Literature DB >> 25138275

Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissues.

Kei-ichiro Inamori1, Tobias Willer2, Yuji Hara2, David Venzke2, Mary E Anderson2, Nigel F Clarke3, Pascale Guicheney4, Carsten G Bönnemann5, Steven A Moore6, Kevin P Campbell7.   

Abstract

Mutations in the LARGE gene have been identified in congenital muscular dystrophy (CMD) patients with brain abnormalities. Both LARGE and its paralog, LARGE2 (also referred to as GYLTL1B) are bifunctional glycosyltransferases with xylosyltransferase (Xyl-T) and glucuronyltransferase (GlcA-T) activities, and are capable of forming polymers consisting of [-3Xyl-α1,3GlcAβ1-] repeats. LARGE-dependent modification of α-dystroglycan (α-DG) with these polysaccharides is essential for the ability of α-DG to act as a receptor for ligands in the extracellular matrix. Here we report on the endogenous enzymatic activities of LARGE and LARGE2 in mice and humans, using a newly developed assay for GlcA-T activity. We show that normal mouse and human cultured cells have endogenous LARGE GlcA-T, and that this activity is absent in cells from the Large(myd) (Large-deficient) mouse model of muscular dystrophy, as well as in cells from CMD patients with mutations in the LARGE gene. We also demonstrate that GlcA-T activity is significant in the brain, heart, and skeletal muscle of wild-type and Large2(-/-) mice, but negligible in the corresponding tissues of the Large(myd) mice. Notably, GlcA-T activity is substantial, though reduced, in the kidneys of both the Large(myd) and Large2(-/-) mice, consistent with the observation of α-DG/laminin binding in these contexts. This study is the first to test LARGE activity in samples as small as cryosections and, moreover, provides the first direct evidence that not only LARGE, but also LARGE2, is vital to effective functional modification of α-DG in vivo.
© 2014 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  Dystroglycan; Extracellular Matrix; Glucuronyltransferase; Glycosyltransferase; LARGE; Laminin; Muscular Dystrophy; Post-translational Modification (PTM)

Mesh:

Substances:

Year:  2014        PMID: 25138275      PMCID: PMC4192470          DOI: 10.1074/jbc.M114.597831

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


  48 in total

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Authors:  Wenli Zhang; Doron Betel; Harry Schachter
Journal:  Biochem J       Date:  2002-01-01       Impact factor: 3.857

2.  Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

Authors:  M Brockington; D J Blake; P Prandini; S C Brown; S Torelli; M A Benson; C P Ponting; B Estournet; N B Romero; E Mercuri; T Voit; C A Sewry; P Guicheney; F Muntoni
Journal:  Am J Hum Genet       Date:  2001-10-08       Impact factor: 11.025

3.  A new beta-1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans.

Authors:  S Takahashi; T Sasaki; H Manya; Y Chiba; A Yoshida; M Mizuno; H Ishida; F Ito; T Inazu; N Kotani; S Takasaki; M Takeuchi; T Endo
Journal:  Glycobiology       Date:  2001-01       Impact factor: 4.313

4.  Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse.

Authors:  P K Grewal; P J Holzfeind; R E Bittner; J E Hewitt
Journal:  Nat Genet       Date:  2001-06       Impact factor: 38.330

5.  Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE.

Authors:  Kei-ichiro Inamori; Takako Yoshida-Moriguchi; Yuji Hara; Mary E Anderson; Liping Yu; Kevin P Campbell
Journal:  Science       Date:  2012-01-06       Impact factor: 47.728

6.  Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.

Authors:  A Yoshida; K Kobayashi; H Manya; K Taniguchi; H Kano; M Mizuno; T Inazu; H Mitsuhashi; S Takahashi; M Takeuchi; R Herrmann; V Straub; B Talim; T Voit; H Topaloglu; T Toda; T Endo
Journal:  Dev Cell       Date:  2001-11       Impact factor: 12.270

Review 7.  Dystroglycanopathies: coming into focus.

Authors:  Caroline Godfrey; A Reghan Foley; Emma Clement; Francesco Muntoni
Journal:  Curr Opin Genet Dev       Date:  2011-03-11       Impact factor: 5.578

8.  Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Authors:  Daniel E Michele; Rita Barresi; Motoi Kanagawa; Fumiaki Saito; Ronald D Cohn; Jakob S Satz; James Dollar; Ichizo Nishino; Richard I Kelley; Hannu Somer; Volker Straub; Katherine D Mathews; Steven A Moore; Kevin P Campbell
Journal:  Nature       Date:  2002-07-25       Impact factor: 49.962

9.  Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.

Authors:  Daniel Beltrán-Valero de Bernabé; Sophie Currier; Alice Steinbrecher; Jacopo Celli; Ellen van Beusekom; Bert van der Zwaag; Hülya Kayserili; Luciano Merlini; David Chitayat; William B Dobyns; Bru Cormand; Ana-Elina Lehesjoki; Jesús Cruces; Thomas Voit; Christopher A Walsh; Hans van Bokhoven; Han G Brunner
Journal:  Am J Hum Genet       Date:  2002-10-04       Impact factor: 11.025

10.  LARGE expression augments the glycosylation of glycoproteins in addition to α-dystroglycan conferring laminin binding.

Authors:  Zhen Zhang; Peng Zhang; Huaiyu Hu
Journal:  PLoS One       Date:  2011-04-20       Impact factor: 3.240

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  8 in total

1.  212th ENMC International Workshop: Animal models of congenital muscular dystrophies, Naarden, The Netherlands, 29-31 May 2015.

Authors:  M Saunier; C G Bönnemann; M Durbeej; V Allamand
Journal:  Neuromuscul Disord       Date:  2016-02-15       Impact factor: 4.296

2.  The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation.

Authors:  Tobias Willer; Kei-Ichiro Inamori; David Venzke; Corinne Harvey; Greg Morgensen; Yuji Hara; Daniel Beltrán Valero de Bernabé; Liping Yu; Kevin M Wright; Kevin P Campbell
Journal:  Elife       Date:  2014-10-03       Impact factor: 8.140

3.  LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans.

Authors:  Kei-Ichiro Inamori; Aaron M Beedle; Daniel Beltrán-Valero de Bernabé; Michael E Wright; Kevin P Campbell
Journal:  Glycobiology       Date:  2016-07-22       Impact factor: 4.313

4.  Identification and Modeling of a GT-A Fold in the α-Dystroglycan Glycosylating Enzyme LARGE1.

Authors:  Benedetta Righino; Manuela Bozzi; Davide Pirolli; Francesca Sciandra; Maria Giulia Bigotti; Andrea Brancaccio; Maria Cristina De Rosa
Journal:  J Chem Inf Model       Date:  2020-05-14       Impact factor: 4.956

5.  Profiling of the muscle-specific dystroglycan interactome reveals the role of Hippo signaling in muscular dystrophy and age-dependent muscle atrophy.

Authors:  Andriy S Yatsenko; Mariya M Kucherenko; Yuanbin Xie; Dina Aweida; Henning Urlaub; Renate J Scheibe; Shenhav Cohen; Halyna R Shcherbata
Journal:  BMC Med       Date:  2020-01-21       Impact factor: 8.775

6.  microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy.

Authors:  Sarah U Morton; Christopher R Sefton; Huanqing Zhang; Manhong Dai; David L Turner; Michael D Uhler; Pankaj B Agrawal
Journal:  Int J Mol Sci       Date:  2021-03-07       Impact factor: 5.923

Review 7.  Molecular and cellular basis of genetically inherited skeletal muscle disorders.

Authors:  James J Dowling; Conrad C Weihl; Melissa J Spencer
Journal:  Nat Rev Mol Cell Biol       Date:  2021-07-13       Impact factor: 94.444

8.  High degree of conservation of the enzymes synthesizing the laminin-binding glycoepitope of α-dystroglycan.

Authors:  Maria Giulia Bigotti; Andrea Brancaccio
Journal:  Open Biol       Date:  2021-09-29       Impact factor: 6.411

  8 in total

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