Direct assignment of the human βB2 and βB3 crystallin genes to 22q11.2→q12: markers for neurofibromatosis 2

Abstract

We have isolated a human probe specific for the βB3 crystallin gene (CRYB3) and hybridized it to Southern blots of human × rodent cell hybrids with known human chromosomal constitution. In this way we could directly assign CRYB3 to chromosome 22. Cell hybrids with translocation chromosomes containing distinct portions of chromosome 22 were used to regionally localize the gene to 22q11.2→q12. Owing to its known close proximity to the βB3 crystallin gene, the βB2-1 crystallin gene (CRYB2-1) also maps in this region. A second βB2 crystallin gene, βB2–2 (CRYB2–2), not linked to the CRYB2-1/CRYB3 cluster, could be localized in the same region. This implies that the three known βB crystallin genes are all within 22q11.2→q12. This small region contains D22S1, the only marker that shows no recombination with neurofibromatosis 2. Therefore, the βB crystallin genes on chromosome 22 might be markers for this disease. Two DNA fragments revealing useful polymorphisms associated with the βB crystallin genes were identified. One detects a two-system MspI restriction fragment length polymorphism specific for the CRYB2-1/CRYB3 cluster. The other detects an informative PstI polymorphism that is in linkage equilibrium with the MspI polymorphism.