Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Feb 1;145(3):dev159178. doi: 10.1242/dev.159178

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2018. Published by The Company of Biologists Ltd

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

PMC Copyright notice

Fig. 2. — Reprogramming of the Notch cellular status by posterior TFCs is for proper CpC specification. (A) Expression of the Notch activity reporter [E(spl)mβ-CD2, green] and Dl protein (red) during the GSC niche formation. The Notch activity reporter and Dl protein are expressed in TFCs at ML3 stage. At LL3 stage, levels of the Notch reporter and the Dl protein are reduced in the most posterior TFC (blue asterisks). Dl appears in vesicles, indicating a Notch signal-sending state. At the prepupal stage, the Notch reporter is active in CpCs (yellow asterisks) and levels of the Notch reporter and Dl protein are reduced in the most posterior TFC (TC, blue asterisks). (B) The potential model of TFC reprograming from the Notch active to Dl-sending status.