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Disruption of LRRK2 does not cause specific loss of dopaminergic neurons in zebrafish.

ABSTRACT: Mutations in LRRK2 are genetically linked to Parkinson's disease (PD) but its normal biological function is largely unknown. Sheng et al. recently reported that deletion of the WD40 domain of LRRK2 in zebrafish specifically causes PD-like loss of neurons and behavior defect. However, our similar early study and recent confirming experiments using the same reagents reported by Sheng et al. failed to reproduce the phenotype of the loss of dopaminergic neurons, although the mRNA of LRRK2 was molecularly disrupted. Our study suggests that function of LRRK2 and its usefulness to generate zebrafish PD model needs further evaluation.

SUBMITTER: Ren G

PROVIDER: S-EPMC3116841 | biostudies-literature | 2011

REPOSITORIES: biostudies-literature

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Disruption of LRRK2 does not cause specific loss of dopaminergic neurons in zebrafish.

Ren Guiqi G Xin Shengchang S Li Song S Zhong Hanbing H Lin Shuo S

PloS one 20110616 6

Mutations in LRRK2 are genetically linked to Parkinson's disease (PD) but its normal biological function is largely unknown. Sheng et al. recently reported that deletion of the WD40 domain of LRRK2 in zebrafish specifically causes PD-like loss of neurons and behavior defect. However, our similar early study and recent confirming experiments using the same reagents reported by Sheng et al. failed to reproduce the phenotype of the loss of dopaminergic neurons, although the mRNA of LRRK2 was molecu ...[more]

PMID: 21698186

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Multiple Pathways of LRRK2-G2019S/Rab10 Interaction in Dopaminergic Neurons.

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| S-EPMC5027571 | biostudies-literature

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