Overexpression of the Salix matsudana SmAP2-17 gene improves Arabidopsis salinity tolerance by enhancing the expression of SOS3 and ABI5.


Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
07 Mar 2022
Historique:
received: 29 07 2021
accepted: 21 02 2022
entrez: 8 3 2022
pubmed: 9 3 2022
medline: 23 3 2022
Statut: epublish

Résumé

Salix matsudana (Koidz.) is a widely planted ornamental allotetraploid tree species. Genetic engineering can be used to enhance the tolerance of this species to soil salinization, endowing varieties with the ability to grow along coastlines, thereby mitigating afforestation and protecting the environment. The AP2/ERF family of transcription factors (TFs) plays multidimensional roles in plant biotic/abiotic stress tolerance and plant development. In this study, we cloned the SmAP2-17 gene and performed functional analysis of its role in salt tolerance. This study aims to identify key genes for future breeding of stress-resistant varieties of Salix matsudana. SmAP2-17 was predicted to be a homolog of AP2-like ethylene-responsive transcription factor ANT isoform X2 from Arabidopsis, with a predicted ORF of 2058 bp encoding an estimated protein of 685 amino acids containing two conserved AP2 domains (PF00847.20). SmAP2-17 had a constitutive expression pattern and was localized to the nucleus. The overexpression of the native SmAP2-17 CDS sequence in Arabidopsis did not increase salt tolerance because of the reduced expression level of ectopic SmAP2-17, potentially caused by salt-induced RNAi. Transgenic lines with high expression of optimized SmAP2-17 CDS under salt stress showed enhanced tolerance to salt. Moreover, the expression of general stress marker genes and important salt stress signaling genes, including RD29A, ABI5, SOS3, AtHKT1, and RBohF, were upregulated in SmAP2-17-overexpressed lines, with expression levels consistent with that of SmAP2-17 or optimized SmAP2-17. Promoter activity analysis using dual luciferase analysis showed that SmAP2-17 could bind the promoters of SOS3 and ABI5 to activate their expression, which plays a key role in regulating salt tolerance. The SmAP2-17 gene isolated from Salix matsudana (Koidz.) is a positive regulator that improves the resistance of transgenic plants to salt stress by upregulating SOS3 and ABI5 genes. This study provides a potential functional gene resource for future generation of salt-resistant Salix lines by genetic engineering.

Sections du résumé

BACKGROUND BACKGROUND
Salix matsudana (Koidz.) is a widely planted ornamental allotetraploid tree species. Genetic engineering can be used to enhance the tolerance of this species to soil salinization, endowing varieties with the ability to grow along coastlines, thereby mitigating afforestation and protecting the environment. The AP2/ERF family of transcription factors (TFs) plays multidimensional roles in plant biotic/abiotic stress tolerance and plant development. In this study, we cloned the SmAP2-17 gene and performed functional analysis of its role in salt tolerance. This study aims to identify key genes for future breeding of stress-resistant varieties of Salix matsudana.
RESULTS RESULTS
SmAP2-17 was predicted to be a homolog of AP2-like ethylene-responsive transcription factor ANT isoform X2 from Arabidopsis, with a predicted ORF of 2058 bp encoding an estimated protein of 685 amino acids containing two conserved AP2 domains (PF00847.20). SmAP2-17 had a constitutive expression pattern and was localized to the nucleus. The overexpression of the native SmAP2-17 CDS sequence in Arabidopsis did not increase salt tolerance because of the reduced expression level of ectopic SmAP2-17, potentially caused by salt-induced RNAi. Transgenic lines with high expression of optimized SmAP2-17 CDS under salt stress showed enhanced tolerance to salt. Moreover, the expression of general stress marker genes and important salt stress signaling genes, including RD29A, ABI5, SOS3, AtHKT1, and RBohF, were upregulated in SmAP2-17-overexpressed lines, with expression levels consistent with that of SmAP2-17 or optimized SmAP2-17. Promoter activity analysis using dual luciferase analysis showed that SmAP2-17 could bind the promoters of SOS3 and ABI5 to activate their expression, which plays a key role in regulating salt tolerance.
CONCLUSIONS CONCLUSIONS
The SmAP2-17 gene isolated from Salix matsudana (Koidz.) is a positive regulator that improves the resistance of transgenic plants to salt stress by upregulating SOS3 and ABI5 genes. This study provides a potential functional gene resource for future generation of salt-resistant Salix lines by genetic engineering.

Identifiants

pubmed: 35255820
doi: 10.1186/s12870-022-03487-y
pii: 10.1186/s12870-022-03487-y
pmc: PMC8900321
doi:

Substances chimiques

Transcription Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102

Subventions

Organisme : National Natural Science Foundation of China
ID : 31971681

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022. The Author(s).

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Auteurs

Yanhong Chen (Y)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Yuanhao Dai (Y)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Yixin Li (Y)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Jie Yang (J)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Yuna Jiang (Y)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Guoyuan Liu (G)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Chunmei Yu (C)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Fei Zhong (F)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Bolin Lian (B)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China.

Jian Zhang (J)

Key Lab of Landscape Plant Genetics and Breeding, School of Life Science, Nantong University, Nantong, Jiangsu Province, China. ntdxylzw@163.com.

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