Abstract
Introduction:
Low temperature is a key environmental factor that threaten sweetpotato growth and development. In-depth studies on the gene functions underlying cold resistance are important for genetic engineering in sweetpotato.
Methods:
The IbXTH16 gene was cloned using a homologous cloning approach. Its expression was detected in sweetpotato leaves subjected to low-temperature stress and brassinosteroid treatment. Subsequently, the IbXTH16 gene was introduced into sweetpotato variety Lizixiang to generate IbXTH16-overexpressing plants, thereby enabling the functional validation of the IbXTH16.
Results and discussion:
The IbXTH16 gene was cloned from the cold-tolerant variety LHS21. Its 879 bp coding sequence encoded a 292 aa protein with a molecular weight of 32.983 kDa and a pI of 8.47. The 2039 bp genomic sequence of IbXTH16 contained two exons and one intron. The IbXTH16 protein was localized in the cell membrane. IbXTH16 was strongly induced by 4°C and brassinosteroid. IbXTH16 positively regulates cold tolerance of sweetpotato by activating the BR and proline pathways.
1 Introduction
Low temperature is a key environmental factor that threaten crop growth and development worldwide (Peng et al., 2014; Shi et al., 2018). Sweetpotato, Ipomoea batatas (L.) Lam., an important cash crop, serves as both a staple food and a bioenergy resource (Zhang et al., 2019). As sweetpotato is native to tropical America, it exhibits sensitivity to low temperature, highlighting the importance of enhancing cold tolerance to ensure sustained productivity (Jin et al., 2017; Yu et al., 2022). The development and cultivation of low-temperature tolerant sweetpotato varieties hold significant importance for addressing temperature-related challenges and ensuring global food security. Therefore, in-depth studies on the gene functions underlying cold resistance are important for genetic engineering in sweetpotato.
The xyloglucan endotransglycosylase/hydrolase (XTH) superfamily is an important protein widely present in plants, mainly catalyzing the endohydrolysis of the β-1,4 glycosidic bond of xyloglucan and the self-connection of the xyloglucan molecule (Rose et al., 2002; Morales-Quintana et al., 2020). The XTH superfamily has been reported to participate in diverse biological processes of plants such as fruit maturation and drought response (Miedes et al., 2010; Wu et al., 2022; Han et al., 2023). In cold stress, AtXTH21 positively modulated the freezing stress resistance and XTH19 mutant exhibited reduced freezing tolerance in Arabidopsis (Shi et al., 2014; Takahashi et al., 2021). In sweetpotato, under cold treatment, only IbXTH02 and IbXTH12 of the XTH family were downregulated expression (Zhang et al., 2023). However, XTHs’ function on cold stress of sweetpotato remain largely unknow.
Brassinolide (BR) refers to a group of polyhydroxy steroids that include BR and its structural analogs (Kim and Russinova, 2020). As a type of steroid hormone, BR is ubiquitously distributed across various plant tissues (Xu et al., 2020). Previous studies have demonstrated that the exogenous application of BR can enhances plant cold tolerance. Specifically, treatment with 2 mg L-1 BR significantly mitigated leaf surface damage in rice plants, improving their resistance to cold stress (Wang et al., 2020). Under exogenous BR treatment, mangoes exhibited an increased proportion of unsaturated fatty acids in cell membranes, which enhanced membrane fluidity and consequently improved cold tolerance (Li et al., 2012). In addition to exogenous BR treatment, endogenous BR signalling pathways in plants also play a crucial role in regulating cold tolerance. The homologous protein CES of brassinosteroid enhanced expression, which acts as a positive regulatory factor in BR signal transduction, can directly interact with downstream CBF proteins and activate the transcription of CBF1 and CBF3, contributing to enhancing plant cold tolerance (Eremina et al., 2016). Overexpression of the BR receptor BRI1, a key activator of BR signalling, has been shown to improve the cold tolerance of tomato plants (Wang et al., 2022). Conversely, BIN2, a negative regulator of BR signalling in Arabidopsis, negatively regulates plant cold tolerance by modulating the activities of BZR1 and phosphorylated ICE1 (Ye et al., 2019).
Proline serves as a critical osmotic regulatory compound that is ubiquitously present in plants and plays a protective role under low temperature stress conditions (Kidokoro et al., 2022; Kim et al., 2024). Specifically, proline helps maintain the stability of biological membranes and various enzymes while regulating the acid-base and redox balance within the cytoplasm (Takagi, 2008; Hayat et al., 2012). In Arabidopsis, the content of proline increases with prolonged exposure to 4°C low temperature treatment (Kaplan et al., 2007). In cucumber, the ICE1 enhances the cold tolerance of transgenic plants by promoting the accumulation of free proline (Liu et al., 2010). In Rosa multiflora, RmZAT10 specifically binds to and activates the promoter of RmP5CS, thereby regulating proline biosynthesis and positively influencing cold resistance (Luo et al., 2022).
In this study, a XTH superfamily gene IbXTH16 was cloned and characterized from sweetpotato. The IbXTH16 gene was introduced into the sweetpotato variety Lizixiang to verify its function. Functional analysis showed that overexpression of IbXTH16 enhanced cold tolerance of sweetpotato by activating the BR and proline pathways.
2 Materials and methods
2.1 Plant materials
The sweetpotato cold-tolerant variety Liaohanshu21 (LHS21) was employed to clone the IbXTH16 gene. The sweetpotato variety LHS21 and cold-susceptible variety Sushu28 (SS28) were employed to analyze the expression level of IbXTH16. The sweetpotato variety Lizixiang was used to identify the function of IbXTH16.
2.2 Cloning and sequence analysis
Total RNA for cDNA generation (TRIzol reagent, CWBIO, Beijing, China) and genomic DNA (Easy Pure Plant Genomic DNA Kit, Trans Gen, Beijing, China) were isolated from the leaves of LHS21 according to Fan et al. (2024). The coding sequence (CDS), genome sequence, and promoter region of IbXTH16 were obtained based on a homologous cloning approach. Phylogenetic analysis was performed with MEGA 11.0 software. The genomic structure of IbXTH16 was analyzed by GSDS 2.0 (http://gsds.gao-lab.org/). The cis-acting regulatory elements of the IbXTH16 promoter region were analyzed by PlantCARE (https://bioinformatics.psb.ugent.be/webtools/plantcare/html/). All primers in this study were showed in Supplementary Table S1.
2.3 Subcellular localization
The CDS of IbXTH16 (without the stop codon) was integrated into the pCAMBIA1300-GFP vector according to Zhang et al. (2020). The pCAMBIA1300-IbXTH16-GFP was introduced into Agrobacterium tumefaciens strain GV3101 and transiently inoculated into Nicotiana benthamiana leaf hypodermal cells. After 48 h of infection, the GFP signals were observed using a confocal fluorescence microscope (LSM880, Zeiss, Jena, Germany).
2.4 Expression analysis
The four-week-old in vitro-grown LHS21 or SS28 plants was treated with cold (4°C) or 100 mM BR for 0, 1, 3, 6, 12, 24 h and the expression of IbXTH16 was quantified with Real-time quantitative polymerase chain reaction (RT-qPCR) (SYBR Green Master Mix, YEASEN, Shanghai, China). Expression of IbXTH16 in leaf, root, and stem tissues four-week-old in vitro-grown LHS21 was quantified with RT-qPCR. The IbACTIN was used as the internal control.
2.5 Production of transgenic sweetpotato plants
The CDS of IbXTH16 (without the stop codon) was integrated into the pCAMBIA1300 vector according to Fan et al. (2024). The pCAMBIA1300-IbXTH16 was introduced into A. tumefaciens strain EHA105, and then infected Lizixiang embryogenic suspension cultures as described by Yu et al. (2007). The transgenic plants were identified with PCR (LA Taq, TaKaRa, Tokyo, Japan) and RT-qPCR.
2.6 Cold tolerance analysis
4-week-old IbXTH16-overexpressing sweetpotato plants and wide type (WT) with the same status were subjected to cold treatment after a week of acclimatization. The cold treated leaves of the IbXTH16-overexpressing sweetpotato plants and WT were used to determine the superoxide dismutase (SOD) (SOD-1-W, Cominbio, Suzhou, China) and peroxidase (POD) activities (POD-1-Y, Cominbio), proline (PRO-1-Y, Cominbio) and malondialdehyde (MDA) contents (MDA-1-Y, Cominbio) according to manufacturer’s instructions. The BR content and relative electrical conductivity were determined by Norminkoda Biotechnology Co., Ltd (Wuhan, China). The expression of IbDWF4, IbDET2, IbBRI1, IbBES1, IbBEE3, IbBIN2, IbP5CR, IbP5CS, IbP5CDH, and IbPDH were quantified with RT-qPCR.
2.7 Statistical analysis
Data are analyzed using one-way ANOVA followed by post-hoc Tukey’s test or Student’s t-test at P < 0.05 or P < 0.01.
3 Results
3.1 Cloning and sequence analysis of IbXTH16 and its promoter
To identify potential regulators of cold resistance in sweetpotato, we cloned IbXTH16 gene from cold-tolerant variety LHS21. Its 879 bp CDS encoded a 292 aa protein with a molecular weight of 32.983 kDa and a pI of 8.47 (Supplementary Table S2). Phylogenetic analysis showed that IbXTH16 shared the closest relationship with AtXTH16 among Arabidopsis homologs (Figure 1A). The 2039 bp genomic sequence of IbXTH16 contained two exons and one intron, which was different from the three exons and two introns of AtXTH16 (Figure 1B). The 800 bp IbXTH16 promoter region contained a low-temperature response element LTR and an ABA-response element ABRE (Figure 1C). To examine the subcellular location of IbXTH16, the IbXTH16-GFP fusion protein was conducted by transiently expressing in N. benthamiana leaf epidermal cells. The results showed that IbXTH16-GFP was localized in the cell membrane (Figure 1D).
FIGURE 1
3.2 Expression analyses of IbXTH16 in sweetpotato
To study the potential role of IbXTH16 in cold resistance of sweetpotato, the expression level of IbXTH16 was analyzed. RT-qPCR assay showed that the expression level of IbXTH16 in LHS21 was much higher than that in SS28 (Figure 2A). Tissue-specific expression assay revealed that the expression level of IbXTH16 was relatively high in the roots of in vitro-grown LHS21 plants (Figure 2B). The expression of IbXTH16 was significantly induced by 4°C and 100 mM BR (Figures 2C,D).
FIGURE 2
3.3 Overexpression of IbXTH16 enhances cold tolerance in sweetpotato
To investigate whether IbXTH16 contributes to cold tolerance in sweetpotato, this gene was transferred into sweetpotato variety Lizixiang via A. tumefaciens-mediated method, and 12 IbXTH16-overexpressing lines (OX-1 to OX-12) were generated (Figures 3A–F). There was no significant difference in the phenotype of sweetpotato storage roots between overexpression lines and WT (Figure 3G). IbXTH16 exhibited increased expression level in the overexpression lines compared with the WT (Figure 3H). Three overexpression lines (OX-2, OX-7, and OX-12) with higher expression levels of IbXTH16 were selected for further study. Furthermore, the overexpression and WT plants were treatment at 4°C and restored at 25°C. The degree of wilting in the overexpression lines at 24 h and 48 h under cold stress was lower compared to that of WT (Figures 4A–C). Additionally, the overexpression lines recovered more rapidly than WT when returned to 25°C (Figure 4D). These results indicated that IbXTH16 functions as a positive regulator of cold tolerance in sweetpotato.
FIGURE 3
FIGURE 4
3.4 IbXTH16 alters the contents of components and expression of genes related to stress response
To further explore how IbXTH16 mediate the cold tolerance in sweetpotato, the contents of stress response-related components were measured. Under 4°C treatments for 24 h and 48 h, higher SOD and POD activities, higher proline and BR contents, and lower relative electrical conductivity and MDA content were found in the overexpression lines relative to WT (Figures 5A–F). In BR biosynthesis and signalling pathway, key enzyme genes IbDWF4 and IbDET2 and positive regulatory factors IbBRI1, IbBES1, and IbBEE3 in the transgenic plants were upregulated under 4°C treatment (Figures 6A–E), while negative regulatory factor IbBIN2 was downregulated (Figure 6F). In proline biosynthesis and signalling pathway, key enzyme genes IbP5CR and IbP5CS in the transgenic plants were upregulated under 4°C treatment (Figures 6G,H), while degradation pathway IbP5CDH and IbPDH were downregulated (Figures 6I,J). These results indicated that IbXTH16 positively regulates cold tolerance of sweetpotato by activating the BR and proline pathways.
FIGURE 5
FIGURE 6
4 Discussion
4.1 IbXTH16 positively regulates cold tolerance of sweetpotato
Many crops are well-suited for growth in tropical or subtropical regions (Chinnusamy et al., 2007). However, the average minimum temperature of most land areas on Earth is <0°C (Rihan et al., 2017). Low temperatures adversely affect crop growth and development, limiting their geographical distribution (Pearce, 2001; Ding et al., 2019). Sweetpotato is an important crop for ensuring national food security, but it is vulnerable to yield reductions caused by low-temperature damage (Jin et al., 2017; Yu et al., 2022). Genetic engineering has emerged as an effective strategy for enhancing sweetpotato’s tolerance to cold stress (Jin et al., 2017; 2021; 2022; Yu et al., 2022). Nevertheless, the function of XTH in cold stress of sweetpotato remains to be further studied. In this study, a novel IbXTH16 gene was cloned from the cold-tolerant variety LHS21 (Figure 1). The plant cell membrane serves as a crucial barrier for maintaining stable cellular metabolism and also plays a key role in sensing low temperatures (Zhang et al., 2019). After plants are exposed to low temperatures, the permeability and fluidity of their cell membranes decline, activating cold-response genes (Muratan, 1997). The localization of IbXTH16 in the cell membrane and the induction of IbXTH16 by cold suggest that IbXTH16 might serve as a signalling molecule in cold tolerance of sweetpotato (Figures 1D, 2C). The expression of IbXTH16 was induced by the BR (Figure 2D), and its overexpression enhanced cold tolerance in sweetpotato (Figure 4). Therefore, IbXTH16 is believed to be involved in the cold tolerance of sweetpotato.
4.2 IbXTH16 activates the biosynthesis of SOD and POD
Under low-temperature stress, plants accumulate excessive reactive oxygen species (ROS), which can be detrimental to plant cells (Guo et al., 2022; Mittler et al., 2022). The ROS scavenging system can detoxify ROS by enhancing the activity of ROS-scavenging enzymes, such as SOD and POD, preventing oxidative damage to plant cells (Gill and Tuteja, 2010; Bose et al., 2014; Choudhury et al., 2017). In Zoysia japonica, overexpression of ZjICE1 conferred cold tolerance in transgenic plants by increasing SOD, POD, and proline contents, as well as decreasing MDA content (Zuo et al., 2019). In Betula platyphylla, overexpression of BpERF13 improved the cold tolerance of transgenic plants by binding to cis-elements of SOD and POD and increasing SOD and POD contents (Lv et al., 2020). In this study, the SOD and POD contents were significantly increased in the transgenic plants under 4°C (Figures 5A,E). It is suggested that overexpression of IbXTH16 enhances cold tolerance by activating the biosynthesis of SOD and POD in transgenic sweetpotato. Previous reports have indicated that the plant hormone ABA is also involved in the cold tolerance of plants (Huang et al., 2017;Ma et al., 2018; Li et al., 2021). The IbXTH16 promoter region contained an ABA-response element ABRE (Figure 1C). However, whether the XTH16 gene regulates cold tolerance in sweetpotato via the ABA pathway requires further investigation.
4.3 IbXTH16 positively regulates BR signalling pathway and proline accumulation
BR signalling not only participates in plant growth and development, but also has been reported in plant resistance to low temperature (Kinoshita et al., 2005; Vriet et al., 2012). In the initial phase when plants are exposed to cold stress, the activity of BIN2 kinase is suppressed, while OST1 kinase is activated, this synergistic regulation stabilizes ICE1, thereby enhancing the expression of CBF and improving the cold tolerance of plants (Barrero-Gil and Salinas, 2018; Ye et al., 2019). In Arabidopsis, compared with the WT, the cold resistance of overexpressing BRI1 plants was enhanced, while that of mutant BRI1 plants was decreased (Eremina et al., 2016). In this study, the transgenic plants showed a significant increase in BR content, which might be due to the overexpression of IbXTH16 increasing the BR biosynthesis of transgenic plants, thus conferring cold tolerance (Figure 5F). Interestingly, the BR content in the transgenic plants was significantly decreased after restoring the room temperature (Figure 5F). The BR biosynthetic pathway involves the participation of a series of genes (Zhao and Li, 2012). In this study, the expression levels of BR biosynthesis and signalling pathway-related positive regulatory factors were significantly upregulated, while negative regulatory factor was significantly downregulated (Figures 6A–F). More proline accumulation can protect plants from low-temperature stress and ROS damage (Ghosh et al., 2022; Kidokoro et al., 2022). In this study, the proline biosynthesis-related genes were significantly upregulated, while degradation pathway-related genes were significantly downregulated (Figures 6G–J). Collectively, these findings suggest that IbXTH16 positively regulates cold tolerance of sweetpotato by activiting BR signalling pathway and proline accumulation (Figure 7).
FIGURE 7
5 Conclusion
Overexpression of the cloned IbXTH16 gene increased cold tolerance of sweetpotato by activating the BR and proline pathways. This study for the first time sheds light on the important role of IbXTH16 in cold tolerance. IbXTH16 has the potential to increase cold tolerance in sweetpotato and other plants.
Statements
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Author contributions
TY: Formal Analysis, Funding acquisition, Investigation, Writing – original draft, Writing – review and editing. JP: Data curation, Investigation, Writing – review and editing. SL: Investigation, Writing – review and editing. ZY: Investigation, Writing – review and editing. ZL: Conceptualization, Funding acquisition, Writing – review and editing.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This research was supported by grants from Potato International Joint Laboratory (2025LHSYS05) and Independent Research Project of Liaoning Academy of Agricultural Sciences (2025XKJBS8507).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
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Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fgene.2025.1629260/full#supplementary-material
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Summary
Keywords
sweetpotato, cold tolerance, IbXTH16, BR, proline
Citation
Yu T, Pan J, Liu S, Yang Z and Liu Z (2025) A xyloglucan endotransglucosylase/hydrolase gene, IbXTH16, increases cold tolerance in transgenic sweetpotato. Front. Genet. 16:1629260. doi: 10.3389/fgene.2025.1629260
Received
15 May 2025
Accepted
09 June 2025
Published
18 June 2025
Volume
16 - 2025
Edited by
Lianjun Wang, Hubei Academy of Agricultural Sciences, China
Reviewed by
Rong Jin, Chinese Academy of Agricultural Sciences, China
Sun Houjun, Xuzhou Institute of Architectural Technology, China
Updates
Copyright
© 2025 Yu, Pan, Liu, Yang and Liu.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhenlei Liu, liuzhenlei@cau.edu.cn
Disclaimer
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