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出 处:《Cell Research》2012年第5期936-940,共5页细胞研究(英文版)
摘 要:The F-box family of proteins (FBPs), the substrate- recognition components of the Skpl-Cull-F-box-protein (SCF) ubiquitin ligase, are evolutionarily conserved in various species and exhibit key roles in a wide array of biological processes, including tumorigenesis and de- velopment [1-3]. Although approximately 70 FBPs have been identified in humans [4, 5], only a few of them have been well characterized. Fbxll4 (F-box and leucine-rich repeat protein 14) has been reported to regulate Snail2 protein during neural crest development ofXenopus lae- vis embryos [6] and to control Snaill protein stability in mammalian cells [7]. There are two homologs of Fbxll4 in zebrafish, namely Fbxll4a and Fbxll4b. In this study, we show that Fbxll4a and Fbxll4b are differential regu- lators of the dorsoventral (DV) patterning of zebrafish embryos and further demonstrate that their roles in axis formation are differentially executed through the modu- lation of MAP kinase phosphatase-3 (Mkp3) ubiquitina- tion and protein levels.
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