Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 24 April 2009:
Vol. 324. no. 5926, pp. 509 - 512
DOI: 10.1126/science.1169498

Reports

Tuning the Activation Threshold of a Kinase Network by Nested Feedback Loops

Quincey A. Justman,1,2,* Zach Serber,3,{dagger} James E. Ferrell, Jr.,3 Hana El-Samad,4,{ddagger} Kevan M. Shokat2,{ddagger}

Determining proper responsiveness to incoming signals is fundamental to all biological systems. We demonstrate that intracellular signaling nodes can tune a signaling network’s response threshold away from the basal median effective concentration established by ligand-receptor interactions. Focusing on the bistable kinase network that governs progesterone-induced meiotic entry in Xenopus oocytes, we characterized glycogen synthase kinase–3β (GSK-3β) as a dampener of progesterone responsiveness. GSK-3β engages the meiotic kinase network through a double-negative feedback loop; this specific feedback architecture raises the progesterone threshold in correspondence with the strength of double-negative signaling. We also identified a marker of nutritional status, L-leucine, which lowers the progesterone threshold, indicating that oocytes integrate additional signals into their cell-fate decisions by modulating progesterone responsiveness.

1 Graduate Group in Biophysics, University of California, San Francisco, CA 94158, USA.
2 Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94158, USA.
3 Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305–5174, USA.
4 Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158, USA.

* Present address: Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

{dagger} Present address: Amyris Biotechnologies, Incorporated, Emeryville, CA 94608, USA.

{ddagger} To whom correspondence should be addressed. E-mail: helsamad{at}biochem.ucsf.edu (H.E.); shokat{at}cmp.ucsf.edu (K.M.S.)

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
To Divide or Not to Divide.
J. M. Skotheim (2009)
Science 324, 476-477
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)