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Breakthrough in study of childhood cataracts
Researchers at ETH Zurich and the University Zurich have identified the chromosomal location and exact molecular defect in the coding region of the gene responsible for a childhood cataract. Until now, no human disease could be associated with this gene. The researchers' results will be published in the 'American Journal of Human Genetics'.
The international team of researchers was able to identify the location and defect in the coding region of the gene through analysis of genetic material (DNA) from members of a large Swiss family, the majority of whom suffered from autosomal dominant juvenile cataract. The corresponding protein belongs to a family of monocarboxylate transporters which move small molecules across cell membranes. Surprisingly, this genetic defect may also lead to the condition of renal glucosuria, a non-pathological kidney defect with elevated levels of glucose in the urine, but not in blood.
New research underway
The search for the molecule that is carried by this new transporter across the membrane has now begun. The researchers suspect that this genetic defect interferes with homeostasis in the lens as well as in the kidney. Since the known environmental risk factors for age-related cataract point to physiological and oxidative damages accumulating over time within the lens, the researchers assume that defects in this newly discovered transporter may also be a cause of age-related cataract. Age-related cataract patients are now being screened to find mutations in this gene. Understanding the exact function of this transporter may open new venues for non-surgical treatment of cataract.
Gradual blurred vision
Cataract, the condition of altered refractive index in the lens of the eye, is the clouding of the eye's normally clear lens and results in blurry vision that frequently includes disturbing glare in the visual field. Successful treatment today involves surgical removal of the affected lens and replacement with an artificial one.
Two conditions of cataract
Age onset of cataract is the distinguishing characteristic between affliction in childhood or in later years. Whereas about 14% of blind children are affected, half of the adult population worldwide aged 60 and older suffers from age-related cataract. Various underlying defects cause its development. Research in molecular and genetic science has enabled identification of several genes that play an important role in structural or regulatory functions in lens cells. Al-though all cataract genes identified to date are known to affect children, genetic factors for age-related cataract continue to remain widely undiscovered.
Original paper:
Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cata-ract with microcornea and renal glucosuria.
Barbara Kloeckener-Gruissem+* 1,2, Kristof Vandekerckhove*3,4, Gudrun Nürnberg5,7, John Neid-hardt1, Christina Zeitz1,8, Peter Nürnberg5,6, Isaak Schipper3 and Wolfgang Berger1
1 Division of Medical Molecular Genetics and Gene Diagnostics, Institute of Medical Genet-ics, University Zurich, Switzerland; 2 Department of Biology, ETH, Zurich, Switzerland; 3 Eye Clinic, Kanton Hospital Luzern, Switzerland; 4 present address: Eye Clinic, Inselspital, Bern, Switzerland; 5 Cologne Center for Genomics, University of Cologne, Germany; 6 Institute for Genetics, University of Cologne, Germany; 7 RZPD Deutsches Ressourcenzentrum für Ge-nomforschung GmbH, Berlin, Germany; 8 present address: UMR S 592, Institut de la Vision, Université Paris, Paris, France
* these authors showed equal contribution
+ Corresponding author
Ref: AJHG-D-07-00111R4, Kloeckener
The first shows an image as seen through a normal lens
Quelle: Photographs by Stephan Labs
Same image as above, but simulated as seen through the lens of a cataract patient with severe cloudi ...
Quelle: Photographs by Stephan Labs
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