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Mutations in ​PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness

Kmoch, S., Majewski, J., Ramamurthy, V., Cao, S., Fahiminiya, S., Ren, H., MacDonald, I. M., Lopez, I., Sun, V., Keser, V., Khan, A., Stránecký, V., Hartmannová, H., Přistoupilová, A., Hodaňová, K., Piherová, L., Kuchař, L., Baxová, A., Chen, R., Barsottini, O. G. P., Pyle, A., Griffin, H., Splitt, M., Sallum, J., Tolmie, J. L., Sampson, Julian Roy, Chinnery, P., Care4Rare, Canada, Banin, E., Sharon, D., Dutta, S., Grebler, R., Helfrich-Foerster, C., Pedroso, J. L., Kretzschmar, D., Cayouette, M. and Koenekoop, R. K. 2015. Mutations in ​PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness. Nature Communications 6 , 5614. 10.1038/ncomms6614

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Abstract

Blindness due to retinal degeneration affects millions of people worldwide, but many disease-causing mutations remain unknown. ​PNPLA6 encodes the ​patatin-like phospholipase domain containing protein 6, also known as ​neuropathy target esterase (​NTE), which is the target of toxic organophosphates that induce human paralysis due to severe axonopathy of large neurons. Mutations in ​PNPLA6 also cause human spastic paraplegia characterized by motor neuron degeneration. Here we identify ​PNPLA6 mutations in childhood blindness in seven families with retinal degeneration, including Leber congenital amaurosis and Oliver McFarlane syndrome. ​PNPLA6 localizes mostly at the inner segment plasma membrane in photoreceptors and mutations in Drosophila ​PNPLA6 lead to photoreceptor cell death. We also report that lysophosphatidylcholine and lysophosphatidic acid levels are elevated in mutant Drosophila. These findings show a role for ​PNPLA6 in photoreceptor survival and identify phospholipid metabolism as a potential therapeutic target for some forms of blindness.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Subjects: R Medicine > R Medicine (General)
Additional Information: PDF uploaded in accordance with publisher's policies at http://www.sherpa.ac.uk/romeo/issn/2041-1723/ (accessed 31.3.16).
Publisher: Nature Publishing Group
ISSN: 2041-1723
Date of First Compliant Deposit: 30 March 2016
Date of Acceptance: 21 October 2014
Last Modified: 13 Jun 2019 12:39
URI: http://orca-mwe.cf.ac.uk/id/eprint/88279

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