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PURPOSE: The macula is essential for visual acuity. It contains many more cone photoreceptors than does the peripheral retina. In this study, macular gene expression was compared with that in the rod-rich peripheral retina. METHODS: Two-millimeter foveomacular and four-millimeter macular punches from human donor eyes, in addition to sections of midperipheral retina, were used to study differential gene expression. Multiple microarray experiments were combined with quantitative PCR and bioinformatic analyses. In the present study, the expression of both known and previously unidentified retinal genes was determined. RESULTS: Several macula enriched transcripts were revealed. Nuclear pore complex interacting protein (NPIP) and eukaryotic translation initiation factor 2alpha kinase (GCN2) were expressed at levels approaching that of red/green cone opsin in the macula. The protein products of several genes highlighted using these expression analyses were also localized in the retina. Both NPIP and histone deacetylase 9 (HDAC9) proteins were detected in cone photoreceptor outer segments. CONCLUSIONS: Characterizing macula enriched transcripts is an important stepping-stone in understanding the molecular basis for visual acuity in the retina. The approach also provides excellent candidates for diseases that affect the macula and fovea such as age-related macular degeneration (AMD). Indeed, several of these transcripts, such as NPIP and GCN2, have genomic loci that are consistent with being candidate genes for AMD.

Original publication

DOI

10.1167/iovs.07-0355

Type

Journal article

Journal

Invest Ophthalmol Vis Sci

Publication Date

12/2007

Volume

48

Pages

5388 - 5396

Keywords

Adult, Aged, Blotting, Northern, Cloning, Molecular, Eye Proteins, Female, Fluorescent Antibody Technique, Indirect, Gene Expression Profiling, Gene Expression Regulation, Histone Deacetylases, Humans, Male, Microscopy, Confocal, Middle Aged, Nuclear Pore Complex Proteins, Oligonucleotide Array Sequence Analysis, Repressor Proteins, Retinal Cone Photoreceptor Cells, Retinal Rod Photoreceptor Cells, Reverse Transcriptase Polymerase Chain Reaction, Transcriptional Activation, eIF-2 Kinase