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Published on: August 24, 2013
Adenomatous polyposis coli is present near the minimal level required for accurate graded responses to the Wingless
Hassina Benchabane1, Edward G Hughes, Carter M Takacs
1Department of Genetics and the Norris Cotton Cancer Center, Dartmouth Medical School, Hanover, NH 03755, USA.
Abstract:
The mechanisms by which the Wingless (Wg) morphogen modulates the activity of the transcriptional activator Armadillo (Arm) to elicit precise, concentration-dependent cellular responses remain uncertain. Arm is targeted for proteolysis by the Axin/Adenomatous polyposis coli (Apc1 and Apc2)/Zeste-white 3 destruction complex, and Wg-dependent inactivation of destruction complex activity is crucial to trigger Arm signaling. In the prevailing model for Wg transduction, only Axin levels limit destruction complex activity, whereas Apc is present in vast excess. To test this model, we reduced Apc activity to different degrees, and analyzed the effects on three concentration-dependent responses to Arm signaling that specify distinct retinal photoreceptor fates. We find that both Apc1 and Apc2 negatively regulate Arm activity in photoreceptors, but that the relative contribution of Apc1 is much greater than that of Apc2. Unexpectedly, a less than twofold reduction in total Apc activity, achieved by loss of Apc2, decreases the effective threshold at which Wg elicits a cellular response, thereby resulting in ectopic responses that are spatially restricted to regions with low Wg concentration. We conclude that Apc activity is not present in vast excess, but instead is near the minimal level required for accurate graded responses to the Wg morphogen.
Insights
Adenomatous polyposis coli (Apc) levels are critical for Wingless (Wg) morphogen signaling. Reduced Apc activity lowers the Wg response threshold, impacting cell fate determination in photoreceptors.
Area of Science:
- Developmental Biology
- Cell Signaling
- Molecular Genetics
Background:
- Wingless (Wg) morphogen signaling regulates cell fate through the transcriptional activator Armadillo (Arm).
- Arm is degraded by the Axin/Adenomatous polyposis coli (Apc)/Zeste-white 3 destruction complex.
- Wg signaling inactivates this complex, stabilizing Arm and initiating cellular responses.
Purpose of the Study:
- To investigate the role of Apc in modulating Arm activity and Wg-dependent cellular responses.
- To test the prevailing model where Apc is in vast excess and Axin is the limiting factor in the destruction complex.
Main Methods:
- Manipulating Apc activity levels in developing photoreceptors.
- Analyzing concentration-dependent responses to Arm signaling.
- Assessing the impact of Apc reduction on Wg signaling thresholds.
Main Results:
- Both Apc1 and Apc2 negatively regulate Arm activity, with Apc1 having a greater contribution.
- A modest reduction in total Apc activity (loss of Apc2) lowered the Wg response threshold.
- This resulted in ectopic Wg responses in areas with low Wg concentration.
Conclusions:
- Apc activity is not in vast excess but is finely tuned for accurate Wg morphogen responses.
- Apc levels are critical for establishing the precise concentration-dependent signaling required for cell fate specification.
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