dickkopf-1 regulates gastrulation movements by coordinated modulation of wnt/ -catenin and wnt/pcp...
TRANSCRIPT
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Dickkopf-1Dickkopf-1 regulates gastrulation regulates gastrulation
movements by coordinated modulationmovements by coordinated modulation
of Wnt/of Wnt/-catenin and Wnt/PCP activities,-catenin and Wnt/PCP activities,
through interaction with the Dally-likethrough interaction with the Dally-like
homolog homolog KnypekKnypek
2007, Genes & Dev
Luca Caneparo
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Roles of Dkk1 in Gastrulation
During gastrulation, anterior territories (neural plate) keep their identities
by moving away from posteriorizing signals or inhibiting them
(Wilson S.W et al, 2004, Dev Biol)
Among the most studied posteriorizing signals are the Wnt molecules(Erter et al, 2001, Development)
Fight against Wnt!
(sFRP, WIF, Cerberus and Dkk)
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Roles of Dkk1 in Gastrulation (continue)
In frog and fish, Dkk1 overexpression is able to anteriorize neural tissue
(Kazanskaya et al, 2000, Development)
The genetic knockout of the mouse dkk1 leads to the formation of headless
(Mukhopadhyay et al, 2001, Dev cell)
embryos due to lack of maintenance of anterior neural identity during gastrulation
But, mechanism by Dkk1 is yet to be unraveled
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Gastrulation movement in zebrafish
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Dkk1 is “Head inducer”
The morphant embryos show a severe reduction of forebrain territories
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Dkk1 is important in rostal population of axial mesendoderm
Dkk1 antibody injected Xenopus embryo, gsc and shh (anterior endoderm marker)
in prechordal plate are down-regulated
(Kazanskaya et al, 2001, Development)
In the mouse dkk1/noggin double mutants, Hesx1 expression is
down-regulated in the presumptive prechordal plate
(del Barco et al, 2003, Genes & Development)
Absence of Dkk1 give the same effect in zebra fish?
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Axial mesendoderm marker
Dkk1 regulates gastrulation movement
dorsal
- Significant reduction of gsc in dkk MO
- Position of the rostal-most limit of the
axial mesendoderm is different
Acceleration of Axial mesendoderm movement?
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Dkk1
Dkk1 MO accelerates gastrulation movement
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- The number of internalized cell/min
- The AP length of the clone - Distance of the rostal-most cell from the posterior margin
Dkk1 MO accelerates gastrulation movement
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How does Dkk1 reduce gastrulation movement?
Two hypothesis
Dkk1
Canonical Wnt signaling block
Interact with LRP5/6 Interact with X
?
Gastrulation defect
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Influence of Dkk1 on gastrulation is Wnt/-catenin independent
Clones are more dispersed
Don’t rescue the phenotype in Dkk1 MO
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Knypek is a Dally-like heparan sulfate proteoglycan
(Dally)
In embryo lacking Knypek, mediolateral intercalations are impaired(Topczewski et al, 2001, Dev cell)
kny mutations exacerbate the CE defect of slb/Wnt11 mutants in a dose-dependent manner
(Lin F. et al, 2005, J cell biol)
And, Kny enhances Wnt11 signaling in overexpression experiments
Kny is a positive modulator of non-canonical Wnt signaling
If Dkk1 interacts with Kny ?
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Dkk1 interacts with Knypek and it regulates propagation of Dkk1
Synergistic effect
Interact with Kny
Require Kny for its propagation
Kny-/- Kny-/- + Dkk1Wt+Dkk1
Propagation is necessary for dkk1 function
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Dkk1 promotes Wnt / PCP pathwayactivin activin+Wnt8 activin+Dkk1
C&E defect
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Dkk1 may act as a switch between the -catenin and PCP pathway
Phenocopy Dkk1 MO
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Dkk1
Canonical Wnt signaling block
Interact with LRP5/6 Interact with knypek
Fine-tuned Gastrulation
Summary
Dkk1 propagation?
Internalization Wnt/PCP activation
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Possible model