Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.

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Published: eLife Sciences Publications, Ltd 2016
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DML
Online Access:http://dx.doi.org/10.7554/elife.14847.011
id crelifesciences:10.7554/elife.14847.011
record_format openpolar
spelling crelifesciences:10.7554/elife.14847.011 2023-07-23T04:19:01+02:00 Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity. (A) Confocal stacks of somites, 6 hr after electroporation of RFP (in red) and SNAI1-GFP (fusion of SNAI1 and GFP, in green) alone or together with NICD. (B) Confocal stacks of somites, 6 hr after electroporation of GSK-3β biosensor (in green) and RFP (in red) alone (left), or together with NICD (right). (C) Confocal stacks of a somite 6 hr after co-electroporation of the GSK-3β biosensor (green) and the NOTCH reporter (red) and immunostained for MYF5 (blue). (D,E) Bar charts showing the% of GSK-3β biosensor-positive cells that activate NOTCH signaling (86.9%, D) and that are MYF5-positive (88.2%, E). (F) Confocal stacks of a somite 6 hr after co-electroporation of a SNAI fused to RFP (in red) and the GSK-3β biosensor (in green). In blue the electroporated cells, identified by H2B-BFP. (G) Bar charts showing 89.4% of DML electroporated cells are GSK-3β biosensor and SNAI1-positive. (H) Confocal stacks of somites and adjacent neural tube electroporated as described in Figure 4H, only in the DML with the GSK-3β biosensor (in green) and H2B-BFP (in blue, left panels) or double-electroporated in the DML with the GSK-3β biosensor (in green) and H2B BFP (in blue) and in the neural tube with DLL1 under the control of a neural crest-specific promoter (right panels). (I) Bar charts showing the% of GSK-3β biosensor-positive cells in the control (26.4%, in white) or with DLL1 expressed in the neural crest (64.6%, in black). (J) Confocal stacks of somites 17 hr after electroporation of GFP as control or DN-GSK-3β and immunostained for MYF5 (red). (K) Bar charts showing the% of electroporated cells that have entered the primary myotome in the control (45.8%, in white) of with the DN-GSK-3β (61.2%, in black). (L) Bar charts showing the% of electroporated cells that are MYF5-positive in the control (23.1%, in white) of with the DN-GSK-3β (57.2%, in black). In each panel are indicated the antigens that were detected by immunostaining, with the exception of native BFP blue fluorescence. Abbreviation: EP: electroporation; NT: neural tube. Scale bars: 50 μm. 2016-06-23T14:51:06Z http://dx.doi.org/10.7554/elife.14847.011 unknown eLife Sciences Publications, Ltd component 2016 crelifesciences https://doi.org/10.7554/elife.14847.011 2023-07-05T08:36:07Z Other/Unknown Material DML eLife (E-Journal - via Crossref)
institution Open Polar
collection eLife (E-Journal - via Crossref)
op_collection_id crelifesciences
language unknown
format Other/Unknown Material
title Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.
spellingShingle Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.
title_short Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.
title_full Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.
title_fullStr Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.
title_full_unstemmed Figure 7. NOTCH regulates SNAI1 degradation through inhibition of GSK-3β activity.
title_sort figure 7. notch regulates snai1 degradation through inhibition of gsk-3β activity.
publisher eLife Sciences Publications, Ltd
publishDate 2016
url http://dx.doi.org/10.7554/elife.14847.011
genre DML
genre_facet DML
op_doi https://doi.org/10.7554/elife.14847.011
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