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Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes
In the CRISPR-Cas systems, Cas13a is an RNA-guided RNA nuclease specifically targeting single strand RNA. We developed a Cas13a mediated CRISPR interference tool to target mRNA for gene silencing in mosquitoes. A Cas13a expressing plasmid was delivered to mosquitoes by intrathoracic injection, and C...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064736/ https://www.ncbi.nlm.nih.gov/pubmed/32190127 http://dx.doi.org/10.7150/jgen.43928 |
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author | Kulkarni, Aditi Yu, Wanqin Moon, Alex S. Pandey, Ashmita Hanley, Kathryn A. Xu, Jiannong |
author_facet | Kulkarni, Aditi Yu, Wanqin Moon, Alex S. Pandey, Ashmita Hanley, Kathryn A. Xu, Jiannong |
author_sort | Kulkarni, Aditi |
collection | PubMed |
description | In the CRISPR-Cas systems, Cas13a is an RNA-guided RNA nuclease specifically targeting single strand RNA. We developed a Cas13a mediated CRISPR interference tool to target mRNA for gene silencing in mosquitoes. A Cas13a expressing plasmid was delivered to mosquitoes by intrathoracic injection, and Cas13a transcripts were detectable at least 10 days post-delivery. The target specific crRNA was synthesized in vitro using T7 RNA polymerase. The Cas13a plasmid and target crRNA can be delivered by intrathoracic injection together, or the Cas13a construct can be provided first, and then target crRNA can be given later when appropriate. The machinery was tested in two mosquito species. In Anopheles gambiae, vitellogenin gene was silenced by Cas13a/Vg-crRNA, which was accompanied by a significant reduction in egg production. In Aedes aegypti, the α- and δ-subunits of COPI genes were silenced by Cas13a/crRNA, which resulted in mortality and fragile midguts, reproducing a phenotype reported previously. Co-silencing genes simultaneously is achievable when a cocktail of target crRNAs is given. No detectable collateral cleavages of non-target transcripts were observed in the study. In addition to dsRNA or siRNA mediated RNA interference, the programmable CRISPR interference method offers an alternative to knock down genes in mosquitoes. |
format | Online Article Text |
id | pubmed-7064736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-70647362020-03-18 Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes Kulkarni, Aditi Yu, Wanqin Moon, Alex S. Pandey, Ashmita Hanley, Kathryn A. Xu, Jiannong J Genomics Research Paper In the CRISPR-Cas systems, Cas13a is an RNA-guided RNA nuclease specifically targeting single strand RNA. We developed a Cas13a mediated CRISPR interference tool to target mRNA for gene silencing in mosquitoes. A Cas13a expressing plasmid was delivered to mosquitoes by intrathoracic injection, and Cas13a transcripts were detectable at least 10 days post-delivery. The target specific crRNA was synthesized in vitro using T7 RNA polymerase. The Cas13a plasmid and target crRNA can be delivered by intrathoracic injection together, or the Cas13a construct can be provided first, and then target crRNA can be given later when appropriate. The machinery was tested in two mosquito species. In Anopheles gambiae, vitellogenin gene was silenced by Cas13a/Vg-crRNA, which was accompanied by a significant reduction in egg production. In Aedes aegypti, the α- and δ-subunits of COPI genes were silenced by Cas13a/crRNA, which resulted in mortality and fragile midguts, reproducing a phenotype reported previously. Co-silencing genes simultaneously is achievable when a cocktail of target crRNAs is given. No detectable collateral cleavages of non-target transcripts were observed in the study. In addition to dsRNA or siRNA mediated RNA interference, the programmable CRISPR interference method offers an alternative to knock down genes in mosquitoes. Ivyspring International Publisher 2020-03-01 /pmc/articles/PMC7064736/ /pubmed/32190127 http://dx.doi.org/10.7150/jgen.43928 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Kulkarni, Aditi Yu, Wanqin Moon, Alex S. Pandey, Ashmita Hanley, Kathryn A. Xu, Jiannong Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes |
title | Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes |
title_full | Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes |
title_fullStr | Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes |
title_full_unstemmed | Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes |
title_short | Programmable CRISPR interference for gene silencing using Cas13a in mosquitoes |
title_sort | programmable crispr interference for gene silencing using cas13a in mosquitoes |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064736/ https://www.ncbi.nlm.nih.gov/pubmed/32190127 http://dx.doi.org/10.7150/jgen.43928 |
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