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

Slides:

Advertisements

Similar presentations

Phenotypic analysis of spo73∆ mutant.

Advertisements

Ocular defects produced by Daam1 mutation and in combination with diabetes. Ocular defects produced by Daam1 mutation and in combination with diabetes.

KIF1Bβ promotes DHX9 nuclear localization.

Defect of cerebellar development and malformation of Purkinje cells in Pex14ΔC/ΔC BL/ICR mice. Defect of cerebellar development and malformation of Purkinje.

ILK knockdown decreases mTOR signaling in PKD kidneys.

Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial cells using live-imaging. Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial.

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.

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

Xp54 helicase is redistributed between the nucleus and the cytoplasm and between large and small complexes during the course of early development. Xp54.

Nephrogenesis in vitro can be rescued in 3D co-cultures by siRNA treatment of Renca cells. Nephrogenesis in vitro can be rescued in 3D co-cultures by siRNA.

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.

Patterns of cell movement in paraxial mesoderm.

No correlation between the position of the gene in the nuclear volume and the transcription levels on each of the alleles. No correlation between the position.

Embryonic corneal defects in E18.5 AP-2β NCC KO mutant embryos.

Ectopic sprouting and proliferation in Rbpj veins.

Challenge with oxazolone results in epithelial hyperplasia and influx of inflammatory cells into the epidermis and dermis and keratosis as observed in.

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

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.

Dany is required for nuclear shape distortion around chromosome territories. Dany is required for nuclear shape distortion around chromosome territories.

Kinetics of induced and non-induced AR, and its relationship to cell death and motility. Kinetics of induced and non-induced AR, and its relationship to.

Severing of trailing arms during meiosis II also resulted in backward movement of acentric fragments. Severing of trailing arms during meiosis II also.

Fcp1 CTD phosphatase affects a broad range of transcripts in the +N and -N media. Fcp1 CTD phosphatase affects a broad range of transcripts in the +N and.

(A) Faucher and Pliska hydrophobicity plot of D2SV protein sequence.

Don1 localization in vps13Δ cells.

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

Morphological defects of hi559 GI tract.

High-affinity binding to the hypervariable region of the β1 I-like domain controls signaling to fibronectin fibrillogenesis. High-affinity binding to the.

ICAM-1 forms distinct complexes with filamin B, α-actinin-4 and cortactin. ICAM-1 forms distinct complexes with filamin B, α-actinin-4 and cortactin. (A)

Chemical chaperone 4-PBA rescues the hi559 GI phenotype.

Defective organ development in mab1 mutants.

High-affinity mutants of β3 integrin fail to stimulate RhoA activity and fibronectin fibrillogenesis. High-affinity mutants of β3 integrin fail to stimulate.

Expression analysis of periostin in DRG

Characterization of anti-N-mPres.

Attenuated STM expression in drn and drnl mutants.

Facilitated migration of implanted Schwann cells infected with Ad-Cdc2 viral vectors in the injured sciatic nerve. Facilitated migration of implanted Schwann.

Analysis of Cdc7p at the end of meiosis.

Subcellular localization of prestin and mutant proteins in type I, II and III cells. Subcellular localization of prestin and mutant proteins in type I,

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.

Shp2 is required for lens and lacrimal gland development.

V-ATPase and proteins involved in late endosomal protein sorting are required for efficient utilization of LDs during growth resumption. V-ATPase and proteins.

Ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis. ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis.

dcn1-deletion results in attenuated cohesin cleavage at anaphase

IGF1R is present in endometrial luminal epithelium at the receptive phase. IGF1R is present in endometrial luminal epithelium at the receptive phase. Endometrial.

Abnormal adherens junctions between hub cells and GSCs in Lar mutants.

E4-ORF1 disrupts proper TJ localization of ZO-1 and ZO-2 in MDCK cells

FRAP and FLIP analysis of GFP-ADAR2 and GFP-ADAR1C-Term.

CENP-F staining in prometaphase and metaphase spermatocytes from B6 and Rb/+ mice. CENP-F staining in prometaphase and metaphase spermatocytes from B6.

EB1 localization to the centrosome is mediated by its C-terminal domain. EB1 localization to the centrosome is mediated by its C-terminal domain. Sections.

Integrin β3 is dispensable for RhoA activity and contractility.

Fig. 5. EGL-20 inhibits anterior and posterior orientation of UNC-40 asymmetric localization and the formation of axons from these sites.(A–D) HSN neurons.

The BRCA1 aggregates exclude large nuclear structures.

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

Mitotic control mutants have altered sensitivity to increased expression of flp1+. Mitotic control mutants have altered sensitivity to increased expression.

Lack of Ctip2 is associated with impaired proliferation and delayed onset of differentiation during early stages of epidermal development. Lack of Ctip2.

Dynamic and polarized recruitment of ERC1a near protrusive sites during migration. Dynamic and polarized recruitment of ERC1a near protrusive sites during.

Lack of LC3–GFP clustering in neurons expressing mutant CHMP2B.

SH3 domain of spectrin accumulates in the early integrin clusters.

Disruption of the tubule formation by immortalized cells during nephrogenesis in vitro. Disruption of the tubule formation by immortalized cells during.

Subnuclear localization of HA-tagged EBNA1 protein.

2DG suppresses of lamellipodia and filopodia and causes disorganization of F-actin filaments in murine endothelial cells. 2DG suppresses of lamellipodia.

Phenotypic characterization of low-Cu-responsive transcription factor Mac1 in A. nidulans. Phenotypic characterization of low-Cu-responsive transcription.

Phenotype of S. pombe cells in the presence of B21P2 or LMB

Recruitment of epiplakin to keratin filaments and aggregates after application of various types of stress. Recruitment of epiplakin to keratin filaments.

Detection of phosphorylated Smad2/3 (pSmad2/3) in the skin of wild-type and transgenic animals during the first hair cycle. Detection of phosphorylated.

Upon challenge with oxazolone, human leukocytes (mainly consisting of T cells) infiltrate the dermis and epidermis. Upon challenge with oxazolone, human.

Effect of overexpression of Gcs1p on mitochondrial morphology.

IKKβ protects adipocytes from HFD-induced cell death.

Activin overexpression leads to keratinocytic cysts and high cell density in the granulation tissue of healed wounds. Activin overexpression leads to keratinocytic.

TDIF-Sensitive Xylem Formation in wox4 Mutants

Fig. 5 C9orf72 knockdown disrupts autophagy induction.

Presentation transcript:

Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells. Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells. Nuclei of strains (A) CRL 152 (wild type), (B) 57-2262 (rec8 mutant) and (C) 88-3485 (rec7 mutant) were stained with Hoechst 33342. Images were taken in a single optical section with 2 minute intervals. Numbers on the left of each image indicate time in minutes. In A, arrows indicate the position of the presumptive telomere cluster. In B, arrows indicate the position of the leading edge of the nucleus. In C, arrows indicate the position of the leading edge of the nucleus; the arrowhead points at the presumptive telomere cluster. Scale bar: 10 μm. Monika Molnar et al. J Cell Sci 2001;114:2843-2853 © The Company of Biologists Limited 2001