Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease
Abstract The familial form of Parkinson’s disease (PD) is linked to mutations in specific genes. The mutations in parkin are one of the most common causes of early-onset PD. Mitochondrial dysfunction is an emerging active player in the pathology of neurodegenerative diseases, because mitochondria ar...
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Online Access: | https://doi.org/10.1186/s40035-020-00229-8 |
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doaj-140c634219994be9ab73f2d3165ae3bc2021-01-24T12:45:52ZengBMCTranslational Neurodegeneration2047-91582021-01-0110111810.1186/s40035-020-00229-8Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s diseaseIryna Kamienieva0Jerzy Duszyński1Joanna Szczepanowska2Nencki Institute of Experimental Biology, Polish Academy of ScienceNencki Institute of Experimental Biology, Polish Academy of ScienceNencki Institute of Experimental Biology, Polish Academy of ScienceAbstract The familial form of Parkinson’s disease (PD) is linked to mutations in specific genes. The mutations in parkin are one of the most common causes of early-onset PD. Mitochondrial dysfunction is an emerging active player in the pathology of neurodegenerative diseases, because mitochondria are highly dynamic structures integrated with many cellular functions. Herein, we overview and discuss the role of the parkin protein product, Parkin E3 ubiquitin ligase, in the cellular processes related to mitochondrial function, and how parkin mutations can result in pathology in vitro and in vivo.https://doi.org/10.1186/s40035-020-00229-8MitochondriaParkinson’s diseaseParkinPINK1MitophagyParkin mutations |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Iryna Kamienieva Jerzy Duszyński Joanna Szczepanowska |
spellingShingle |
Iryna Kamienieva Jerzy Duszyński Joanna Szczepanowska Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease Translational Neurodegeneration Mitochondria Parkinson’s disease Parkin PINK1 Mitophagy Parkin mutations |
author_facet |
Iryna Kamienieva Jerzy Duszyński Joanna Szczepanowska |
author_sort |
Iryna Kamienieva |
title |
Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease |
title_short |
Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease |
title_full |
Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease |
title_fullStr |
Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease |
title_full_unstemmed |
Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease |
title_sort |
multitasking guardian of mitochondrial quality: parkin function and parkinson’s disease |
publisher |
BMC |
series |
Translational Neurodegeneration |
issn |
2047-9158 |
publishDate |
2021-01-01 |
description |
Abstract The familial form of Parkinson’s disease (PD) is linked to mutations in specific genes. The mutations in parkin are one of the most common causes of early-onset PD. Mitochondrial dysfunction is an emerging active player in the pathology of neurodegenerative diseases, because mitochondria are highly dynamic structures integrated with many cellular functions. Herein, we overview and discuss the role of the parkin protein product, Parkin E3 ubiquitin ligase, in the cellular processes related to mitochondrial function, and how parkin mutations can result in pathology in vitro and in vivo. |
topic |
Mitochondria Parkinson’s disease Parkin PINK1 Mitophagy Parkin mutations |
url |
https://doi.org/10.1186/s40035-020-00229-8 |
work_keys_str_mv |
AT irynakamienieva multitaskingguardianofmitochondrialqualityparkinfunctionandparkinsonsdisease AT jerzyduszynski multitaskingguardianofmitochondrialqualityparkinfunctionandparkinsonsdisease AT joannaszczepanowska multitaskingguardianofmitochondrialqualityparkinfunctionandparkinsonsdisease |
_version_ |
1724325423283699712 |