A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

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Abstract
Paragangliomas of the head and neck are show growing tumors which rarely show malignant progression. Familial transmission has been described consistent with an autosomal dominant mode of inheritance. Clinical manifestations of hereditary parangliomas are determined by the sex of the transmitting parent. All affected individuals have inherited the disease gene from their father, expression of the phenotype is not observed in the offspring of an affected female until subsequent transmittance of the gene through a male carrier. This finding strongly suggests that genomic imprinting is involved. We report the results of a linkage study on a large Dutch pedigree with hereditary paragangliomas. Highly significant evidence for genetic linkage to chromosome 11q23-qter with the anonymous DNA marker D11S147 was detected with a peak lod score of 6.0 at a recombination fraction θ= 0.0. Likelihood calculations yielded an odds ratio of 2.7 · 106 in favor of genomic imprinting versus the absence of genomic imprinting.