Analysis of differentially expressed genes in retinitis pigmentosa retinas Altered expression of clusterin mRNA
- 6 April 1992
- journal article
- research article
- Published by Wiley in FEBS Letters
- Vol. 300 (3) , 279-282
- https://doi.org/10.1016/0014-5793(92)80863-c
Abstract
The molecular and cellular processes underlying photoreceptor degeneration in retinitis pigmentosa (RP) are unknown. We have investigated gene expression in diseased retinas using differential hybridization screening of a retinal cDNA library with probes derived from normal and RP retinal RNA. Most differential clones detected corresponded to transcripts absent from the dystrophic state, including e.g. opsin. However, one clone was noticeably increased in RP in comparison with the control; partial sequencing showed it encoded clusterin. Increased expression of clusterin has been identified in several cases of tissues undergoing apoptosis (programmed cell death), and our finding suggests that the degenerative changes in advanced RP may represent another example or apoptosis, possibly with common causative mechanisms.Keywords
This publication has 27 references indexed in Scilit:
- A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosaNature, 1991
- Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaNature, 1991
- Effect of chronic adrenalectomy on neuron loss and distribution of sulfated glycoprotein-2 in the dentate gyrus of prepubertal ratsExperimental Neurology, 1991
- Apolipoprotein J: structure and tissue distributionBiochemistry, 1990
- Abnormalities in expression of human retinal mRNA in retinitis pigmentosaNeurochemistry International, 1990
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- Characterization and cloning of androgen-repressed mRNAs from rat ventral prostateBiochemical and Biophysical Research Communications, 1987
- Molecular cloning of the S-antigen cDNA from bovine retinaBiochemical and Biophysical Research Communications, 1987
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979