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Molecular Cloning, Subcellular Localization and Expression Analyses of PdbHLH57 Transcription Factor in Colored-Leaf Poplar

Yuhang Li1, Li Sun1, Tao Wang1, Bingjun Yu2, Zhihong Gao3, Xiaochun Shu1, Tengyue Yan1, Weibing Zhuang1,2,*, Zhong Wang1,*

1 Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, 210014, China
2 College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China
3 College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China

* Corresponding Authors: Weibing Zhuang. Email: email; Zhong Wang. Email: email

Phyton-International Journal of Experimental Botany 2025, 94(4), 1211-1223. https://doi.org/10.32604/phyton.2025.063647

Abstract

bHLH transcription factors, widely exist in various plants, and are vital for the growth and development of these plants. Among them, many have been implicated in anthocyanin biosynthesis across various plants. In the present study, a PdbHLH57 gene, belonging to the bHLH IIIf group, was characterized, which was isolated and cloned from the colored-leaf poplar ‘Zhongshancaiyun’ (ZSCY). The cDNA sequence of PdbHLH57 was 1887 base pairs, and the protein encoded by PdbHLH57 had 628 amino acids, the isoelectric point and molecular weight of which were 6.26 and 69.75 kDa, respectively. Through bioinformatics analysis, PdbHLH57 has been classified into the IIIf bHLH subgroup, with many members of this subgroup known to participate in anthocyanin biosynthesis. The subcellular localization analysis conducted in the leaf protoplasts of ‘ZSCY’ revealed that the PdbHLH57 protein is specifically localized in the nucleus. The transcription activation analysis was also conducted, and the results showed that the PdbHLH57 protein had self-transcription activation. To better explore the functions of the PdbHLH57 protein, two parts of this protein (PdbHLH57-1, PdbHLH57-2) were split to detect their transcriptional activation activity. The results indicated that PdbHLH57-1 (1-433aa) had self-transcription activation, and PdbHLH57-2 (433-628aa) had no transcription activation. The expression of PdbHLH57 peaked in June during different developmental stages in ‘ZSCY’, and it was most highly expressed in the phloem among various tissues. These findings offer a basis for understanding the role of PdbHLH57 in colored-leaf poplar.

Keywords

Transcription factors; PdbHLH57; subcellular localization; transcription activation analysis; expression pattern; colored-leaf poplar

Supplementary Material

Supplementary Material File

Cite This Article

APA Style
Li, Y., Sun, L., Wang, T., Yu, B., Gao, Z. et al. (2025). Molecular Cloning, Subcellular Localization and Expression Analyses of PdbHLH57 Transcription Factor in Colored-Leaf Poplar. Phyton-International Journal of Experimental Botany, 94(4), 1211–1223. https://doi.org/10.32604/phyton.2025.063647
Vancouver Style
Li Y, Sun L, Wang T, Yu B, Gao Z, Shu X, et al. Molecular Cloning, Subcellular Localization and Expression Analyses of PdbHLH57 Transcription Factor in Colored-Leaf Poplar. Phyton-Int J Exp Bot. 2025;94(4):1211–1223. https://doi.org/10.32604/phyton.2025.063647
IEEE Style
Y. Li et al., “Molecular Cloning, Subcellular Localization and Expression Analyses of PdbHLH57 Transcription Factor in Colored-Leaf Poplar,” Phyton-Int. J. Exp. Bot., vol. 94, no. 4, pp. 1211–1223, 2025. https://doi.org/10.32604/phyton.2025.063647



cc Copyright © 2025 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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