Helen Strutt

ORCID: 0000-0003-4365-2271
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About
Contact & Profiles
Research Areas
  • Wnt/β-catenin signaling in development and cancer
  • Developmental Biology and Gene Regulation
  • Hippo pathway signaling and YAP/TAZ
  • Cellular Mechanics and Interactions
  • Neurobiology and Insect Physiology Research
  • Microtubule and mitosis dynamics
  • Genomics and Chromatin Dynamics
  • Epigenetics and DNA Methylation
  • Cancer therapeutics and mechanisms
  • Skin and Cellular Biology Research
  • Cancer-related gene regulation
  • DNA Repair Mechanisms
  • Insect and Arachnid Ecology and Behavior
  • RNA and protein synthesis mechanisms
  • Polyomavirus and related diseases
  • Plant Molecular Biology Research
  • RNA Research and Splicing
  • Hedgehog Signaling Pathway Studies
  • Cellular transport and secretion
  • Protist diversity and phylogeny
  • Connective tissue disorders research
  • Neutropenia and Cancer Infections
  • Insect Resistance and Genetics
  • Ubiquitin and proteasome pathways
  • Chromosomal and Genetic Variations

University of Sheffield
2014-2024

Heidelberg University
1997-2007

University of British Columbia
1998

Max Planck Institute for Biophysical Chemistry
1998

MRC Laboratory of Molecular Biology
1995

Medical Research Council
1995

Cancer Research UK
1991-1994

University of Cambridge
1991-1994

Planar polarity decisions in the wing of Drosophila involve assembly asymmetric protein complexes containing conserved receptor Frizzled. In this study, we analyse role Van Gogh/strabismus gene formation these and cell polarisation. We find that Strabismus becomes asymmetrically localised to proximal edge cells. absence strabismus activity, planar proteins Dishevelled Prickle are mislocalised cell. show binds directly is able recruit them membranes. Furthermore, demonstrate putative...

10.1242/dev.00526 article EN Development 2003-05-20

Camptothecin is a specific topoisomerase I poison and highly cytotoxic to eukaryotic cells. In the present study, we show, using pulse field gel electrophoresis assay, that camptothecin induces DNA double strand breaks (DSBs) specifically in newly replicated DNA. these replication associated DSBs dose-dependent manner. At levels of drug which are toxic cell, long-lived, still measurable 24 hr after treatment. Both induced cytotoxicity prevented by co-exposure with aphidicolin--a result...

10.1093/nar/19.12.3295 article EN Nucleic Acids Research 1991-01-01

The subcellular three-dimensional distribution of three polycomb-group (PcG) proteins—polycomb, polyhomeotic and posterior sex combs—in fixed whole-mount Drosophila embryos was analyzed by multicolor confocal fluorescence microscopy. All proteins are localized in complex patterns 100 or more loci throughout most the interphase nuclear volume. rather narrow protein intensities vast majority argues against a PcG-mediated sequestration repressed target genes aggregation into subnuclear domains....

10.1083/jcb.141.2.469 article EN The Journal of Cell Biology 1998-04-20

BackgroundThe planar polarization of developing tissues is controlled by a conserved set core polarity proteins. In the Drosophila pupal wing, these proteins adopt distinct proximal and distal localizations in apicolateral junctions that act as subcellular cues to control morphological events. The protein Flamingo (Fmi) localizes both cell boundaries known have asymmetric activity, but molecular basis this activity unknown.ResultsWe examine role Fmi controlling localization wing cells. We...

10.1016/j.cub.2008.08.063 article EN cc-by Current Biology 2008-09-19

The core planar polarity proteins localize asymmetrically to the adherens junctions of epithelial cells, where they have been hypothesized assemble into intercellular complexes. Here, we show that are preferentially distributed discrete membrane subdomains ("puncta"), form asymmetric contacts between neighboring cells. Using an antibody internalization assay and fluorescence recovery after photobleaching in prepupal pupal wings, investigated turnover two key proteins, Flamingo Frizzled, find...

10.1016/j.devcel.2011.03.018 article EN cc-by Developmental Cell 2011-04-01

10.1016/s1534-5807(02)00363-5 article EN publisher-specific-oa Developmental Cell 2002-12-01

In Drosophila the Polycomb group genes are required for long-term maintenance of repressed state many developmental regulatory genes. Their gene products thought to function in a common multimeric complex that associates with response elements (PREs) target and regulates higher-order chromatin structure. We show chromodomain is necessary protein-protein interactions within Polycomb-Polyhomeotic complex. addition, Posterior Sex Combs protein coimmunoprecipitates Polyhomeotic, indicating they...

10.1128/mcb.17.12.6773 article EN Molecular and Cellular Biology 1997-12-01

During planar polarity patterning of the Drosophila wing, a "core" group genes has been identified which acts downstream global cues to locally coordinate cell and specify trichome production at distal edges. These encode protein products that assemble into asymmetric apicolateral complexes straddle proximodistal junctional region between adjacent cells. We have carried out detailed genetic analysis experiments, analysing requirements each complex component for patterning. find three...

10.1016/j.ydbio.2006.09.026 article EN cc-by Developmental Biology 2006-09-19

Polarised tissue elongation during morphogenesis involves cells within epithelial sheets or tubes making and breaking intercellular contacts in an oriented manner. Growing evidence suggests that cell adhesion can be modulated by endocytic trafficking of E-cadherin (E-cad), but how this process polarised individual is poorly understood. The Frizzled (Fz)-dependent core planar polarity pathway a major regulator rearrangements processes such as gastrulation, has also been implicated regulation...

10.1242/dev.088724 article EN cc-by-nc-sa Development 2013-01-31

Highlights•Planar polarity proteins form signalosome-like complexes of variable stoichiometry•Flamingo and Frizzled a stoichiometric nucleus within the complex•Asymmetric localization core is robust to changes in complex composition•Core protein stability not dependent on stoichiometrySummaryIn developing epithelia, planar physically interact with each other localize asymmetrically at opposite cell ends, forming intercellular that link neighboring cells. Using quantitative imaging examine...

10.1016/j.celrep.2016.11.021 article EN cc-by Cell Reports 2016-12-01

Four-jointed (fj) is required for proximodistal growth and planar polarity in Drosophila tissues. It encodes a predicted type II transmembrane protein with putative signal peptidase sites its domain, C terminus secreted. Fj has therefore been proposed to act as secreted signalling molecule. We show that graded distribution eye wing imaginal discs, largely localised the Golgi vivo transfected cells. Forms of are constitutively or anchored were assayed function vivo. find cleavage secretion...

10.1242/dev.00996 article EN cc-by Development 2004-02-02

The asymmetric localisation of core planar polarity proteins at apicolateral junctions is required to specify cell in the plane epithelia. This distribution proposed require amplification an initial asymmetry by feedback loops. In addition, generation appears regulation protein levels, but importance such and underlying mechanisms unknown. Here we show that ubiquitylation acts through more than one mechanism control levels Drosophila, without this cellular compromised. Levels Dishevelled are...

10.1242/dev.089656 article EN cc-by-nc-sa Development 2013-03-14

The core planar polarity proteins are required to specify the orientation of structures that polarised in plane epithelium. In Drosophila melanogaster wing, localise asymmetrically at either proximal or distal cell edges. Asymmetric localisation is thought be biased by long-range cues, causing asymmetric complexes become aligned with tissue axes. Core then participate feedback interactions necessary amplify asymmetry, and order for such operate correctly, levels junctions must tightly...

10.1371/journal.pgen.1003654 article EN cc-by PLoS Genetics 2013-07-18
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