Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2008-5-2
pubmed:abstractText
Nephropathic cystinosis is a lysosomal disorder caused by functional defects of cystinosin, which mediates cystine efflux into the cytosol. The protein sequence contains at least two signals that target the protein to the lysosomal compartment, one of which is located at the carboxy terminal tail (GYDQL). We have isolated from a human kidney cDNA library a cystinosin isoform, which is generated by an alternative splicing of exon 12 that removes the GYDQL motif. Based on its last three amino acids, we have termed this protein cystinosin-LKG. Contrary to the lysosomal cystinosin isoform, expression experiments performed by transient transfection of green fluorescent protein fusion plasmids in HK2 cells showed that cystinosin-LKG is expressed in the plasma membrane, in lysosomes, and in other cytosolic structures. This subcellular localization of the protein was confirmed by transmission electron microscopy. In addition, immunogold labeling was observed in the endoplasmic reticulum and in the Golgi apparatus. Expression of the protein in renal tubular structures was also directly demonstrated by immunostaining of normal human kidney sections. The plasma membrane localization of cystinosin-LKG was directly tested by [(35)S]cystine flux experiments in COS-1 cells. In the presence of a proton gradient, a marked enhancement of intracellular cystine transport was observed in cells overexpressing this isoform. These data indicate that the expression of the gene products encoded by the CTNS gene is not restricted to the lysosomal compartment. These finding may help elucidate the mechanisms of cell dysfunction in this disorder.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1931-857X
pubmed:author
pubmed:issnType
Print
pubmed:volume
294
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
F1101-8
pubmed:dateRevised
2011-4-28
pubmed:meshHeading
pubmed-meshheading:18337546-Amino Acid Sequence, pubmed-meshheading:18337546-Amino Acid Transport Systems, Neutral, pubmed-meshheading:18337546-Animals, pubmed-meshheading:18337546-Cell Line, pubmed-meshheading:18337546-Cell Membrane, pubmed-meshheading:18337546-Cloning, Molecular, pubmed-meshheading:18337546-Cystine, pubmed-meshheading:18337546-Cytosol, pubmed-meshheading:18337546-DNA, Complementary, pubmed-meshheading:18337546-Endoplasmic Reticulum, pubmed-meshheading:18337546-Endosomes, pubmed-meshheading:18337546-Exons, pubmed-meshheading:18337546-Golgi Apparatus, pubmed-meshheading:18337546-Humans, pubmed-meshheading:18337546-Immunoenzyme Techniques, pubmed-meshheading:18337546-Isomerism, pubmed-meshheading:18337546-Lysosomes, pubmed-meshheading:18337546-Mice, pubmed-meshheading:18337546-Microscopy, Fluorescence, pubmed-meshheading:18337546-Microscopy, Immunoelectron, pubmed-meshheading:18337546-Molecular Sequence Data, pubmed-meshheading:18337546-Plasmids, pubmed-meshheading:18337546-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:18337546-Subcellular Fractions, pubmed-meshheading:18337546-Transfection
pubmed:year
2008
pubmed:articleTitle
Identification and subcellular localization of a new cystinosin isoform.
pubmed:affiliation
Department of Nephrology and Urology, Division of Nephrology, Ospedale Bambino Gesù Children's Hospital and Research Insitute, Rome, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't