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Cloning and functional analysis of the PLkF3H2 promoter in Larix kaempferi

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Abstract

The flavanone 3-hydroxy-lase2 (F3H2) gene is one of the key genes in flavonoid biosynthesis pathways in Larix kaempferi (Lam.) Carrière (Japanese larch). However, the transcriptional regulation mechanism of this gene in flavonoid metabolism has not been studied. In this study, we cloned a 2398 bp upstream promoter sequence and tested its transcriptional activity in larch protoplasts using transient transformation. We also constructed the 5’ shortened fragments of this sequence into the upstream of the β-glucuronidase (GUS) gene in the pBI121 expression vector. In transient and stable transgenic tobacco, GUS expression could be initiated by both full-length and shortened promoters, but its activity gradually decreased as the 5’ end was continuously removed. The GUS histochemical staining revealed that the key promoter region was located from − 526 bp to − 429 bp. Moreover, in transgenic tobacco, the PLkF3H2 promoter responded to environmental signals and hormones, such as methyl jasmonate (MeJA), abscisic acid (ABA), NaCl, and low temperature. The NaCl and low-temperature responsive elements were located at − 2325 bp ~ − 1570 bp and − 526 bp ~ − 429 bp, respectively. But in larch, LkF3H2 gene expression was positively regulated by MeJA, ABA, and NaCl via PLkF3H2 promoter elements, while it was negatively regulated by low temperature. Our study provides a theoretical reference for the use of the PLkF3H2 in biological adversity resistance as well as the functional verification of the LkF3H2 gene and regulation of flavonoid synthesis in Japanese larch.

Key message

This study discovered the transcriptional activity and function of the PLkF3H2 promoter in Larix kaempferi, which was expected to be used in stress resistance in the future.

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Data Availability

All data generated or analysed during this study are included in this published article (and its additional files). Requests for material should be made to the corresponding authors.

Abbreviations

GUS:

β-glucuronidase

GFP:

Green fluorescent protein

F3H:

flavanone 3-hydroxy-lase

MeJA:

methyl jasmonate

ABA:

abscisic acid

LkF3H2:

Larix kaempferi gene

PLkF3H2:

promoter in Larix kaempferi

MS:

Murashige Skoog nutrient medium

Kana:

Kanamycin

Rif:

Rifampicin

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Acknowledgements

We thank LetPub for its linguistic assistance during the preparation of this manuscript.

Funding

This work was supported by the National Key R&D Program of China (2022YFD2200100-03-04).

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Authors

Contributions

YG and XNJ designed the study. CL conducted the experiments, and CL and WTJ analyzed the data. CL and YG wrote the paper. All authors read and approved the manuscript.

Corresponding author

Correspondence to Ying Gai.

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The authors declare that the research was conducted in the absence of any potential conflict of interest.

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Informed consent was not required as no human or animals was involved.

Research involving human and animal rights

Our study has no research involved human participants or animals.

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Communicated by Goetz Hensel.

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Li, C., Jiang, W., Jiang, X. et al. Cloning and functional analysis of the PLkF3H2 promoter in Larix kaempferi. Plant Cell Tiss Organ Cult 154, 481–491 (2023). https://doi.org/10.1007/s11240-023-02467-w

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  • DOI: https://doi.org/10.1007/s11240-023-02467-w

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