Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.

Glaucoma is the world's second leading cause of bilateral blindness with progressive loss of vision due to retinal ganglion cell death. Myocilin has been associated with congenital glaucoma and 2-4% of primary open angle glaucoma (POAG) cases, but the pathogenic mechanisms remain largely unknow...

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Main Authors: Mary Anna Carbone, Julien F Ayroles, Akihiko Yamamoto, Tatiana V Morozova, Steven A West, Michael M Magwire, Trudy F C Mackay, Robert R H Anholt
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2615221?pdf=render
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author Mary Anna Carbone
Julien F Ayroles
Akihiko Yamamoto
Tatiana V Morozova
Steven A West
Michael M Magwire
Trudy F C Mackay
Robert R H Anholt
author_facet Mary Anna Carbone
Julien F Ayroles
Akihiko Yamamoto
Tatiana V Morozova
Steven A West
Michael M Magwire
Trudy F C Mackay
Robert R H Anholt
author_sort Mary Anna Carbone
collection DOAJ
description Glaucoma is the world's second leading cause of bilateral blindness with progressive loss of vision due to retinal ganglion cell death. Myocilin has been associated with congenital glaucoma and 2-4% of primary open angle glaucoma (POAG) cases, but the pathogenic mechanisms remain largely unknown. Among several hypotheses, activation of the unfolded protein response (UPR) has emerged as a possible disease mechanism.We used a transgenic Drosophila model to analyze whole-genome transcriptional profiles in flies that express human wild-type or mutant MYOC in their eyes. The transgenic flies display ocular fluid discharge, reflecting ocular hypertension, and a progressive decline in their behavioral responses to light. Transcriptional analysis shows that genes associated with the UPR, ubiquitination, and proteolysis, as well as metabolism of reactive oxygen species and photoreceptor activity undergo altered transcriptional regulation. Following up on the results from these transcriptional analyses, we used immunoblots to demonstrate the formation of MYOC aggregates and showed that the formation of such aggregates leads to induction of the UPR, as evident from activation of the fluorescent UPR marker, xbp1-EGFP. CONCLUSIONS / SIGNIFICANCE: Our results show that aggregation of MYOC in the endoplasmic reticulum activates the UPR, an evolutionarily conserved stress pathway that culminates in apoptosis. We infer from the Drosophila model that MYOC-associated ocular hypertension in the human eye may result from aggregation of MYOC and induction of the UPR in trabecular meshwork cells. This process could occur at a late age with wild-type MYOC, but might be accelerated by MYOC mutants to account for juvenile onset glaucoma.
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spelling doaj.art-d3e0cb21ecd74cbfa320e04f2083bc0e2022-12-21T23:50:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0141e421610.1371/journal.pone.0004216Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.Mary Anna CarboneJulien F AyrolesAkihiko YamamotoTatiana V MorozovaSteven A WestMichael M MagwireTrudy F C MackayRobert R H AnholtGlaucoma is the world's second leading cause of bilateral blindness with progressive loss of vision due to retinal ganglion cell death. Myocilin has been associated with congenital glaucoma and 2-4% of primary open angle glaucoma (POAG) cases, but the pathogenic mechanisms remain largely unknown. Among several hypotheses, activation of the unfolded protein response (UPR) has emerged as a possible disease mechanism.We used a transgenic Drosophila model to analyze whole-genome transcriptional profiles in flies that express human wild-type or mutant MYOC in their eyes. The transgenic flies display ocular fluid discharge, reflecting ocular hypertension, and a progressive decline in their behavioral responses to light. Transcriptional analysis shows that genes associated with the UPR, ubiquitination, and proteolysis, as well as metabolism of reactive oxygen species and photoreceptor activity undergo altered transcriptional regulation. Following up on the results from these transcriptional analyses, we used immunoblots to demonstrate the formation of MYOC aggregates and showed that the formation of such aggregates leads to induction of the UPR, as evident from activation of the fluorescent UPR marker, xbp1-EGFP. CONCLUSIONS / SIGNIFICANCE: Our results show that aggregation of MYOC in the endoplasmic reticulum activates the UPR, an evolutionarily conserved stress pathway that culminates in apoptosis. We infer from the Drosophila model that MYOC-associated ocular hypertension in the human eye may result from aggregation of MYOC and induction of the UPR in trabecular meshwork cells. This process could occur at a late age with wild-type MYOC, but might be accelerated by MYOC mutants to account for juvenile onset glaucoma.http://europepmc.org/articles/PMC2615221?pdf=render
spellingShingle Mary Anna Carbone
Julien F Ayroles
Akihiko Yamamoto
Tatiana V Morozova
Steven A West
Michael M Magwire
Trudy F C Mackay
Robert R H Anholt
Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.
PLoS ONE
title Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.
title_full Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.
title_fullStr Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.
title_full_unstemmed Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.
title_short Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.
title_sort overexpression of myocilin in the drosophila eye activates the unfolded protein response implications for glaucoma
url http://europepmc.org/articles/PMC2615221?pdf=render
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