The CRISPR/Cas9-mediated modulation of SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE 8 in alfalfa leads to distinct phenotypic outcomes
The CRISPR/Cas9-mediated modulation of SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE 8 in alfalfa leads to distinct phenotypic outcomes
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- creativework.keywords - en
- Crop improvement
- Cultures--Amélioration
- Luzerne--Résistance à la sécheresse
- Alfalfa--Drought tolerance
- creativework.keywords - fr
- Fourrage
- Forage
- Édition génomique
- Genome editing
- dc.contributor.author
- Singer, Stacy D.
- Burton Hughes, Kimberley
- Subedi, Udaya
- Dhariwal, Gaganpreet Kaur
- Kader, Kazi
- Acharya, Surya
- Chen, Guanqun
- Hannoufa, Abdelali
- dc.date.accepted
- 2021-12-10
- dc.date.accessioned
- 2024-06-07T18:27:36Z
- dc.date.available
- 2024-06-07T18:27:36Z
- dc.date.issued
- 2022-01-05
- dc.date.submitted
- 2021-09-11
- dc.description.abstract - en
- Alfalfa (Medicago sativa L.) is the most widely grown perennial leguminous forage and is an essential component of the livestock industry. Previously, the RNAi-mediated down-regulation of alfalfa SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE 8 (MsSPL8) was found to lead to increased branching, regrowth and biomass, as well as enhanced drought tolerance. In this study, we aimed to further characterize the function of MsSPL8 in alfalfa using CRISPR/Cas9-induced mutations in this gene. We successfully generated alfalfa genotypes with small insertions/deletions (indels) at the target site in up to three of four MsSPL8 alleles in the first generation. The efficiency of editing appeared to be tightly linked to the particular gRNA used. The resulting genotypes displayed consistent morphological alterations, even with the presence of up to two wild-type MsSPL8 alleles, including reduced leaf size and early flowering. Other phenotypic effects appeared to be dependent upon mutational dosage, with those plants with the highest number of mutated MsSPL8 alleles also exhibiting significant decreases in internode length, plant height, shoot and root biomass, and root length. Furthermore, MsSPL8 mutants displayed improvements in their ability to withstand water-deficit compared to empty vector control genotypes. Taken together, our findings suggest that allelic mutational dosage can elicit phenotypic gradients in alfalfa, and discrepancies may exist in terms of MsSPL8 function between alfalfa genotypes, growth conditions, or specific alleles. In addition, our results provide the foundation for further research exploring drought tolerance mechanisms in a forage crop.
- dc.identifier.citation
- Singer, S. D., Burton Hughes, K., Subedi, U., Dhariwal, G. K., Kader, K., Acharya, S., Chen, G., & and Hannoufa, A. (2022). The CRISPR/Cas9-mediated modulation of SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE 8 in alfalfa leads to distinct phenotypic outcomes. Frontiers in Plant Science, 12, Article 774146. https://doi.org/10.3389/fpls.2021.774146
- dc.identifier.doi
- https://doi.org/10.3389/fpls.2021.774146
- dc.identifier.issn
- 1664-462X
- dc.identifier.uri
- https://open-science.canada.ca/handle/123456789/2573
- dc.language.iso
- en
- dc.publisher
- Frontiers Media S.A.
- dc.rights - en
- Creative Commons Attribution 4.0 International (CC BY 4.0)
- dc.rights - fr
- Creative Commons Attribution 4.0 International (CC BY 4.0)
- dc.rights.openaccesslevel - en
- Gold
- dc.rights.openaccesslevel - fr
- Or
- dc.rights.uri - en
- https://creativecommons.org/licenses/by/4.0/
- dc.rights.uri - fr
- https://creativecommons.org/licenses/by/4.0/deed.fr
- dc.subject - en
- Agriculture
- dc.subject - fr
- Agriculture
- dc.subject.en - en
- Agriculture
- dc.subject.fr - fr
- Agriculture
- dc.title - en
- The CRISPR/Cas9-mediated modulation of SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE 8 in alfalfa leads to distinct phenotypic outcomes
- dc.type - en
- Article
- dc.type - fr
- Article
- local.acceptedmanuscript.articlenum
- 774146
- local.article.journaltitle
- Frontiers in Plant Science
- local.article.journalvolume
- 12
- local.pagination
- 1-17
- local.peerreview - en
- Yes
- local.peerreview - fr
- Oui
- local.requestdoi
- No
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