Expression defect of ornithine aminotransferase gene in gyrate atrophy

G. Inana, Y. Hotta, C. Zintz, K. Takki, Richard Weleber, N. G. Kennaway, K. Nakayasu, A. Nakajima, T. Shiono

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

A generalized deficiency in the mitochondrial enzyme, ornithine aminotransferase (OAT: EC 2.6.1.13), is the hallmark of gyrate atrophy (GA), a hereditary degenerative disease of the choroid and retina of the eye that leads to blindness. A human OAT cDNA, previously constructed and characterized in our laboratory, and anti-human OAT antibody were used as probes to examine the OAT gene, mRNA and protein of GA patients. A blot analysis of the genomic DNAs, RNAs and proteins of 14 GA patients identified a case with a partial heterozygous deletion of the functional OAT gene located on chromosome 10, no detectable OAT mRNA, and a barely detectable level of OAT antibody-reactive protein. The rest of the cases showed grossly normal OAT gene, mRNA, and variably reduced levels of OAT protein. A restriction fragment length polymorphism (RFLP) was identified in the functional OAT gene sequence with EcoRI which may be useful for prenatal diagnosis of GA. RFLPs were also identified in the OAT-related gene sequences located on the X chromosome with Hind III and Pst I which may potentially show linkage to X-linked retinitis pigmentosa locus. The finding of an OAT gene, mRNA, and protein defect in a GA case constitutes the first real demonstration of the molecular genetic defect of OAT in GA.

Original languageEnglish (US)
Pages (from-to)1001-1005
Number of pages5
JournalInvestigative Ophthalmology and Visual Science
Volume29
Issue number7
StatePublished - 1988
Externally publishedYes

Fingerprint

Gyrate Atrophy
Ornithine-Oxo-Acid Transaminase
Genes
Messenger RNA
Proteins
Restriction Fragment Length Polymorphisms
Chromosomes, Human, Pair 10
Inborn Genetic Diseases
Retinitis Pigmentosa
Choroid
Antibodies
X Chromosome
Blindness
Prenatal Diagnosis
Retina
Molecular Biology
Complementary DNA
RNA
DNA
Enzymes

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Inana, G., Hotta, Y., Zintz, C., Takki, K., Weleber, R., Kennaway, N. G., ... Shiono, T. (1988). Expression defect of ornithine aminotransferase gene in gyrate atrophy. Investigative Ophthalmology and Visual Science, 29(7), 1001-1005.

Expression defect of ornithine aminotransferase gene in gyrate atrophy. / Inana, G.; Hotta, Y.; Zintz, C.; Takki, K.; Weleber, Richard; Kennaway, N. G.; Nakayasu, K.; Nakajima, A.; Shiono, T.

In: Investigative Ophthalmology and Visual Science, Vol. 29, No. 7, 1988, p. 1001-1005.

Research output: Contribution to journalArticle

Inana, G, Hotta, Y, Zintz, C, Takki, K, Weleber, R, Kennaway, NG, Nakayasu, K, Nakajima, A & Shiono, T 1988, 'Expression defect of ornithine aminotransferase gene in gyrate atrophy', Investigative Ophthalmology and Visual Science, vol. 29, no. 7, pp. 1001-1005.
Inana, G. ; Hotta, Y. ; Zintz, C. ; Takki, K. ; Weleber, Richard ; Kennaway, N. G. ; Nakayasu, K. ; Nakajima, A. ; Shiono, T. / Expression defect of ornithine aminotransferase gene in gyrate atrophy. In: Investigative Ophthalmology and Visual Science. 1988 ; Vol. 29, No. 7. pp. 1001-1005.
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