Literature DB >> 16221665

Lunatic fringe, manic fringe, and radical fringe recognize similar specificity determinants in O-fucosylated epidermal growth factor-like repeats.

Raajit Rampal1, Annie S Y Li, Daniel J Moloney, Stephanie A Georgiou, Kelvin B Luther, Aleksandra Nita-Lazar, Robert S Haltiwanger.   

Abstract

Notch signaling is a component of a wide variety of developmental processes in many organisms. Notch activity can be modulated by O-fucosylation (mediated by protein O-fucosyltransferase-1) and Fringe, a beta1,3-N-acetylglucosaminyltransferase that modifies O-fucose in the context of epidermal growth factor-like (EGF) repeats. Fringe was initially described in Drosophila, and three mammalian homologues have been identified, Manic fringe, Lunatic fringe, and Radical fringe. Here for the first time we have demonstrated that, similar to Manic and Lunatic, Radical fringe is also a fucose-specific beta1,3-N-acetylglucosaminyltransferase. The fact that three Fringe homologues exist in mammals raises the question of whether and how these enzymes differ. Although Notch contains numerous EGF repeats that are predicted to be modified by O-fucose, previous studies in our laboratory have demonstrated that not all O-fucosylated EGF repeats of Notch are further modified by Fringe, suggesting that the Fringe enzymes can differentiate between them. In this work, we have sought to identify specificity determinants for the recognition of an individual O-fucosylated EGF repeat by the Fringe enzymes. We have also sought to determine differences in the biochemical behavior of the Fringes with regard to their in vitro enzymatic activities. Using both in vivo and in vitro experiments, we have found two amino acids that appear to be important for the recognition of an O-fucosylated EGF repeat by all three mammalian Fringes. These amino acids provide an initial step toward defining sequences that will allow us to predict which O-fucosylated EGF repeats are modified by the Fringes.

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Year:  2005        PMID: 16221665     DOI: 10.1074/jbc.M509552200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  46 in total

Review 1.  Role of glycans and glycosyltransferases in the regulation of Notch signaling.

Authors:  Hamed Jafar-Nejad; Jessica Leonardi; Rodrigo Fernandez-Valdivia
Journal:  Glycobiology       Date:  2010-04-05       Impact factor: 4.313

2.  Deciphering the Fringe-Mediated Notch Code: Identification of Activating and Inhibiting Sites Allowing Discrimination between Ligands.

Authors:  Shinako Kakuda; Robert S Haltiwanger
Journal:  Dev Cell       Date:  2017-01-12       Impact factor: 12.270

3.  Deletion of Pofut1 in Mouse Skeletal Myofibers Induces Muscle Aging-Related Phenotypes in cis and in trans.

Authors:  Deborah A Zygmunt; Neha Singhal; Mi-Lyang Kim; Megan L Cramer; Kelly E Crowe; Rui Xu; Ying Jia; Jessica Adair; Isabel Martinez-Pena Y Valenzuela; Mohammed Akaaboune; Peter White; Paulus M Janssen; Paul T Martin
Journal:  Mol Cell Biol       Date:  2017-05-02       Impact factor: 4.272

4.  O-glucose trisaccharide is present at high but variable stoichiometry at multiple sites on mouse Notch1.

Authors:  Nadia A Rana; Aleksandra Nita-Lazar; Hideyuki Takeuchi; Shinako Kakuda; Kelvin B Luther; Robert S Haltiwanger
Journal:  J Biol Chem       Date:  2011-07-08       Impact factor: 5.157

5.  Site-specific O-glucosylation of the epidermal growth factor-like (EGF) repeats of notch: efficiency of glycosylation is affected by proper folding and amino acid sequence of individual EGF repeats.

Authors:  Hideyuki Takeuchi; Joshua Kantharia; Maya K Sethi; Hans Bakker; Robert S Haltiwanger
Journal:  J Biol Chem       Date:  2012-08-07       Impact factor: 5.157

6.  O-Glycosylation modulates the stability of epidermal growth factor-like repeats and thereby regulates Notch trafficking.

Authors:  Hideyuki Takeuchi; Hongjun Yu; Huilin Hao; Megumi Takeuchi; Atsuko Ito; Huilin Li; Robert S Haltiwanger
Journal:  J Biol Chem       Date:  2017-07-20       Impact factor: 5.157

7.  Fringe-mediated extension of O-linked fucose in the ligand-binding region of Notch1 increases binding to mammalian Notch ligands.

Authors:  Paul Taylor; Hideyuki Takeuchi; Devon Sheppard; Chandramouli Chillakuri; Susan M Lea; Robert S Haltiwanger; Penny A Handford
Journal:  Proc Natl Acad Sci U S A       Date:  2014-05-06       Impact factor: 11.205

8.  Impaired O-linked N-acetylglucosaminylation in the endoplasmic reticulum by mutated epidermal growth factor (EGF) domain-specific O-linked N-acetylglucosamine transferase found in Adams-Oliver syndrome.

Authors:  Mitsutaka Ogawa; Shogo Sawaguchi; Takami Kawai; Daita Nadano; Tsukasa Matsuda; Hirokazu Yagi; Koichi Kato; Koichi Furukawa; Tetsuya Okajima
Journal:  J Biol Chem       Date:  2014-12-08       Impact factor: 5.157

Review 9.  Role of unusual O-glycans in intercellular signaling.

Authors:  Kelvin B Luther; Robert S Haltiwanger
Journal:  Int J Biochem Cell Biol       Date:  2008-10-08       Impact factor: 5.085

Review 10.  A Notch updated.

Authors:  An-Chi Tien; Akhila Rajan; Hugo J Bellen
Journal:  J Cell Biol       Date:  2009-03-02       Impact factor: 10.539

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