Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.

Abstract

zeta-Crystallin is a lens protein that has been associated with autosomal dominant congenital cataracts in guinea pigs and thus is a candidate for human congenital cataracts. We have assigned the zeta-crystallin gene (CRYZ) to human chromosome 1 using a Southern panel of 17 human-mouse somatic cell hybrids and regionally localized it to 1p22-p31 by fluorescence in situ hybridization. Five restriction fragment length polymorphisms were identified by analyzing the DNA from 10 unrelated, unaffected individuals. Our results will permit evaluation of its role in human cataractogenesis.

• Authors: C Heinzmann, T L Kojis, P Gonzalez, P V Rao, J S Zigler Jr, M H Polymeropoulos, I Klisak, R S Sparkes, T Mohandas, J B Bateman
• Journal: Genomics (Genomics) Vol. 23 Issue 2 Pg. 403-7 (Sep 15 1994) ISSN: 0888-7543 [Print] United States
• PMID: 7835889 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Crystallins

Topics

• Alleles
• Animals
• Cataract (congenital, genetics)
• Chromosome Mapping
• Chromosomes, Human, Pair 1
• Crystallins (genetics)
• Genetic Linkage
• Guinea Pigs
• Humans
• Hybrid Cells
• In Situ Hybridization, Fluorescence
• Mice
• Polymorphism, Restriction Fragment Length