Abstract
The current agriculture main challenge is to maintain food production while
facing multiple threats such as increasing world population, temperature
increase, lack of agrochemicals due to health issues and uprising of weeds
resistant to herbicides. Developing novel, alternative, and safe methods is hence
of paramount importance. Here, we show that complementary peptides (cPEPs)
fromany gene can be designed to target specifically plant coding genes. External
application of synthetic peptides increases the abundance of the targeted protein,
leading to related phenotypes. Moreover, we provide evidence that cPEPs
can be powerful tools in agronomy to improve plant traits, such as growth,
resistance to pathogen or heat stress, without the needs of genetic approaches.
Finally, by combining their activity they can also be used to reduce weed growth.
facing multiple threats such as increasing world population, temperature
increase, lack of agrochemicals due to health issues and uprising of weeds
resistant to herbicides. Developing novel, alternative, and safe methods is hence
of paramount importance. Here, we show that complementary peptides (cPEPs)
fromany gene can be designed to target specifically plant coding genes. External
application of synthetic peptides increases the abundance of the targeted protein,
leading to related phenotypes. Moreover, we provide evidence that cPEPs
can be powerful tools in agronomy to improve plant traits, such as growth,
resistance to pathogen or heat stress, without the needs of genetic approaches.
Finally, by combining their activity they can also be used to reduce weed growth.
Originalsprog | Engelsk |
---|---|
Artikelnummer | 254 |
Tidsskrift | Nature Communications |
Vol/bind | 14 |
Antal sider | 13 |
ISSN | 2041-1723 |
DOI | |
Status | Udgivet - 2023 |
Bibliografisk note
Funding Information:This work was funded by the French ANR project BiomiPEP (ANR-16-CE12-0018-01). B.F. has been supported by the Fondation ARC pour la recherche sur le cancer. The work (proteomics) was funded in part by grants from the Région Occitanie, European funds (Fonds Européens de Développement Régional, FEDER), Toulouse Métropole, and the French Ministry of Research with the Investissement d’Avenir Infrastructures Nationales en Biologie et Santé program (ProFI, Proteomics French Infrastructure project, ANR-10-INBS-08). We thank Christian Mazars (LRSV, Auzeville-Tolosane, France) for valuable advice about CPK3, Marc Knight (Durham University, UK) for Arabidopsis ABRE Luciferase lines, and Camille Ribeyre (Micropep Technologies) for Botrytis cinerea spores. This work was supported by UPVD University through the utilization of the NextSeq 550 device at the Bioenvironment Platform.
Funding Information:
This work was funded by the French ANR project BiomiPEP (ANR-16-CE12-0018-01). B.F. has been supported by the Fondation ARC pour la recherche sur le cancer. The work (proteomics) was funded in part by grants from the Région Occitanie, European funds (Fonds Européens de Développement Régional, FEDER), Toulouse Métropole, and the French Ministry of Research with the Investissement d’Avenir Infrastructures Nationales en Biologie et Santé program (ProFI, Proteomics French Infrastructure project, ANR-10-INBS-08). We thank Christian Mazars (LRSV, Auzeville-Tolosane, France) for valuable advice about CPK3, Marc Knight (Durham University, UK) for Arabidopsis ABRE Luciferase lines, and Camille Ribeyre (Micropep Technologies) for Botrytis cinerea spores. This work was supported by UPVD University through the utilization of the NextSeq 550 device at the Bioenvironment Platform.
Publisher Copyright:
© 2023, The Author(s).