Identification and characterization of human Golgi nucleotide sugar transporter SLC35D2, a novel member of the SLC35 nucleotide sugar transporter family

Genomics ◽  
2005 ◽  
Vol 85 (1) ◽  
pp. 106-116 ◽  
Author(s):  
Nobuhiro Ishida ◽  
Toshiyasu Kuba ◽  
Kazuhisa Aoki ◽  
Shoichiro Miyatake ◽  
Masao Kawakita ◽  
...  
Biochimie ◽  
2003 ◽  
Vol 85 (3-4) ◽  
pp. 245-260 ◽  
Author(s):  
Ivan Martinez-Duncker ◽  
Rosella Mollicone ◽  
Patrice Codogno ◽  
Rafael Oriol

2004 ◽  
Vol 279 (25) ◽  
pp. 26469-26474 ◽  
Author(s):  
Takeshi Suda ◽  
Shin Kamiyama ◽  
Masayuki Suzuki ◽  
Norihiro Kikuchi ◽  
Ken-ichi Nakayama ◽  
...  

Blood ◽  
2006 ◽  
Vol 109 (4) ◽  
pp. 1533-1540 ◽  
Author(s):  
Sreenivasulu Chintala ◽  
Jian Tan ◽  
Rashi Gautam ◽  
Michael E. Rusiniak ◽  
Xiaoli Guo ◽  
...  

Abstract Platelet dense granules are lysosome-related organelles which contain high concentrations of several biologically important low-molecular-weight molecules. These include calcium, serotonin, adenine nucleotides, pyrophosphate, and polyphosphate, which are necessary for normal blood hemostasis. The synthesis of dense granules and other lysosome-related organelles is defective in inherited diseases such as Hermansky-Pudlak syndrome (HPS) and Chediak-Higashi syndrome (CHS). HPS and CHS mutations in 8 human and at least 16 murine genes have been identified. Previous studies produced contradictory findings for the function of the murine ashen (Rab27a) gene in platelet-dense granules. We have used a positional cloning approach with one line of ashen mutants to establish that a new mutation in a second gene, Slc35d3, on mouse chromosome 10 is the basis of this discrepancy. The platelet-dense granule defect is rescued in BAC transgenic mice containing the normal Slc35d3 gene. Thus, Slc35d3, an orphan member of a nucleotide sugar transporter family, specifically regulates the contents of platelet-dense granules. Unlike HPS or CHS genes, it has no apparent effect on other lysosome-related organelles such as melanosomes or lysosomes. The ash-Roswell mouse mutant is an appropriate model for human congenital-isolated delta-storage pool deficiency.


2018 ◽  
Author(s):  
Beibei Jing ◽  
Toshiki Ishikawa ◽  
Nicole Soltis ◽  
Noriko Inada ◽  
Yan Liang ◽  
...  

AbstractThe Golgi lumen is the site of many different glycosylation events, including cell wall polysaccharide biosynthesis and lipid glycosylation. Transporters are necessary for the import of the substrates required for glycosylation (nucleotide sugars) from the cytosol where they are synthesized. Plants use four GDP-linked sugars to glycosylate macromolecules: GDP-L-Fucose, GDP-D-Mannose, GDP-L-Galactose and GDP-D-Glucose. Of the predicted fifty-one members of the nucleotide sugar transporter/triose phosphate transporter family in Arabidopsis, only four appear to contain the conserved motif needed for the transport of GDP-linked sugars, GOLGI LOCALIZED NUCLEOTIDE SUGAR TRANSPORTER (GONST) 1-4. Previously, we have demonstrated that GONST1 provides GDP-D-Mannose for glycosylation of a class of sphingolipids, the glycosylinositolphosphorylceramides (GIPCs). Here, we characterize its closest homologue, GONST2, and conclude that it also specifically provides substrate for GIPC glycosylation. Expression of GONST2 driven by the GONST1 promoter is able to rescue the severe growth phenotype of gonst1. Loss of GONST2 exacerbates the gonst1 constitutive hypersensitive response, as well as the reduced cell wall cellulose content. The gonst2 mutant grows normally under standard conditions, but has enhanced resistance to the powdery mildew-causing fungus Golovinomyces orontii.


Sign in / Sign up

Export Citation Format

Share Document