| Literature DB >> 27633991 |
Zhigang Jin1, Tyler Schwend1, Jia Fu1, Zehua Bao2, Jing Liang2, Huimin Zhao2, Wenyan Mei1, Jing Yang3.
Abstract
Hedgehog (Hh) signaling is fundamentally important for development and adult tissue homeostasis. It is well established that in vertebrates Sufu directly binds and inhibits Gli proteins, the downstream mediators of Hh signaling. However, it is unclear how the inhibitory function of Sufu towards Gli is regulated. Here we report that the Rusc family of proteins, the biological functions of which are poorly understood, form a heterotrimeric complex with Sufu and Gli. Upon Hh signaling, Rusc is displaced from this complex, followed by dissociation of Gli from Sufu. In mammalian fibroblast cells, knockdown of Rusc2 potentiates Hh signaling by accelerating signaling-induced dissociation of the Sufu-Gli protein complexes. In Xenopus embryos, knockdown of Rusc1 or overexpression of a dominant-negative Rusc enhances Hh signaling during eye development, leading to severe eye defects. Our study thus uncovers a novel regulatory mechanism controlling the response of cells to Hh signaling in vertebrates.Entities:
Keywords: Gli; Hedgehog signaling; Human; Mouse; Rusc; Sufu; Xenopus
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Year: 2016 PMID: 27633991 PMCID: PMC5117142 DOI: 10.1242/dev.138917
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868