CRISPR/Cas9‐mediated grna gene knockout leads to neurodevelopmental defects and motor behavior changes in zebrafish. Issue 3 (15th February 2021)
- Record Type:
- Journal Article
- Title:
- CRISPR/Cas9‐mediated grna gene knockout leads to neurodevelopmental defects and motor behavior changes in zebrafish. Issue 3 (15th February 2021)
- Main Title:
- CRISPR/Cas9‐mediated grna gene knockout leads to neurodevelopmental defects and motor behavior changes in zebrafish
- Authors:
- Zhu, Jiuling
Xu, Huimin
Song, Hui
Li, Xiang
Wang, Ning
Zhao, Junli
Zheng, Xiaojing
Kim, Kwang‐Youn
Zhang, Hui
Mao, Qinwen
Xia, Haibin - Abstract:
- Abstract: Progranulin (PGRN) is a secreted glycoprotein with multiple biological functions in early embryogenesis, anti‐inflammation, and neurodegeneration. A good model for the functional study of PGRN is the zebrafish with knockdown or knockout of grn, the gene encoding PGRN. Morpholino oligonucleotides (MOs) and zinc finger nucleases have been used to generate zebrafish grn models, yet they have shown inconsistent phenotypes due to either the neurotoxicity of the MOs or possible genetic compensation responses during gene editing. In this study, we generated stable grna (one of the major grn homologues of zebrafish) knockout zebrafish by using CRISPR/Cas9‐mediated genome editing. A grna sgRNA was designed to target the similar repeated sequence shared by exon 13, exon 15, and exon 19 in zebrafish. The F1 generation with the frameshift mutation of + 4 bp (the addition of 4 bp to exon15), which causes a premature termination, was obtained and subjected to morphological and behavioral evaluation. The grna knockout zebrafish showed neurodevelopmental defects, including spinal motor neurons with shorter axons, decreased sensory hair cells, thinning of the outer nuclear layer and thickening of the inner nuclear layer of the retina, decreased expression of rhodopsin in the cone cells, and motor behavior changes. Moreover, the phenotypes of grna knockout zebrafish could be rescued with the Tol2 system carrying the grna gene. The grna knockout zebrafish model generated in thisAbstract: Progranulin (PGRN) is a secreted glycoprotein with multiple biological functions in early embryogenesis, anti‐inflammation, and neurodegeneration. A good model for the functional study of PGRN is the zebrafish with knockdown or knockout of grn, the gene encoding PGRN. Morpholino oligonucleotides (MOs) and zinc finger nucleases have been used to generate zebrafish grn models, yet they have shown inconsistent phenotypes due to either the neurotoxicity of the MOs or possible genetic compensation responses during gene editing. In this study, we generated stable grna (one of the major grn homologues of zebrafish) knockout zebrafish by using CRISPR/Cas9‐mediated genome editing. A grna sgRNA was designed to target the similar repeated sequence shared by exon 13, exon 15, and exon 19 in zebrafish. The F1 generation with the frameshift mutation of + 4 bp (the addition of 4 bp to exon15), which causes a premature termination, was obtained and subjected to morphological and behavioral evaluation. The grna knockout zebrafish showed neurodevelopmental defects, including spinal motor neurons with shorter axons, decreased sensory hair cells, thinning of the outer nuclear layer and thickening of the inner nuclear layer of the retina, decreased expression of rhodopsin in the cone cells, and motor behavior changes. Moreover, the phenotypes of grna knockout zebrafish could be rescued with the Tol2 system carrying the grna gene. The grna knockout zebrafish model generated in this study provides a useful tool to study PGRN function and has potential for high‐throughput drug screening for disease therapy. Abstract : Progranulin (PGRN) is a secreted, cysteine‐enriched glycoprotein with multiple important biological functions. So far, no reliable grn zebrafish models have been available to study PGRN function. In this study, we generated stable grna knockout zebrafish ( grna being one of the major grn homologues of zebrafish) by using CRISPR/Cas9‐mediated genome editing. The grna knockout zebrafish showed neurodevelopmental defects, including spinal motor neurons with shorter axons, thinning of the outer nuclear layer and thickening of the inner nuclear layer of the retina, decreased expression of rhodopsin in the cone cells, and motor behavior changes. This grna knockout zebrafish model provides a reliable tool to study the function of PGRN. SpMN, spinal motor neuron. … (more)
- Is Part Of:
- Journal of neurochemistry. Volume 157:Issue 3(2021)
- Journal:
- Journal of neurochemistry
- Issue:
- Volume 157:Issue 3(2021)
- Issue Display:
- Volume 157, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 157
- Issue:
- 3
- Issue Sort Value:
- 2021-0157-0003-0000
- Page Start:
- 520
- Page End:
- 531
- Publication Date:
- 2021-02-15
- Subjects:
- CRISPR/Cas9 -- grn -- knockout -- PGRN -- phenotype -- zebrafish
Neurochemistry -- Periodicals
616.8042 - Journal URLs:
- http://www.blackwell-synergy.com/loi/jnc ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jnc.15307 ↗
- Languages:
- English
- ISSNs:
- 0022-3042
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5021.500000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23604.xml