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이강한  |  2019-03-14 19:07 조회 25   
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Modeling neurodegenerative Spinocerebellar Ataxia type 13 in zebrafish using a Purkinje neuron specific tunable co-expression system
Journal of Neuroscience, https://doi.org/10.1523/JNEUROSCI.1862-18.2019
http://www.jneurosci.org/content/early/2019/03/12/JNEUROSCI.1862-18.2019
Email: kanghanl(at).naver.com

논문요청드립니다.
Modeling neurodegenerative Spinocerebellar Ataxia type 13 in zebrafish using a Purkinje neuron specific tunable co-expression system

Kazuhiko Namikawa, Alessandro Dorigo, Marta Zagrebelsky, Giulio Russo, Toni Kirmann, Wieland Fahr, Stefan Dübel, Martin Korte and Reinhard W. Köster

Abstract

Purkinje cells (PCs) are primarily affected in neurodegenerative Spinocerebellar Ataxias (SCAs). For generating animal models for SCAs, genetic regulatory elements specifically targeting PCs are required, thereby linking pathological molecular effects with impaired function and organismic behavior. Because cerebellar anatomy and function are evolutionary conserved, zebrafish represent an excellent model to study SCAs in vivo.

We have isolated a 258bp cross-species PC-specific enhancer element that can be used in a bidirectional manner for bioimaging of transgene-expressing PCs in zebrafish (both sexes) with variable copy numbers for tuning expression strength. Emerging ectopic expression at high copy numbers can be further eliminated by repurposing microRNA-mediated posttranslational mRNA regulation.

Subsequently, we generated a transgenic SCA type 13 (SCA13) model, using a zebrafish-variant mimicking a human pathological SCA13R420H mutation, resulting in cell-autonomous progressive PC degeneration linked to cerebellum-driven eye-movement deficits as observed in SCA-patients. This underscores that investigating PC-specific cerebellar neuropathologies in zebrafish allows for interconnecting bioimaging of disease mechanisms with behavioral analysis suitable for therapeutic compound testing.

SIGNIFICANCE STATEMENT

SCA13 patients carrying a KCNC3R420H allele have been shown to display mid- onset progressive cerebellar atrophy, but genetic modeling of SCA13 by expressing this pathogenic mutant in different animal models has not resulted in neuronal degeneration so far - likely because the transgene was expressed in heterologous cell types. We developed a genetic system for tunable PC specific coexpression of several transgenes to manipulate and simultaneously monitor cerebellar PCs. We modeled a SCA13 zebrafish accessible for bio-imaging to investigate disease progression, revealing robust PC degeneration, resulting in impaired eye movement. Our transgenic zebrafish mimicking both neuropathological and behavioral changes manifested in SCA-affected patients will be suitable for investigating causes of cerebellar diseases in vivo from the molecular to the behavioral level.


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회원작성글 수수수  (2019-03-15 19:33)
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