-cell–inflamed phenotype and increased T-cell activation. Socs1 KD tumors exhibit a more T-cell–inflamed phenotype and.
LIMK1 inhibition protects against Aβ-induced neuronal hyperexcitability. LIMK1 inhibition protects against Aβ-induced neuronal hyperexcitability. (A) Representative.
Ventral mouse V-SVZ cells exhibit higher mTORC1 activity than dorsal cells and are responsive to rapamycin. Ventral mouse V-SVZ cells exhibit higher mTORC1.
Validation of GFP and BMP-2 expression in lentivirus-transduced neonatal human skin fibroblasts. Validation of GFP and BMP-2 expression in lentivirus-transduced.
TOR, but not OSP, blocks STx2B transport and alters endosomal dynamics
MPP+-induced toxicity in cultured SN and VTA DA neurons.
Socs1 KD tumors exhibit a more T cell–inflamed phenotype and increased CD8+ T cell activation. Socs1 KD tumors exhibit a more T cell–inflamed phenotype.
RECQL4 depletion or malfunction increases inter-kinetochore distance.
Chd5-deficient NSCs generate excessive astrocytes at the expense of neurons. Chd5-deficient NSCs generate excessive astrocytes at the expense of neurons.
Association of NM-HA and NM-GFP with SGs is transient.
FUT1 and STAM are required for the retrograde transport of STx2B to the Golgi. FUT1 and STAM are required for the retrograde transport of STx2B to the.
Metformin (Met) reduces membrane-associated TRPA1 levels in rat DRG neurons. Metformin (Met) reduces membrane-associated TRPA1 levels in rat DRG neurons.
Sensory neurons grow and downregulate UCHL1 expression levels during postnatal maturation. Sensory neurons grow and downregulate UCHL1 expression levels.
SiRNA directed at Ngn1 inhibited differentiation of inner ear stem cells to β-III tubulin-positive cells. a, Inner ear stem cells treated with siRNA to.
LILRA3 increased density of synaptic contacts in mouse cortical neurons cultured for 21 days. LILRA3 increased density of synaptic contacts in mouse cortical.
Knockdown of ZBP1 in hippocampal neurons decreases dendritic branching
PTZ-induced neuronal activity visualized by IEGs
PDL-coated beads induce the formation of functional presynaptic terminals within 24 h. PDL-coated beads induce the formation of functional presynaptic.
Knock-out of NSG2 decreases mEPSC frequency.
S-Affs colocalize with SUMO in mammalian cells.
Activity regulates eEF2K-dependent spine morphogenesis.
Akt overexpression rescues Aβ42-induced toxicity without affecting levels of intraneuronal Aβ. Akt overexpression rescues Aβ42-induced toxicity without.
RUNX3 depletion induces cellular senescence and inflammatory cytokine expression in cells undergoing TGFβ-mediated EMT. A, Cells were transfected with.
Presentation transcript:

Nucleolar poly-GR/PR alter nucleolar organization and inhibit translation. Nucleolar poly-GR/PR alter nucleolar organization and inhibit translation. GFP, GFP-(GR)53, GFP-(GR)149, or (PR)175-GFP were transduced in primary rat neurons. (A) Images show fibrillarin immunofluorescence staining of hippocampal neurons. Left two columns represent GFP signal and fibrillarin staining in different DPR species as indicated. Right column shows merge with additional nuclear DAPI staining in blue. Scale bar denotes 20 μm. (B) LDH release assay detects significant cell death on lentiviral expression of (PR)175-GFP and GFP-(GR)53 but not GFP-(GR)149 compared with GFP control in primary rat neurons (DIV7 + 14) (n = 3 independent experiments with six replicates each; box plot is shown with 25th percentile, median, and 75th percentile; and whiskers represent minimum and maximum; exact P-values: GFP versus GFP-GR53, P = 0.0011; GFP versus GFP-GR149, P = 0.9954; and GFP versus PR175-GFP, P = 0.0001 in one-way ANOVA with Dunnett’s posttest). (C) SUnSET experiment in GFP-(GR)53–, GFP-(GR)149–, (PR)175-GFP–, or GFP–expressing primary cortical neurons (DIV6+7) as in Fig 6C. Cells were incubated with 1 μM puromycin (puro) for 10 min or not treated (nt). Note the reduced incorporation of puromycin in neurons expressing GFP-(GR)53 and (PR)175-GFP. (D) Quantification of puromycin signal normalized to calnexin (n = 6 from three independent experiments, mean ± SEM, exact P-values: GFP versus GFP-GR53, P = 0.0022; GFP versus GFP-GR149, P = 0.8638; and GFP versus PR175-GFP, P = 0.0005 in one-way ANOVA with Dunnett’s posttest). (E) Quantification of fibrillarin distribution within the nucleolus from (A). n = 6 to 16 images were analyzed. Hannelore Hartmann et al. LSA 2018;1:e201800070 © 2018 Hartmann et al.