Cherqui S, Kalatzis V, Forestier L, Poras I, Antignac C
Inserm U423,Université René Descartes, Hôpital Necker-Enfants Malades, 75743 Paris Cedex 15, France.
BMC Genomics. 2000;1:2. doi: 10.1186/1471-2164-1-2. Epub 2000 Dec 6.
Cystinosis is an autosomal recessive disorder characterised by an intralysosomal accumulation of cystine, and affected individuals progress to end-stage renal failure before the age of ten. The causative gene, CTNS, was cloned in 1998 and the encoded protein, cystinosin, was predicted to be a lysosomal membrane protein.
We have cloned the murine homologue of CTNS, Ctns, and the encoded amino acid sequence is 92.6% similar to cystinosin. We localised Ctns to mouse chromosome 11 in a region syntenic to human chromosome 17 containing CTNS. Ctns is widely expressed in all tissues tested with the exception of skeletal muscle, in contrast to CTNS.
We have isolated, characterised and localised Ctns, the murine homologue of CTNS underlying cystinosis. Furthermore, our work has brought to light the existence of a differential pattern of expression between the human and murine homologues, providing critical information for the generation of a mouse model for cystinosis.
胱氨酸贮积症是一种常染色体隐性疾病,其特征为溶酶体内胱氨酸蓄积,患病个体在十岁前会发展为终末期肾衰竭。致病基因CTNS于1998年被克隆,其编码的蛋白质胱氨酸转运体被预测为溶酶体膜蛋白。
我们克隆了CTNS的小鼠同源基因Ctns,其编码的氨基酸序列与胱氨酸转运体有92.6%的相似性。我们将Ctns定位到小鼠11号染色体上与包含CTNS的人类17号染色体同线的区域。与CTNS不同,Ctns在除骨骼肌外的所有检测组织中广泛表达。
我们已经分离、鉴定并定位了Ctns,即胱氨酸贮积症相关基因CTNS的小鼠同源基因。此外,我们的工作揭示了人类和小鼠同源基因之间存在不同的表达模式,为建立胱氨酸贮积症小鼠模型提供了关键信息。