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PMID: 18836446 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.

Nature genetics ·Vol. 40 ·No. 11 ·2008-11-00 ·Pages 1285-7

Abd El-Aziz MM, Barragan I, O'Driscoll CA, Goodstadt L, Prigmore E, Borrego S, Mena M, Pieras JI, El-Ashry MF, Safieh LA, Shah A, Cheetham ME, Carter NP, Chakarova C, Ponting CP, Bhattacharya SS, Antinolo G

Abstract

Using a positional cloning approach supported by comparative genomics, we have identified a previously unreported gene, EYS, at the RP25 locus on chromosome 6q12 commonly mutated in autosomal recessive retinitis pigmentosa. Spanning over 2 Mb, this is the largest eye-specific gene identified so far. EYS is independently disrupted in four other mammalian lineages, including that of rodents, but is well conserved from Drosophila to man and is likely to have a role in the modeling of retinal architecture.

MeSH Terms
Animals Cell Line Chromosomes, Human, Pair 6/genetics Drosophila Proteins/chemistry Drosophila melanogaster/chemistry Eye Proteins/chemistry,genetics,metabolism Gene Expression Profiling Gene Expression Regulation Genes, Recessive Humans Mutation/genetics Protein Structure, Tertiary Protein Transport Retinitis Pigmentosa/genetics Sequence Homology, Amino Acid
Chemicals
Drosophila Proteins EYS protein, human Eye Proteins eys protein, Drosophila
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Abd El-Aziz Mai M
Department of Molecular Genetics, Institute of Ophthalmology, London EC1V 9EL, UK.
Barragan Isabel
O'Driscoll Ciara A
Goodstadt Leo
Prigmore Elena
Borrego Salud
Mena Marcela
Pieras Juan I
El-Ashry Mohamed F
Safieh Leen Abu
Shah Amna
Cheetham Michael E
Carter Nigel P
Chakarova Christina
Ponting Chris P
Bhattacharya Shomi S
Antinolo Guillermo
References (13)
13 references, click to expand
  1. Using genomic data to unravel the root of the placental mammal phylogeny.
    Genome Res. 2007 Apr;17(4):413-21 PMID: 17322288
  2. A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa.
    Ann Hum Genet. 2007 May;71(Pt 3):281-94 PMID: 17156103
  3. Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
    Nat Genet. 2007 Jul;39(7):889-95 PMID: 17546029
  4. Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 interval.
    Ann Hum Genet. 2008 Jul;72(Pt 4):463-77 PMID: 18510646
  5. Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.
    Ann Hum Genet. 2008 Jul;72(Pt 4):454-62 PMID: 18510647
  6. Rodent phylogeny and a timescale for the evolution of Glires: evidence from an extensive taxon sampling using three nuclear genes.
    Mol Biol Evol. 2002 Jul;19(7):1053-65 PMID: 12082125
  7. Transforming the architecture of compound eyes.
    Nature. 2006 Oct 12;443(7112):696-9 PMID: 17036004
  8. Evolutionary conservation and selection of human disease gene orthologs in the rat and mouse genomes.
    Genome Biol. 2004;5(7):R47 PMID: 15239832
  9. Nonsense-mediated decay approaches the clinic.
    Nat Genet. 2004 Aug;36(8):801-8 PMID: 15284851
  10. A major locus for autosomal recessive retinitis pigmentosa on 6q, determined by homozygosity mapping of chromosomal regions that contain gamma-aminobutyric acid-receptor clusters.
    Am J Hum Genet. 1998 Jun;62(6):1452-9 PMID: 9585594
  11. Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.
    Am J Hum Genet. 1999 Aug;65(2):571-4 PMID: 10417302
  12. Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa.
    Ophthalmic Res. 2005 Mar-Apr;37(2):89-93 PMID: 15746564
  13. The agrin/perlecan-related protein eyes shut is essential for epithelial lumen formation in the Drosophila retina.
    Dev Cell. 2006 Oct;11(4):483-93 PMID: 17011488
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1546-1718
Published
2008-11-00
Epub
2008-00-05
Pages
1285-7
Language
English
Region
United States
NLM ID
9216904
PMCID
PMC2719291
Subset
IM
Grants
Wellcome Trust · 077008 · United Kingdom
Medical Research Council · MC_U137761446 · United Kingdom
Corrections
CommentIn
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