Oa1 knock-out

New insights on the pathogenesis of ocular albinism type 1

Barbara Incerti, Katia Cortese, Alessandro Pizzigoni, Enrico M. Surace, Simona Varani, Massimiliano Coppola, Glen Jeffery, Mathias Seeliger, Gesine Jaissle, Dorothy C. Bennett, Valeria Marigo, Maria Vittoria Schiaffino, Carlo Tacchetti, Andrea Ballabio

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

Ocular albinism type I (OA1) is an X-linked disorder characterized by severe reduction of visual acuity, strabismus, photophobia and nystagmus. Ophthalmologic examination reveals hypopigmentation of the retina, foveal hypoplasia and iris translucency. Microscopic examination of both retinal pigment epithelium (RPE) and skin melanocytes shows the presence of large pigment granules called giant melanosomes or macromelanosomes. In this study, we have generated and characterized Oa1-deficient mice by gene targeting (KO). The KO males are viable, fertile and phenotypically indistinguishable from the wild-type littermates. Ophthalmologic examination shows hypopigmentation of the ocular fundus in mutant animals compared with wild-type. Analysis of the retinofugal pathway reveals a reduction in the size of the uncrossed pathway, demonstrating a misrouting of the optic fibres at the chiasm, as observed in OA1 patients. Microscopic examination of the RPE shows the presence of giant melanosomes comparable with those described in OA1 patients. Ultrastructural analysis of the RPE cells, suggests that the giant melanosomes may form by abnormal growth of single melanosomes, rather than the fusion of several, shedding light on the pathogenesis of ocular albinism.

Original languageEnglish
Pages (from-to)2781-2788
Number of pages8
JournalHuman Molecular Genetics
Volume9
Issue number19
Publication statusPublished - Nov 22 2000

Fingerprint

Melanosomes
Retinal Pigment Epithelium
Hypopigmentation
Ocular Albinism
Photophobia
Gene Targeting
Strabismus
Melanocytes
Iris
Giant Cells
Visual Acuity
Retina
Skin
Ocular Albinism type 1
Growth

ASJC Scopus subject areas

  • Genetics

Cite this

Incerti, B., Cortese, K., Pizzigoni, A., Surace, E. M., Varani, S., Coppola, M., ... Ballabio, A. (2000). Oa1 knock-out: New insights on the pathogenesis of ocular albinism type 1. Human Molecular Genetics, 9(19), 2781-2788.

Oa1 knock-out : New insights on the pathogenesis of ocular albinism type 1. / Incerti, Barbara; Cortese, Katia; Pizzigoni, Alessandro; Surace, Enrico M.; Varani, Simona; Coppola, Massimiliano; Jeffery, Glen; Seeliger, Mathias; Jaissle, Gesine; Bennett, Dorothy C.; Marigo, Valeria; Schiaffino, Maria Vittoria; Tacchetti, Carlo; Ballabio, Andrea.

In: Human Molecular Genetics, Vol. 9, No. 19, 22.11.2000, p. 2781-2788.

Research output: Contribution to journalArticle

Incerti, B, Cortese, K, Pizzigoni, A, Surace, EM, Varani, S, Coppola, M, Jeffery, G, Seeliger, M, Jaissle, G, Bennett, DC, Marigo, V, Schiaffino, MV, Tacchetti, C & Ballabio, A 2000, 'Oa1 knock-out: New insights on the pathogenesis of ocular albinism type 1', Human Molecular Genetics, vol. 9, no. 19, pp. 2781-2788.
Incerti B, Cortese K, Pizzigoni A, Surace EM, Varani S, Coppola M et al. Oa1 knock-out: New insights on the pathogenesis of ocular albinism type 1. Human Molecular Genetics. 2000 Nov 22;9(19):2781-2788.
Incerti, Barbara ; Cortese, Katia ; Pizzigoni, Alessandro ; Surace, Enrico M. ; Varani, Simona ; Coppola, Massimiliano ; Jeffery, Glen ; Seeliger, Mathias ; Jaissle, Gesine ; Bennett, Dorothy C. ; Marigo, Valeria ; Schiaffino, Maria Vittoria ; Tacchetti, Carlo ; Ballabio, Andrea. / Oa1 knock-out : New insights on the pathogenesis of ocular albinism type 1. In: Human Molecular Genetics. 2000 ; Vol. 9, No. 19. pp. 2781-2788.
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