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A role for prenylated rab acceptor 1 in vertebrate photoreceptor development

BACKGROUND: The rd1 mouse retina is a well-studied model of retinal degeneration where rod photoreceptors undergo cell death beginning at postnatal day (P) 10 until P21. This period coincides with photoreceptor terminal differentiation in a normal retina. We have used the rd1 retina as a model to in...

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Autores principales: Dickison, Virginia M, Richmond, Angela M, Abu Irqeba, Ameair, Martak, Joshua G, Hoge, Sean CE, Brooks, Matthew J, Othman, Mohammed I, Khanna, Ritu, Mears, Alan J, Chowdhury, Adnan Y, Swaroop, Anand, Ogilvie, Judith Mosinger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576285/
https://www.ncbi.nlm.nih.gov/pubmed/23241222
http://dx.doi.org/10.1186/1471-2202-13-152
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author Dickison, Virginia M
Richmond, Angela M
Abu Irqeba, Ameair
Martak, Joshua G
Hoge, Sean CE
Brooks, Matthew J
Othman, Mohammed I
Khanna, Ritu
Mears, Alan J
Chowdhury, Adnan Y
Swaroop, Anand
Ogilvie, Judith Mosinger
author_facet Dickison, Virginia M
Richmond, Angela M
Abu Irqeba, Ameair
Martak, Joshua G
Hoge, Sean CE
Brooks, Matthew J
Othman, Mohammed I
Khanna, Ritu
Mears, Alan J
Chowdhury, Adnan Y
Swaroop, Anand
Ogilvie, Judith Mosinger
author_sort Dickison, Virginia M
collection PubMed
description BACKGROUND: The rd1 mouse retina is a well-studied model of retinal degeneration where rod photoreceptors undergo cell death beginning at postnatal day (P) 10 until P21. This period coincides with photoreceptor terminal differentiation in a normal retina. We have used the rd1 retina as a model to investigate early molecular defects in developing rod photoreceptors prior to the onset of degeneration. RESULTS: Using a microarray approach, we performed gene profiling comparing rd1 and wild type (wt) retinas at four time points starting at P2, prior to any obvious biochemical or morphological differences, and concluding at P8, prior to the initiation of cell death. Of the 143 identified differentially expressed genes, we focused on Rab acceptor 1 (Rabac1), which codes for the protein Prenylated rab acceptor 1 (PRA1) and plays an important role in vesicular trafficking. Quantitative RT-PCR analysis confirmed reduced expression of PRA1 in rd1 retina at all time points examined. Immunohistochemical observation showed that PRA1-like immunoreactivity (LIR) co-localized with the cis-Golgi marker GM-130 in the photoreceptor as the Golgi translocated from the perikarya to the inner segment during photoreceptor differentiation in wt retinas. Diffuse PRA1-LIR, distinct from the Golgi marker, was seen in the distal inner segment of wt photoreceptors starting at P8. Both plexiform layers contained PRA1 positive punctae independent of GM-130 staining during postnatal development. In the inner retina, PRA1-LIR also colocalized with the Golgi marker in the perinuclear region of most cells. A similar pattern was seen in the rd1 mouse inner retina. However, punctate and significantly reduced PRA1-LIR was present throughout the developing rd1 inner segment, consistent with delayed photoreceptor development and abnormalities in Golgi sorting and vesicular trafficking. CONCLUSIONS: We have identified genes that are differentially regulated in the rd1 retina at early time points, which may give insights into developmental defects that precede photoreceptor cell death. This is the first report of PRA1 expression in the retina. Our data support the hypothesis that PRA1 plays an important role in vesicular trafficking between the Golgi and cilia in differentiating and mature rod photoreceptors.
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spelling pubmed-35762852013-02-20 A role for prenylated rab acceptor 1 in vertebrate photoreceptor development Dickison, Virginia M Richmond, Angela M Abu Irqeba, Ameair Martak, Joshua G Hoge, Sean CE Brooks, Matthew J Othman, Mohammed I Khanna, Ritu Mears, Alan J Chowdhury, Adnan Y Swaroop, Anand Ogilvie, Judith Mosinger BMC Neurosci Research Article BACKGROUND: The rd1 mouse retina is a well-studied model of retinal degeneration where rod photoreceptors undergo cell death beginning at postnatal day (P) 10 until P21. This period coincides with photoreceptor terminal differentiation in a normal retina. We have used the rd1 retina as a model to investigate early molecular defects in developing rod photoreceptors prior to the onset of degeneration. RESULTS: Using a microarray approach, we performed gene profiling comparing rd1 and wild type (wt) retinas at four time points starting at P2, prior to any obvious biochemical or morphological differences, and concluding at P8, prior to the initiation of cell death. Of the 143 identified differentially expressed genes, we focused on Rab acceptor 1 (Rabac1), which codes for the protein Prenylated rab acceptor 1 (PRA1) and plays an important role in vesicular trafficking. Quantitative RT-PCR analysis confirmed reduced expression of PRA1 in rd1 retina at all time points examined. Immunohistochemical observation showed that PRA1-like immunoreactivity (LIR) co-localized with the cis-Golgi marker GM-130 in the photoreceptor as the Golgi translocated from the perikarya to the inner segment during photoreceptor differentiation in wt retinas. Diffuse PRA1-LIR, distinct from the Golgi marker, was seen in the distal inner segment of wt photoreceptors starting at P8. Both plexiform layers contained PRA1 positive punctae independent of GM-130 staining during postnatal development. In the inner retina, PRA1-LIR also colocalized with the Golgi marker in the perinuclear region of most cells. A similar pattern was seen in the rd1 mouse inner retina. However, punctate and significantly reduced PRA1-LIR was present throughout the developing rd1 inner segment, consistent with delayed photoreceptor development and abnormalities in Golgi sorting and vesicular trafficking. CONCLUSIONS: We have identified genes that are differentially regulated in the rd1 retina at early time points, which may give insights into developmental defects that precede photoreceptor cell death. This is the first report of PRA1 expression in the retina. Our data support the hypothesis that PRA1 plays an important role in vesicular trafficking between the Golgi and cilia in differentiating and mature rod photoreceptors. BioMed Central 2012-12-15 /pmc/articles/PMC3576285/ /pubmed/23241222 http://dx.doi.org/10.1186/1471-2202-13-152 Text en Copyright © 2012 Dickison et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dickison, Virginia M
Richmond, Angela M
Abu Irqeba, Ameair
Martak, Joshua G
Hoge, Sean CE
Brooks, Matthew J
Othman, Mohammed I
Khanna, Ritu
Mears, Alan J
Chowdhury, Adnan Y
Swaroop, Anand
Ogilvie, Judith Mosinger
A role for prenylated rab acceptor 1 in vertebrate photoreceptor development
title A role for prenylated rab acceptor 1 in vertebrate photoreceptor development
title_full A role for prenylated rab acceptor 1 in vertebrate photoreceptor development
title_fullStr A role for prenylated rab acceptor 1 in vertebrate photoreceptor development
title_full_unstemmed A role for prenylated rab acceptor 1 in vertebrate photoreceptor development
title_short A role for prenylated rab acceptor 1 in vertebrate photoreceptor development
title_sort role for prenylated rab acceptor 1 in vertebrate photoreceptor development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576285/
https://www.ncbi.nlm.nih.gov/pubmed/23241222
http://dx.doi.org/10.1186/1471-2202-13-152
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