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Genome-wide identification, phylogeny and expression analysis of AP2/ERF transcription factors family in sweet potato

BMC Genomics volume 22, Article number: 748 (2021) Cite this article

A Correction to this article was published on 16 February 2022

This article has been updated

Abstract

Background

In recent years, much attention has been given to AP2/ERF transcription factors because they play indispensable roles in many biological processes, such as plant development and biotic and abiotic stress responses. Although AP2/ERFs have been thoroughly characterised in many plant species, the knowledge about this family in the sweet potato, which is a vital edible and medicinal crop, is still limited. In this study, a comprehensive genome-wide investigation was conducted to characterise the AP2/ERF gene family in the sweet potato.

Results

Here, 198 IbAP2/ERF transcription factors were obtained. Phylogenetic analysis classified the members of the IbAP2/ERF family into three groups, namely, ERF (172 members), AP2 (21 members) and RAV (5 members), which was consistent with the analysis of gene structure and conserved protein domains. The evolutionary characteristics of these IbAP2/ERF genes were systematically investigated by analysing chromosome location, conserved protein motifs and gene duplication events, indicating that the expansion of the IbAP2/ERF gene family may have been caused by tandem duplication. Furthermore, the analysis of cis-acting elements in IbAP2/ERF gene promoters implied that these genes may play crucial roles in plant growth, development and stress responses. Additionally, the available RNA-seq data and quantitative real-time PCR (qRT-PCR) were used to investigate the expression patterns of IbAP2/ERF genes during sweet potato root development as well as under multiple forms of abiotic stress, and we identified several developmental stage-specific and stress-responsive IbAP2/ERF genes. Furthermore, g59127 was differentially expressed under various stress conditions and was identified as a nuclear protein, which was in line with predicted subcellular localization results.

Conclusions

This study originally revealed the characteristics of the IbAP2/ERF superfamily and provides valuable resources for further evolutionary and functional investigations of IbAP2/ERF genes in the sweet potato.

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Introduction

One of the largest gene families in plants is the AP2/ERF transcription factor (TF) superfamily, which includes at least one APETALA2 (AP2) domain comprising approximately 60 amino acid residues and is significant to the regulation of plant development and the response to various types of stress [1, 2]. By the rule of the components of conserved domains, AP2/ERF TFs can be separated into ERF, AP2 and RAV gene subfamilies [3,4,5]. Most AP2/ERF TFs belong to the ERF subfamily, which contains one conserved AP2 domain, and the AP2 subfamily encodes proteins with two AP2 domains. Additionally, with the exception of one single AP2 domain, the RAV subfamily also includes a B3 DNA binding domain that is conserved in other plant-specific transcription factors [6]. Although the sequences of the AP2 domain are highly conserved, the DNA binding elements of each subfamily are totally different. Generally, based on the DNA binding motifs, the ERF subfamily can be further subdivided into two groups: the ERF group, including B1 to B6 subgroups, can bind to the GCC-box (AGCCGCC element); and the DREB group, including A1 to A6 subgroups, can bind to the DRE/CRT (dehydration responsive element/C-repeat, RCCGCC element) element [7, 8].. The AP2 subfamily cannot bind to the CCGA/CC element, which is a core element interacting with the ERF subfamily, but can bind to the GCAC(A/G)N(A/T)TCCC(A/G)ANG(C/T) sequence [9, 10]. Additionally, the binding sequences of the RAV subfamily can be CACCTG and CAACA elements [11].

Extensive studies have been conducted to investigate the significant roles of AP2/ERF genes in regulating diverse developmental processes, stress responses and plant hormone signal transduction, including ethylene, auxin, salicylic acid and jasmonic acid [12,13,14]. Several members of the ERF subfamily have been revealed as viable candidates to enhance plant abiotic stress tolerance and display different response patterns under abiotic stress, including cold (AtCBF1, PtERF109) [15, 16], heat (ZmDREB2A, AtDREB1A) [17, 18], osmotic stress (CkDREB) [19], drought (OsDREB1, IbRAP2–12) [20,21,22], and high-salt stress (CaDREBLP1, LkERF-B2, IbERF5) [23,24,25]. Members of the AP2 subfamily play vital roles in the regulation of organ architecture and development, such as floral organ patterning [26,27,28], leaf development [29] and embryo development [30], while RAV subfamily genes are the main factors involved in plant hormone signal transduction [31], including that of brassinosteroids [32], ethylene [33] and auxin [34], and are the main regulators of multiple stress responses [11, 35, 36]. Thus, identification and analysis of the AP2/ERF gene family are crucial to understanding the mechanisms of many developmental processes and various stress responses.

The sweet potato [37], which originated in Central America and belongs to the Convolvulaceae family, is an important food crop grown globally and has significant medicinal value [38]. Additionally, with the release of sweet potato genome data and the advancement of transgenic technology, it has become possible to identify and investigate important gene families at the whole genome level. Beta-galactosidase family members of the sweet potato have been identified at the genome-wide level [37]. Additionally, genome-wide characterisations of several potassium absorption-related gene families, such as the HAK K+ transport family [39] and the Shaker K+ channel family [40], have also been investigated.

Due to the significance of AP2/ERF genes in many biological processes, it is crucial to systematically investigate the AP2/ERF gene family in the sweet potato. The functions of AP2/ERF TFs have been well studied in many species, but there are few investigations in the sweet potato. IbDREB1 was identified and can respond to several abiotic stressors, including dehydration, salt and cold stress [41]. A previous report showed that two ERF members, IbERF1 and IbERF2, are involved in different types of abiotic stress and in response to pathogens, and can activate the transcription of defence genes in tobacco [42]. IbCBF3 can strengthen the drought and cold tolerance of the sweet potato [43]. Another IbAP2/ERF gene, IbRAP2–12, responded to salt and drought stress in transgenic Arabidopsis [22]. Recently, sweet potato IbERF4 also played a vital role in regulating of abiotic stress [44].

In this study, through analysis of genome-wide biological information, the evolutionary characteristics of sweet potato AP2/ERF TFs were revealed. The expression profiles of IbAP2/ERF genes at different root developmental stages and under multiple forms of stress were further investigated by analysing RNA-seq and qRT-PCR data. This work lays a solid foundation for subsequent functional studies of the AP2/ERF gene family in the sweet potato.

Methods

Identification and classification of the AP2/ERF gene family in the sweet potato genome

Whole sweet potato genome data were downloaded from the Ipomoea Genome Hub (https://ipomoea-genome.org/). The AP2 domain (PF00847) was retrieved from the PFAM database (http://pfam.xfam.org/), and was used as the query for the HMM (hidden Markov model) search, which was conducted using the HMMER 3.0 programme with E < 1e− 5 as the threshold. Furthermore, the BLASTP programme with an e-value of 1e− 5 and identity of 50% as the threshold was used to search against the sweet potato protein dataset by using the AP2/ERF protein sequences of rice and Arabidopsis obtained from the plant transcription factor database (http://plntfdb.bio.uni-potsdam.de/v3.0/) as the query. Then, we used the NCBI-CDD web server (http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/Structure/cdd/wrpsb.cgi) and the SMART database (http://smart.embl-heidelberg.de/) to further verify the existence of the AP2 domain in all IbAP2/ERF proteins. The ExPASy server (http://www.expasy.org/) was used to calculate the MW (molecular weight) and PI (theoretical isoelectric point) of the retrieved proteins using the compute pI/Mw tool. The Cell-PLoc 2.0 web server (http://www.csbio.sjtu.edu.cn/bioinf/plant-multi/) was used to predict the subcellular localization of the retrieved proteins.

Multiple sequence alignment and phylogenetic analysis

ClustalW with default parameters was used to perform the multiple sequence alignment of obtained AP2/ERF protein sequences. Phylogenetic and molecular evolutionary analyses were performed using MEGA7 with the neighbour-joining (NJ) algorithm. Phylogenetic trees were constructed using the retrieved conserved domains of AP2/ERF proteins. The bootstrap value was 1000. IbAP2/ERF genes were partitioned into three different groups based on the number of AP2 domains and the presence of B3 domains. The ERF subfamily was further subdivided into 12 groups (DREB A1-A6 and ERF B1-B6) based on the homologues of the corresponding genes in Arabidopsis.

Sequence analysis

The Gene Structure Display Server (GSDS: http://gsds.gao-lab.org/index.php) was used to determine the exon-intron structure of these IbAP2/ERF genes. The structural differences among IbAP2/ERF proteins were investigated by studying the conserved protein domains. Additionally, the MEME programme was used to predict the conserved motifs of IbAP2/ERF proteins.

Chromosome distribution, gene duplication and cis-acting elements in the promoters of IbAP2/ERF genes

From the genome annotation information, the chromosome distribution of all IbAP2/ERF genes was acquired and then confirmed by BLASTn search. Multiple collinear scanning toolkits (MCScanX) were used to evaluate gene replication events. Furthermore, we obtained the AP2/ERF protein sequences of Arabidopsis thaliana, Oryza sativa, Manihot esculenta, Glycine max, Vitis vinifera and Zea mays from the Phytozome database (https://phytozome.jgi.doe.gov/pz/portal.html#!search). Dual Synteny Plotter software (https://github.com/CJ-Chen/TBtools) was used to analyse the syntenic relationships among AP2/ERF genes in different selected plants. The 2000-bp genomic sequence was extracted from the upstream of the start codon of each IbAP2/ERF gene as the putative promoter region. Then, we used the PlantCARE database (http://bioinformatics.psb.ugent.be/webtools/plantcare/html) to predict cis-acting elements.

Transcriptome data source and bioinformation analysis

High-throughput RNA-seq data (accession numbers PRJNA533954, PRJNA515432, PRJNA413661 and PRJNA631585) of the sweet potato were downloaded from the SRA database (http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/sra) and used to analyse the expression profiles of IbAP2/ERF genes by FPKM analysis. We used various quality parameters to assess the raw sequence data and used the NGS QC Toolkit (v2.3) [45] to filter the high-quality reads. Mapping onto the sweet potato genome of filtered high-quality reads was conducted by TopHat (v2.0.0) using the default parameters. The FPKM value and read counts of each sweet potato gene were obtained through Cufflinks (v2.0.2) using the mapped output. Read counts were used to detect differentially expressed genes with false discovery rate (FDR) < 0.01 and fold change > 2 through DESeq. The stage-specific/preferential genes in each stage were identified with the SS scoring algorithm, which compares the expression of a gene in a given stage with its maximum expression level in other stages as described previously [46]. A higher SS score of a gene in a particular stage signifies its more specific expression at that stage. A total of 15 RNA-seq datasets of sweet potato roots at different developmental stages, including fibrous roots (root diameters of approximately 1 mm) and storage roots (D1, D3, D5 and D10; root diameters of 1 cm, 3 cm, 5 cm and 10 cm, respectively), were used. Additionally, 9 RNA-seq datasets of sweet potato storage roots stored at 4 °C for 0 (control), 2, and 6 weeks were used to investigate the expression pattern of IbAP2/ERF genes under low temperature. Eight RNA-seq datasets of sweet potato leaves at 0 (control), 6, 12 and 24 h after 30% polyethylene glycol (PEG) treatment were used to explore the expression profile of IbAP2/ERF genes under drought stress. Moreover, 6 RNA-seq datasets of sweet potato roots at 0 (control) and 24 h after 150 mM NaCl treatment were used to analyse the transcript patterns of IbAP2/ERF genes in response to salt stress.

Plant abiotic stress and low temperature treatment

Sweet potato (Ipomoea batatas L.) Cv. Taizhong6 seedlings were planted in early May in the Wushe Plantation for Transgenic Crops in Shanghai, China (31°13,948.0099 N, 121°28,912.0099E). Fibrous roots (S1, root diameter of 2 mm), pencil roots (S2, root diameter of 5 mm) and storage roots at two stages (S3 and S4; root diameters of 15 mm and 25 mm, respectively) were collected from the sweet potato plants in early November to cover the entire storage root initiation and development processes. Then, for low-temperature treatment, the collected storage roots (S4) were stored at 4 °C as described [47]. Tuberous roots were collected at 0 (control), 1, and 2 weeks after treatment. All samples were frozen in liquid nitrogen and stored at − 70 °C for mRNA extraction.

For abiotic treatments, sweet potato seedlings were incubated in quarter-strength Hoagland solution in a greenhouse (16 h/8 h of light/dark, 30 °C/22 °C day/night). The treatment assays were conducted as described in a previous report [25] with some modifications. Cold stress was performed by culturing seedlings at 4 °C, and the roots were collected. Dehydration and salt experiments were carried out by immersing the adventitious roots in 20% PEG6000 or 150 mM NaCl solutions, respectively, and the roots were harvested. All samples were collected at 0 (control), 1, 12, 24, and 48 h after each treatment and immediately frozen in liquid nitrogen for mRNA extraction.

RNA extraction and quantitative real-time polymerase chain reaction (qRT-PCR) analysis

RNA Extraction Kits (TianGen, Beijing, China) were used to extract total RNA from samples according to the manufacturer’s instructions. Two micrograms of RNA was reverse-transcribed using ReverTra Ace qPCR RT Master Mix (TOYOBO, Shanghai, China). qRT-PCR analysis was performed as described earlier [48] with three biological replicates for each tissue sample and at least triplicates of each biological replicate. The gene-specific primers designed using Primer Express (v3.0) software are listed in Table S7. Each gene was normalized to the β-Actin internal control gene, and the fold change was calculated using the 2−∆∆CT method.

Analysis of subcellular localization

For the subcellular localization experiment, a construct coding for a g59127-GFP fusion protein was generated under the control of the CaMV 35S promoter, which was then introduced into tobacco leaves through Agrobacterium-mediated transformation. Finally, the leaves were observed under an Olympus FV1000 microscope (Olympus, Japan). The primers used in this study are listed in Table S7.

Statistical analysis

Samples were collected from three independent plants. Data from at least three replicates are presented as the mean ± SD. Analysis of independent samples with Student’s t-test was performed using SPSS software, version 17 (SPSS Inc., Chicago, IL, USA). An alpha value of P < 0.05 was statistically significant.

Results

Identification of AP2/ERF family transcription factors in the sweet potato

All possible IbAP2/ERF genes were excavated from the sweet potato genome using a genome-wide search for AP2 domains including proteins. In total, 198 distinct IbAP2/ERF putative transcription factors were identified after removing redundant and alternative forms of the same gene (Table S1). The chromosome distribution results showed that these IbAP2/ERF genes were located on all 15 chromosomes in the sweet potato. In detail, IbAP2/ERF genes were most abundant on chromosome 7 with 23 IbAP2/ERF genes, while 22 and 17 IbAP2/ERF genes were distributed on the chromosomes 2 and 11, respectively. Otherwise, chromosome 14, with only 6 genes, had the fewest number of IbAP2/ERF TFs.

Gene characteristics were further investigated. Analysis of the coding sequence length (CDS) showed that g60090 yielded the largest protein with 5064 bp (1687 amino acids), while g532 yielded the smallest protein, with 309 bp (102 amino acids). The isoelectric point (pI) of these proteins ranged from 4.17 (g20630) to 11.65 (g54236), and the protein molecular weight (MW) ranged from 11.3 to 177.45 kDa. In addition, predicted subcellular localization analysis showed that the majority of IbAP2/ERF TFs were localized to the nucleus, with 157 genes, and 17 genes were localised to chloroplast. The remaining genes were predicted to be localised to mitochondria, peroxisomes, the plasma membrane and the cytoplasm.

Phylogenetic relationship, gene structure and conserved motif analysis

To explore the phylogenetic relationship of sweet potato AP2/ERF proteins, the multiple sequence alignment results of 198 sweet potato AP2/ERF proteins and 141 Arabidopsis AP2/ERF proteins were used to construct a phylogenetic tree by using the neighbour-joining (NJ) method. All the AP2/ERF genes were clustered into three major clades (ERF, AP2 and RAV) based on their domain composition (Fig. 1). There were 172 genes assigned to the ERF subfamily, which contains one single AP2 domain, and all these genes can be subdivided into two groups: DREB [A1 (4), A2 (10), A3 (1), A4 (15), A5 (14), A6 (11)] and ERF [B1 (38), B2 (20), B3 (40), B4 (5), B5 (4), B6 (10)], which is consistent with a previous report [25] (Table S2). The AP2 subfamily had 21 genes with two AP2 DNA binding domains. Only 5 genes encoding a single AP2 domain and a B3 domain were grouped into the RAV family. Interestingly, the g34948, g56186 and g60806 genes belonged to the ERF subfamily members; however, these genes showed high similarity with the AP2 subfamily.

Fig. 1
figure 1

The phylogenetic tree constructed by the neighbor-joining method represents the relationships among AP2/ERF proteins of sweet potato and Arabidopsis. The proteins of sweet potato and Arabidopsis are marked in red and black respectively. Red, green and blue colored branches indicate ERF, AP2 and RAV subfamily

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To further understand the gene structural composition, the intron and exon structures of IbAP2/ERF genes were analysed by comparing the genomic DNA sequences (Fig. 2a, b). Most members of the ERF subfamily contained no or few introns, except for eight genes with intron numbers ranging from 7 to 12. Interestingly, 7 of those genes, including g5177, g60806, g16798, g34948, g56186, g14188 and g551886, showed high similarity with the AP2 subfamily. Additionally, the RAV subfamily contained no or one intron. Compared with the ERF and RAV subfamilies, the members of the AP2 subfamily had at least 5 introns. Among AP2 subfamily genes, g54878 contained the most introns (14). The highly diverse gene structure indicated that there was extensive differentiation during the formation and evolution of the sweet potato genome.

Fig. 2
figure 2

Architecture of phylogenetic tree, gene structure and protein conserved motifs in the IbAP2/ERF superfamily from sweet potato. (a) Phylogenetic relationships of IbAP2/ERF proteins in sweet potato. Members of ERF, AP2 and RAV subfamily were filled in yellow, blue and green respectively. (b) Exon-intron structure of IbAP2/ERF genes. Green boxes indicate exons; black lines indicate introns. (c) The motif pattern of IbAP2/ERF proteins. The different colors represent different motifs with the number 1–10. The sequence information of each motif is provided in Additional file 1: Table S3. The protein length can be estimated using the scale at the bottom

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Furthermore, characteristic region analysis of IbAP2/ERF proteins was conducted (Fig. S1). These proteins have a highly conserved AP2 domain, which is the typical pattern in the AP2/ERF family, especially in the AP2 subfamily, which contains two conserved AP2 domains. In addition to the AP2 domain, RAV subfamily members also contained the B3 domain consisting of 100–120 amino acids. Moreover, other conserved regions were also detected in individual proteins. For example, the PRA1 domain, the ribosomal-S9 domain and the Metallophos domain were detected in the g5338 protein, g50554 protein and g54878 protein, respectively.

The conserved motifs of IbAP2/ERF proteins were further characterised by MEME software (Table S3). The results showed that a total of 10 conserved motifs were identified (Fig. 2a, c). Among these motifs, motifs 1, 2, 3, 4, 5, 6, 7 and 9 were located in the AP2 conserved domain regions. Besides, ERF subfamily members contained motifs 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10, of which motif 9 was detected in most genes (100), and motif 6 was detected in the fewest genes (6). In the AP2 subfamily members, motifs 1, 2, 3, 4, 6 and 7 were detected, of which motifs 2, 4 and 6 were found in almost all the members of the AP2 subfamily. Motif 1 was detected in g54878, motif 3 in g29817, and motif 7 in g28895. In the RAV subfamily, motif 4 was the only shared motif. Generally, many conserved motifs detected in these IbAP2/ERF proteins may participate in the expression regulation of genes with the potential DNA binding sites, which can be further examined. The similar composition of gene structure and conserved motifs in a specific subfamily further verified the reliability of the phylogenetic tree and clustering.

Chromosome distribution, gene duplication and synteny analysis of the IbAP2/ERF gene family

To investigate the chromosome distribution of the IbAP2/ERF genes, the latest sweet potato genome database was used for analysis. A total of 198 IbAP2/ERF genes were distributed unevenly on 15 sweet potato chromosomes (Fig. 3). Chromosome 7 had the largest number of IbAP2/ERF TFs (27 genes), which accounted for approximately 11.6% of the total number of IbAP2/ERF genes. Chromosome 2 contained 22 IbAP2/ERF genes, which accounted for approximately 11% of the total number of IbAP2/ERF genes, while the smallest number of IbAP2/ERF TFs was found on chromosome 14, with 6 genes. The ERF subfamily was detected on all chromosomes, of which chromosomes 14 and 15 contained only ERF subfamily members. In addition, no AP2 subfamily members were found on chromosomes 2, 9, 14 or 15, while the members of the RAV subfamily were distributed on chromosomes 2, 3, 4, 9 and 12. Furthermore, some IbAP2/ERF TFs that have similar conserved structures were localised on the same chromosome, which has also been observed in Arabidopsis thaliana [5], Vitis vinifera [49], Chinese cabbage [50] and Tartary buckwheat genomes [51], indicating that ancestral polyploidy events may result in these homologous fragments. In addition, we analysed the duplication events of IbAP2/ERF genes because gene duplication is a key mechanism in gene expansion and the emergence of novel functions. Tandem replication was defined as 200 kb-range chromosomal regions that included more than one homologous gene. Six IbAP2/ERF gene clusters containing twenty-six tandem duplicated genes were identified in sweet potato linkage groups (LGs) 2, 3, 7, 10 and 11. LG7 had two clusters, one of which contained the most genes (8 genes), indicating hot spots of IbAP2/ERF gene distribution. Interestingly, each cluster contained only genes belonging to the ERF subfamily.

Fig. 3
figure 3

Chromosomal distribution of sweet potato IbAP2/ERF genes. The chromosome number is marked on the left of each chromosome. The red lines represent duplicated IbAP2/ERF gene pairs

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Apart from tandem duplication events, we also found many pairs of segmental duplications in the sweet potato chromosomes (Fig. 4), since the analysis of homologous genes is significant in exploring the kinship of evolution. Several pairs of homologous genes were found on different sweet potato chromosomes, further confirming that the IbAP2/ERF gene family is highly conserved. According to the above data, some IbAP2/ERF genes might be the result of gene replication, which might be the main evolutionary driving force of IbAP2/ERF genes.

Fig. 4
figure 4

Interchromosomal relationships of sweet potato IbAP2/ERF genes. Grey lines indicate all syntenic blocks in the sweet potato genome. Red lines indicate collinear blocks of IbAP2/ERF genes in the sweet potato genome

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Evolutionary analysis of AP2/ERF genes in the sweet potato and several different species

Since the phylogenetic mechanisms of the IbAP2/ERF family were uncertain, we constructed syntenic maps of the sweet potato compared with six different species including three monocotyledonous plants (grape, corn, rice) and three dicotyledonous plants (soybean, Arabidopsis, and cassava). The results showed that the AP2/ERF genes in the sweet potato have homologous genes in these reference plants, of which Manihot esculenta had the most syntenic conservation (158 syntenic gene pairs located on chr1 - chr18), followed by Arabidopsis thaliana (119 orthologous gene pairs distributed on chr1 - chr5) and Glycine Max (109 syntenic gene pairs distributed on chr1 – chr9 and chr20) (Fig. 5). When comparing between the sweet potato and Manihot esculenta, the syntenic results of AP2/ERF genes showed that g13132, g13922, g46272, g55039 and g60882 were connected with more than two orthologous gene pairs, indicating that these genes might be of great significance in AP2/ERF family evolution (Table S4). According to the above results, sweet potato AP2/ERF genes are closer to those in cassava and may evolve from a common ancestor in various plants.

Fig. 5
figure 5

Syntenic analysis of AP2/ERF genes between sweet potato and six representative plant species. Gray lines in the background indicate the collinear blocks within sweet potato and other plant genomes, whereas red lines highlight syntenic AP2/ERF gene pairs

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Cis-acting elements of sweet potato IbAP2/ERF genes

To further infer the potential function of sweet potato IbAP2/ERF genes, cis-acting elements were analysed using the promoters of these genes (Fig. 6). Many cis-acting elements, such as hormone-responsive, stress-responsive and light-responsive elements, were observed in the promoters of IbAP2/ERF genes. Light-responsive elements (1418) were the most enriched cis-elements in the promoters of IbAP2/ERF genes. Hormone-responsive elements (748), such as methyl jasmonate (MeJA, 538), SA (85) and auxin (125), were often detected in the promoters of IbAP2/ERF genes. The promoters also included stress-related elements for anaerobic induction (339), low-temperature responsiveness (85), defence and stress responsiveness (75) and wound responsiveness (3). Additionally, endosperm expression (42), circadian control (38) and cell cycle regulation (9) promoter elements were also detected. These results implied that the IbAP2/ERF genes may be regulated through various cis-acting elements and play significant roles during plant development and stress responses.

Fig. 6
figure 6

Predicted cis-acting elements in the promoter of the IbA2/ERF genes. The 2.0 kb region upstream of ATG was analysed using the PlantCARE software

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Expression patterns of IbAP2/ERF genes during root development and under multiple forms of abiotic stress

To determine the functional roles of IbAP2/ERF genes during root development, the expression profiles of these genes at different root developmental stages (F, fibrous roots; D1, pencil roots with a diameter of 1 cm; D3, storage roots with a diameter of 3 cm; D5, storage roots with a diameter of 5 cm; D10, storage roots with a diameter of 10 cm) were analysed using RNA-seq data through FPKM analysis. In the results, 191 IbAP2/ERF genes were examined in these data, and the expression levels of these genes had high variance, indicating that the IbAP2/ERF genes had multiple potential functions in sweet potato root development (Fig. 7a and Table S5). Generally, among these genes, 44, 7, 6 and 2 genes were relatively highly expressed in the F, D1, D5 and D10 stages, respectively. In detail, g15856, g25314, g38193, g40768, g14059, g20630 and g25967 were specifically expressed in the early developmental stages (D1), with extremely low expression levels in the other stages. We presumed that these genes may mainly affect the early development of roots and may be used as marker genes during early root developmental stages. In addition, several genes showed relatively high expression at each stage of root development, such as g31279, g6122, g54463, g59147, g60949, g60090, g34543, g30808, g670 and g20475, indicating that they may play indispensable roles in regulating tuber development. However, g38291, g39445, g39452, g38698, g47478, g51568, g6437 and g20397 were not expressed in any of the tested samples.

Fig. 7
figure 7

The expression profiles of IbAP2/ERF genes in the sweet potato at different root developmental stages and under multiple forms of stress analysed by the available RNA-Seq data. (a) The expression profiles of IbAP2/ERF genes in the sweet potato roots at different developmental stages. F, fibrous roots; D1, the pencil roots (diameter: 1 cm); D3, the storage roots (diameter: 3 cm); D5, the storage roots (diameter: 5 cm); D10, the storage roots (diameter: 10 cm). (b) The expression profiles of IbAP2/ERF genes in the root under cold stress. w, week. (c) The expression profiles of IbAP2/ERF genes in the leaves under 30% PEG treatment. h, hour. (d) The expression profiles of IbAP2/ERF genes in the roots under salt treatment. h, hour. For each row, blue and red correspond to low and high values of gene expression, respectively

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We found low-temperature responsive elements in the promoters of IbAP2/ERF genes, indicating that IbAP2/ERF TFs might play indispensable roles in responding to low temperatures. To further analyse the physiological function of IbAP2/ERF genes under cold stress, the available RNA-seq data of sweet potato roots under cold stress were used to study the expression profiles of these genes (Fig. 7b and Table S5). In the results, 56 IbAP2/ERF genes were detected, and there were 29 differentially expressed genes, of which 16 genes were upregulated and 4 genes were downregulated under cold stress at 2 weeks. The expression level of g60059 increased quickly under cold stress at 2 weeks and increased continuously to 6 weeks. A large proportion of TFs, such as g13922, g41901, g34543, g59147, g670, g5499 and g12377, also increased quickly under cold stress at 2 weeks, but their expression levels irregularly changed at 6 weeks. The expression levels of g19784 and g25314 decreased quickly under cold stress at 2 weeks and decreased continuously to 6 weeks. Additionally, some genes, such as g5103 and g12458 exhibited decreased expression patterns under cold stress at 2 weeks, but their expression levels increased at 6 weeks. These results implied that the IbAP2/ERF TFs might play indispensable roles in the response to cold stress.

For dehydration stress, the expression patterns of IbAP2/ERF genes were investigated by RNA-seq data of sweet potato leaves under 30% PEG treatment (Fig. 7c and Table S5). A total of 52 IbAP2/ERF genes were detected, wherein 18 genes including 17 upregulated genes and 1 downregulated gene were differentially expressed at 6 h. There was only one gene (g54428) differentially expressed at 12 h. At 24 h, 5 genes and 2 genes were upregulated or downregulated, respectively. Among these genes, g54428 was differentially expressed at all the time points, implying that it might contribute to the sweet potato response to drought stress. Additionally, 155 IbAP2/ERF genes were examined in the RNA-seq data of sweet potato roots under salt stress (Fig. 7d and Table S5). The transcript level of 21 genes were increased at 24 h, while there were 9 downregulated genes at 24 h. g35344 and g43542 might be key regulators of the response to salt stress because they exhibited the highest induction level under salt stress with approximately a 64-fold change.

To validate the RNA-seq results, we performed qRT-PCR analysis of 15 main abiotic stress-induced genes with high transcriptional expression levels based on the RNA-seq data (Fig. 8a-b and Fig. 9a). The results showed that abiotic stress can lead to dramatic alterations in these selected genes. The expression profiles revealed by qRT-PCR were similar to those obtained by RNA-seq (Fig. 7a-d), indicating the accuracy of RNA-seq data and the potential contribution of the tested genes to root development and in response to abiotic stress. Among these genes, g670, g8319, g17206, g29674, g28855, g28895, g30588, g41901, g43908, g59127 and g60392 were more highly expressed at early root developmental stages (S1 and S2), while g1018 was more highly expressed at later stages (S3 and S4), indicating that different genes might play various roles during the root developmental process (Fig. 8a). Under salt stress, g8319 was the most significantly induced (approximately 55-fold), followed by g59127 (30-fold), g13657 (9-fold), g41901 (6-fold) and g29674 (3.5-fold). However, g670, g41968 and g54428 expression was inhibited, implying that these genes might be key regulators of the response to salt stress (Fig. 9a). For dehydration stress, the highest induction level was observed in g59127 at 80-fold. Expression of g60392 also increased (approximately 12-fold), whereas that of g670, g30588 and g41968 was inhibited (Fig. 9a). For cold stress, g8319 had the most significant induction level (at approximately 6-fold), followed by g29674 (at approximately 4-fold). In contrast, many of the analysed genes, including g670, g13657, g17206, g30588, g41968, g41901, g54428 and g60392, were inhibited when subjected to cold stress (Fig. 9a). Collectively, the significant and diverse expression patterns of these genes implied that they might play a role in responding to abiotic stress.

Fig. 8
figure 8

The expression profiles of IbAP2/ERF genes in the roots at different developmental stages (a) and during storage process at low temperature (b) analyzed by qRT-PCR. Fibrous roots (S1, root diameter of 2 mm), pencil roots (S2, root diameter of 5 mm) and storage roots at two stages (S3 and S4; root diameters of 15 mm and 25 mm respectively) from the sweet potato plants were harvested at six months after planting. Then, the collected storage roots were stored at 4 °C. Tuberous roots were collected at 0 (control), 2, and 6 weeks after low temperature treatment. The expression data were normalized to 1 in S1 and unstressed plants (0 w). Bars represent the mean of replicates ± standard error. * and ** indicate a significant difference at P < 0.05 and < 0.01, respectively, determined by Student’s t-test

Full size image
Fig. 9
figure 9

The expression profiles of IbAP2/ERF genes detected by qRT-PCR under various types of abiotic stress and the subcellular localization of g59127 protein. (a) The expression profiles of IbAP2/ERF genes detected by qRT-PCR under NaCl, dehydration, and cold stress. The sweet potato seedlings were submerged in 150 mM NaCl and 20% (w/v) PEG6000 solutions, respectively, and then adventitious roots were harvested. Cold assays were carried out by incubating the seedlings at 4 °C, and then roots were collected. The expression data were normalized to 1 in unstressed plants (0 h). Bars represent the mean of replicates ± standard error. * indicates a significant difference at P < 0.05, determined by Student’s t-test. (b) Analysis of the subcellular localization of g59127 protein. Localization of g59127-YFP fusion protein in tobacco (Nicotiana L.) cells. g59127-YFP expression was visualized using a confocal laser scanning microscope. Bar, 20 μm

Full size image

Analysis of subcellular localization of g59127 protein

Because the transcriptional expression of the g59127 gene showed obvious alterations during root development and could be markedly affected by most forms of abiotic stress, including cold, dehydration and salt stress, it was selected for further molecular characterisation analyses. The g59127 protein was predicted to be in the nucleus (Table S1), and a vector with the translational fusion of g59127 to GFP was constructed to confirm this result. As shown in Fig. 9b, the free GFP protein was both nuclear and cytoplasmic, but the g59127-GFP fusion protein was only displayed in the nucleus, which was consistent with the bioinformatics results.

Discussion

The AP2/ERF superfamily is one of the largest families of plant-specific transcription factors and plays important roles in a variety of biological processes. Many works have been performed to identify members of the AP2/ERF superfamily in several plants with sequenced genomes, such as Arabidopsis [5], maize [52], peach [53] and foxtail millet [54]. Nevertheless, no detailed study of this superfamily has been carried out in the sweet potato at the whole genome level until now. In this study, extensive identification of AP2/ERF genes throughout the sweet potato genome was conducted. A total of 198 sweet potato AP2/ERF genes were discovered (Table S1), accounting for 0.31% of all the sweet potato genes, which is lower than the results observed in rice (0.43%), maize (0.44%), foxtail millet (0.44%) and Brachypodium distachyon (0.45%). Compared with other plants, the AP2/ERF gene number in the sweet potato (198) was greater than that in barley (121), longan (125), tomato (146), Arabidopsis (148) and rice (167) but lower than that in poplar (202) and Chinese cabbage (291). It has been reported that the number of AP2/ERF genes is determined by the number of ERF subfamily members to a certain extent [55]. There were 172 ERF subfamily genes in the sweet potato and 122, 132 and 158 in Arabidopsis, rice and maize, respectively. Gene evolution and duplication have been revealed to cause this variance in plants [56, 57]. Additionally, there was no significant variance in the number of AP2 and RAV family members among these plant species, with values of 24, 25, 26, 28 and 34 in Arabidopsis, maize, sweet potato, Brachypodium distachyon and rice, respectively.

In the gene intron/exon structure of the 198 IbAP2/ERF genes, the AP2 subfamily had more introns, while the ERF subfamily had fewer introns, and no intron was found in the RAV subfamily (Fig. 2a, b), which resembles that of AP2/ERF genes in other plant species, including cauliflower and radish [58, 59]. Some studies have revealed that plant evolution is related to intron number and distribution [6], and the intron number of ERF subfamily genes is probably lost during plant evolution [60, 61]. Herein, no intron was observed in 92 of the 172 ERF subfamily members (53%), but a higher number was reported for Tartary buckwheat [51]. The variance of the gene structure among AP2, ERF and RAV subfamily members indicated that there might have been extensive differentiation and numerous functional discrepancies between these subfamilies during the evolution of the sweet potato genome. In addition, conserved domains and motifs play important roles in regulatory functions, which are associated with transcriptional activity, DNA binding and protein interactions [62, 63]. Previous reports have shown that in addition to an N-terminal DNA-binding domain, the C-terminal activation domain of AP2/ERF proteins can regulate the transcription of their target genes in Arabidopsis and rice [3]. AP2/ERF genes with ERF-associated amphiphilic repression (EAR) motifs (LxLxL or DLNxxP sequence) or B3 repression domains (BRD, R/KLFGV sequence) have a repressive effect on their target genes [64, 65]. The EDLL motif identified from AtERF98 can override the repressive effect mediated by the EAR motif [66]. In this study, 41 IbAP2/ERFs had the EAR motif, and 4 IbAP2/ERFs had the B3 motif (Table S6), implying that these genes might be involved in negative regulatory functions. Additionally, the EDLL motif was detected in 4 IbAP2/ERFs (Table S6), suggesting that the regulation of these genes may be complex, but further experimental verification is needed. Moreover, another 10 motifs were found in IbAP2/ERF proteins based on the MEME results: eight of the 10 motifs (motifs 1–7, 9) were related to the AP2 domain, and only 2 conserved motifs were located outside the AP2 domain (Fig. 2, Fig. S1 and Table S3). The ERF subfamily members had all 10 motifs, of which motif-9 was shared by most genes (100). Motif-9 was detected in the AP2 domain and enriched many DNA binding sites, indicating that this motif may be essential for the DNA binding abilities of these TFs [67]. Additionally, AP2 subfamily members harboured numerous motifs, ranging from 1 to 4 and 6 to 7, whereas the RAV family members only had motif-4. Based on these results, although high conservation was observed in some motifs of the IbAP2/ERF family, the unique motifs of different subgroups might be involved in more special functions in each IbAP2/ERF subfamily, and their functions require more work to clarify.

The latest sweet potato genome database was used to analyse the chromosome distribution of the IbAP2/ERF genes, and these genes were unevenly anchored on 15 chromosomes (LGs) (Fig. 3 and Fig. 4). Hot regions existed in most chromosomes, which indicated that IbAP2/ERF gene family expansion might be caused by tandem duplication and segmental duplications, which is in accordance with previous studies [55, 68]. In total, 26 paralogous pairs were found in the sweet potato, more were discovered in rice (41), Arabidopsis (51) and grape (76), and less were discovered in jujube (18). Furthermore, using MCScanX, there were 38,290 collinear gene pairs in the sweet potato genome, and 683 IbAP2/ERF collinear gene pairs were recognised, indicating that the sweet potato genome experienced a whole genome duplication event that might also underlie the expansion of the IbAP2/ERF family (Fig. 5 and Table S4).

Previous reports have shown that AP2/ERF TFs can be potential candidates for crop improvement because they are key regulators in different plant development processes and various stress responses [43, 69,70,71,72]. Nevertheless, IbAP2/ERF gene functions in the sweet potato are still not well known, and it is essential to analyse the transcriptional regulation of IbAP2/ERFs to utilise them to improve the quality and abiotic stress tolerance of the sweet potato. Here, we systematically analysed the expression profiles of these genes during root development and under multiple types of stress to determine their potential functions in biological processes. In this study, a total of 191 IbAP2/ERFs were expressed at different root developmental stages, implying that they might be widely associated with the regulation of root growth and development (Fig. 7a and Table S5). Furthermore, prominent temporal expression patterns of IbAP2/ERF genes were also observed. Forty-four IbAP2/ERF genes were specifically expressed in fibrous roots and 2 IbAP2/ERF genes showed preferential expression in the mature storage root (D10). Additionally, the expression levels of 60 IbAP2/ERF genes increased gradually during root development, indicating that these genes might play crucial roles in the process. In particular, g20630 showed a continuous upregulation profile, and its homologous gene AtCRF3 was reported to regulate lateral root development in Arabidopsis [73], implying that g20630 might have a similar function in sweet potato root development, thus confirming the reliability of our results. Furthermore, AP2/ERF TFs were reported to regulate the expression of target genes that respond to stress by binding to GCC-box or DRE motifs [74, 75]. Our results showed that there were 85 low-temperature responsive and 75 defence- and stress-responsive cis-elements in the promoter regions of IbAP2/ERF genes (Fig. 6). Moreover, compared to the control, IbAP2/ERF genes were specifically induced or repressed under multiple types of stress (Fig. 7b-d, Fig. 8b, Fig. 9a and Table S5). In particular, the expression of g25316, which encodes the IbDREB1/IbCBF3 protein, showed a remarkable reduction under cold stress and a significant increase under drought stress, which is consistent with a previous study [41, 43]; and the function of its homologue AtCBF3 in Arabidopsis [76], further confirming the reliability of our results. IbERF1 (g35249) and IbERF7 (g55038) was induced by salt stress, which is in accordance with a previous report [25, 42]. Moreover, IbRAP2–12 (g60949) showed increased patterns under both drought and salt stress, which is similar to published results [22]. IbERF4 (g30808) showed a similarly increased profile under drought stress compared with a previous report [44]. In addition, a previous report showed that AtERF113 (RAP2.6 L) can be activated by drought and salt stress, and enhance the tolerance to these stressors in Arabidopsis [77]. Our results found that the homologous genes of AtERF113 in the sweet potato, including g28064, g60059 and g52248, showed similar expression patterns to those in a previous report [25], indicating that these genes may play similar roles in the sweet potato stress response. Based on the above data, we speculated that cis-elements might be crucial regulatory factors for the spatial and temporal expression of IbAP2/ERF genes, which could form a complex regulatory network with other functional proteins during development and stress response processes [78]. These identified developmental stage-specific and stress-induced IbAP2/ERF genes might be valuable candidates for systematic functional investigations of these genes in the sweet potato and other tuberous crops.

The bioinformatics analysis of the subcellular localization of IbAP2/ERF TFs showed that most of these genes were in the nucleus (157), while others were distributed in chloroplasts (17), the cytoplasm (15), mitochondria (6) and peroxisomes (3) (Table S1). The results of the subcellular localization experiment verified that g59127 localised to the nucleus, which was in line with predicted results. In summary, our present study identified and characterised IbAP2/ERF TFs in the sweet potato. By conducting a genome-wide search, 198 IbAP2/ERF TFs were identified. The phylogenetic relationship, exon-intron structure, conserved motif composition, chromosome distribution and gene duplication of these IbAP2/ERF TFs were systematically discussed and compared. IbAP2/ERFs could be clustered into three major subfamilies, which was consistent with the number of AP2 domains and gene structure. The cis-acting elements in the promoter regions of the IbAP2/ERF genes were analysed, and we further clarified the expression patterns of these genes at different root developmental stages and under multiple forms of abiotic stress. Several storage root developmental stage-specific or abiotic stress-responsive IbAP2/ERF TFs were identified, which might be ideal candidate genes for further functional study of the corresponding biological processes and the development of high-quality and stress-tolerant sweet potatos by genetic engineering. Our study originally discovered the components, structures, evolution and expression profiles of the IbAP2/ERF superfamily, which could facilitate further functional analyses of IbAP2/ERF genes and a better understanding of the molecular mechanisms in developmental processes and stress responses in the sweet potato.

Availability of data and materials

Public datasets from SRA database (http://www.ncbi.nlm.nih.gov/sra) were used in this study. For RNA-seq data, we used root development data of sweet potato (PRJNA515432), chilling response data (PRJNA533954), drought response data (PRJNA413661) and salt response data (PRJNA350623). All of the datasets supporting the results of this article are included within the article and its additional files. The collection of sweet potato materials was permitted and complied with relevant institutional, national, and international guidelines and legislation.

Change history

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Acknowledgements

We are grateful to Dr. Luonan Chen, Dr. Chuanchao Zhang and Dr. Qianqian Shi for their constructive suggestion on data analysis. This work was partially supported by National Key R&D Program of China (2018YFD1000705). We appreciate the editor and reviewers for critically evaluating this manuscript and providing constructive comments for its improvement.

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Author notes

  1. Shutao He and Xiaomeng Hao contributed equally to this work.

Authors and Affiliations

  1. State Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, CAS Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, 200031, China

    Shutao He

  2. National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, 200032, China

    Xiaomeng Hao & Peng Zhang

  3. University of Chinese Academy of Sciences, Beijing, 100049, China

    Xiaomeng Hao

  4. Jining College Affiliated Senior High School, Jining, 272004, China

    Shuli He

  5. Tsinghua University, Beijing, 100084, China

    Xiaoge Hao

  6. Beihang University, Beijing, 100191, China

    Xiaonan Chen

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Contributions

Shutao He, Peng Zhang and Xiaonan Chen designed and conceived this project; Shutao He, Xiaomeng Hao, Xiaoge Hao and Shuli He performed the analysis and experiments; Shutao He and Xiaomeng Hao prepared the figure and drafted the manuscript; Xiaonan Chen, Xiaoge Hao and Shuli He analyzed the data and revised the manuscript with input from the other authors. All authors contributed to and approved the final manuscript.

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The original version of this article was revised: Peng Zhang was not included in the original authorship list.

Supplementary Information

Additional file 1: Table S1.

Complete list of IbAP2/ERF genes identified in the sweet potato genome. Table S2. One-to-one corresponding relationships of IbAP2/ERF genes between this study and previous report. Table S3. Analysis and distribution of conserved motifs in sweet potato IbAP2/ERF proteins. Table S4. One-to-one orthologous relationships between sweet potato and other species. Table S5. Expression profiles of IbAP2/ERF genes at different root developmental stages and under multiple types of abiotic stress. Table S6. Analysis and distribution of known motifs in sweet potato IbAP2ERF proteins. Table S7. Primer pairs used in this study.

Additional file 2: Fig. S1.

Phylogenetic relationships and conserved domains in IbAP2/ERF proteins from sweet potato.

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He, S., Hao, X., He, S. et al. Genome-wide identification, phylogeny and expression analysis of AP2/ERF transcription factors family in sweet potato. BMC Genomics 22, 748 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s12864-021-08043-w

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BMC Genomics

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