PuSH - Publication Server of Helmholtz Zentrum München

Siemiatkowska, A.M.* ; Arimadyo, K.* ; Moruz, L.M.* ; Astuti, G.D.* ; de Castro-Miró, M.* ; Zonneveld, M.N.* ; Strom, T.M. ; de Wijs, I.J.* ; Hoefsloot, L.H.* ; Faradz, S.M.* ; Cremers, F.P.* ; den Hollander, A.I.* ; Collin, R.W.*

Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping.

Mol. Vis. 17, 3013-3024 (2011)
Publ. Version/Full Text Volltext
Free journal
Creative Commons Lizenzvertrag
Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous retinal disorder. Despite tremendous knowledge about the genes involved in RP, little is known about the genetic causes of RP in Indonesia. Here, we aim to identify the molecular genetic causes underlying RP in a small cohort of Indonesian patients, using genome-wide homozygosity mapping. METHODS: DNA samples from affected and healthy individuals from 14 Indonesian families segregating autosomal recessive, X-linked, or isolated RP were collected. Homozygosity mapping was conducted using Illumina 6k or Affymetrix 5.0 single nucleotide polymorphism (SNP) arrays. Known autosomal recessive RP (arRP) genes residing in homozygous regions and X-linked RP genes were sequenced for mutations. RESULTS: In ten out of the 14 families, homozygous regions were identified that contained genes known to be involved in the pathogenesis of RP. Sequence analysis of these genes revealed seven novel homozygous mutations in ATP-binding cassette, sub-family A, member 4 (ABCA4), crumbs homolog 1 (CRB1), eyes shut homolog (Drosophila) (EYS), c-mer proto-oncogene tyrosine kinase (MERTK), nuclear receptor subfamily 2, group E, member 3 (NR2E3) and phosphodiesterase 6A, cGMP-specific, rod, alpha (PDE6A), all segregating in the respective families. No mutations were identified in the X-linked genes retinitis pigmentosa GTPase regulator (RPGR) and retinitis pigmentosa 2 (X-linked recessive; RP2). CONCLUSIONS: Homozygosity mapping is a powerful tool to identify the genetic defects underlying RP in the Indonesian population. Compared to studies involving patients from other populations, the same genes appear to be implicated in the etiology of recessive RP in Indonesia, although all mutations that were discovered are novel and as such may be unique for this population.
Additional Metrics?
Edit extra informations Login
Publication type Article: Journal article
Document type Scientific Article
Keywords Lebers congenital amaurosis; Ligand-binding domain; Nuclear receptor; Missense mutations; Crystal-structure; Linkage Analyses; Acid; identification; Dystrophy; ABCR
ISSN (print) / ISBN 1090-0535
e-ISSN 1090-0535
Quellenangaben Volume: 17, Issue: , Pages: 3013-3024 Article Number: , Supplement: ,
Publisher Sun Yat-sen University, P.R. China
Reviewing status Peer reviewed