Literature DB >> 31286677

Bone and connective tissue disorders caused by defects in glycosaminoglycan biosynthesis: a panoramic view.

Chiara Paganini1, Rossella Costantini1, Andrea Superti-Furga2, Antonio Rossi1.   

Abstract

Glycosaminoglycans (GAGs) are a heterogeneous family of linear polysaccharides that constitute the carbohydrate moiety covalently attached to the protein core of proteoglycans, macromolecules present on the cell surface and in the extracellular matrix. Several genetic disorders of bone and connective tissue are caused by mutations in genes encoding for glycosyltransferases, sulfotransferases and transporters that are responsible for the synthesis of sulfated GAGs. Phenotypically, these disorders all reflect alterations in crucial biological functions of GAGs in the development, growth and homoeostasis of cartilage and bone. To date, up to 27 different skeletal phenotypes have been linked to mutations in 23 genes encoding for proteins involved in GAG biosynthesis. This review focuses on recent genetic, molecular and biochemical studies of bone and connective tissue disorders caused by GAG synthesis defects. These insights and future research in the field will provide a deeper understanding of the molecular pathogenesis of these disorders and will pave the way for developing common therapeutic strategies that might be targeted to a range of individual phenotypes.
© 2019 Federation of European Biochemical Societies.

Entities:  

Keywords:  Golgi; endoplasmic reticulum; genotype phenotype correlation; glycosaminoglycans; glycosyltransferases; proteoglycans; skeletal disorders; sulfotransferases

Year:  2019        PMID: 31286677     DOI: 10.1111/febs.14984

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  17 in total

1.  Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.

Authors:  Jonathan J Rios; Bruce Beutler; Kristin Denton; Jamie Russell; Julia Kozlitina; Carlos R Ferreira; Amy F Lewanda; Joshua E Mayfield; Eva Moresco; Sara Ludwig; Miao Tang; Xiaohong Li; Stephen Lyon; Anas Khanshour; Nandina Paria; Aysha Khalid; Yang Li; Xudong Xie; Jian Q Feng; Qian Xu; Yongbo Lu; Robert E Hammer; Carol A Wise
Journal:  J Bone Miner Res       Date:  2021-05-10       Impact factor: 6.390

2.  CANT1 deficiency in a mouse model of Desbuquois dysplasia impairs glycosaminoglycan synthesis and chondrocyte differentiation in growth plate cartilage.

Authors:  Kazuki Kodama; Hiroaki Takahashi; Nobuyasu Oiji; Kenta Nakano; Tadashi Okamura; Kimie Niimi; Eiki Takahashi; Long Guo; Shiro Ikegawa; Tatsuya Furuichi
Journal:  FEBS Open Bio       Date:  2020-04-23       Impact factor: 2.693

3.  Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6.

Authors:  Stefano Giuseppe Caraffi; Ilenia Maini; Ivan Ivanovski; Marzia Pollazzon; Sara Giangiobbe; Maurizia Valli; Antonio Rossi; Silvia Sassi; Silvia Faccioli; Maja Di Rocco; Cinzia Magnani; Belinda Campos-Xavier; Sheila Unger; Andrea Superti-Furga; Livia Garavelli
Journal:  Genes (Basel)       Date:  2019-10-12       Impact factor: 4.096

4.  Growth patterns for untreated individuals with MPS I: Report from the international MPS I registry.

Authors:  David Viskochil; Lorne A Clarke; Luisa Bay; Hillary Keenan; Joseph Muenzer; Nathalie Guffon
Journal:  Am J Med Genet A       Date:  2019-10-22       Impact factor: 2.802

Review 5.  Nucleotide Sugars in Chemistry and Biology.

Authors:  Satu Mikkola
Journal:  Molecules       Date:  2020-12-06       Impact factor: 4.411

6.  Novel lamprey antibody recognizes terminal sulfated galactose epitopes on mammalian glycoproteins.

Authors:  Tanya R McKitrick; Steffen M Bernard; Alexander J Noll; Bernard C Collins; Christoffer K Goth; Alyssa M McQuillan; Jamie Heimburg-Molinaro; Brantley R Herrin; Ian A Wilson; Max D Cooper; Richard D Cummings
Journal:  Commun Biol       Date:  2021-06-03

Review 7.  Supply chain logistics - the role of the Golgi complex in extracellular matrix production and maintenance.

Authors:  John Hellicar; Nicola L Stevenson; David J Stephens; Martin Lowe
Journal:  J Cell Sci       Date:  2022-01-13       Impact factor: 5.285

8.  A Dominant Heterozygous Mutation in COG4 Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling.

Authors:  Zhi-Jie Xia; Xin-Xin I Zeng; Mitali Tambe; Bobby G Ng; P Duc S Dong; Hudson H Freeze
Journal:  Front Cell Dev Biol       Date:  2021-09-14

9.  Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities.

Authors:  Pauline E Schneeberger; Leonie von Elsner; Emma L Barker; Peter Meinecke; Iris Marquardt; Malik Alawi; Katharina Steindl; Pascal Joset; Anita Rauch; Petra J G Zwijnenburg; Marjan M Weiss; Catherine L R Merry; Kerstin Kutsche
Journal:  Am J Hum Genet       Date:  2020-11-06       Impact factor: 11.025

Review 10.  Skeletal Dysplasias Caused by Sulfation Defects.

Authors:  Chiara Paganini; Chiara Gramegna Tota; Andrea Superti-Furga; Antonio Rossi
Journal:  Int J Mol Sci       Date:  2020-04-14       Impact factor: 5.923

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