Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding (Q34405965)

2 August 2017

title

Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding (English)

1 reference

2 August 2017

Santosh K Patnaik

1

1 reference

2 August 2017

Pamela Stanley

series ordinal

2

1 reference

2 August 2017

language of work or name

English

0 references

publication date

23 March 2005

1 reference

Journal of Biological Chemistry

2 August 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

2 August 2017

volume

280

1 reference

2 August 2017

issue

21

1 reference

2 August 2017

page(s)

20851-20859

1 reference

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Cranin: a laminin-binding protein of cell membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

A stoichiometric complex of neurexins and dystroglycan in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Influence of core protein sequence on glycosaminoglycan assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Purification of cranin, a laminin binding membrane protein. Identity with dystroglycan and reassessment of its carbohydrate moieties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Core 1 glycans on alpha-dystroglycan mediate laminin-induced acetylcholine receptor clustering but not laminin binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Molecular recognition by LARGE is essential for expression of functional dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

The role of defective glycosylation in congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Defective glycosylation in congenital muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Phenotypic spectrum associated with mutations in the fukutin-related protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Chinese hamster ovary cells selected for resistance to the cytotoxicity of phytohemagglutinin are deficient in a UDP-N-acetylglucosamine--glycoprotein N-acetylglucosaminyltransferase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Chinese hamster ovary cell mutants with multiple glycosylation defects for production of glycoproteins with minimal carbohydrate heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Two Chinese hamster ovary glycosylation mutants affected in the conversion of GDP-mannose to GDP-fucose

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Mutant of Chinese hamster ovary cells with altered mannose 6-phosphate receptor activity is unable to synthesize mannosylphosphoryldolichol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

HUNT: launch of a full-length cDNA database from the Helix Research Institute

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

The Lec4A CHO glycosylation mutant arises from miscompartmentalization of a Golgi glycosyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Prediction, conservation analysis, and structural characterization of mammalian mucin-type O-glycosylation sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Cloning and characterization of mammalian UDP-glucose glycoprotein: glucosyltransferase and the development of a specific substrate for this enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Two homologues encoding human UDP-glucose:glycoprotein glucosyltransferase differ in mRNA expression and enzymatic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Temporal and spatial appearance of α‐dystroglycan in differentiated mouse myoblasts in culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Five Lec1 CHO cell mutants have distinct Mgat1 gene mutations that encode truncated N-acetylglucosaminyltransferase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Differential involvement of cell surface sialic acid residues in wheat germ agglutinin binding to parental and wheat germ agglutinin-resistant Chinese hamster ovary cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Mutants of the CMP-sialic acid transporter causing the Lec2 phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Point mutations identified in Lec8 Chinese hamster ovary glycosylation mutants that inactivate both the UDP-galactose and CMP-sialic acid transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

alpha(1,3)fucosyltransferases expressed by the gain-of-function Chinese hamster ovary glycosylation mutants LEC12, LEC29, and LEC30.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Molecular cloning and expression of GDP-D-mannose-4,6-dehydratase, a key enzyme for fucose metabolism defective in Lec13 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Molecular cloning of human GDP-mannose 4,6-dehydratase and reconstitution of GDP-fucose biosynthesis in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Molecular characterization of eukaryotic polysialyltransferase-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Lec3 Chinese Hamster Ovary Mutants Lack UDP-N-acetylglucosamine 2-Epimerase Activity Because of Mutations in the Epimerase Domain of the Gne Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

A single point mutation resulting in an adversely reduced expression of DPM2 in the Lec15.1 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Protein C-mannosylation is enzyme-catalysed and uses dolichyl-phosphate-mannose as a precursor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Molecular cloning and expression of a novel beta-1, 6-N-acetylglucosaminyltransferase that forms core 2, core 4, and I branches

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Dystrophin and the membrane skeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Specific disruption of a schwann cell dystrophin-related protein complex in a demyelinating neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Dystroglycan complex in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

CDD: a database of conserved domain alignments with links to domain three-dimensional structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

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/10.1074%2FJBC.M500069200

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Deletions on chromosome 22 in sporadic meningioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M500069200

21 January 2018

Identifiers

DOI

10.1074/JBC.M500069200

1 reference

2 August 2017

1 reference