Subcellular localization of FZR-1 during the first cell cycle.

Slides:

Advertisements

Similar presentations

Recruitment of VAMP3 to the phagocytic cup F-actin (red) and nuclei (blue) were stained in macrophages expressing GFP-VAMP3 (green) before confocal imaging.

Advertisements

An analysis of Plk4 centriolar dynamics.

Intracellular EBV‐encoded LMP1 localizes to late endosomes.

Carly I. Dix, Jordan W. Raff Current Biology

Volume 23, Issue 11, Pages (June 2013)

Volume 7, Issue 6, Pages (December 2004)

Direct fusion lines allow fluorescent visualization of plasmatocyte nuclei, the cytoplasm, or the cytoskeleton in embryos from stage (St) 8 onwards. Direct.

And the Dead Shall Rise: Actin and Myosin Return to the Spindle

Renzhi Yang, Jessica L. Feldman Current Biology

Flies without Centrioles

Overexpressing Centriole-Replication Proteins In Vivo Induces Centriole Overduplication and De Novo Formation Nina Peel, Naomi R. Stevens, Renata Basto,

Cdk1 Modulation Ensures the Coordination of Cell-Cycle Events during the Switch from Meiotic Prophase to Mitosis Dai Tsuchiya, Soni Lacefield Current.

Candidates with a PVM localization.

Plk1 negatively regulates NuMA cortical localization by phosphorylating at its C-terminus. Plk1 negatively regulates NuMA cortical localization by phosphorylating.

Lysozyme expression in isolated Paneth cells and linage tracing of Notch1+ cells Lysozyme expression in isolated Paneth cells and linage tracing of Notch1+

Plk1 inhibition or depletion causes robust cortical NuMA localization in mitosis. Plk1 inhibition or depletion causes robust cortical NuMA localization.

Time-lapse microscopy of a growing single cell with fluorescently labeled cell wall. Time-lapse microscopy of a growing single cell with fluorescently.

Volume 23, Issue 4, Pages (April 2018)

FLP-mediated removal of extraneous sequences (A) Schematic representation of FLP-mediated removal of extraneous sequences. FLP-mediated removal of extraneous.

A. A. The two independent mutations identified in the structural gene of pqn-82 are shown above the gene. The genomic coordinates for the altered base.

Stabilization of Cartwheel-less Centrioles for Duplication Requires CEP295-Mediated Centriole-to-Centrosome Conversion Denisse Izquierdo, Won-Jing Wang,

Maintenance of Miranda Localization in Drosophila Neuroblasts Involves Interaction with the Cognate mRNA Anne Ramat, Matthew Hannaford, Jens Januschke

Volume 6, Issue 4, Pages (April 2004)

RNA-FISH validation of male and female markers.

Volume 3, Issue 5, Pages (November 2002)

Volume 119, Issue 2, Pages (October 2004)

Identification of one type of RGCs with large somas.

Loss of FZR-1 results in elevated SAS-5 levels.

The Subcellular Distribution of a Sar1-YFP Fusion Is Altered by the Expression of Golgi Markers.(A) and (B) Cytoplasm of a tobacco leaf epidermal cell.

KIN-3 depletion leads to increased levels of centrosomal ZYG-1

CK2 is required for early cell divisions in C. elegans embryos

Localization of PBANKA_ and PBANKA_ during blood and liver stage development. Localization of PBANKA_ and PBANKA_ during blood.

Mitosis-Resistant Adhesions Provide Molecular Memory to Dividing Cells

The first two principal components for the islet gene expression data for the 181 microarray probes that map to the chromosome 6 trans-eQTL hotspot with.

Recruitment of PH-Akt-GFP to the leading edge of the cell during chemotaxis. Recruitment of PH-Akt-GFP to the leading edge of the cell during chemotaxis.

Coalescent analysis of nucleotide differentiation between high and low latitude samples. Coalescent analysis of nucleotide differentiation between high.

Polyploidy Experimental Hematology

Distribution of protrusive activity.

Patterns of cell movement in paraxial mesoderm.

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.

The expression of histone H1. X::GFP in C

Mesenchymal behavior of epidermal cells in clint1 mutants.

Fig. 2. Morphological analysis of acentriolar mitotic spindles

Leukocyte infiltration of epidermis and phagocytosis of debris in clint1 mutants. Leukocyte infiltration of epidermis and phagocytosis of debris in clint1.

Frequency distribution of total leaf number for an F2 population derived from a cross of Van-0 with Ler, grown in long days. Frequency distribution of.

RECQL4 is a MAP with a spindle function.

Spatial distribution of individual genotypes in a subpart (of size 500 grid units × 700 grid units) of the total grid after the last cycle in one replicate.

Depleting CK2 restores centrosomal ZYG-1 levels in zyg-1(it25) embryos

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.

Properties of cBAF-overexpressing cells.

Fibroblasts from Rothmund–Thomson syndrome patients have abnormal spindle axis and more micronuclei. Fibroblasts from Rothmund–Thomson syndrome patients.

Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells.

dcn1-deletion results in attenuated cohesin cleavage at anaphase

Tcf4 is highly expressed and Tcf4GFPCre+neo genetically labels muscle connective tissue fibroblasts in culture. Tcf4 is highly expressed and Tcf4GFPCre+neo.

Effect of FGF8 on R-C marker expression.

Association of NM-HA and NM-GFP with SGs is transient.

Analysis of centromere and kinetochore function after depletion of DmSMC4. Analysis of centromere and kinetochore function after depletion of DmSMC4. (A)

Large pericentromeres colocalize more frequently with H3S10P foci than small pericentromeres. Large pericentromeres colocalize more frequently with H3S10P.

TAC-1, a Regulator of Microtubule Length in the C. elegans Embryo

Fig 1. Unenhanced axial T1-weighted MR image (728/15/2 [TR/TE/excitations]; matrix, 256 × 512; section thickness, 4 mm) shows an abnormally thickened second.

S-Affs colocalize with SUMO in mammalian cells.

An ipRGC axon collateral colocalized with the presynaptic marker bassoon makes contact with TH-positive DAC processes. An ipRGC axon collateral colocalized.

mEGFP:Pp3c12_24670 Fusion Protein Resides in Cytoplasmic Vesicles.

TAG-1 is expressed by oligodendrocytes and accumulates at the juxtaparanodal region. TAG-1 is expressed by oligodendrocytes and accumulates at the juxtaparanodal.

Volume 7, Issue 6, Pages (December 2004)

Cdk1 Modulation Ensures the Coordination of Cell-Cycle Events during the Switch from Meiotic Prophase to Mitosis Dai Tsuchiya, Soni Lacefield Current.

ESCRT-0 component Hrs is an effector of Rab35.

Centrosome anomalies characterize colorectal cancer with rhabdoid phenotype. Centrosome anomalies characterize colorectal cancer with rhabdoid phenotype.

Fgfr1a, fgfr1b, and fgfr2 function redundantly to regulate pectoral fin development. fgfr1a, fgfr1b, and fgfr2 function redundantly to regulate pectoral.

Fig. 3 4n hybrids undergo bipolar and tripolar mitosis.

Presentation transcript:

Subcellular localization of FZR-1 during the first cell cycle. Subcellular localization of FZR-1 during the first cell cycle. (A) Still images from time-lapse movie of an embryo expressing GFP::FZR-1 and mCherry::tubulin. Movie was acquired at 1-min intervals. GFP::FZR-1 localizes at nuclei, mitotic spindles, and centrosomes (arrows). Expression of mCherry::tubulin used as a subcellular land-marker. (B) Embryo expressing GFP::FZR-1 and mCherry::SPD-2 displays that GFP::FZR-1 localizes to mitotic spindles and centrosomes (arrows) that colocalize with mCherry-SPD-2, a centrosome marker. Bar, 5 μm. Jeffrey C. Medley et al. G3 2017;7:3937-3946 ©2017 by Genetics Society of America