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PMID: 11733058 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes.

Cell ·Vol. 107 ·No. 5 ·2001-11-30 ·Pages 579-89

Blackshaw S, Fraioli RE, Furukawa T, Cepko CL

Abstract

To identify the full set of genes expressed by mammalian rods, we conducted serial analysis of gene expression (SAGE) by using libraries generated from mature and developing mouse retina. We identified 264 uncharacterized genes that were specific to or highly enriched in rods. Nearly half of all cloned human retinal disease genes are selectively expressed in rod photoreceptors. In silico mapping of the human orthologs of genes identified in our screen revealed that 86 map within intervals containing uncloned retinal disease genes, representing 37 different loci. We expect these data will allow identification of many disease genes, and that this approach may be useful for cloning genes involved in classes of disease where cell type-specific expression of disease genes is observed.

MeSH Terms
Animals Blotting, Northern Expressed Sequence Tags Gene Expression Profiling/methods Gene Expression Regulation Gene Library Homeodomain Proteins/genetics,metabolism Humans Hypothalamus/physiology In Situ Hybridization Mice Mice, Inbred C57BL Mice, Knockout RNA, Messenger/genetics,metabolism Retina/cytology,physiology Retinal Diseases/genetics Retinal Rod Photoreceptor Cells/physiology Trans-Activators/genetics,metabolism
Chemicals
Homeodomain Proteins RNA, Messenger Trans-Activators cone rod homeobox protein
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Blackshaw S
Department of Genetics, Howard Hughes Medical Institute, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
Fraioli R E
Furukawa T
Cepko C L
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
2001-11-30
Pages
579-89
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NEI NIH HHS · EY0976 · United States
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