Literature DB >> 16344554

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

Bo Thomsen1, Per Horn, Frank Panitz, Emøke Bendixen, Anette H Petersen, Lars-Erik Holm, Vivi H Nielsen, Jørgen S Agerholm, Jens Arnbjerg, Christian Bendixen.   

Abstract

The extensive use of a limited number of elite bulls in cattle breeding can lead to rapid spread of recessively inherited disorders. A recent example is the globally distributed syndrome Complex Vertebral Malformation (CVM), which is characterized by misshapen and fused vertebrae around the cervico-thoracic junction. Here, we show that CVM is caused by a mutation in the Golgi-resident nucleotide-sugar transporter encoded by SLC35A3. Thus, the disease showed complete cosegregation with the mutation in a homozygous state, and proteome patterns indicated abnormal protein glycosylation in tissues of affected animals. In addition, a yeast mutant that is deficient in the transport of UDP-N-acetylglucosamine into its Golgi lumen can be rescued by the wild-type SLC35A3 gene, but not by the mutated gene. These results provide the first demonstration of a genetic disorder associated with a defective SLC35A3 gene, and reveal a new mechanism for malformation of the vertebral column caused by abnormal nucleotide-sugar transport into the Golgi apparatus.

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Year:  2005        PMID: 16344554      PMCID: PMC1356133          DOI: 10.1101/gr.3690506

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  61 in total

1.  Localized and transient transcription of Hox genes suggests a link between patterning and the segmentation clock.

Authors:  J Zákány; M Kmita; P Alarcon; J L de la Pompa; D Duboule
Journal:  Cell       Date:  2001-07-27       Impact factor: 41.582

Review 2.  Dissecting glycoprotein quality control in the secretory pathway.

Authors:  C M Cabral; Y Liu; R N Sifers
Journal:  Trends Biochem Sci       Date:  2001-10       Impact factor: 13.807

3.  The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.

Authors:  K Lühn; M K Wild; M Eckhardt; R Gerardy-Schahn; D Vestweber
Journal:  Nat Genet       Date:  2001-05       Impact factor: 38.330

4.  Molecular characterization of human UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter, a novel nucleotide sugar transporter with dual substrate specificity.

Authors:  M Muraoka; M Kawakita; N Ishida
Journal:  FEBS Lett       Date:  2001-04-20       Impact factor: 4.124

5.  Complex vertebral malformation in holstein calves.

Authors:  J S Agerholm; C Bendixen; O Andersen; J Arnbjerg
Journal:  J Vet Diagn Invest       Date:  2001-07       Impact factor: 1.279

6.  Complex vertebral malformation in a holstein calf: report of a case in the USA.

Authors:  R B Duncan; C B Carrig; J S Agerholm; C Bendixen
Journal:  J Vet Diagn Invest       Date:  2001-07       Impact factor: 1.279

7.  The UDPase activity of the Kluyveromyces lactis Golgi GDPase has a role in uridine nucleotide sugar transport into Golgi vesicles.

Authors:  M D Lopez-Avalos; D Uccelletti; C Abeijon; C B Hirschberg
Journal:  Glycobiology       Date:  2001-05       Impact factor: 4.313

8.  FGF signaling controls somite boundary position and regulates segmentation clock control of spatiotemporal Hox gene activation.

Authors:  J Dubrulle; M J McGrew; O Pourquié
Journal:  Cell       Date:  2001-07-27       Impact factor: 41.582

9.  Dual role of the fringe connection gene in both heparan sulphate and fringe-dependent signalling events.

Authors:  E M Selva; K Hong; G H Baeg; S M Beverley; S J Turco; N Perrimon; U Häcker
Journal:  Nat Cell Biol       Date:  2001-09       Impact factor: 28.824

10.  UDP-sugar transporter implicated in glycosylation and processing of Notch.

Authors:  S Goto; M Taniguchi; M Muraoka; H Toyoda; Y Sado; M Kawakita; S Hayashi
Journal:  Nat Cell Biol       Date:  2001-09       Impact factor: 28.824

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  54 in total

1.  Disease-promoting and -protective genomic loci on mouse chromosomes 3 and 19 control the incidence and severity of autoimmune arthritis.

Authors:  T T Glant; V A Adarichev; F Boldizsar; T Besenyei; A Laszlo; K Mikecz; T A Rauch
Journal:  Genes Immun       Date:  2012-03-08       Impact factor: 2.676

Review 2.  Role of glycans and glycosyltransferases in the regulation of Notch signaling.

Authors:  Hamed Jafar-Nejad; Jessica Leonardi; Rodrigo Fernandez-Valdivia
Journal:  Glycobiology       Date:  2010-04-05       Impact factor: 4.313

3.  Inhibition of Golgi apparatus glycosylation causes endoplasmic reticulum stress and decreased protein synthesis.

Authors:  Yu-Xin Xu; Li Liu; Carolina E Caffaro; Carlos B Hirschberg
Journal:  J Biol Chem       Date:  2010-06-07       Impact factor: 5.157

4.  Conserved Glu-47 and Lys-50 residues are critical for UDP-N-acetylglucosamine/UMP antiport activity of the mouse Golgi-associated transporter Slc35a3.

Authors:  M Agustina Toscanini; M Belén Favarolo; F Luis Gonzalez Flecha; Berit Ebert; Carsten Rautengarten; Luis M Bredeston
Journal:  J Biol Chem       Date:  2019-05-22       Impact factor: 5.157

5.  Single nucleotide polymorphisms in candidate genes and their relation with somatic cell scores in Argentinean dairy cattle.

Authors:  Juan P Nani; Maria A Raschia; Hugo Carignano; Mario A Poli; Luis F Calvinho; Ariel F Amadio
Journal:  J Appl Genet       Date:  2015-03-18       Impact factor: 3.240

6.  Independent and simultaneous translocation of two substrates by a nucleotide sugar transporter.

Authors:  Carolina E Caffaro; Carlos B Hirschberg; Patricia M Berninsone
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-23       Impact factor: 11.205

Review 7.  The role of nucleotide sugar transporters in development of eukaryotes.

Authors:  Li Liu; Yu-Xin Xu; Carlos B Hirschberg
Journal:  Semin Cell Dev Biol       Date:  2010-02-06       Impact factor: 7.727

8.  Biosynthesis of GlcNAc-rich N- and O-glycans in the Golgi apparatus does not require the nucleotide sugar transporter SLC35A3.

Authors:  Bozena Szulc; Paulina Sosicka; Dorota Maszczak-Seneczko; Edyta Skurska; Auhen Shauchuk; Teresa Olczak; Hudson H Freeze; Mariusz Olczak
Journal:  J Biol Chem       Date:  2020-09-16       Impact factor: 5.157

9.  Screening for bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, complex vertebral malformation, bovine citrullinaemia, and factor XI deficiency in Holstein cows reared in Turkey.

Authors:  Hasan Meydan; Mehmet A Yildiz; Jørgen S Agerholm
Journal:  Acta Vet Scand       Date:  2010-10-07       Impact factor: 1.695

10.  Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene.

Authors:  Bo Thomsen; Peter H Nissen; Jørgen S Agerholm; Christian Bendixen
Journal:  Neurogenetics       Date:  2009-08-28       Impact factor: 2.660

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