Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models
Tauopathy refers to a group of progressive neurodegenerative diseases, including frontotemporal lobar degeneration and Alzheimer’s disease, which correlate with the malfunction of microtubule-associated protein Tau (MAPT) due to abnormal hyperphosphorylation, leading to the formation of intracellula...
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doaj-3762338fa52d4bb797380125d71c53112021-08-26T13:51:30ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-08-01228465846510.3390/ijms22168465Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> ModelsHoi-Khoanh Giong0Manivannan Subramanian1Kweon Yu2Jeong-Soo Lee3Disease Target Structure Research Center, KRIBB, 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, KoreaDisease Target Structure Research Center, KRIBB, 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, KoreaDisease Target Structure Research Center, KRIBB, 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, KoreaDisease Target Structure Research Center, KRIBB, 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, KoreaTauopathy refers to a group of progressive neurodegenerative diseases, including frontotemporal lobar degeneration and Alzheimer’s disease, which correlate with the malfunction of microtubule-associated protein Tau (MAPT) due to abnormal hyperphosphorylation, leading to the formation of intracellular aggregates in the brain. Despite extensive efforts to understand tauopathy and develop an efficient therapy, our knowledge is still far from complete. To find a solution for this group of devastating diseases, several animal models that mimic diverse disease phenotypes of tauopathy have been developed. Rodents are the dominating tauopathy models because of their similarity to humans and established disease lines, as well as experimental approaches. However, powerful genetic animal models using <i>Drosophila</i>, zebrafish, and <i>C. elegans</i> have also been developed for modeling tauopathy and have contributed to understanding the pathophysiology of tauopathy. The success of these models stems from the short lifespans, versatile genetic tools, real-time in-vivo imaging, low maintenance costs, and the capability for high-throughput screening. In this review, we summarize the main findings on mechanisms of tauopathy and discuss the current tauopathy models of these non-rodent genetic animals, highlighting their key advantages and limitations in tauopathy research.https://www.mdpi.com/1422-0067/22/16/8465tauopathypathophysiology<i>Drosophila</i>zebrafish<i>C. elegans</i>advantages |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hoi-Khoanh Giong Manivannan Subramanian Kweon Yu Jeong-Soo Lee |
spellingShingle |
Hoi-Khoanh Giong Manivannan Subramanian Kweon Yu Jeong-Soo Lee Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models International Journal of Molecular Sciences tauopathy pathophysiology <i>Drosophila</i> zebrafish <i>C. elegans</i> advantages |
author_facet |
Hoi-Khoanh Giong Manivannan Subramanian Kweon Yu Jeong-Soo Lee |
author_sort |
Hoi-Khoanh Giong |
title |
Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models |
title_short |
Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models |
title_full |
Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models |
title_fullStr |
Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models |
title_full_unstemmed |
Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of <i>Drosophila</i>, Zebrafish, and <i>C. elegans</i> Models |
title_sort |
non-rodent genetic animal models for studying tauopathy: review of <i>drosophila</i>, zebrafish, and <i>c. elegans</i> models |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2021-08-01 |
description |
Tauopathy refers to a group of progressive neurodegenerative diseases, including frontotemporal lobar degeneration and Alzheimer’s disease, which correlate with the malfunction of microtubule-associated protein Tau (MAPT) due to abnormal hyperphosphorylation, leading to the formation of intracellular aggregates in the brain. Despite extensive efforts to understand tauopathy and develop an efficient therapy, our knowledge is still far from complete. To find a solution for this group of devastating diseases, several animal models that mimic diverse disease phenotypes of tauopathy have been developed. Rodents are the dominating tauopathy models because of their similarity to humans and established disease lines, as well as experimental approaches. However, powerful genetic animal models using <i>Drosophila</i>, zebrafish, and <i>C. elegans</i> have also been developed for modeling tauopathy and have contributed to understanding the pathophysiology of tauopathy. The success of these models stems from the short lifespans, versatile genetic tools, real-time in-vivo imaging, low maintenance costs, and the capability for high-throughput screening. In this review, we summarize the main findings on mechanisms of tauopathy and discuss the current tauopathy models of these non-rodent genetic animals, highlighting their key advantages and limitations in tauopathy research. |
topic |
tauopathy pathophysiology <i>Drosophila</i> zebrafish <i>C. elegans</i> advantages |
url |
https://www.mdpi.com/1422-0067/22/16/8465 |
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