28.11.2012 Views

Annual Report 2009 - Department of Zoology - University of ...

Annual Report 2009 - Department of Zoology - University of ...

Annual Report 2009 - Department of Zoology - University of ...

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Tulay Atamert: Fly stocks maintenance<br />

Paul Avery: RNA stability in Drosophila<br />

Marcus Bisch<strong>of</strong>f: Morphogenesis and pattern formation <strong>of</strong><br />

the abdomen <strong>of</strong> Drosophila<br />

Jose Casal: Planar polarity in Drosophila<br />

Bhavna Chanana: The function <strong>of</strong> tumour suppressor<br />

pathways in early development<br />

Barry Denholm: Cell patterning and morphogenesis in<br />

renal tissues<br />

Nan Hu: Cell specification in renal tubules<br />

Joanna Krzemień: Development <strong>of</strong> adult muscles in the<br />

abdomen <strong>of</strong> Drosophila<br />

Philippe Loiseau: Intracellular transport cargo recognition<br />

by conventional kinesin<br />

18<br />

Isabel Peset-Martin: The function <strong>of</strong> motors in<br />

establishing cell polarities<br />

Pedro Saavedra: Planar polarity in Drosophila<br />

Ada Repiso: Molecular analysis <strong>of</strong> planar polarity<br />

molecules<br />

Aditya Saxena: Regulation <strong>of</strong> tubule morphogenesis<br />

Catherine Scahill: Cell specification and tissue<br />

morphogenesis<br />

Susan Wan: Intercellular signaling and branching<br />

morphogenesis<br />

Lucy Williams: The function <strong>of</strong> Kinesin-1<br />

Helen Weavers: Cell interactions underlying tissue<br />

pathfinding<br />

c) Xenopus Development<br />

The research group <strong>of</strong> John Gurdon concentrates on mechanisms <strong>of</strong> nuclear reprogramming as a route towards personspecific<br />

cell replacement. This group is analyzes the molecular mechanisms by which eggs and oocytes re-set the gene<br />

expression pattern <strong>of</strong> the somatic cell nucleus to that <strong>of</strong> an embryo cell, including the transcriptional activation <strong>of</strong> pluripotency<br />

genes. Methods include nuclear transplantation to eggs and oocytes, mutant mouse cell lines, as well as imaging<br />

and FRAP analyses.<br />

Carolina Astrand: Histone mobility<br />

Nigel Garrett: Genetic manipulation<br />

Richard Halley-Stott: Chromatin decondensation<br />

Jerome Jullien: Linker histone exchange<br />

Vincent Pasque: X-chromosomal inactivation<br />

Ilenia Simeoni: Gene transcription in oocytes<br />

Four-jointed can modify the activity <strong>of</strong> both Dachsous and Fat in vivo<br />

Jose Casal<br />

These images provide evidence that a Golgi protein kinase, Fourjointed,<br />

interacts with both Dachsous and Fat — these are large cadherin<br />

molecules. Fat and Dachsous link together as heterodimers, with Fat in<br />

one cell contacting Dachsous in a neighbouring cell. We believe that the<br />

asymmetric distribution <strong>of</strong> these heterodimers within a cell is read out as the<br />

planar polarity <strong>of</strong> that cell. What we see here are clones <strong>of</strong> cells that lack<br />

all endogenous Fat and Dachsous, but have one <strong>of</strong> these proteins added<br />

back. If the clone contains only Dachsous, then Fat is drawn to the apposing<br />

membranes <strong>of</strong> the adjacent wildtype cells and, consequently those cells<br />

are repolarised (posterior to the clone). If the clone contains only Fat, then<br />

Dachsous is drawn to the apposing membranes <strong>of</strong> the adjacent wildtype cells and this also causes repolarisation (but<br />

now anterior to the clone). Repolarisation can propagate beyond the neighbouring wildtype cells because, if Dachsous is<br />

drawn to one side <strong>of</strong> a cell it becomes depleted from the other side, and this will affect the distribution <strong>of</strong> heterodimers in<br />

the next, more outlying, wildtype cells.<br />

When Four-jointed is over-expressed in the clone expressing Dachsous, then the affinity <strong>of</strong> Dachsous for Fat is<br />

diminished, less Fat is attracted to the adjacent membrane and repolarisation <strong>of</strong> the wildtype cells is reduced.<br />

When Four-jointed is over-expressed in the clone expressing Fat, then the affinity <strong>of</strong> Fat for Dachsous is increased,<br />

more Dachsous is attracted to the adjacent membrane and repolarisation <strong>of</strong> the wildtype cells is extended. Four-jointed<br />

molecules with a change in the kinase domain <strong>of</strong> the protein have much reduced effects, arguing that Four-jointed acts<br />

as a kinase to phosphorylate both Dachsous and Fat. We have provided additional in vitro evidence is provided for these<br />

conclusions.<br />

The clones <strong>of</strong> cells are genetically marked with a mutation that makes each cell produce an increased number <strong>of</strong> very<br />

small hairs. The cells surrounding the clones and their changed polarities can be seen in the orientation <strong>of</strong> the wildtype<br />

hairs.<br />

Reference:<br />

Brittle, A.L., Repiso, A. Casal, J., Lawrence, P.A. and Strutt, D. (2010). Four-jointed modulates growth and planar polarity<br />

by reducing the affinity <strong>of</strong> Dachsous for Fat. Curr. Biol. 20, 803-810.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!