{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,22]],"date-time":"2026-10-22T06:29:48Z","timestamp":1792650588396,"version":"4.5.0"},"reference-count":67,"publisher":"The Company of Biologists","issue":"11","license":[{"start":{"date-parts":[[2020,9,3]],"date-time":"2020-09-03T00:00:00Z","timestamp":1599091200000},"content-version":"vor","delay-in-days":672,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"funder":[{"name":"Department of Biotechnology, Ministry of Science and Technology","award":["BT\/PR6423\/GBD\/27\/437\/2012"],"award-info":[{"award-number":["BT\/PR6423\/GBD\/27\/437\/2012"]}]},{"name":"Department of Biotechnology, Ministry of Science and Technology","award":["BT\/RLF\/Re-entry\/34\/2010"],"award-info":[{"award-number":["BT\/RLF\/Re-entry\/34\/2010"]}]},{"name":"Department of Biotechnology, Ministry of Science and Technology","award":["BT\/HRD\/35\/02\/2009"],"award-info":[{"award-number":["BT\/HRD\/35\/02\/2009"]}]},{"name":"University Grants Commission"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,11,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n               <jats:p>Mucopolysaccharidosis VII (MPS VII) is a recessively inherited lysosomal storage disorder caused by \u03b2-glucuronidase enzyme deficiency. The disease is characterized by widespread accumulation of non-degraded or partially degraded glycosaminoglycans, leading to cellular and multiple tissue dysfunctions. The patients exhibit diverse clinical symptoms, and eventually succumb to premature death. The only possible remedy is the recently approved enzyme replacement therapy, which is an expensive, invasive and lifelong treatment procedure. Small-molecule therapeutics for MPS VII have so far remained elusive primarily due to lack of molecular insights into the disease pathogenesis and unavailability of a suitable animal model that can be used for rapid drug screening. To address these issues, we developed a Drosophila model of MPS VII by knocking out the CG2135 gene, the fly \u03b2-glucuronidase orthologue. The CG2135\u2212\/\u2212 fly recapitulated cardinal features of MPS VII, such as reduced lifespan, progressive motor impairment and neuropathological abnormalities. Loss of dopaminergic neurons and muscle degeneration due to extensive apoptosis was implicated as the basis of locomotor deficit in this fly. Such hitherto unknown mechanistic links have considerably advanced our understanding of the MPS VII pathophysiology and warrant leveraging this genetically tractable model for deeper enquiry about the disease progression. We were also prompted to test whether phenotypic abnormalities in the CG2135\u2212\/\u2212 fly can be attenuated by resveratrol, a natural polyphenol with potential health benefits. Indeed, resveratrol treatment significantly ameliorated neuromuscular pathology and restored normal motor function in the CG2135\u2212\/\u2212 fly. This intriguing finding merits further preclinical studies for developing an alternative therapy for MPS VII.<\/jats:p>\n               <jats:p>This article has an associated First Person interview with the first author of the paper.<\/jats:p>","DOI":"10.1242\/dmm.036954","type":"journal-article","created":{"date-parts":[[2018,11,20]],"date-time":"2018-11-20T22:36:44Z","timestamp":1542753404000},"source":"Crossref","is-referenced-by-count":37,"title":["Neuromuscular degeneration and locomotor deficit in a <i>Drosophila<\/i> model of mucopolysaccharidosis VII is attenuated by treatment with resveratrol"],"prefix":"10.1242","volume":"11","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5591-8749","authenticated-orcid":false,"given":"Sudipta","family":"Bar","sequence":"first","affiliation":[{"name":"Indian Institute of Science Education and Research (IISER) Kolkata Department of Biological Sciences , , Mohanpur 741246, West Bengal , India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3254-0541","authenticated-orcid":false,"given":"Mohit","family":"Prasad","sequence":"additional","affiliation":[{"name":"Indian Institute of Science Education and Research (IISER) Kolkata Department of Biological Sciences , , Mohanpur 741246, West Bengal , India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1820-9251","authenticated-orcid":false,"given":"Rupak","family":"Datta","sequence":"additional","affiliation":[{"name":"Indian Institute of Science Education and Research (IISER) Kolkata Department of Biological Sciences , , Mohanpur 741246, West Bengal , India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2018,11,20]]},"reference":[{"key":"2024061302111142500_DMM036954C1","doi-asserted-by":"publisher","first-page":"865","DOI":"10.1126\/science.1067389","article-title":"Chaperone suppression of alpha -Synuclein toxicity in a Drosophila model for Parkinson's disease","volume":"295","author":"Auluck","year":"2002","journal-title":"Science (80-.)"},{"key":"2024061302111142500_DMM036954C2","doi-asserted-by":"publisher","first-page":"1195","DOI":"10.1016\/j.bbadis.2014.09.011","article-title":"Neuroprotective action of resveratrol","volume":"1852","author":"Bastianetto","year":"2015","journal-title":"Biochim. 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