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.

Slides:



Advertisements
Similar presentations
TIA-1 Self-Multimerization, Phase Separation, and Recruitment into Stress Granules Are Dynamically Regulated by Zn2+  Joseph B. Rayman, Kevin A. Karl,
Advertisements

Cycloheximide inhibits arsenite‐induced stress granule formation and prevents the decreased number of senescent cells mediated by repeated arsenite treatment.
Sec1p requires Boi1/2p for proper localization.
Phenotypic analysis of spo73∆ mutant.
Colocalization of the human trimethylguanosine synthase 1 and survival of motor neuron proteins. Colocalization of the human trimethylguanosine synthase.
Loss of USP8 or HIF1α impairs endocytic recycling required for ciliogenesis Kinetic analysis of transferrin recycling measured by flow cytometry. Loss.
Calcium regulates ERK nuclear association, but not its activation.
STAU1/2 and YBX1 recruit poly-GR/PR into large cytoplasmic granules.
M6A signal increases in response to oxidative stress and accumulates in SGs. m6A signal increases in response to oxidative stress and accumulates in SGs.
Exposure to stress and SGs formation.
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.
Cytoplasmic poly-GR/PR inclusions resemble stress granules in vitro.
Poly-GR mainly co-localizes with nucleolar ribosomes.
SUPPLEMENTAL TABLE 1. Cell cycle profiles of HeLa cells treated
DNA degradation is strictly controlled in wild-type, but not in recA cells. DNA degradation is strictly controlled in wild-type, but not in recA cells.
Direct fusion lines allow fluorescent visualization of plasmatocyte nuclei, the cytoplasm, or the cytoskeleton in embryos from stage (St) 8 onwards. Direct.
Endogenous SRP19 is localized to the nucleus and the nucleolus.
Confocal images of negative controls for Aβ42, Synaptophysin (syp), and PSD95 in hippocampal neurons. Confocal images of negative controls for Aβ42, Synaptophysin.
DNA and membrane binding of MinD are interconnected.
STED microscopy of MINOS
Candidates with a PVM localization.
DC-derived EV differentiate monocytes.
Marker identification and quantification by StrataQuest, and confocal analysis of EV-containing tissue sections. Marker identification and quantification.
Subcellular localization of UUKV, HRTV, and SFTSV NSs
Juxtaposition of GFP-Rab1b with IRES-containing RNA.
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.
Endolysosomal proteins are exported from the Golgi complex in two distinct populations of transport carriers. Endolysosomal proteins are exported from.
TIA-1 Self-Multimerization, Phase Separation, and Recruitment into Stress Granules Are Dynamically Regulated by Zn2+  Joseph B. Rayman, Kevin A. Karl,
Cortical NuMA enrichment upon Plk1 inhibition is dynein independent.
Defect of cerebellar development and malformation of Purkinje cells in Pex14ΔC/ΔC BL/ICR mice. Defect of cerebellar development and malformation of Purkinje.
DIA1(R1204X) induces elongated and thick microvilli in HeLa cells
Mitotic chromosome misalignment is independent of DNA replication.
FAM134B-2 colocalizes with SERCA2 and SEC62.
Plk1 inhibition affects the NuMA turnover at the spindle pole.
Characterization of SYNCRIP-SMN1 methylation–dependent interaction.
Methylation dependency of SNYCRIP protein interactions.
Differential intracellular localization of ISS in human PDCs
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
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.
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.
FGF/ERK inhibition accelerates neural fate conversion of EpiSCs.
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. 6. Comparison of Plk4 with Sas-6 localization
Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.
DDR1 inhibition does not prevent establishment of apicobasal polarity in 2D culture but delays the maturation/polarization process. DDR1 inhibition does.
ArfGAP1 expression alters GBF1 recruitment to Golgi membranes.
Ezrin in its open, activated conformation binds and colocalizes with MISP at the cell cortex. Ezrin in its open, activated conformation binds and colocalizes.
Inhibition of DNA replication and induction of DNA damage does not cause chromosome misalignment. Inhibition of DNA replication and induction of DNA damage.
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.
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.
RECQL4 is required for microtubule stability.
hADAR1 and hADAR2 co-localize within the nucleolus.
The microtubule-binding region of RECQL4 is required for chromosome alignment. The microtubule-binding region of RECQL4 is required for chromosome alignment.
Lysine residues in the cytoplasmic region of TfR are involved in the MARCH8-induced downregulation of TfR. Lysine residues in the cytoplasmic region of.
Wrch-1 localizes to focal adhesions.
RECQL4 depletion or malfunction increases inter-kinetochore distance.
The N-terminal α-helices of YopM mediate cellular uptake and are able to deliver proteins as cargo. The N-terminal α-helices of YopM mediate cellular uptake.
LC8 and its binding partners display broad cellular localization.
Fibril-induced NM prions do not evolve from SGs.
Association of NM-HA and NM-GFP with SGs is transient.
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
Recruitment of epiplakin to keratin filaments and aggregates after application of various types of stress. Recruitment of epiplakin to keratin filaments.
Ca2+-mediated differentiation of primary mouse keratinocytes is independent of epiplakin. Ca2+-mediated differentiation of primary mouse keratinocytes.
Fig. 3 C9ORF72 interacts with SMCR8 in a DENN domain–dependent manner.
Microfluidic platform for cell phenotype and gene function analysis
The activity of MRP1-EYFP is analogous to wild-type MRP1.
Presentation transcript:

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 after diverse stresses. (A) Extended panel from Fig 3D. HeLa cells, either untreated or incubated for 1 h at 44°C, were stained for EYFP (using a GFP antibody), endogenous SMN, and TIA-1 as marker for stress granules and analyzed by confocal microscopy. (B) HeLa cells, either untreated or incubated for 30 min with 0.5-mM arsenite, were stained for endogenous SMN and TIA-1 as marker for stress granules and analyzed by confocal microscopy. DAPI used to stain the nucleus. Scale bar indicates 20 μm. Jonathan Woodsmith et al. LSA 2018;1:e201800178 © 2018 Stelzl et al.