Sedoheptulokinase deficiency due to a 57-kb deletion in cystinosis patients causes urinary accumulation of sedoheptulose:: Elucidation of the CARKL gene
Sedoheptulokinase deficiency due to a 57-kb deletion in cystinosis patients causes urinary accumulation of sedoheptulose:: Elucidation of the CARKL gene
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DOI：
10.1002/humu.20685
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发表时间：
2008-04-01
期刊：
影响因子：
3.9
通讯作者：
Wevers, Ron A.
中科院分区：
文献类型：
--
作者：
Wamelink, Mirjam M. C.;Struys, Eduard A.;Wevers, Ron A.
The most common mutation in the nephropathic cystinosis (CTNS) gene is a homozygous 57-kb deletion that also includes an adjacent gene carbohydrate kinase-like (CARKL). The latter gene encodes a protein that is predicted to function as a carbohydrate kinase. Cystinosis patients with the common 57-kb deletion had strongly elevated urinary concentrations of sedoheptulose (28-451 mmol/mol creatinine; controls and other cystinosis patients < 9) and erythritol (234-1110 mmol/mol creatinine; controls and other cystinosis patients < 148). Enzyme studies performed on fibroblast homogenates derived from patients carrying the 57-kb deletion revealed 80% reduction in their sedoheptulose phosphorylating activity compared to cystinosis patients with other mutations and controls. This indicates that the CARKL,encoded protein, sedoheptulokinase (SHK), is responsible for the reaction: sedoheptulose + ATP -> secloheptulose-7-phosphate + ADP and that deletion of CARKL causes urinary accumulation of sedoheptulose and erythritol.
