Literature DB >> 26246518

Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses.

Sali M K Farhan1, Jian Wang2, John F Robinson2, Asuri N Prasad3, C Anthony Rupar4, Victoria M Siu4, Robert A Hegele1.   

Abstract

BACKGROUND: Heparan sulfate proteoglycans are vital components of the extracellular matrix and are essential for cellular homeostasis. Many genes are involved in modulating heparan sulfate synthesis, and when these genes are mutated, they can give rise to early-onset developmental disorders affecting multiple body systems. Herein, we describe a consanguineous family of four sibs with a novel disorder, which we designate as seizures-scoliosis-macrocephaly syndrome, characterised by seizures, intellectual disability, hypotonia, scoliosis, macrocephaly, hypertelorism and renal dysfunction.
METHODS: Our application of autozygosity mapping and whole-exome sequencing allowed us to identify mutations in the patients. To confirm the autosomal-recessive mode of inheritance, all available family members were genotyped. We also studied the effect of these mutations on protein expression and function in patient cells and using an in vitro system.
RESULTS: We identified two homozygous mutations p.Met87Arg and p.Arg95 Cys in exostosin 2, EXT2, a ubiquitously expressed gene that encodes a glycosyltransferase required for heparan sulfate synthesis. In patient cells, we observed diminished EXT2 expression and function. We also performed an in vitro assay to determine which mutation has a larger effect on protein expression and observed reduced EXT2 expression in constructs expressing either one of the mutations but a greater reduction when both residues were mutated.
CONCLUSIONS: In short, we have unravelled the genetic basis of a new recessive disorder, seizures-scoliosis-macrocephaly syndrome. Our results have implicated a well-characterised gene in a new developmental disorder and have further illustrated the spectrum of phenotypes that can arise due to errors in glycosylation. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  EXT2; Heparan sulfate; Intellectual disability; NDST1; Whole-exome sequencing

Mesh:

Substances:

Year:  2015        PMID: 26246518     DOI: 10.1136/jmedgenet-2015-103279

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 in total

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Journal:  J Inherit Metab Dis       Date:  2017-05-08       Impact factor: 4.982

2.  Equivocal evidence for a link between megalencephaly-related genes and primate brain size evolution.

Authors:  Alex R DeCasien; Amber E Trujillo; Mareike C Janiak; Etta P Harshaw; Zosia N Caes; Gabriela A Galindo; Rachel M Petersen; James P Higham
Journal:  Sci Rep       Date:  2022-06-28       Impact factor: 4.996

3.  Early pregnancy dyslipidemia is associated with placental DNA methylation at loci relevant for cardiometabolic diseases.

Authors:  Marion Ouidir; Xuehuo Zeng; Tsegaselassie Workalemahu; Deepika Shrestha; Katherine L Grantz; Pauline Mendola; Cuilin Zhang; Fasil Tekola-Ayele
Journal:  Epigenomics       Date:  2020-07-17       Impact factor: 4.778

4.  Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome.

Authors:  Machteld M Oud; Paul Tuijnenburg; Maja Hempel; Naomi van Vlies; Zemin Ren; Sacha Ferdinandusse; Machiel H Jansen; René Santer; Jessika Johannsen; Chiara Bacchelli; Marielle Alders; Rui Li; Rosalind Davies; Lucie Dupuis; Catherine M Cale; Ronald J A Wanders; Steven T Pals; Louise Ocaka; Chela James; Ingo Müller; Kai Lehmberg; Tim Strom; Hartmut Engels; Hywel J Williams; Phil Beales; Ronald Roepman; Patricia Dias; Han G Brunner; Jan-Maarten Cobben; Christine Hall; Taila Hartley; Polona Le Quesne Stabej; Roberto Mendoza-Londono; E Graham Davies; Sérgio B de Sousa; Davor Lessel; Heleen H Arts; Taco W Kuijpers
Journal:  Am J Hum Genet       Date:  2017-01-26       Impact factor: 11.025

5.  A De Novo POLD1 Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome.

Authors:  Linda R Wang; Aleksandar Radonjic; Allison A Dilliott; Adam D McIntyre; Robert A Hegele
Journal:  J Investig Med High Impact Case Rep       Date:  2018-07-12

6.  Liver Involvement in Congenital Disorders of Glycosylation: A Systematic Review.

Authors:  Rossella Colantuono; Elisa D'Acunto; Daniela Melis; Pietro Vajro; Hudson H Freeze; Claudia Mandato
Journal:  J Pediatr Gastroenterol Nutr       Date:  2021-10-01       Impact factor: 3.288

Review 7.  Epigenetic Regulation of the Biosynthesis & Enzymatic Modification of Heparan Sulfate Proteoglycans: Implications for Tumorigenesis and Cancer Biomarkers.

Authors:  Elizabeth E Hull; McKale R Montgomery; Kathryn J Leyva
Journal:  Int J Mol Sci       Date:  2017-06-26       Impact factor: 5.923

8.  Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy.

Authors:  Sali M K Farhan; Kevin C J Nixon; Michelle Everest; Tara N Edwards; Shirley Long; Dmitri Segal; Maria J Knip; Heleen H Arts; Rana Chakrabarti; Jian Wang; John F Robinson; Donald Lee; Seyed M Mirsattari; C Anthony Rupar; Victoria M Siu; Michael O Poulter; Robert A Hegele; Jamie M Kramer
Journal:  Hum Mol Genet       Date:  2017-11-01       Impact factor: 6.150

  8 in total

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