Dual functions of DP1 promote biphasic Wnt-on and Wnt-off states during anteroposterior neural patterning.


Autoria(s): Kim W.T.; Kim H.; Katanaev V.L.; Joon Lee S.; Ishitani T.; Cha B.; Han J.K.; Jho E.H.
Data(s)

2012

Resumo

DP1, a dimerization partner protein of the transcription factor E2F, is known to inhibit Wnt/β-catenin signalling along with E2F, although the function of DP1 itself was not well characterized. Here, we present a novel dual regulatory mechanism of Wnt/β-catenin signalling by DP1 independent from E2F. DP1 negatively regulates Wnt/β-catenin signalling by inhibiting Dvl-Axin interaction and by enhancing poly-ubiquitination of β-catenin. In contrast, DP1 positively modulates the signalling upon Wnt stimulation, via increasing cytosolic β-catenin and antagonizing the kinase activity of NLK. In Xenopus embryos, DP1 exerts both positive and negative roles in Wnt/β-catenin signalling during anteroposterior neural patterning. From subcellular localization analyses, we suggest that the dual roles of DP1 in Wnt/β-catenin signalling are endowed by differential nucleocytoplasmic localizations. We propose that these dual functions of DP1 can promote and stabilize biphasic Wnt-on and Wnt-off states in response to a gradual gradient of Wnt/β-catenin signalling to determine differential cell fates.

Identificador

http://serval.unil.ch/?id=serval:BIB_6888DB2531B0

isbn:1460-2075 (Electronic)

pmid:22773187

doi:10.1038/emboj.2012.181

isiid:000307879700004

Idioma(s)

en

Fonte

EMBO Journal, vol. 31, no. 16, pp. 3384-3397

Palavras-Chave #Animals; Body Patterning; Gene Expression Regulation, Developmental; Signal Transduction; Transcription Factor DP1/metabolism; Wnt Proteins/metabolism; Xenopus/embryology; beta Catenin/metabolism
Tipo

info:eu-repo/semantics/article

article