Candidate locus for a nuclear modifier gene for maternally iherited deafness

Yelena Bykhovskaya, Xavier P. Estivill, Kent Taylor, Tieu Hang, Melanie Hamon, Rosaria A M S Casano, Huiying Yang, Jerome I. Rotter, Mordechai Shohat, Nathan Fischel-Ghodsian

Research output: Contribution to journalArticle

91 Citations (Scopus)

Abstract

Maternally inherited deafness associated with the A1555G mutation in the mitochondrial 12S ribosomal RNA (rRNA) gene appears to require additional environmental or genetic changes for phenotypic expression. Aminoglycosides have been identified as one such environmental factor. In one large Arab- Israeli pedigree with congenital hearing loss in some of the family members with the A1555G mutation and with no exposure to aminoglycosides, biochemical evidence has suggested the role of nuclear modifier gene(s), but a genomewide search has indicated the absence of a single major locus having such an effect. Thus it has been concluded that the penetrance of the mitochondrial mutation appears to depend on additive effects of several nuclear genes. We have now investigated 10 multiplex Spanish and Italian families with 35 members with the A1555G mutation and sensorineural deafness. Parametric analysis of a genomewide screen again failed to identify significant evidence for linkage to a single autosomal locus. However, nonparametric analysis supported the role of the chromosomal region around marker D8S277. The combined maximized allele-sharing LOD score of 3.1 in Arab- Israeli/Spanish/Italian families represents a highly suggestive linkage result. We suggest that this region should be considered a candidate for containing the first human nuclear modifier gene for a mitochondrial DNA disorder. The locus operates in Arab-Israeli, Spanish, and Italian families, resulting in the deafness phenotype on a background of the mitochondrial A1555G mutation. No obvious candidate genes are located in this region.

Original languageEnglish
Pages (from-to)1905-1910
Number of pages6
JournalAmerican Journal of Human Genetics
Volume66
Issue number6
DOIs
Publication statusPublished - 2000
Externally publishedYes

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Modifier Genes
Deafness
Mutation
Aminoglycosides
Genes
Mitochondrial Diseases
Penetrance
Pedigree
Mitochondrial DNA
Hearing Loss
Alleles
Phenotype

ASJC Scopus subject areas

  • Genetics

Cite this

Bykhovskaya, Y., Estivill, X. P., Taylor, K., Hang, T., Hamon, M., Casano, R. A. M. S., ... Fischel-Ghodsian, N. (2000). Candidate locus for a nuclear modifier gene for maternally iherited deafness. American Journal of Human Genetics, 66(6), 1905-1910. https://doi.org/10.1086/302914

Candidate locus for a nuclear modifier gene for maternally iherited deafness. / Bykhovskaya, Yelena; Estivill, Xavier P.; Taylor, Kent; Hang, Tieu; Hamon, Melanie; Casano, Rosaria A M S; Yang, Huiying; Rotter, Jerome I.; Shohat, Mordechai; Fischel-Ghodsian, Nathan.

In: American Journal of Human Genetics, Vol. 66, No. 6, 2000, p. 1905-1910.

Research output: Contribution to journalArticle

Bykhovskaya, Y, Estivill, XP, Taylor, K, Hang, T, Hamon, M, Casano, RAMS, Yang, H, Rotter, JI, Shohat, M & Fischel-Ghodsian, N 2000, 'Candidate locus for a nuclear modifier gene for maternally iherited deafness', American Journal of Human Genetics, vol. 66, no. 6, pp. 1905-1910. https://doi.org/10.1086/302914
Bykhovskaya, Yelena ; Estivill, Xavier P. ; Taylor, Kent ; Hang, Tieu ; Hamon, Melanie ; Casano, Rosaria A M S ; Yang, Huiying ; Rotter, Jerome I. ; Shohat, Mordechai ; Fischel-Ghodsian, Nathan. / Candidate locus for a nuclear modifier gene for maternally iherited deafness. In: American Journal of Human Genetics. 2000 ; Vol. 66, No. 6. pp. 1905-1910.
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