Literature DB >> 12068947

Developmental roles of heparan sulfate proteoglycans: a comparative review in Drosophila, mouse and human.

Marc Princivalle1, Ariane de Agostini.   

Abstract

In recent years, progress in the fields of development and proteoglycan biology have produced converging evidence of the role of proteoglycans in morphogenesis. Numerous studies have demonstrated that proteoglycans are involved in several distinct morphogenetic pathways upon which they act at different levels. In particular, proteoglycans can determine the generation of morphogen gradients and be required for their signal transduction. The surface of most cells and the extracellular matrix are decorated by heparan sulfates which are the most common glycosaminoglycans, normally present as heparan sulfate proteoglycans. Considerable structural heterogeneity is generated in proteoglycans by the biosynthetic modification of their heparan sulfate chains as well as by the diverse nature of their different core proteins. This heterogeneity provides an impressive potential for protein-protein and protein-carbohydrate interactions, and can partly explain the diversity of proteoglycan involvement in different morphogenetic pathways. In this review, we summarize the current knowledge about mutations affecting heparan sulfate proteoglycans that influence the function of growth factor pathways essential for tissue assembly, differentiation and development. The comparison of data obtained in Drosophila, rodents and humans reveals that mutations affecting the proteoglycan core proteins or one of the biosynthetic enzymes of their heparan sulfate chains have profound effects on growth and morphogenesis. Further research will complete the picture, but current evidence shows that at the very least, heparan sulfate proteoglycans need to be counted as legitimate elements of morphogenetic pathways that have been maintained throughout evolution as determinant mechanisms of pattern formation.

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Year:  2002        PMID: 12068947

Source DB:  PubMed          Journal:  Int J Dev Biol        ISSN: 0214-6282            Impact factor:   2.203


  14 in total

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2.  Involvement of chondroitin sulfate synthase-3 (chondroitin synthase-2) in chondroitin polymerization through its interaction with chondroitin synthase-1 or chondroitin-polymerizing factor.

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Review 3.  A starting place for the road to function.

Authors:  Jeremiah E Silbert; Geetha Sugumaran
Journal:  Glycoconj J       Date:  2002 May-Jun       Impact factor: 2.916

4.  A missense mutation in the bovine SLC35A3 gene, encoding a UDP-N-acetylglucosamine transporter, causes complex vertebral malformation.

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Journal:  Genome Res       Date:  2005-12-12       Impact factor: 9.043

5.  Signaling network involved in the GPC3-induced inhibition of breast cancer progression: role of canonical Wnt pathway.

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7.  Spatiotemporal distribution of heparan sulfate epitopes during murine cartilage growth plate development.

Authors:  Ronald R Gomes; Toin H Van Kuppevelt; Mary C Farach-Carson; Daniel D Carson
Journal:  Histochem Cell Biol       Date:  2006-07-12       Impact factor: 4.304

Review 8.  Unlocking the secrets of syndecans: transgenic organisms as a potential key.

Authors:  Robert Bellin; Ishan Capila; John Lincecum; Pyong Woo Park; Ofer Reizes; Merton R Bernfield
Journal:  Glycoconj J       Date:  2002 May-Jun       Impact factor: 2.916

9.  Regulation of xylosyltransferase I gene expression by interleukin 1β in human primary chondrocyte cells: mechanism and impact on proteoglycan synthesis.

Authors:  Mostafa Khair; Mustapha Bourhim; Lydia Barré; Dong Li; Patrick Netter; Jacques Magdalou; Sylvie Fournel-Gigleux; Mohamed Ouzzine
Journal:  J Biol Chem       Date:  2012-12-05       Impact factor: 5.157

10.  Structure of a UDP-glucose dehydrogenase from the hyperthermophilic archaeon Pyrobaculum islandicum.

Authors:  Haruhiko Sakuraba; Tomoyuki Kawai; Kazunari Yoneda; Toshihisa Ohshima
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-08-29
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