|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
2
|
|
pubmed:dateCreated |
1999-10-19
|
|
pubmed:databankReference |
|
|
pubmed:abstractText |
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5 million people worldwide. Affected individuals suffer from a progressive degeneration of the photoreceptors, eventually resulting in severe visual impairment. To isolate candidate genes for chorioretinal diseases, we cloned cDNAs specifically or preferentially expressed in the human retina and the retinal pigment epithelium (RPE) through a novel suppression subtractive hybridization (SSH) method. One of these cDNAs (RET3C11) mapped to chromosome 1q31-q32.1, a region harbouring a gene involved in a severe form of autosomal recessive RP characterized by a typical preservation of the para-arteriolar RPE (RP12; ref. 3). The full-length cDNA encodes an extracellular protein with 19 EGF-like domains, 3 laminin A G-like domains and a C-type lectin domain. This protein is homologous to the Drosophila melanogaster protein crumbs (CRB), and denoted CRB1 (crumbs homologue 1). In ten unrelated RP patients with preserved para-arteriolar RPE, we identified a homozygous AluY insertion disrupting the ORF, five homozygous missense mutations and four compound heterozygous mutations in CRB1. The similarity to CRB suggests a role for CRB1 in cell-cell interaction and possibly in the maintenance of cell polarity in the retina. The distinct RPE abnormalities observed in RP12 patients suggest that CRB1 mutations trigger a novel mechanism of photoreceptor degeneration.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
1061-4036
|
|
pubmed:author |
pubmed-author:BergerA EAE,
pubmed-author:BhattacharyaS SSS,
pubmed-author:Bleeker-WagemakersE MEM,
pubmed-author:BrunnerH GHG,
pubmed-author:CremersF PFP,
pubmed-author:DeutmanA FAF,
pubmed-author:HeckenlivelyJ RJR,
pubmed-author:HoyngC BCB,
pubmed-author:KellnerUU,
pubmed-author:PayneA MAM,
pubmed-author:WesterveldAA,
pubmed-author:de KokY JYJ,
pubmed-author:den HollanderA IAI,
pubmed-author:ten BrinkJ BJB,
pubmed-author:van DrielM AMA,
pubmed-author:van SoestSS,
pubmed-author:van de PolD JDJ,
pubmed-author:van den BornL ILI
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
23
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
217-21
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:10508521-Alu Elements,
pubmed-meshheading:10508521-Amino Acid Sequence,
pubmed-meshheading:10508521-Amino Acid Substitution,
pubmed-meshheading:10508521-Animals,
pubmed-meshheading:10508521-Base Sequence,
pubmed-meshheading:10508521-Blotting, Northern,
pubmed-meshheading:10508521-Cell Line,
pubmed-meshheading:10508521-Chromosome Mapping,
pubmed-meshheading:10508521-Chromosomes, Human, Pair 1,
pubmed-meshheading:10508521-DNA, Complementary,
pubmed-meshheading:10508521-DNA Mutational Analysis,
pubmed-meshheading:10508521-Drosophila Proteins,
pubmed-meshheading:10508521-Drosophila melanogaster,
pubmed-meshheading:10508521-Eye Proteins,
pubmed-meshheading:10508521-Family Health,
pubmed-meshheading:10508521-Female,
pubmed-meshheading:10508521-Gene Expression Regulation, Developmental,
pubmed-meshheading:10508521-Homozygote,
pubmed-meshheading:10508521-Humans,
pubmed-meshheading:10508521-Male,
pubmed-meshheading:10508521-Membrane Proteins,
pubmed-meshheading:10508521-Molecular Sequence Data,
pubmed-meshheading:10508521-Mutagenesis, Insertional,
pubmed-meshheading:10508521-Mutation,
pubmed-meshheading:10508521-Pedigree,
pubmed-meshheading:10508521-Point Mutation,
pubmed-meshheading:10508521-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:10508521-RNA, Messenger,
pubmed-meshheading:10508521-Retinitis Pigmentosa,
pubmed-meshheading:10508521-Sequence Analysis, DNA,
pubmed-meshheading:10508521-Tissue Distribution
|
|
pubmed:year |
1999
|
|
pubmed:articleTitle |
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
|
|
pubmed:affiliation |
Department of Human Genetics, University Hospital Nijmegen, Geert Grooteplein 10, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
