Contribution of EXT1, EXT2, and EXTL3 to heparan sulfate chain elongation (Q24338759)

Exostosin glycosyltransferase 2

GOA release 2020-03-11

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heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process

GOA release 2020-03-11

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GOA release 2020-03-11

author

Marion Kusche-Gullberg

7

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Marta Busse

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Maria Wilén

4

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Lena Kjellén

6

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Jenny Presto

3

object named as

Jenny Presto

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author name string

Marta Busse

1

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Almir Feta

2

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Mona Grønning

Journal of Biological Chemistry

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language of work or name

English

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publication date

9 November 2007

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published in

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volume

282

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issue

45

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page(s)

32802-10

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cites work

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Axon sorting in the optic tract requires HSPG synthesis by ext2 (dackel) and extl3 (boxer).

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Hereditary multiple exostoses and heparan sulfate polymerization

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Heparan sulfate abnormalities in exostosis growth plates

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Formation of anhydrosugars in the chemical depolymerization of heparin

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Overexpression of different isoforms of glucosaminyl N-deacetylase/N-sulfotransferase results in distinct heparan sulfate N-sulfation patterns

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Expression of heparan sulphate L-iduronyl 2-O-sulphotransferase in human kidney 293 cells results in increased D-glucuronyl 2-O-sulphation

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Substrate specificities of mouse heparan sulphate glucosaminyl 6-O-sulphotransferases

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Biosynthesis of heparin. The D-glucuronosyl- and N-acetyl-D-glucosaminyltransferase reactions and their relation to polymer modification

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Human tumor suppressor EXT gene family members EXTL1 and EXTL3 encode alpha 1,4- N-acetylglucosaminyltransferases that likely are involved in heparan sulfate/ heparin biosynthesis

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The putative tumor suppressors EXT1 and EXT2 form a stable complex that accumulates in the Golgi apparatus and catalyzes the synthesis of heparan sulfate

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Accumulation of a pentasaccharide terminating in alpha-N-acetylglucosamine in an animal cell mutant defective in heparan sulfate biosynthesis

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Domain structure of heparan sulfates from bovine organs

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Regulated diversity of heparan sulfate

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Heparan sulfate synthesized by mouse embryonic stem cells deficient in NDST1 and NDST2 is 6-O-sulfated but contains no N-sulfate groups

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Location of the glucuronosyltransferase domain in the heparan sulfate copolymerase EXT1 by analysis of Chinese hamster ovary cell mutants

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In vitro heparan sulfate polymerization: crucial roles of core protein moieties of primer substrates in addition to the EXT1-EXT2 interaction

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In vitro polymerization of heparan sulfate backbone by the EXT proteins

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Embryonic fibroblasts with a gene trap mutation in Ext1 produce short heparan sulfate chains

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Characterizing the non-reducing end structure of heparan sulfate

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Heparin and heparan sulfate biosynthesis

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Interactions between heparan sulfate and proteins: the concept of specificity

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Etiological point mutations in the hereditary multiple exostoses gene EXT1: a functional analysis of heparan sulfate polymerase activity

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The EXT1/EXT2 tumor suppressors: catalytic activities and role in heparan sulfate biosynthesis

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A PCR primer bank for quantitative gene expression analysis

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Differentiation-induced loss of heparan sulfate in human exostosis derived chondrocytes

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Genotype-phenotype correlation in hereditary multiple exostoses

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Order out of chaos: assembly of ligand binding sites in heparan sulfate

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Molecular diversity of heparan sulfate

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Three Drosophila EXT genes shape morphogen gradients through synthesis of heparan sulfate proteoglycans

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Distinct and collaborative roles of Drosophila EXT family proteins in morphogen signalling and gradient formation

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Abrogation of heparan sulfate synthesis in Drosophila disrupts the Wingless, Hedgehog and Decapentaplegic signaling pathways

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Mice deficient in Ext2 lack heparan sulfate and develop exostoses

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