Affiliation:
1. Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., C3-168, P.O. Box 19024, Seattle, Washington 98109-1024
2. Department of Neurology, University of Washington Medical Center, Seattle, Washington 98195
Abstract
ABSTRACT
Siamois is the transcriptional mediator of the dorsal Wnt signaling pathway and is necessary for formation of the Spemann organizer and dorsoanterior development in
Xenopus
. We have determined that XIC, a
Xenopus
I-mfa domain protein that regulates Tcf3 binding, is required for dorsoaxial development and specifically for Siamois activity in establishing the dorsal organizer. In loss-of-function studies, we found that embryos injected with a morpholino to
XIC
mRNA (
XIC
morphpolino) are missing head structures, neural tube, notochord, and paraxial mesoderm as well as
NCAM
and
XMyoD
expression. Although
Siamois
,
Twin
, and
Xnr3
expression is normal in morpholino-injected embryos, levels of downstream organizer factors, including
goosecoid
,
Xnot
,
Cerberus
, and
chordin
, are severely reduced. Ectopic axis formation induced by Siamois is repressed by injection of the
XIC
morpholino and further repressed by coinjection of β-catenin or a constitutively active Tcf3/HMG/G4A fusion. Activation of reporters driven by the Siamois-responsive proximal element of the
goosecoid
promoter is inhibited in the presence of the morpholino and can be rescued by murine I-mfa and by a dominant-negative Tcf3. The data indicate a role for XIC in limiting Tcf3-dependent repression of Siamois activities that are required for
goosecoid
transcription and for dorsal organizer formation.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
10 articles.
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