Larger Image

Fig. S2. XSeb4R gain- and loss-of-function in the embryos. Pigmented and albino embryos were unilaterally injecetd with XSeb4R capped-RNA (200 pg/blastomere) or XSeb4R-MO (20 ng/blastomere), using LacZ mRNA as a tracer (200 pg/blastomere). Embryos were cultured and fixed at neurula stage 18 and at tadpole stage. X-gal staining were performed (blue color) and the albino embryos were analyzed by WMISH. Note differential distribution of the blue color, recapitulating the sites of XSeb4R overexpression (A) or depletion (B). Neural crest (NC) formation was investigated targeting Slug expression (B). XSeb4R-MO revealed no significant effect on the intensity of Slug expression but rather a marked clustering of signal that reflects NC cells migration inhibition (100%, n = 32).

Image published in: Bentaya S et al. (2012)

Copyright © 2012. Image reproduced with permission of the Publisher, Elsevier B. V.

GeneSynonymsSpeciesStage(s)Tissue
snai2.Lslug, snai2-a, snai2-b, Snail2, xSlu, xslug, XSnail2X. laevisThroughout NF stage 18neural crest
migratory neural crest cell
premigratory neural crest cell

Image source: Published

Experiment + Assay Source Phenotypes and Disease
Xla Wt + rbm38 + NF37/38 (morphology) fig.S2.a
Anatomical Phenotype
abnormal bending of anterior-posterior axis
abnormal head morphology
absent eye
increased pigmentation in the trunk
increased size of the ventral trunk
Xla Wt + rbm38 MO + NF18 (morphology) fig.S2.b
Anatomical Phenotype
abnormal cell migration in neural crest
Expression Phenotype
mislocalised snai2.L expression in migratory neural crest cell

Permanent Image Page
Printer Friendly View

XB-IMG-78848