Journal Article

Link between a novel human γD-crystallin allele and a unique cataract phenotype explained by protein crystallography

Stanislav Kmoch, Jirí Brynda, Befekadu Asfaw, Karel Bezouška, Petr Novák, Pavlína Řezáčová, Lenka Ondrová, Martin Filipec, Juraj Sedláček and Milan Elleder

in Human Molecular Genetics

Volume 9, issue 12, pages 1779-1786
Published in print July 2000 | ISSN: 0964-6906
Published online July 2000 | e-ISSN: 1460-2083 | DOI: http://dx.doi.org/10.1093/hmg/9.12.1779
Link between a novel human γD-crystallin allele and a unique cataract phenotype explained by protein crystallography

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We describe a 5-year-old boy with a unique congenital cataract caused by deposition of numerous birefringent, pleiochroic and macroscopically prismatic crystals. Crystal analysis with subsequent automatic Edman degradation and matrix-associated laser desorption ionization time-of-flight mass spectrometry have identified the crystal-forming protein as γD-crystallin (CRYGD) lacking the N-terminal methionine. Sequencing of the CRYGD gene has shown a heterozygous C→A transversion in position 109 of the inferred cDNA (36R→S transversion of the processed, N-terminal methionine-lacking CRYGD). The lens protein crystals were X-ray diffracting, and our crystal structure solution at 2.25 Å suggests that mutant R36S CRYGD has an unaltered protein fold. In contrast, the observed crystal packing is possible only with the mutant protein molecules that lack the bulky Arg36 side chain. This is the first described case of human cataract caused by crystallization of a protein in the lens. It involves the third known mutation in the CRYGD gene but offers, for the first time, a causative explanation of the phenotype.

Journal Article.  4819 words.  Illustrated.

Subjects: Genetics and Genomics

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