(Q38266217)

1 September 2017

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title

Glycobiology of α-dystroglycan and muscular dystrophy (English)

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1 September 2017

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Tamao Endo

1

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1 September 2017

publication date

7 November 2014

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1 September 2017

published in

Journal of Biochemistry

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1 September 2017

volume

157

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1 September 2017

issue

1

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1 September 2017

page(s)

1-12

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Membrane organization of the dystrophin-glycoprotein complex

1 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Molecular recognition by LARGE is essential for expression of functional dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Decoding arenavirus pathogenesis: essential roles for alpha-dystroglycan-virus interactions and the immune response.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-linked or 2,6-linked hexose (mannose).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

High prevalence of 2-mono- and 2,6-di-substituted manol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Role of N-glycans in maintaining the activity of protein O-mannosyltransferases POMT1 and POMT2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Futile protein folding cycles in the ER are terminated by the unfolded protein O-mannosylation pathway.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Structure-function analysis of human protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 1, POMGnT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Effects of length and amino acid sequence of O-mannosyl peptides on substrate specificity of protein O-linked mannose β1,2-N-acetylglucosaminyltransferase 1 (POMGnT1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

O-glycosylation of the non-canonical T-cadherin from rabbit skeletal muscle by single mannose residues

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

A novel β(1,6)‐N‐acetylglucosaminyltransferase V (GnT‐VB)1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Molecular cloning and characterization of human GnT-IX, a novel beta1,6-N-acetylglucosaminyltransferase that is specifically expressed in the brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

N-Acetylglucosaminyltransferase IX acts on the GlcNAc beta 1,2-Man alpha 1-Ser/Thr moiety, forming a 2,6-branched structure in brain O-mannosyl glycan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Loss of branched O-mannosyl glycans in astrocytes accelerates remyelination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Receptor tyrosine phosphatase beta (RPTPbeta) activity and signaling are attenuated by glycosylation and subsequent cell surface galectin-1 binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

beta4GalT-II is a key regulator of glycosylation of the proteins involved in neuronal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate transfer regulates laminin-binding glycans on α-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

LARGE2 generates the same xylose- and glucuronic acid-containing glycan structures as LARGE

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

A stoichiometric complex of neurexins and dystroglycan in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Dystroglycan organizes axon guidance cue localization and axonal pathfinding

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Tissue-specific heterogeneity in alpha-dystroglycan sialoglycosylation. Skeletal muscle alpha-dystroglycan is a latent receptor for Vicia villosa agglutinin b4 masked by sialic acid modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

O-glycosylation pattern of CD24 from mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Neurofascin 186 is O-mannosylated within and outside of the mucin domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

The lecticans of mammalian brain perineural net are O-mannosylated

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAc

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Expression cloning of cDNA encoding a human beta-1,3-N-acetylglucosaminyltransferase that is essential for poly-N-acetyllactosamine synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Cloning, expression and characterization of the pig liver GDP-mannose pyrophosphorylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Expression and characterization of a human cDNA ...

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

A dystroglycan mutation associated with limb-girdle muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Tumor suppressor function of laminin-binding alpha-dystroglycan requires a distinct beta3-N-acetylglucosaminyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

A truncating mutation in B3GNT1 causes severe Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJB%2FMVU066

21 January 2018

Identifiers

DOI

10.1093/JB/MVU066

1 reference

1 September 2017

1 reference