Sökning: onr:"swepub:oai:DiVA.org:umu-140877" > DJ-1 is a redox sen...
Fältnamn | Indikatorer | Metadata |
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000 | 04611naa a2200553 4500 | |
001 | oai:DiVA.org:umu-140877 | |
003 | SwePub | |
008 | 171120s2017 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1408772 URI |
024 | 7 | a https://doi.org/10.1093/hmg/ddx2942 DOI |
040 | a (SwePub)umu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Piston, Dominik4 aut |
245 | 1 0 | a DJ-1 is a redox sensitive adapter protein for high molecular weight complexes involved in regulation of catecholamine homeostasis |
264 | c 2017-07-25 | |
264 | 1 | b Oxford University Press,c 2017 |
338 | a electronic2 rdacarrier | |
500 | a Correction: Dominik Piston, Lydia Alvarez-Erviti, Vikas Bansal, Daniela Gargano, Zhi Yao, Gyorgy Szabadkai, Mark Odell, M Rhyan Puno, Benny Björkblom, Jodi Maple-Grødem, Peter Breuer, Oliver Kaut, Jan Petter Larsen, Stefan Bonn, Simon Geir Møller, Ullrich Wüllner, Anthony H V Schapira, Matthew E Gegg. DJ-1 is a redox sensitive adapter protein for high molecular weight complexes involved in regulation of catecholamine homeostasis. Human Molecular Genetics. Volume 27, Issue 3, 1 February 2018, Pages 576. DOI: 10.1093/hmg/ddx425 | |
520 | a DJ-1 is an oxidation sensitive protein encoded by the PARK7 gene. Mutations in PARK7 are a rare cause of familial recessive Parkinson's disease (PD), but growing evidence suggests involvement of DJ-1 in idiopathic PD. The key clinical features of PD, rigidity and bradykinesia, result from neurotransmitter imbalance, particularly the catecholamines dopamine (DA) and noradrenaline. We report in human brain and human SH-SY5Y neuroblastoma cell lines that DJ-1 predominantly forms high molecular weight (HMW) complexes that included RNA metabolism proteins hnRNPA1 and PABP1 and the glycolysis enzyme GAPDH. In cell culture models the oxidation status of DJ-1 determined the specific complex composition. RNA sequencing indicated that oxidative changes to DJ-1 were concomitant with changes in mRNA transcripts mainly involved in catecholamine metabolism. Importantly, loss of DJ-1 function upon knock down (KD) or expression of the PD associated form L166P resulted in the absence of HMW DJ-1 complexes. In the KD model, the absence of DJ-1 complexes was accompanied by impairment in catecholamine homeostasis, with significant increases in intracellular DA and noraderenaline levels. These changes in catecholamines could be rescued by re-expression of DJ-1. This catecholamine imbalance may contribute to the particular vulnerability of dopaminergic and noradrenergic neurons to neurodegeneration in PARK7-related PD. Notably, oxidised DJ-1 was significantly decreased in idiopathic PD brain, suggesting altered complex function may also play a role in the more common sporadic form of the disease. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Cell- och molekylärbiologi0 (SwePub)301082 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Cell and Molecular Biology0 (SwePub)301082 hsv//eng |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinsk bioteknologix Medicinsk bioteknologi0 (SwePub)304012 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Medical Biotechnologyx Medical Biotechnology0 (SwePub)304012 hsv//eng |
700 | 1 | a Alvarez-Erviti, Lydia4 aut |
700 | 1 | a Bansal, Vikas4 aut |
700 | 1 | a Gargano, Daniela4 aut |
700 | 1 | a Yao, Zhi4 aut |
700 | 1 | a Szabadkai, Gyorgy4 aut |
700 | 1 | a Odell, Mark4 aut |
700 | 1 | a Puno, M. Rhyan4 aut |
700 | 1 | a Björkblom, Bennyu Umeå universitet,Kemiska institutionen4 aut0 (Swepub:umu)bebj0009 |
700 | 1 | a Maple-Grodem, Jodi4 aut |
700 | 1 | a Breuer, Peter4 aut |
700 | 1 | a Kaut, Oliver4 aut |
700 | 1 | a Larsen, Jan Petter4 aut |
700 | 1 | a Bonn, Stefan4 aut |
700 | 1 | a Moller, Simon Geir4 aut |
700 | 1 | a Wuellner, Ullrich4 aut |
700 | 1 | a Schapira, Anthony H. V.4 aut |
700 | 1 | a Gegg, Matthew E.4 aut |
710 | 2 | a Umeå universitetb Kemiska institutionen4 org |
773 | 0 | t Human Molecular Geneticsd : Oxford University Pressg 26:20, s. 4028-4041q 26:20<4028-4041x 0964-6906x 1460-2083 |
856 | 4 | u https://umu.diva-portal.org/smash/get/diva2:1158427/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print |
856 | 4 | u https://academic.oup.com/hmg/article-pdf/26/20/4028/24339317/ddx294.pdf |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-140877 |
856 | 4 8 | u https://doi.org/10.1093/hmg/ddx294 |
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