| Literature DB >> 27350215 |
Miho Fujiwara1, Shintaro Kato1, Yuki Niwa1, Takehiro Suzuki2, Miyu Tsuchiya1, Yukiko Sasazawa1, Naoshi Dohmae2, Siro Simizu1.
Abstract
R-spondin3 (Rspo3) is a secreted protein, which acts as an agonist of canonical Wnt/β-catenin signaling that plays an important role in embryonic development and homeostasis. In this study, we focused on C-mannosylation, a unique type of glycosylation, of human Rspo3. Rspo3 has two putative C-mannosylation sites at Trp(153) and Trp(156) ; however, it had been unclear whether these sites are C-mannosylated or not. We demonstrated that Rspo3 was C-mannosylated at both Trp(153) and Trp(156) by mass spectrometry. Using C-mannosylation-defective Rspo3 mutant-overexpressing cell lines, we found that C-mannosylation of Rspo3 promotes its secretion and activates Wnt/β-catenin signaling.Entities:
Keywords: C-mannosylation; R-spondin3; Wnt/β-catenin signaling; glycobiology; mass spectrometry; signal transduction
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Year: 2016 PMID: 27350215 DOI: 10.1002/1873-3468.12274
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124