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A novel Sugarcane bacilliform virus promoter confers gene expression preferentially in the vascular bundle and storage parenchyma of the sugarcane culm

  • †1,
  • †2,
  • †2,
  • 3,
  • 1,
  • 1 and
  • 2Email author
†Contributed equally
Biotechnology for Biofuels201710:172

https://doi.org/10.1186/s13068-017-0850-9

©  The Author(s) 2017

  • Received: 9 January 2017
  • Accepted: 16 June 2017
  • Published:

Abstract

Background

Saccharum species such as sugarcane and energy cane are key players in the expanding bioeconomy for sugars, bioenergy, and production of high-value proteins. Genomic tools such as culm-regulated promoters would be of great value in terms of improving biomass characteristics through enhanced carbon metabolism for sugar accumulation and/or fiber content for biofuel feedstock. Unlike the situation in dicots, monocot promoters currently used are limited and mostly derived from highly expressed constitutive plant genes and viruses. In this study, a novel promoter region of Sugarcane bacilliform virus (SCBV; genus Badnavirus, family Caulimoviridae), SCBV21 was cloned and mapped by deletion analysis and functionally characterized transiently in monocot and dicot species and stably in sugarcane.

Results

In silico analysis of SCBV21 [1816 base pair (bp)] identified two putative promoter regions (PPR1 and PPR2) with transcription start sites (TSS1 and TSS2) and two TATA-boxes (TATAAAT and ATATAA), and several vascular-specific and regulatory elements. Deletion analysis revealed that the 710 bp region spanning PPR2 (with TSS2 and ATATAA) at the 3′ end of SCBV21 retained the full promoter activity in both dicots and monocots, as shown by transient expression of the enhanced yellow fluorescent protein (EYFP) gene. In sugarcane young leaf segments, SCBV21 directed a 1.8- and 2.4-fold higher transient EYFP expression than the common maize ubiquitin 1 (Ubi1) and Cauliflower mosaic virus 35S promoters, respectively. In transgenic sugarcane, SCBV21 conferred a preferential expression of the β-glucuronidase (GUS) gene in leaves and culms and specifically in the culm storage parenchyma surrounding the vascular bundle and in vascular phloem cells. Among the transgenic events and tissues characterized in this study, the SCBV21 promoter frequently produced higher GUS activity than the Ubi1 or 35S promoters in a manner that was not obviously correlated with the transgene copy number.

Conclusions

The newly developed plant viral SCBV21 promoter is distinct from the few existing SCBV promoters in its sequence and expression pattern. The potential of SCBV21 as a tissue-regulated promoter with a strong activity in the culm vascular bundle and its storage parenchyma makes it useful in sugarcane engineering for improved carbon metabolism, increased bioenergy production, and enhanced stress tolerance.

Keywords

  • Sugarcane bacilliform virus promoter
  • Tissue-regulated expression
  • Culm preferential expression
  • Storage parenchyma
  • Vascular bundle
  • Saccharum spp. hybrids

Background

The development of genomic tools such as promoters that differ in their ability to regulate the temporal and spatial expression patterns of transgenes constitute a major priority for the genetic improvement of major crops and the production of new products at levels useful for commercialization. The use of promoters with different expression patterns is particularly desirable to minimize the risk of transgene silencing in multigene transformation, routinely applied to achieve more complex, and ambitious phenotypes in transgenic crops [1, 2]. Unlike the situation in dicots, monocot promoters currently used are relatively few and mostly derived from highly expressed constitutive plant genes, such as the Ubiquitin (Ubi) promoters, maize Ubi1 [3], sugarcane ub4 and ub9 [4], rice RUBQ2 [5], Porteresia coarctata Ubi2.3 [6], and Erianthus arundinaceus Eriubi D7 [7]. To date, tissue-specific monocot promoters have been developed that target gene expression in leaf and root, but only few are functional in stems. This is a crucial deficit for sugarcane (Saccharum spp. hybrids), a major sugar and biomass producer accounting for about 40% of the biofuel production worldwide [8]. Promoters functional in the sugarcane culm include sugarcane dirigent and o-methyltransferase from putative defense and fiber biosynthesis-related genes [9], maize phosphoenolpyruvate carboxylase [10, 11], and sugarcane Loading Stem Gene [12].

Intergenic regions of plant pararetroviruses (family Caulimoviridae) have the potential to be used as promoters and could be exploited in the expression of transgenes in monocots or dicots. These include the various enhanced 35S promoters from the dicot-infecting DNA Cauliflower mosaic virus (CaMV) [13] or the promoters of monocot-infecting DNA viruses like Rice tungro bacilliform virus (RTBV) [14, 15], Commelina yellow mottle virus [16], Taro bacilliform virus [17], Banana streak virus (BSV) [18], and Sugarcane bacilliform virus (SCBV) [19, 20]. Viral promoters derived from monocot-infecting DNA viruses are of particular interest because they tend to confer a tissue-specific gene expression, specifically in the vascular system [14, 16–20].

SCBV (genus Badnavirus, family Caulimoviridae), serologically related to BSV, have a double-stranded DNA genome of around 7.3–7.9 kilobase pair (kb) in size, encoding three open reading frames (ORFs) whose transcription is directed by a single promoter residing between ORF3 (3′ end) and ORF1 (5′ end) [21–25]. SCBV promoters previously examined are derived from two distinct SCBV species recognized by the International Committee on Taxonomy of Viruses, Sugarcane bacilliform MO virus (SCBMOV-MOR) and Sugarcane bacilliform IM virus (SCBIMV-QLD), originating from Morocco and Australia, respectively [21, 22, 26, 27]. SCBV isolates display a high degree of variability in their nucleotide (nt) sequence [23, 24, 28, 29], and SCBV promoters confer different patterns of gene expression in various plant species [30]. The natural diversity of SCBV could be exploited to isolate additional SCBV promoters with distinct expression patterns.

Few studies have been directed towards investigating the expression pattern of SCBV promoters in sugarcane. The successful use of such promoters depends to a large extent on overcoming the ability of highly polyploid species such as sugarcane to silence transgenes [31–34]. In this study, we report the development of a novel plant viral promoter, SCBV21, isolated from a commercial sugarcane variety (CP72-1210) infected with a Texan SCBV isolate (SCBV-TX) and functionally active in sugarcane. Stable expression analyses demonstrated that SCBV21 conferred a tissue-regulated gene expression, preferentially in leaves and culms and mainly in the storage parenchyma surrounding the vascular bundle and in vascular phloem and sclerenchyma of the sugarcane culm. It is further shown that SCBV21 exhibited significantly higher levels of gene expression than the common maize Ubi1 and CaMV 35S promoters. The value of the SCBV21 promoter in functional gene analysis and in engineering high-biomass producers such as sugarcane and other monocot species for improved carbon metabolism, enhanced stress tolerance, and bioenergy production, is discussed.

Methods

Isolation and sequence analysis of the SCBV21 promoter

The intergenic region of the viral genome in the family Caulimoviridae is a potential promoter region (PPR) [27]. Hence, a set of primers, Prom-F and Prom-R (Additional file 1: Table S1) were designed from the conserved sites flanking the PPR based on multiple alignment of the nucleotide sequences of the two published SCBMOV-MOR and SCBIMV-QLD promoters and an unpublished potential SCBV promoter fragment (~2 kb) (kindly provided by Dr. Guo-Hui Zhou, South China Agricultural University). A 1816-base pair (bp) fragment containing the SCBV21 promoter was PCR amplified from leaf genomic DNA of commercial sugarcane variety CP72-1210 infected with SCBV-TX isolate, using the Prom-F and Prom-R primers. PCR was performed in a total reaction volume of 20 µL using Taq DNA polymerase (NEB BioLabs, Ipswich, MA, USA) following the manufacturer’s recommendation with the cycling conditions: one cycle at 94 °C for 4 min, 35 cycles each at 94 °C for 30 s, 52 °C for 30 s, and 72 °C for 2 min, and one cycle at 72 °C for 5 min. The nt sequence of the amplified SCBV21 (Additional file 2: Figure S1) was deposited into GenBank under accession number KY031904. The PPR and transcription start site (TSS) of SCBV21 was identified in silico with Neural Network Promoter Prediction (http://www.fruitfly.org/seq_tools/promoter.html) [35], and putative cis-acting elements were predicted by PlantCARE (http://bioinformatics.psb.ugent.be/webtools/plantcare) [36] and PLACE database for plant cis-acting regulatory DNA elements (https://sogo.dna.affrc.go.jp/cgi-bin/) [37]. Motifs for plant transcription factors (TFs) associated with phloem or xylem histogenesis were identified in SCBV21 by the plant TF database PlantTFDB version 4.0 (http://planttfdb.cbi.pku.edu.cn) [38]. Partial reverse transcriptase/ribonuclease H (RT/RNAse H) nt sequences (782 nt) from the SCBV21 promoter and corresponding regions of 12 SCBV and three BSV genomes from GenBank were aligned with the ClustalW algorithm implemented in MEGA 6.0 [39]. Nucleotide sequences of the promoter regions of SCBV21, SCBIMV-QLD, and SCBMOV-MOR were also aligned using the same algorithm. Nucleotide sequence identities were estimated by pair-wise sequence comparison using BioEdit programs [40].

Expression vectors

The amplified SCBV21 promoter was subcloned into pGEM-T Easy vector (Promega, Madison, WI, USA) as SCBV21/pGEM-T. Three EYFP expression vectors were generated with SCBV21, Pr4 [Ubi1 without heat-shock elements, a deletion of 25 bp (5′-TGGACCCCTCTCGAGAGTTCCGCTC-3′) at the 5′ end of Ubi1] and CaMV 35S promoters (Additional file 3: Figure S2). The SCBV21:EYFP/pSK vector was produced by cloning the SalΙ/NcoΙ-released SCBV21 fragment of SCBV21/pGEM-T as a transcriptional fusion with the EYFP gene in the SalΙ/NcoΙ-digested CaMV 2×35S:EYFP-NOS/pSK (pBluescript) vector [41], replacing the CaMV 2×35S promoter. The Pr4:EYFP/pSK construct was assembled by cloning the HindШ/NcoΙ-released Pr4 fragment of Pr4:GUS/pUC19 (Invitrogen, Carlsbad, CA, USA) as a transcriptional fusion with EYFP into the HindШ/NcoΙ-digested EYFP-NOS/pSK, replacing the CaMV 2×35S promoter. The 35S:EYFP-NOS/pSK vector was constructed by cloning the HindШ/BamHΙ-released CaMV 35S fragment from pBI221 (Clontech, Takara Bio USA, Inc., Mountain View, CA, USA) as a transcriptional fusion with the EYFP gene in the Ubi1:EYFP-NOS/pSK vector [41] after digestion with two sets of restriction enzymes, BamHΙ and EcoRΙ, and EcoRΙ and HindШ, replacing the Ubi1 promoter.

Three GUS expression vectors were generated with SCBV21, Ubi1, and CaMV 35S promoters. The SCBV21:GUS/pUC19 was constructed by cloning the NotΙ-released SCBV21 fragment from SCBV21/pGEM-T as a transcriptional fusion with the GUS gene to the SphΙ/XbaΙ-digested and blunt ended pBI221, replacing the CaMV 35S promoter. Ubi1:GUS/pUC19 (pAHC27) [3] and pBI221 (CaMV 35S:GUS) were used.

A series of SCBV21 deletion constructs were generated from SCBV21:EYFP-NOS/pSK, using the three restriction enzymes XhoI, NcoI, and StuI. XhoI and NcoI sites were incorporated at the 5′ end of forward (SCBV-MF1 and SCBV-MF2) and reverse (SCBV-MR1 and SCBV-MR2) primers, respectively (Additional file 1: Table S1). Deletion fragment ∆nt1014–nt1837 (deletion A) was generated by deleting the region between SutI and NcoI in SCBV21:EYFP-NOS/pSK, followed by blunt ending using the Klenow enzyme (NEB BioLabs). Deletion fragments ∆nt1–nt1010 (deletion B), ∆nt1–nt1105 (deletion C), ∆nt1–nt1010 and ∆nt1732–nt1837 (deletion D), and ∆nt1–nt1105 and ∆nt1732–nt1837 (deletion E) were PCR amplified from SCBV21:EYFP-NOS/pSK using the four sets of primers MF1/MR1, MF2/MR1, MF1/MR2, and MF2/MR2, respectively, and cloned in the blunt ended EYFP-NOS/pSK, replacing full-length SCBV21. All constructs were sequenced prior to further use to ensure integrity.

Preparation of target tissue

Transient EYFP and GUS gene expression assays were performed on sugarcane (Saccharum spp. hybrids) tissues (young leaf, top culm, and root), sweet sorghum (Sorghum vulgare) leaves, tobacco (Nicotiana benthamiana) leaves, and lima bean (Phaseolus lunatus L.) cotyledons. Sugarcane young leaf segment, leaf roll and top culm were collected from field-grown varieties CP72-1210 and CP84-1198 and prepared as previously described [34, 41]. Leaf segments and rolls were cultured on MS0.6 medium [42, 43] for 3–4 and 7–10 days in the dark before transformation, respectively. The top young shoot culms were excised approximately 1 cm thick and used immediately. Roots, collected from 3 month-old greenhouse-grown plants, were sterilized in 10% (v/v) commercial bleach for 20 min and rinsed three times with sterile water before transformation.

Young leaf segments of field-grown sweet sorghum were prepared the same way as sugarcane [34, 41] and incubated on MS0.6 medium for 3–4 days in the dark prior to transformation. N. benthamiana seeds were sterilized and germinated on MS medium for 1–2 months before seedling leaves were excised and transformed. Cotyledonary tissue from germinating lima bean seeds was prepared according to Chiera et al. [44]. Briefly, seeds were sterilized in 10% (v/v) commercial bleach for 20 min, washed three times with sterile water, and kept in Magenta GA7 containers between layers of a folded white paper towel saturated with sterile water (25 mL) for 4 days at 26 ± 1 °C under 16 h of illumination (40 µEm−2/s). The light green cotyledons were excised from the germinating seedlings prior to transformation.

Plant transformation and generation of transgenics

All tissues were incubated on MSO medium (MS0.6 with 36.44 g/L d-mannitol and 36.44 g/L d-sorbitol) prior to transformation by particle bombardment. DNA coating for bombardment was performed according to Beyene et al. [41]. Briefly, tungsten particles (1.1 µm, Bio-Rad Laboratories, Hercules, CA, USA) (1 mg) were coated separately with plasmid DNA (1.0 µg) of different constructs using calcium chloride (33.4 µL of 2.5 M) and spermidine (13.4 µL of 0.1 M). A total of 4 μL of the DNA particle suspension (0.5 µg of plasmid DNA per bombardment) was placed in the center of a syringe filter and delivered into tissue with a particle inflow gun using a 1100 psi rupture disk, 26 in. Hg vacuum and 7 cm target distance. Bombarded tissue was maintained on MS0.6 medium at 26 ± 1 °C in the dark until analysis.

For stable gene expression, Ubi1:bar (pAHC20) [3] was co-bombarded with the target construct into leaf roll discs. Following bombardment, leaf roll discs were maintained on MS0.6 medium for 7 days in the dark without selection, and then broken into small pieces and incubated on MS0.6 with Bialaphos (4 mg/L) selection for 2 weeks. Subsequently, resistant calli derived from leaf rolls were placed on MS with kinetin (2 mg/L), naphthalene acetic acid (2 mg/L), and Bialaphos (4 mg/L) for 6–8 weeks under a 16 h light/8 h dark cycle. Shoots were produced and transferred to MS rooting medium containing indole-3-butyric acid (4 mg/L) and Bialaphos (4 mg/L). After 4 weeks, rooted seedlings were transplanted into pots in the greenhouse. Screening of seedlings for presence of the selection marker Bialaphos was done by spraying with the herbicide glufosinate ammonium (11.33%) (15 mL/L). Seedlings that survived were grown in the greenhouse for 2–12 months for further analysis.

Southern blot analysis

Identification of independent transgenic lines was done by Southern blot analysis. Genomic DNA was isolated from leaves using the SDS method [45]. Genomic DNA (10 µg) was digested overnight with HindIII, separated on a 1% (w/v) agarose gel and blotted onto a nylon membrane in 0.4 M alkaline solution [46]. A GUS probe was generated from Pr4:GUS/pUC19 by BbsI/SacI digestion and labeled with [α-32P] dCTP using the Random Primers DNA Labeling kit (Invitrogen, Carlsbad, CA). Pre-hybridization, hybridization, washing, and detection of DNA gel blots were conducted as described by Sambrook et al. [47] and Mangwende et al. [48], using Church’s buffer.

Analysis of β-glucuronidase activity

Histochemical analysis of β-glucuronidase (GUS) activity was performed mainly as described by Jefferson et al. [49], using GUS buffer [0.1% (v/v) Triton X-100 and 50 mM sodium phosphate buffer, pH 7.0] with X-Gluc (5-bromo-4-chloro-3-indolyl-β-d-glucuronic acid) (1.0 mM, dissolved in DMF) and the oxidation catalysts, potassium ferricyanide, and potassium ferrocyanide (0.5 mM each, dissolved in 10 mM EDTA, pH 8.0). Stained plant tissues were photographed with a zoom stereomicroscope (Olympus SZX7, Olympus, Center Valley, PA, USA). Quantitative GUS activity was carried out using 4-methylumbelliferyl-β-d-glucuronide (Rose Scientific Ltd., Alberta, Canada) [34, 49]). Fluorescence (emission of 455 nm and excitation of 365 nm) was measured with a VersaFluor (Bio-Rad Laboratories). Protein concentrations were determined with the Bio-Rad protein assay kit.

Evaluation of EYFP expression

Images of different tissues expressing EYFP were collected at 48 h post-DNA bombardment using a stereomicroscope (Olympus SZX7, Olympus) fitted with YFPHQ filters (excitation of 490–500 nm and emission of 515–560 nm) and a DP71 digital camera (Olympus). Colored RGB images (4080 × 3072 pixels) of leaf segments were collected using the same stereomicroscope (15×). EYFP expression analysis was quantified using the ImageJ software (Rasband 1997–2009) as described by Chiera et al. [44]. The detailed protocol was provided by Gao et al. [34].

Statistical analysis

The GLM procedure of Statistical Analysis System (8.0 version, SAS Institute, USA) was used for statistical analysis. Multiple comparisons of the means were conducted by the Student–Newman–Keuls (SNK) Test. Pearson correlation analysis (SAS software) was performed on GUS activity and GUS copy number (as identified by Southern blot analysis) of the generated GUS transgenic lines.

Results

Sequence analysis of SCBV21

The 1826-bp SCBV21 amplified fragment (from SCBV-TX isolate), located at the 3′ end of the SCBV genome, consisted of partial RT/RNAse H genomic (~0.8 kb near the 5′ end) and ~1.0 kb promoter regions (Additional file 2: Figure S1). In silico analysis of SCBV21 sequence with Neural Network Promoter Prediction (NNPP, version 2.2) identified two PPRs, PPR1 (1055–1105 nt) with transcription start site TSS1 (Fig. 1a; Additional file 2: Figure S1), and PPR2 (1737–1787 nt) with transcription start site TSS2 (Fig. 1b; Additional file 2: Figure S1). Two TATA-boxes (TATAAAT and ATATAA) were observed in PPR1 and PPR2, respectively. Seven CAAT-box and one CAT-box common cis-acting elements related to enhancer elements and meristem expression [50, 51], respectively, were found in SCBV21 (Table 1).
Fig. 1
Fig. 1

Multiple nucleotide sequence alignments of SCBV21 [two potential promoter regions (PPRs)], 12 SCBV, and three BSV published isolates using DNAMAN 8.0. The sequence of isolate SCBV-TX (KY031904) was determined in this study, while sequences of isolates SCBMOV-MOR (NC_008017), SCBIMV-QLD (NC_003031), SCBV-CHN1 (KM214357), SCBV-CHN2 (KM214358), SCBV-BO91 (JN377533), SCBV-Iscam (JN377534), SCBV-BB (JN377535), SCBV-BT (JN377536), SCBV-BRU (JN377537), SCBGAV-R570 (FJ824813), SCBGAV-B51129 (FJ824814), SCBGDV-Batavia (FJ439817), BSOLV-NI (NC_003381), BSMYV-AUS (NC_006955), and BSGFV-EC (NC_007002) were obtained from the GenBank database. a, b Two PPRs of SCBV21 were identified by Neural Network Promoter Prediction (NNPP, version 2.2). The two TATA-boxes (TATAAAT and ATATAA) that were predicted by PlantCARE and PLACE databases are indicated in a red box. Nucleotides that are highlighted in black have the highest percentage identity

Table 1

Putative regulatory motifs enriched in the SCBV21 promoter

Motif name and sequencea

Occurrence and position of motifb

Function

Tissue-specific motifs

 

Expression in phloem, shoot, root, meristem

 ASL-box: CTTTA

2 (844; 1631)

Plant transcription factor motifs

 

Biological process phloem or xylem biogenesis

 Motif 1: AAAAGGGAGCAAAAGGATTAA

1 (298–318)

 Motif 2: TTGAACGATGATTAT

1 (1288–1302)

 Motif 3: ATAAAGAAGCTAAAGCTGAAT

1 (1252–1272)

 Motif 4: TGAAGAAGGATAAAGAAGCTA

1 (1243–1263)

Enhancer element motif

 

Enhancement of gene expression

 CAAT-box: CAAT

7 (909; 1075; 1201; 1475; 1511; 1540; 1558)

Meristem-regulated motif

 

Meristem-regulated gene expression

 CAT-box: CAT

1 (1087)

aMotifs were identified by PlantCARE motif sampler (http://bioinformatics.psb.ugent.be/webtools/plantcare) and PLACE for plant cis-acting regulatory DNA elements (https://sogo.dna.affrc.go.jp/cgi-bin/). Plant transcription factor motifs were identified by PlantTFDB version 4.0 (http://planttfdb.cbi.pku.edu.cn)

bThe motif position is given by the number corresponding to the SCBV21 promoter nucleotide sequence provided in Additional file 2: Figure S1

Multiple nt sequence alignment of the two PPRs of SCBV21 and those of 12 SCBV and three BSV published isolates comprising BSGFV-EC, BSMYV-AUS, and BSOLV-NI revealed that the TATAAAT sequence in PPR1 of SCBV21 was found only in SCBV-TX and SCBV-BB isolates (Fig. 1a), whereas the ATATAA sequence in PPR2 of SCBV21 was conserved among the different SCBV and BSV isolates (Fig. 1b). Since the difference (>20%) in RT/RNase H nt sequence is used as a species demarcation criterion in the Badnavirus genus [27], the pair-wise sequence comparison of the partial RT/RNase H sequences of SCBV21 and the published SCBV and BSV isolates showed that the RT/RNAse H of SCBV21 shared only 56.5–88.7 and 56.0–60.0% sequence identities with the 12 SCBV and three BSV published isolates, respectively (Additional file 4: Table S2). Sequence identities of 78.4 and 88.7% were observed between SCBV-TX and SCBMOV-MOR and SCBIMV-IM, respectively, based on the RT/RNAse H analysis (Additional file 4: Table S2). Furthermore, SCBV-TX shared only 76.4 and 61.4% nt sequence identity with the published SCBIMV-QLD and SCBMOV-MOR promoters, respectively, based on analysis of the full promoter regions (~1826 bp) (Additional file 2: Figure S1).

The SCBV21 core region is PPR2

In order to map an active promoter region within the cloned 1816-bp SCBV21 fragment, a series of deletions were made around the two putative promoter regions, PPR1 and PPR2 (Fig. 2a). Each deletion was fused to EYFP and its promoter activity was tested transiently in sugarcane young leaf segments (Fig. 2b, c). As shown in Fig. 2b, c, a deletion of 824 nt at the 3′ end of SCBV21 containing PPR1 and PPR2 (deletion A: ∆nt1014–nt1837) abolished its promoter activity. On the other hand, a deletion of 1010 nt at the 5′ end of SCBV21 (deletion B: ∆nt1–nt1010) with a longer deletion containing PPR1 at the 5′ end of deletion B (deletion C: ∆nt1–nt1105) did not affect the promoter activity. However, deletion of PPR2 located at the 3′ end of SCBV21 (deletion D: ∆nt1–nt1010 and ∆nt1732–nt1837 and deletion E: ∆nt1–nt1105 and ∆nt1732–nt1837) showed a significant decrease in EYFP expression.
Fig. 2
Fig. 2

Transient EYFP gene expression as directed by SCBV21 and its deletions in sugarcane. a Schematic map of full-length SCBV21 [1816 base pair (bp)] and its deletions. Nucleotide (nt) 1 is the first nt at the 5′ end of SCBV21. Deletions are indicated by dotted lines and their nt position of each deletion is indicated above the dotted line. The region between SCBV21 and EYFP, marked with an asterisk (*) in deletion A, is derived from the multicloning site of pGEM T-Easy vector and is removed from all deletion fragments. In deletions C and D, the guanine base (G) at nt 1816 was deleted during cloning. Three important restriction enzyme sites, XhoI, StuI, and NcoI used for deletions are marked in deletion A. The two potential promoter regions (PPR1 and PPR2) of SCBV21, which are 632 bp apart from each other, are shown with unfilled square boxes. The approximate position of primers used to generate deletions is indicated with filled arrowheads. b, c Monitoring of transient EYFP expression as directed by SCBV21 and its deletions in sugarcane young leaf segments. Representative images were collected with a stereomicroscope (Olympus SZX7, Olympus) fitted with YFPHQ filters (excitation of 490–500 nm and emission of 515–560 nm) and a DP71 digital camera (Olympus) (×15 magnification) for 48 h post-DNA bombardment (scale bar 2.0 mm). EYFP expression levels were scored as high (+++), medium (++), low (+), and none (−), based on the EYFP focus count and EYFP expression level (mean gray value × pixels)

SCBV21 directs transient EYFP gene expression in monocots and dicots

To check if SCBV21 is active in monocots and dicots, each of SCBV21:EYFP and SCBV21:GUS DNA (Additional file 3: Figure S2) was bombarded into leaf roll, stem and root of sugarcane, sweet sorghum young leaf, N. benthamiana leaf, and cotyledons of germinating seeds of lima bean. Tissue bombardment experiments demonstrated that SCBV21 directed EYFP and GUS gene expression transiently in all tested tissue types (leaves, stems, and roots) in both monocots (sugarcane and sweet sorghum) and dicots (N. benthamiana and lima bean) (Additional file 5: Figure S3).

To compare the activity of SCBV21 with that of four common promoters, CaMV 35S, CaMV 2×35S, Ubi1, and Pr4, EYFP were fused to each promoter (Additional file 3: Figure S2) and its expression was measured in sugarcane young leaf segments post-DNA bombardment (Fig. 3). The kinetics of EYFP gene expression revealed that the maximum level of expression was at 48 h post-DNA bombardment (data not shown). Based on the EYFP foci count and signal intensity as quantified with ImageJ [34], the activity of SCBV21 and CaMV 2×35S was significantly (p < 0.05) stronger than that of Ubi1, Pr4 and CaMV 35S (Fig. 3). The EYFP foci count for Ubi1, Pr4 and CaMV 35S were about 75.5, 70.2 and 66.4% of that of SCBV21, and the EYFP expression value was 54.8, 45.9 and 42.2% of that of SCBV21, respectively (Fig. 3). However, EYFP expression levels driven by SCBV21 in sugarcane leaf segments were as high as those driven by CaMV 2×35S.
Fig. 3
Fig. 3

Quantitative assessment of transient EYFP gene expression as directed by SCBV21, Ubi1, Pr4, CaMV 35S or enhanced CaMV 35S (2×35S) in sugarcane young leaf segments. Values of a EYFP focus count and b total EYFP expression level (104) (mean gray value × pixels) were collected from representative images monitored with a stereomicroscope (Olympus SZX7, Olympus) fitted with YFPHQ filters (excitation of 490–500 nm and emission of 515–560 nm) and a DP71 digital camera (Olympus) (×15 magnification) at 48 h post-DNA bombardment and calculated using ImageJ software as described in “Methods”. Values represent means with standard error from three independent experiments and nine replicates per experiment. Means with the same letter are not significantly different at p > 0.05

SCBV21 directs GUS gene expression in a tissue-regulated manner in transgenic sugarcane

Several sugarcane lines transgenic for SCBV21:GUS, Ubi1:GUS, and CaMV 35S:GUS were generated, as identified by Southern blot analysis with a range of GUS copy number of 8–14, 13–19, and 4–23, respectively (Table 2). No significant (p > 0.05) correlation between GUS activity and GUS copy number of the SCBV21:GUS, Ubi1:GUS, and 35S:GUS lines was found.
Table 2

The SCBV21 promoter drives expression of the GUS gene preferentially in the sugarcane culm and leaf

Transgenic line

GUS copy number

GUS activity (pmol of 4-methylumbelliferone/min/µg protein)a

Culm

Leaf

Root

SCBV21:GUS

8–14

2649.1 ± 41.3 (2466.3–3252.1)

1260.0 ± 201.8 (1127.9–1384.8)

165.3 ± 4.8 (126.0–233.9)

Ubi1:GUS

13–19

23.6 ± 1.5 (18.3–42.5)

46.6 ± 2.6 (31.6–57.4)

58.1 ± 9.0 (37.1–80.1)

35S:GUS

4–23

3.8 ± 0.9 (2.0–5.4)

1.3 ± 0.2 (0.4–3.0)

7.2 ± 0.3 (5.5–9.0)

Nontransformed

 

8.8 ± 0.5 (0.5–13.0)

0.5 ± 0.03 (0.05–0.1)

3.9 ± 0.1 (3.6–4.3)

aAverage GUS activity was measured in culms, leaves and roots of 1 year-old sugarcane transgenic for SCBV21:GUS. Ubi1:GUS and 35S:GUS lines were included as a positive control. The number of independent SCBV21:GUS, Ubi1:GUS and 35S:GUS transgenic lines tested were 5, 5 and 7, respectively. GUS activity represents three technical repetitions and is reported with the standard error. The range of GUS activities for each set of experiments is indicated in parentheses

Quantitative analysis indicated that GUS activity levels of SCBV21:GUS sugarcane plants were significantly higher in culms than in leaves and roots (Table 2). Increases in GUS activity of SCBV21:GUS sugarcane culms were 2.1-fold higher compared to leaves and 16.0-fold higher compared to roots. GUS activity driven by SCBV21 increased 112-fold in culm and 27.0-fold in leaf compared to that driven by Ubi1 and 697-fold in culm and 969-fold in leaf, compared to that directed by CaMV 35S (Table 2). GUS activity driven by SCBV21 was enhanced by 2.8- and 23.0-fold in root compared to that driven by Ubi1 and CaMV 35S, respectively (Table 2). SCBV21 conferred high GUS activity in sugarcane culm tissue, irrespective of different spatial positions (top, middle, and bottom) (Table 3) and no significant difference in GUS activity was detected among the SCBV21:GUS transgenics (Table 3).
Table 3

The SCBV21 promoter drives high levels of GUS gene expression in the sugarcane culm

SCBV21:GUS transgenic line

GUS activity (pmol of 4-methylumbelliferone/min/µg protein)a

Top

Middle

Bottom

5A (CP84-1198)

2648.8 ± 27.5

2535.4 ± 48.6

2466. 3 ± 59.3

3501 (CP72-1210)

2560.0 ± 49.4

2500.8 ± 40.4

2574.8 ± 34.6

3512 (CP72-1210)

2668.5 ± 13.1

2668.5 ± 9.9

2688.3 ± 58.9

3515 (CP72-1210)

2653.7 ± 39.5

2569.9 ± 74.6

3252.1 ± 42.2

35123 (CP72-1210)

2693.2 ± 21.5

2651.3 ± 65.3

2604.4 ± 34.6

Nontransformed (CP72-1210)

6.7 ± 0.5

10.4 ± 0.6

9.2 ± 0.4

aAverage GUS activity was measured in culm top, middle and bottom sections of 1-year-old sugarcane transgenic for SCBV21:GUS. The number of independent SCBV21:GUS transgenic lines tested was five (The range of copy number of GUS in these lines is 8–14). GUS activity represents six technical repetitions and is reported with the standard error

Significant GUS expression was histochemically detected in culms, especially in nodes and vascular bundles of transgenic sugarcane carrying SCBV21:GUS (Fig. 4a–c). GUS expression was also detected in leaves (Fig. 4d) and root tips (Fig. 4e).
Fig. 4
Fig. 4

The SCBV21 promoter directs GUS gene expression in a semi-constitutive manner in sugarcane. GUS activity was analyzed histochemically in transgenic sugarcane carrying SCBV21:GUS in a–c culms, d leaves and e roots. a longitudinal culm section, b culm with nodes, and c transverse culm section

SCBV21 confers GUS gene expression in the sugarcane culm vascular bundle and storage parenchyma

Histochemical GUS localization of SCBV21-driven GUS expression revealed that the SCBV21 promoter conferred vascular GUS expression in the culm (Fig. 4), associated with the phloem and sclerenchyma cells of the vascular complex and with the storage parenchymatous tissue surrounding the vascular bundle (Fig. 5a, b). In silico analysis of the SCBV21 sequence predicted the presence of the ASL-box (CTTTA repeat) [52, 53] and four motifs of plant TFs previously associated with phloem histogenesis [54, 55] (Table 1), with three located at nt 1243–1302 between PPR1 and PPR2 and one in the RT/RNAse H region (Table 1).
Fig. 5
Fig. 5

The SCBV21 promoter directs GUS gene expression in the sugarcane culm vasculature and storage parenchyma. GUS activity was analyzed histochemically in transverse sections of a, b transgenic sugarcane culms carrying SCBV21:GUS, and in c nontransformed sugarcane culms. x, xylem; px, protoxylem; mx, metaxylem; p, phloem; s, sclerenchyma; spa, storage parenchyma. Scale bar 50 μm

Discussion

We have expanded the repertoire of promoters available for use in monocots by developing a novel plant viral promoter, SCBV21, that is preferentially expressed in the culm vascular bundle and the storage parenchyma surrounding the bundle. The activity of SCBV21 in monocots and dicots was evaluated by adopting a transient gene expression assay, previously shown to be rapid, quantifiable, and reproducible for the comparative analysis of the activity of different promoters [34, 41]. Transient and stable expression analyses using SCBV21 fusions to EYFP and GUS genes (SCBV21:EYFP and SCBV21:GUS) showed that the promoter is functional in both monocots (sugarcane and sweet sorghum) and dicots (N. benthamiana and lima bean), consistent with the activity of the SCBV promoters from SCBMOV-MOR [19, 20, 30, 56] and SCBIMV-QLD species [57].

Sequence relatedness of SCBV21 to other related SCBV and BSV

Similar to other badnaviruses, SCBV are genetically diverse, and the large pool of SCBV variants present in sugarcane is probably due to the vegetative nature of propagation of the host and its long history of movement and cultivation [57]. The extensive genetic diversity of SCBV has been reported in the promoter [57], RT/RNase H [29], and full genomic [25] sequences. In this study, we cloned, mapped, and functionally characterized a novel SCBV promoter, SCBV21, in addition to two SCBV promoters previously developed from SCBIMV-QLD [57] and SCBMOV-MOR [19, 20]. SCBV21 shared low nt sequence identity with the published SCBIMV-QLD and SCBMOV-MOR promoters, respectively based on the full promoter sequence, showing that it is a distinct promoter [58]. SCBV21 is also different in its RT/RNase H region (872 nt), a common taxonomic marker for species demarcation in the family Caulimoviridae [27], since it shared only 56.5–88.7 and 56.0–60.0% nt sequence identity with 12 other SCBV and three BSV published isolates. Furthermore, the SCBV21 sequence in the genomic intergenic region (a PPR), particularly in the first TATA-box motif showed more divergence than that of the other SCBV and BSV isolates.

Regulatory region of SCBV21

Common core promoter sequences usually contain an initiator and a TATA-box as well as specific cis-acting regulatory elements interacting with various enhancers or TFs [2]. Our deletion analysis revealed that the 710-nt region containing PPR2 [with TSS2 and TATA-box (ATATAA)] at the 3′ end of SCBV21 retained the full promoter activity, suggesting that the RT/RNase H coding region and putative PPR1 [with TSS1 and TATA-box (TATAAAT)] may not be required for SCBV21 activity. Similarly, previous studies have reported that RT/RNase H was not influenced by important promoter motifs, such as those identified in the SCBMOV-MOR or SCBIMV-QLD promoters [19, 57]. However, SCBMOV-MOR-derived promoters ScBV-1 and ScBV-2, which lacked the TATA-box sequence at PPR2 conferred a decreased GUS expression level [19]. Furthermore, deletion of the 5′ end of ScBV-3 promoter did not affect GUS expression until it was close to the 254 bp upstream of the TATA-box at PPR2 [59]. The SCBV839 promoter, derived from SCBIMV-QLD and containing 770 bp upstream of transcript start site (T) conferred a higher GUS activity than SCBV576 (containing 507 bp prior to T) and SCBV333 (containing 264 bp prior to T), indicating that putative enhancer sequences are present in the region prior to the TSS [60]. Alternatively, SCBV537 or SCBV282, which contained putative enhancer sequences with no PPR2, increased GUS activity when fused with the truncated maize alcohol dehydrogenase 1 promoter [60]. These results demonstrate that PPR2 is critical for promoter activity, and some enhancer sequences upstream PPR2 are potential regulatory elements. Alignment of PPR2 sequence of SCBV21 with those of 12 SCBV and 3 BSV published isolates revealed that the TATA-box (ATATAA) motif has conserved cis-acting elements.

Semi-constitutive gene expression

Histochemical localization of GUS expression in situ and quantitative assessment of GUS activity in transgenic sugarcane provides evidence for a higher activity of SCBV21 in the culm than the leaf and root. The SCBV21 promoter is different in its semi-constitutive expression pattern from the two previously developed SCBV promoters. For instance, the SCBMOV-MOR promoter was shown to confer high levels of constitutive GUS expression in vegetative and reproductive tissues of both monocots (sugarcane, banana, oat, barley, and wheat) and dicots (Arabidopsis and tobacco) [18–20]. However, differences in SCBMOV-MOR promoter specificity were detected among species and tissues, i.e., stronger GUS activity in most tissues of oat and barley than in wheat [30]; and mainly vascular GUS activity in root of banana but constitutive in tobacco [20]. The SCBIMV-QLD promoter was reported to be the strongest in driving reporter gene expression in the leaves, meristems, and roots of glasshouse-grown sugarcane [57]. The SCBV21 promoter shares more nt sequence homology with the SCBIMV-QLD promoter and, similarly, it is active in leaves and roots and contains several putative meristem-regulated motifs (CAT-box) and enhancer elements (CAAT-box) [50, 51]. However, the activity of SCBV21 in these tissues is stronger than that of the SCBIMV-QLD promoter, which conferred equal to or non-significantly higher expression levels of the neomycin phosphotransferase II gene than those measured for Ubi1 in sugarcane [57].

Preferential gene expression in the culm vascular bundle and storage parenchyma

The vascular-regulated GUS expression pattern of SCBV21 is similar to the one displayed by other badnavirus-derived promoters [14, 16–20]. Some badnaviruses are limited to the vascular tissue like RTBV that replicates only in phloem cells of its host and its promoter drives a strong phloem-specific gene expression [14]. However, other badnaviruses like SCBV, infecting economically important species in the Poaceae family, are not phloem-limited [19]; for instance, the expression profile of the SCBV21 promoter in the vascular bundle, including the phloem cells and the storage parenchyma provides evidence for a more widespread vascular expression than that of RTBV. In addition, SCBV21 displays a significant strong activity in the culm storage parenchyma, not reported for the existing SCBV promoters from SCBIMV-QLD and SCBMOV-MOR species.

The vascular-regulated activity of SCBV21 in the culm correlates with the presence of vascular tissue-specific regulatory motifs in its sequence. These motifs include the ASL-box (CTTTA repeat), present in phloem-specific promoters [52, 53] as well as four motifs of plant TFs associated with biological process of phloem histogenesis [54, 55], with three harbored in the PPR1 and PPR2 region. Phloem-regulated expression can be beneficial in imposing a decreased metabolic load on the plant by incorporation of additional phloem-derived cells to ensure proper transport of organic nutrients to cells involved in the reinforcement of the plant axis to counteract the increased weight of the growing plant [61].

The significant SCBV21-driven expression in the storage parenchyma of the vascular bundle of the culm is of major importance to the economic value of crops like sugarcane, energy cane, and other high biomass and fiber producers. The economic yield of sugarcane is determined by accumulation of sucrose in the culm, and the sucrose and hexoses are taken up by the storage parenchyma cells [62]. Under conditions favoring sucrose accumulation, the storage parenchyma tissue of sugarcane can store sucrose up to the maximum value of 62% dry weight or 27% fresh weight in theory [62, 63]. SCBV21 could be advantageous in manipulating certain aspects of sucrose transport and fiber synthesis, and the spatial separation or partitioning between sucrose accumulation and cell wall fiber synthesis. In particular, the GUS expression pattern of SCBV21 is similar to the green fluorescent protein expression pattern displayed by the promoter of the cell wall synthesis gene ShCesA7 in the storage parenchyma of the maturing culm internode of sugarcane [64]. The use of SCBV21 in co-targeting an elevated expression of primary cell wall synthesis genes (ShCesA1, ShCesA7, ShCesA9 and Shbk2l3) and sugar transporter genes (ShPST2a, ShPST2b, and ShSUT4) [64] in the storage parenchyma would maximize sucrose production and biomass accumulation.

The vascular-regulated expression may be also exploited to develop virus-resistant lines by fusing antiviral constructs to SCBV21 to control monocot viruses that multiply and translocate in the vascular tissue [65], or to improve plant tolerance to important pests such as the neonate sugarcane borer (Diatraea saccharalis F.) larvae by driving the expression of the Bacillus thuringiensis δ-endotoxin [66]. SCBV21 is also potentially useful in other sugarcane biotechnology applications, such as in enhancing the expression of high-value recombinant proteins in the culm of high biomass producers like sugarcane and energy cane [67].

Conclusions

In this study, a novel plant viral promoter, SCBV21 (1816 bp) was PCR amplified from the genomic DNA of a commercial sugarcane variety infected with a Texan SCBV isolate, with the aim to expand the repertoire of promoters available for use in monocots such as sugarcane, a major sucrose accumulator and biomass producer. Deletion analysis of SCBV21 revealed that the 710-nt region containing PPR2 [with TSS2 and TATA-box (ATATAA)] at its 3′ end retained the full promoter activity, suggesting that the RT/RNase H region and putative PPR1 may not be required for SCBV21 activity. Stable expression analyses demonstrated that SCBV21 conferred a preferential GUS gene expression in the storage parenchyma surrounding the vascular bundle and in vascular phloem and sclerenchyma of the sugarcane culm. It is further shown that SCBV21 exhibited significantly higher levels of GUS gene expression than the common maize Ubi1 and CaMV 35S promoters. The novel SCBV21 promoter expression pattern is distinct from that of the few existing SCBV promoters in its strong activity in the culm vascular bundle and its storage parenchyma, making it valuable for metabolic engineering to improve plant biomass characteristics through enhanced carbon metabolism for sugar accumulation or increased fiber content for biofuel feedstock.

Notes

Abbreviations

BSV: 

Banana streak virus

CaMV: 

Cauliflower mosaic virus

DMF: 

N,N-dimethylformamide

EDTA: 

ethylenediaminetetraacetic acid

EYFP: 

enhanced yellow fluorescent protein

GUS: 

β-glucuronidase

NOS: 

Agrobacterium tumefaciens nopaline synthase

MS: 

Murashige and Skoog medium

pSK: 

pBluescript

RT/RNase H: 

reverse transcriptase/ribonuclease H

PPR: 

potential promoter region

RTBV: 

Rice tungro bacilliform virus

SCBIMV-QLD: 

Sugarcane bacilliform IM virus-Queensland

SCBMOV-MOR: 

Sugarcane bacilliform MO virus-Morocco

TF: 

transcription factor

TSS: 

transcription start site

Ubi1: 

maize ubiquitin 1

X-Gluc: 

5-bromo-4-chloro-3-indolyl-β-d-glucuronic acid

Declarations

Authors’ contributions

SJG, MBD, and JWP performed most of the experiments, acquisition and interpretation of data, and crafting and critical revision of the manuscript. XBW and SRS were involved in carrying out part of the experimental study and data analysis. RKC participated in critical revision of the manuscript. TEM acted as a coordinator of the project, designed this study, analyzed experimental data, drafted, and revised the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We gratefully acknowledge Denise Rossi, Soledad Al-Varez and Hyun Park Kang for excellent technical assistance. We sincerely thank Dr. Guo-Hui Zhou (South China Agricultural University) for kindly providing the Prom-F and Prom-R primers and Dr. Xiaofeng Wang (Virginia Tech University) for his constructive suggestions in manuscript preparation.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The datasets supporting the conclusions of this manuscript are included within the article and its additional files.

Funding

This study was funded in part by an Earmark Fund from the China Agriculture Research System (CARS-20-2-4) and the Major Science and Technology Project of Fujian Province (No. 2015NZ0002-2) in China.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
National Engineering Research Center for Sugarcane, Fujian Agriculture and Forestry University, Fuzhou, 350002, Fujian, China
(2)
Texas A&M AgriLife Research, Weslaco, TX 78596, USA
(3)
Guangdong Key Lab of Sugarcane Improvement & Biorefinery, Guangzhou Sugarcane Industry Research Institute, Guangzhou, 510316, Guangdong, China

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