A missense mutation in the bovine SLC35A3 gene, encoding a UDP-N-acetylglucosamine transporter, causes complex vertebral malformation
Open Access
- 12 December 2005
- journal article
- Published by Cold Spring Harbor Laboratory in Genome Research
- Vol. 16 (1) , 97-105
- https://doi.org/10.1101/gr.3690506
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.Keywords
This publication has 63 references indexed in Scilit:
- Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporterBlood, 2005
- Identification and characterization of human Golgi nucleotide sugar transporter SLC35D2, a novel member of the SLC35 nucleotide sugar transporter familyGenomics, 2005
- Loss of srf-3-encoded Nucleotide Sugar Transporter Activity in Caenorhabditis elegans Alters Surface Antigenicity and Prevents Bacterial AdherenceJournal of Biological Chemistry, 2004
- Practical genetics: alpha-1-antitrypsin deficiency and the serpinopathiesEuropean Journal of Human Genetics, 2003
- An NDPase links ADAM protease glycosylation with organ morphogenesis in C. elegansNature Cell Biology, 2003
- The underglycosylation of plasma alpha1-antitrypsin in congenital disorders of glycosylation type I is not randomGlycobiology, 2002
- Listening to silence and understanding nonsense: exonic mutations that affect splicingNature Reviews Genetics, 2002
- Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1Nature Genetics, 1997
- Transporters of nucleotide sugars, nucleotide sulfate and ATP in the Golgi apparatusTrends in Biochemical Sciences, 1997
- Guanosine diphosphatase is required for protein and sphingolipid glycosylation in the Golgi lumen of Saccharomyces cerevisiaeThe Journal of cell biology, 1993