Germline excision of transgenes in Aedes aegypti by homing endonucleases
dc.contributor.author | Aryan, Azadeh | en |
dc.contributor.author | Anderson, Michelle A. E. | en |
dc.contributor.author | Myles, Kevin M. | en |
dc.contributor.author | Adelman, Zach N. | en |
dc.contributor.department | Entomology | en |
dc.contributor.department | Fralin Life Sciences Institute | en |
dc.date.accessed | 2014-06-13 | en |
dc.date.accessioned | 2014-06-16T14:11:23Z | en |
dc.date.available | 2014-06-16T14:11:23Z | en |
dc.date.issued | 2013-04 | en |
dc.description.abstract | Aedes (Ae.) aegypti is the primary vector for dengue viruses (serotypes1-4) and chikungunya virus. Homing endonucleases (HEs) are ancient selfish elements that catalyze double-stranded DNA breaks (DSB) in a highly specific manner. In this report, we show that the HEs Y2-I-AniI, I-CreI and I-SceI are all capable of catalyzing the excision of genomic segments from the Ae. aegypti genome in a heritable manner. Y2-I-AniI demonstrated the highest efficiency at two independent genomic targets, with 20-40% of Y2-I-AniI-treated individuals producing offspring that had lost the target transgene. HE-induced DSBs were found to be repaired via the single-strand annealing (SSA) and non-homologous end-joining (NHEJ) pathways in a manner dependent on the availability of direct repeat sequences in the transgene. These results support the development of HE-based gene editing and gene drive strategies in Ae. aegypti, and confirm the utility of HEs in the manipulation and modification of transgenes in this important vector. | en |
dc.description.sponsorship | NIH-NIAID AI071208 | en |
dc.description.sponsorship | Fralin Life Science Institute and College of Agriculture and Life Sciences at Virginia Tech | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.citation | Aryan, A.; Anderson, M. A. E.; Myles, K. M.; Adelman, Z. N., "Germline excision of transgenes in Aedes aegypti by homing endonucleases," Scientific Reports 3:1603, (2013). DOI: 10.1038/srep01603. | en |
dc.identifier.doi | https://doi.org/10.1038/srep01603 | en |
dc.identifier.issn | 2045-2322 | en |
dc.identifier.uri | http://hdl.handle.net/10919/48929 | en |
dc.identifier.url | http://www.nature.com/srep/2013/130403/srep01603/full/srep01603.html | en |
dc.language.iso | en | en |
dc.publisher | Nature Publishing Group | en |
dc.rights | In Copyright | en |
dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
dc.subject | engineered male mosquitos | en |
dc.subject | yellow-fever mosquito | en |
dc.subject | homologous | en |
dc.subject | recombination | en |
dc.subject | directed evolution | en |
dc.subject | anopheles-gambiae | en |
dc.subject | dna breaks | en |
dc.subject | gene | en |
dc.subject | drosophila | en |
dc.subject | sequences | en |
dc.subject | populations | en |
dc.subject | multidisciplinary sciences | en |
dc.title | Germline excision of transgenes in Aedes aegypti by homing endonucleases | en |
dc.title.serial | Scientific Reports | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
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