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Genes & Dev. 13 (21): 2828-2837
Copyright © 1999 by Cold Spring Harbor Laboratory Press.
Vol. 13, No. 21, pp. 2828-2837, November 1, 1999
RESEARCH PAPER
Protein kinase A antagonizes Hedgehog signaling by regulating both the activator and repressor forms of Cubitus interruptus
Gelin
Wang,
Bing
Wang, and
Jin
Jiang1
Center for Developmental Biology and Department of Pharmacology,
University of Texas Southwestern Medical Center,
Dallas, Texas 75235-9133 USA
The Hedgehog (Hh) family of secreted proteins controls many aspects
of animal development. In Drosophila, Hh transduces its signal
via Cubitus interruptus (Ci), a transcription factor present in two
forms: a full-length activator and a carboxy-terminally truncated
repressor that is derived from the full-length form by proteolytic
processing. The proteolytic processing of Ci is promoted by the
activities of protein kinase A (PKA) and Slimb, whereas it is inhibited
by Hh. Here we show that PKA inhibits the activity of the full-length
Ci in addition to its role in regulating Ci proteolysis. Whereas Ci
processing is blocked in both PKA and slimb mutant
cells, the accumulated full-length Ci becomes activated only in
PKA but not in slimb mutant cells. Moreover, PKA
inhibits an uncleavable activator form of Ci. These observations suggest that PKA regulates the activity of the full-length Ci independent of its proteolytic processing. We also provide evidence that PKA regulates both the proteolytic processing and transcriptional activity of Ci by directly phosphorylating Ci. We propose that phosphorylation of Ci by PKA has two separable roles: (1) It blocks the
transcription activity of the full-length activator form of Ci, and (2)
it targets Ci for Slimb-mediated proteolytic processing to generate the
truncated form that functions as a repressor.
[Key Words:
PKA; Ci; Hedgehog; Slimb; proteolysis; limb
development]
GENES & DEVELOPMENT 13:2828-2837 © 1999 by Cold Spring Harbor Laboratory Press ISSN 0890-9369/99 $5.00
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