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First published online 20 February 2008
doi: 10.1242/dev.020289


Development 135, 1215-1221 (2008)
Published by The Company of Biologists 2008


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Silencing of Smedcatenin1 generates radial-like hypercephalized planarians

Marta Iglesias1, Jose Luis Gomez-Skarmeta2, Emili Saló1 and Teresa Adell1,*

1 Departament de Genètica, Universitat de Barcelona, 08028 Barcelona, Spain.
2 Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide-CSIC, 41013 Sevilla, Spain.


Figure 1
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Fig. 1. Smed-βcatenin1 silencing induces a gradual anteriorization of regenerating planarians. (A-E) Stereomicroscope views of regenerating trunk pieces showing the different phenotypes. (F-W,A'-H') Several markers were used at different regeneration stages to characterize the phenotype. Analysis of opsin (F-I), cintillo (J-M) and H.10.2f (N-Q) revealed the differentiation of ectopic anterior structures in the posterior blastema, which subsequently expanded throughout the periphery of the planarian body. Anti-arrestin immunostaining (R,S) showed that, in radial-like hypercephalized planarians, all photoreceptors were connected through ectopic visual axons. Synapsin immunostaining (T,U) and in situ hybridization for GluR (V,W) and H.10.2f (P,Q) demonstrated that the cephalic ganglia (cg) and ventral nerve cords (vnc) are transformed into a thick ring from which cephalic branches ectopically differentiate all around the body of radial-like hypercephalized planarians. (A'-H') Defects in the pattering of gut and secretory cells were visualized with anti-P-Tyr (green) and anti-arrestin (pink pseudocolour) antibodies. A control planarian viewed at the level of the gut has one anterior and two posterior gut branches (gb; B',F'), along with more dorsal secretory cells (sc) in the pre-pharyngeal but not the post-pharyngeal region (D',H'). The two posterior gut branches converge into one in Smed-bcatenin1-silenced planarians (E'), and secretory cells ectopically differentiate in the post-pharyngeal region (G'). (I') The dose dependence of the phenotype and a quantification of the different degrees of anteriorization (1, 2 or 3d x 3inj/d indicates that planarians were injected three times during 1, 2 or 3 consecutive days, respectively). Anterior is shown to the left in those cases where an anteroposterior axis is present. (R-U,A'-H') Confocal z-projections. Yellow asterisk indicates the pharynx. Yellow/black arrows and red arrows indicate the differentiation of anterior structures in normal and ectopic positions, respectively. d, days after wounding; a, anterior; p, posterior. Scale bar in A: 270 µm in A-C,E,F,N; 180 µm in D; 250 µm in H,L,P,R,T,W; 395 µm in J; 437 µm in K; 300 µm in all other images.

 

Figure 2
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Fig. 2. Trunk and tail identities are lost in Smed-bcatenin1-silenced planarians, whereas the dorsoventral axis remains unaffected. (A-F) Analysis of Smed-HoxD (A-D) and Smed-AbdBa (E,F) reveals the disappearance of tail and trunk identities, including the mouth (m). (G,H) Expression of Smed-TCEN49 almost disappears in radial-like hypercephalized planarians. (I-P) Analysis of Septin (I-L) and Eye53 (M-P) expression demonstrates that the dorsoventral axis is not affected. Eye53 is also expressed in the eyes (black arrowheads in the control, N), revealing the ectopic eyes around the treated animal (M). Anterior is shown to the left in those cases where an anteroposterior axis is present. Yellow/black asterisks indicate the pharynx. d, dorsal view; v, ventral view. Scale bar in A: 270 µm in A,E; 250 µm in C,G,I,K,M,O; 300 µm in all other images.

 

Figure 3
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Fig. 3. Smed-βcatenin1-silenced intact planarians transform to radial-like hypercephalized planarians. (A-C) Stereomicroscope views showing two different stages. (D-S) Several markers were used at different days after Smedcatenin1 silencing to characterize the phenotype. Anti-arrestin (D-F), cintillo (G-I), H.10.2f (J-L), synapsin (M-O), Smed-TCEN49 (P,Q) and Smed-HoxD (R,S). (T) Quantification of the different phenotypes observed after Smed-bcatenin1 silencing, showing that the anteriorization started in most of the animals in the posterior region. Anterior is to the left in those cases where an anteroposterior axis is present. Confocal z-projections (D-F,M-O). Yellow asterisks indicate the pharynx. Yellow/black arrows and red arrows indicate the differentiation of anterior structures in normal and ectopic positions, respectively. d, days after silencing. Scale bar in A: 200 µm in B,E,H,K,N,P,R; 300 µm in all other images.

 

Figure 4
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Fig. 4. mRNA injection of Smed-βcatenin1 but not Smed-βcatenin2 induces a secondary axis in Xenopus embryos. (A,B) Xenopus embryos injected with Smedcatenin1 (A) or Smedcat2 RNA (B), showing Otx2 (forebrain, red arrow), Krox20 (rhombomeres 3 and 5, green arrows) and Cad3 (spinal cord, white arrows) expression, along with muscle staining with the antibody 12/101 (brown signal). A schematic representation of the structure of each β-catenin is shown under the corresponding image. GSK3-binding domain and adhesion domains are shown with red and blue boxes, respectively. (C-H) Neurula (C-F) and tailbud (G,H) stage embryos injected with GFP-tagged constructs for both Schmidtea mediterranea β-catenins. (I,J) Smed-βcatenin1 but not Smed-βcatenin2 is found preferentially in the cell nucleus. (K) Quantification of the secondary axis obtained after each Smed-βcatenin injection (Xenopus β-catenin was used as a control).

 





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