- Original article
- Open Access
Whole plastid transcriptomes reveal abundant RNA editing sites and differential editing status in Phalaenopsis aphrodite subsp. formosana
Botanical Studies volume 58, Article number: 38 (2017)
RNA editing is a process of post-transcriptional level of gene regulation by nucleotide modification. Previously, the chloroplast DNA of Taiwan endemic moth orchid, P. aphrodite subsp. formosana was determined, and 44 RNA editing sites were identified from 24 plastid protein-coding transcripts of leaf tissue via RT-PCR and then conventional Sanger sequencing. However, the RNA editing status of whole-plastid transcripts in leaf and other distinct tissue types in moth orchids has not been addressed. To sensitively and extensively examine the plastid RNA editing status of moth orchid, RNA-Seq was used to investigate the editing status of whole-plastid transcripts from leaf and floral tissues by mapping the sequence reads to the corresponding cpDNA template. With the threshold of at least 5% C-to-U or U-to-C conversion events observed in sequence reads considered as RNA editing sites.
In total, 137 edits with 126 C-to-U and 11 U-to-C conversions, including 93 newly discovered edits, were identified in plastid transcripts, representing an average of 0.09% of the nucleotides examined in moth orchid. Overall, 110 and 106 edits were present in leaf and floral tissues, respectively, with 79 edits in common. As well, 79 edits were involved in protein-coding transcripts, and the 58 nucleotide conversions caused the non-synonymous substitution. At least 32 edits showed significant (≧20%) differential editing between leaf and floral tissues. Finally, RNA editing in trnM is required for the formation of a standard clover-leaf structure.
We identified 137 edits in plastid transcripts of moth orchid, the highest number reported so far in monocots. The consequence of RNA editing in protein-coding transcripts mainly cause the amino acid change and tend to increase the hydrophobicity as well as conservation among plant phylogeny. RNA editing occurred in non-protein-coding transcripts such as tRNA, introns and untranslated regulatory regions could affect the formation and stability of secondary structure, which might play an important role in the regulation of gene expression. Furthermore, some unidentified tissue-specific factors might be required for regulating RNA editing in moth orchid.
RNA editing represents a process of post-transcriptional level of gene regulation by modification of the nucleotide sequence. Two distinct types of RNA editing are identified: insertion/deletion and conversion/substitution. In plant organelles, most of the RNA editing causes C-to-U and rarely U-to-C conversions. The consequence of RNA editing occurring at first or second codon positions can increase proteomic diversity but usually leads to the conservation of amino acid sequences among plant phylogeny. Some RNA editing events could result in the creation of translation initiation or termination codons or repair internal stop codons (Bock 2000; Fiebig et al. 2004; Wolf et al. 2004). Several events occurring in non-coding regions such as tRNA, 5′/3′ untranslated regulatory regions (UTR) or introns might affect RNA stability or splicing by modifying the secondary structure (Drescher et al. 2002; Farre et al. 2012; Zeng et al. 2007). The significance of RNA editing in regulating plant organellar gene expression has been demonstrated, with the alteration of some editing sites having deleteriously effects on plant growth, development, and fertility (Hammani and Giege 2014).
The current model for plant organellar RNA editing requires at least three components: the cis-acting elements recognized by trans-acting factors, subsequently recruiting the editing enzyme to catalyze the nucleotide conversion (Takenaka et al. 2012). The cis-elements include approximately 20–40 nucleotides (−30/+10) spanning the editing site, and the upstream 20 nucleotides are more important than downstream nucleotides (Bock 2000; Hammani and Giege 2014; Hirose and Sugiura 2001; Yagi et al. 2013); however, the cis-elements surrounding organellar editing sites are not generally conserved. The site-specific cis-elements are recognized by an editosome that consists of at least four nuclear-encoded protein factors (Sun et al. 2016). The pentatricopeptide repeat (PPR) protein is a large family with more than 400 members in most species of land plants (Barkan and Small 2014). The CRR4 protein, required for site-specific editing at the initiation codon of chloroplast ndhD transcripts, was the first identified PPR protein in Arabidopsis (Kotera et al. 2005). In addition, another group of small family proteins, multiple organellar RNA editing factors or RNA editing-interacting proteins (MORF/RIP), is required for plant organelle RNA editing (Bentolila et al. 2012, 2013; Takenaka et al. 2012, 2013, 2014). The MORF/RIP proteins could interact with PPR proteins and might serve as a bridge to connect PPR proteins and editing enzymes, but the actual function is not clear (Bentolila et al. 2012; Takenaka et al. 2013). Furthermore, a zinc finger protein, organelle zinc finger 1 (OZ1), directly interacts with organelle RNA recognition motif-containing protein 1 (ORRM1), which in turn could bind to RIPs, is also required for some C targets (Sun et al. 2013, 2015). The editing enzyme responsible for deamination or amination remains unidentified. Because of a highly conserved motif resembling the zinc-binding active site of nucleotide deaminases and essential for editing, the DYW motif of PPR protein was hypothesized to be responsible for the catalytic reaction but is still debated (Boussardon et al. 2014; Takenaka et al. 2014; Yagi et al. 2013; Wagoner et al. 2015).
The organellar RNA editing sites have been investigated in more than a dozen plant species by traditional Sanger methods, through sequencing cDNA and comparing with corresponding genomic DNA. In plastids of seed plants, the number of editing sites is relatively constant, 21 to 44 which account for less than 0.07% of genome (Sasaki et al. 2003, 2006; Zeng et al. 2007), and mostly occur in protein-coding transcripts. However, the number of mitochondrial editing sites is abundant, from 189 to 635, but varies among species (Grimes et al. 2014; Picardi et al. 2010; Sloan et al. 2010). The editing efficiency of plastid transcripts varies among ecotypes, tissue types, developmental stages and environmental factors (Bentolila et al. 2005; Tseng et al. 2013). Recently, by applying next-generation sequencing (NGS), organellar RNA editing sites have been identified more rapidly and economically and have been extensively examined at the whole transcriptome level (Bentolila et al. 2013; Grimes et al. 2014; Picardi et al. 2010). Besides the fast and large-scale detection of RNA editing sites, NGS technology has provided depth of coverage (DOC) per reference nucleotide and qualities of base call. It could overcome the existing limitations of standard Sanger methodology to sensitively revealing previously undiscovered tissue-specific or low-level partial editing sites. For instance, NGS revealed many new editing sites in the mitochondria of Arabidopsis and tobacco from leaf and/or floral tissues (Bentolila et al. 2013; Grimes et al. 2014; Picardi et al. 2010). In addition, re-addressing RNA editing status in the leaf chloroplasts of Arabidopsis and pnp mutant by NGS revealed several novel editing sites (Bentolila et al. 2013; Ruwe et al. 2013).
The Orchidaceae family contains approximately 25,000 species and represents one of the most diverse families in flowering plants (Dressler 2005). The Phalaenopsis (moth orchids) genus comprises approximately 66 endemic species (Christenson 2001; Lin et al. 2016). Moth orchids are among the top-traded blooming potted plants in the world, with more than 32,000 hybrids bred and registered in the Royal Horticultural Society (Lin et al. 2015a, b; Liu et al. 2016). The chloroplast DNAs (cpDNAs) of two endemic moth orchids, P. aphrodite subsp. formosana and P. equestris, have been determined (Chang et al. 2006; Jheng et al. 2012); 44 plastid RNA editing sites were identified from 24 protein-coding transcripts of leaf tissues in P. aphrodite subsp. formosana by conventional Sanger sequencing (Zeng et al. 2007); and 43 editing sites were bioinformatically predicted in P. equestris (Jheng et al. 2012). However, the RNA editing status of whole-plastid transcripts in leaf and other distinct tissue types in moth orchids has not been addressed.
In this study, we used NGS for transcriptome analysis to extensively study the RNA editing status in whole-plastid transcripts from leaf and floral tissues of P. aphrodite subsp. formosana. Our results revealed 93 new plastid edits and significantly differential editing status between the two tissue types.
Plant material and RNA extraction
The seedlings of 1.5-year-old P. aphrodite subsp. formosana cultivar TS97 were purchased from TaiSugar Corporation (Tainan, Taiwan). Approximately 50–100 g tissues from leaves or flowers was used to isolate plastids as described (Hrubec et al. 1985; Schwitzguebel and Siegenthaler 1984) with slight modification. Plastid-enriched RNA was extracted with Trizol reagent (Omic Bio, Taiwan). To eliminate DNA contamination, RNA samples were treated with DNase by use of the RapidOut DNA removal kit (Thermo, USA). The RNA quality was checked by PCR and RT-PCR before RNA-sequencing (RNA-Seq).
Plastid-enriched RNA from leaf and floral tissues underwent NGS with Ion Proton and Illumina Hiseq 2000 platforms, respectively (Yourgene Bioscience, Taiwan). In brief, ribosomal RNA was depleted from total RNA by using RiboMinus™ eukaryote kit (Life technologies, USA), and subsequently RNA was fragmented using RNase III. The fragmented RNA was then hybridized and ligated with adaptor mixture. Subsequently, the reverse transcription was performed. The cDNA was amplified using Platinum PCR SuperMix High Fidelity reaction mix, and then the library was sequenced. In total, two independent libraries from leaf and one from floral tissue were constructed and sequenced (Additional file 1: Table S1). Short-sequenced reads were trimmed with a minimal of 35-bp read and error probability <0.05. Approximately 49,722,976 reads with average 114.9 bp and 29,726,302 reads with average 111.7 bp were obtained from two independent libraries of leaf tissues, respectively, and 21,207,630 reads with average 95.8 bp in length were obtained from floral tissues (Additional file 1: Table S1). The raw sequence reads data were submitted to the Sequence Read Archive (http://trace.ncbi.nlm.nih.gov/Traces/sra/) with BioSample Accession Numbers SRR4996537, SRR4098109 and SRR4098702.
Determination of RNA editing sites and gene expression profile
Transcriptome analysis involved use of CLC Genomic Workbench 7.5.1 (CLC Bio, Aarhus, Denmark) as described with modification (Suzuki et al. 2013). In brief, quality control was adjusted with the mapping parameters of length fraction 0.98 and similarity 0.98 to eliminate undesirable fragment reads. The sequence reads were mapped to the cpDNA (Accession AY916449) template of P. aphrodite (Chang et al. 2006). The low frequency variant detection parameters were set to 5% for required significance, and the minimum coverage, minimum count and minimum frequency was set to 10, 2, and 5% respectively. Then, the position of RNA editing sites, total read counts and coverage depth were identified. The level of nucleotide conversion for each site was calculated according to the number of reads with nucleotide conversion divided by number of total reads, and frequency >5% of C-to-U or U-to-C conversions at specific nucleotide positions was defined as an RNA editing site as described in Wang et al. (2015). In addition, we manually inspect for the edits located in the regions of homopolymer runs of more than five to eliminate potentially cause by sequencing errors. Reads per kilobase of exon model per million mapped reads (RPKM) values was measured to estimate the gene expression profile as described (Mortazavi et al. 2008). To compare and validate the obtained RNA editing sites from flower tissue, we alternatively conducted a bioinformatic analysis using RES-scanner (Wang et al. 2016). In brief, the quality of RNA-seq reads from flower tissue was checked, and then trimmed using Trimmomatic (Bolger et al. 2014) version 0.33 with the following parameters: CROP:90 HEADCROP:10 LEADING:30 TRAILING:30 SLIDINGWINDOW:4:20 MINLEN:50. Subsequently, the RNA-seq reads were mapped to the reference cpDNA using RES-scanner (Wang et al. 2016) with the parameters of Phred-scaled base quality score cutoff 30 and mapping quality score cutoff 39. The RNA editing sites were filtered, and then defined the same as described above.
Prediction of RNA structure
The tRNA structure was predicted by tRNA-scanning (Schattner et al. 2005). The secondary structure of non-coding transcripts of 100 nt in length with 50 nt extending from both upstream and downstream of indicated editing sites were predicted by using CLC Genomic Workbench 7.5.1.
Plastid RNA edits in moth orchid
Previously, 44 RNA edits were identified from plastid protein-coding transcripts of leaf tissues in P. aphrodite subsp. formosana via RT-PCR and then conventional Sanger sequencing (Zeng et al. 2007). To sensitively and extensively examine the plastid RNA editing status of moth orchid, RNA-Seq was used to investigate the editing status of whole-plastid transcripts from leaf and floral tissues by mapping the sequence reads to the corresponding cpDNA in P. aphrodite subsp. formosana. Two independent libraries from leaf and one from floral tissue were sequenced (Additional file 1: Table S1). We mapped 805,063 (leaf-1), 1,751,673 reads (leaf-2) and 7,177,146 reads (flower) to the chloroplast DNA, which account for 1.5, 5.9 and 33% of total reads, respectively. The average genomic coverage is 591 (leaf-1), 1174 (leaf-2) and 4645 (flower) folds, respectively (Additional file 1: Table S1). The NGS libraries with genome coverage more than 1000 folds were further used for RNA editing analysis. With the threshold of at least 5% C-to-U or U-to-C conversion events observed in sequence reads considered as RNA editing sites, 137 RNA edits with 126 C-to-U and 11 U-to-C conversions, which include 93 newly discovered edits, were identified in plastid transcripts, representing an average of 0.09% of the nucleotides examined in moth orchid (Table 1; Additional file 1: Table S2). Overall, 110 and 106 edits were present in leaf and floral tissue, respectively; 79 edits, including 44 previously identified edits (Zeng et al. 2007), were commonly present in both leaf and floral tissues, whereas 31 and 27 edits were specific to leaf or floral tissues, respectively (Table 1). According to the edited proportion of each nucleotide in sequence reads with a C-to-U or U-to-C conversion after mapping to the corresponding DNA template over the total reads in that nucleotide position, the efficiency of RNA editing for each edit was further classified into five groups. Full editing was defined as >90% efficiency, high partial editing 60–90% efficiency, medium partial editing 40–60% efficiency, low partial editing 20–40% efficiency, and poor partial editing 5–20% efficiency. Overall, 10 (9.1%) and 18 (17%) fully edited sites were present in leaf and floral tissue, respectively; 26 (23.6%) and 30 (28.3%) high partially edited sites; 15 (13.6%) and 11 (10.4%) medium partially edited sites; 14 (12.7%) and 6 (5.7%) low partially edited sites; and 45 (40.9%) and 41 (39.6%) poor partially edited sites (Additional file 1: Figure S1, Table S2).
RNA editing in protein-coding transcripts
In total, 42 protein-coding transcripts were responsible for 79 edits, and 67 and 69 edits were present in leaf and floral tissues, respectively, with 57 edits in common (Table 1). In particular, the psbN and petL transcripts had the highest density of RNA editing sites in both tissues, with more than 1.5% of nucleotides having various levels of RNA editing. In contrast, ycf1, rpoC2 and psaB transcripts had the lowest density (Additional file 1: Figure S2). However, 17 edits including two newly identified sites (rpoB-55; rpoC1-1638) from the rpo transcripts showed the highest number among functional gene categories, and three edits (rpoB-55, rpoC1-203, rpoC1-1638) were unique to moth orchids as compared with 17 other species of seed plants (Additional file 1: Tables S2 and S3). Among the 79 edits that involved codons, 12 (15%) were in the first position and 55 (70%) in the second position, which resulted in 12 (15%) synonymous substitutions and 67 (85%) nonsynonymous substitutions (Table 1 and Additional file 1: Figure S3A, B). This result is consistent with previous reports regarding genome-wide RNA editing across widely divergent taxa, showing a bias in favor of second codon-position edits (Zeng et al. 2007). The most frequently edited codon was Ser converted to Leu (28%), followed by Ser to Phe (18%), and Pro to Leu (15%) resulting from nonsynonymous substitution (Additional file 1: Figure S3C). In addition, the consequence of amino acid substitution results in the increase of hydrophobicity (Additional file 1: Figure S3D).
Seven edits in six protein coding transcripts having relatively high editing efficiency (>40%) were previous unidentified in moth orchid (Additional file 1: Table S2). Two edits, petL-56 and rps12-221 are in high editing level (>83%) both in leaf and floral tissues. Editing of the corresponding orchid petL-56 causing the conversion of Ser to Leu was not reported in other eight plant species which they encode Pro or Ser in the genome except rice and cycas already coding for Leu (Fig. 1a). The orchid rps12-221 (S → L) edit also occurred in Amborella (Hein et al. 2016), and the consequence of nucleotide substitution increase the amino acid conservation among plant species (Fig. 1b). Three edits psbN-29, psbN-30 and ccsA-336 are in medium editing level (45–54%) in leaf, but poor (8–9%) in flower. Editing of psbN-29 and psbN-30 (S → F) in moth orchid tend to increase the amino acid conservation with tobacco and Arabidopsis, and ccsA-336 (F → F) is a silent edit (Fig. 1c, d). In contrast, petG-56 and rps3-583 are in high editing level (64–72%) in flower, but relatively low (30–35%) in leaf. Editing of petG-56 (T → I) result in the increase of amino acid hydrophobicity in moth orchid, and the corresponding site encoding Ala was not edited for other eight species of seed plant (Fig. 1e). In contrast, the editing of rps3-583 (H → Y) in moth orchid tends to increase the amino acid conservation among plants except coconut and cycas (Fig. 1f).
One medium (42%) or high partial editing (71%) was involved in the creation of the rpl2 start codon in leaf and floral tissue, respectively. In contrast, six C-to-U conversions could result in stop codons (Table 1), but their conversion efficiency was poor (Additional file 1: Table S2). For instance, the C-to-U conversion of ndhE-106 and rpl20-40 resulted in stop codons, but the editing efficiency was poor (5–20%) in both leaf and floral tissues. In addition, ccsA-652 and ycf2-3868 showed poor partial editing (11–16%) in leaf and much less editing level (0–3%) in floral tissue. In contrast, ndhB-106, rpoB-55 and ycf4-163 showed poor partial editing (5–10%) for the creation of a stop codon in floral tissue, but the level was much less in leaf (1–4%).
RNA editing status in transcripts of two long conserved open reading frames, ycf1 and ycf2, have not been investigated in moth orchid. We found one edit and six edits for ycf1 and ycf2 transcripts, respectively (Additional file 1: Table S2), but the editing efficiency was poor (5–23%) in both leaf and floral tissues. Ndh genes, encoding the subunits of NADH dehydrogenase complex, have various degrees of nucleotide insertion/deletion and were non-functional pseudogenes in moth orchids (Chang et al. 2006; Jheng et al. 2012). Previously, only one edit was found in the ndhB transcripts (1977) (Zeng et al. 2007). In this study, four more edits (ndhB-106, ndhD-528, ndhD-740 and ndhE-106) were discovered in ndh transcripts. The editing level of ndhB-1977 was medium (~57%) in both leaf and floral tissues but the editing efficiency of other four newly identified sites was poor (5–17%).
RNA editing in non-protein coding transcripts
The plastid RNA editing status of tRNA, rRNA and non-coding transcripts was previously unexplored in moth orchid, with the exception of one edit reported in the 5′UTR of psbH transcripts (Zeng et al. 2007). In this study, we identified 59 edits with 22 common edits present in non-protein-coding transcripts of moth orchid; 21 and 16 edits were specific to leaf and floral tissues, respectively (Table 1; Additional file 1: Table S2). Among them, one common edit was found in tRNA, seven (four in leaf and five in floral tissue, two in common) in introns, and 51 (38 in leaf and 32 in floral tissue, 19 in common) in intergenic spacer (IGS) or untranslated regions (UTRs), but no edit was found in rRNA. Previously, chloroplast protein-coding transcripts including moth orchid showed a nearest-neighbor bias towards a U_A context immediately before and after RNA editing sites (Zeng et al. 2007). However, the condition surrounding edits in non-protein-coding transcripts have not been analyzed. In this study, we found a similar U_A context bias surrounding plastid edits in both protein-coding and non–protein-coding transcripts in moth orchid (Additional file 1: Figure S4).
Both leaf and floral tissue showed high efficiency editing (>63%) at 52,826 genomic position in trnM (cau) transcripts. The consequence of this C-to-U conversion in trnM (cau) of moth orchid resulted in increased nucleotide conservation among plant phylogeny (Fig. 2a). In addition, after being edited, despite no difference in free energy change (ΔG), the clover-leaf structure was restored as predicted by tRNAscan-SE 1.21 (Fig. 2b), which implied the functional importance of RNA editing for the trnM. Furthermore, we found relatively high-level editing (>48%) in the rps12 intron (100,611) and ycf3 intron (44,389; 45,108) (Additional file 1: Table S2). To determine whether the C-to-U conversion in these precursor transcripts affected the RNA secondary structure, the sequence extending 50 nt to both upstream and downstream of the edit in its edited and unedited form was analyzed. The secondary structures and free energy of these two transcripts, rps12 intron (100,611) and ycf3 intron (45,108) did not change before and after editing (Additional file 1: Figure S5A, B). In contrast, the secondary structure of ycf3 intron (44,389) transcript was energetically more stable after editing (Additional file 1: Figure S5C).
Previously, the edit of the psbT-psbH (76,156 position) IGS, which also located in the 5′UTR of psbH (−30 position), resulted in the formation of an energetically less stable secondary structure (Zeng et al. 2007). We found very high efficiency editing (>82%) for this psbH 5′UTR edit in both leaf and floral tissues. In addition, at least a 50% editing level was found in the following seven IGS edits clpP-rpl20 (70,142), psaI-ycf4 (60,764), psbB-psbT (75,495), psbM-rpoB (27,736), rps16-matK (3095), trnD-psbM (31,129), and trnN-rps12 (130,345) (Additional file 1: Table S2), which most of them might locate in the 5′ or 3′ UTRs and play an important role in regulation of gene expression. To determine whether the nucleotide substitution in these transcripts affected the RNA secondary structure, the sequence extending 50 nt to each side of the edit was predicted in its edited and unedited form. The secondary structure was energetically less stable in edited than non-edited transcripts of psaI-ycf4 (60,764) and rps16-matK (3095). In contrast, the secondary structure was energetically more stable in edited than non-edited forms of clpP-rpl20 (70,142), psbM-rpoB (27,736) as well as trnD-psbM (31,129) transcripts, but with no significant difference in edited and non-edited forms of the psbB-psbT (75,495) and trnN-rps12 (130,345) transcripts were observed (Additional file 1: Figure S5D–J).
Differential status of RNA editing
Among 137 edits, we found significantly differential efficiency (>20%) of RNA editing for at least 32 edits between leaf and floral tissue, with 10 edits upregulated and 22 edits downregulated in comparing leaf and floral tissues (Fig. 3; Additional file 1: Table S2). Among 79 edits in protein-coding transcripts, 4 edits were significantly upregulated from 20 to 46%, and 17 edits were significantly downregulated, from 20 to 72% in comparing leaf and floral tissues (Fig. 3; Additional file 1: Table S2). In particular, two edits (psbN-29, 30) in psbN transcripts were upregulated to more than 42%, and the ccsA-336 edit was upregulated by 36%. In contrast, rpoB-614, rpoB-629, rpoB-686, atpF-92 and rpoC1-638 were downregulated by 72, 68, 66, 63 and 58%, respectively, in comparing leaf and floral tissues. These results suggested the involvements of unidentified tissue-specific factors in editing of protein-coding transcripts in moth orchid.
The trnM (52,826) is the only edit occurred in tRNA transcripts, which it is high partial editing (64%) in floral tissue and was upregulated 29% to nearly fully edited in leaf tissue (Fig. 3; Additional file 1: Table S2). Among 7 edits in introns, one edit at ycf3 intron (44,389) showed significant differential editing up to 43% between the two tissue types (Fig. 3; Additional file 1: Table S2). Among 51 edits in IGS, 9 differential (>20%) edits were identified: 5 edits were significantly upregulated from 20 to 71%, and 4 edits were significantly downregulated from 20 to 40% in comparing leaf and floral tissues (Fig. 3; Additional file 1: Table S2). For example, the efficiency of C-to-U conversion in the IGSs of trnT-psbD (33,566) and trnN-rps12 (130,345) was upregulated to 33, and 71%, respectively, in comparing leaf and floral tissues, with the editing barely detectable in floral tissue. In contrast, the C-to-U conversion efficiency in the IGSs of ndhJ-trnT (49,716) and rbcL-accD (57,773) was downregulated by 40 and 37%, respectively, in comparing leaf and floral tissues. Meanwhile, the former edit were specific for floral tissue. Those analyses suggested the involvements of unknown tissue-specific factors in editing of none-protein-coding transcripts in moth orchid.
Expression profile of plastid protein-coding genes in moth orchids
RNA-Seq was used to investigate the relative steady-state expression of 68 plastid protein-coding genes from leaf and floral tissues of moth orchid by RPKM analysis. In both leaf and floral tissues, photosynthesis-related genes were most highly expressed. For instance, four genes (psbA, rbcL, psaC and petB) were the most highly expressed, with RPKM > 20,000 in leaf and four genes (psbA, psaC, rbcL and psbD) were the most highly expressed, with RPKM > 2250 in flower (Fig. 4a). The expression of psbA was highest in both leaf and floral tissues (Fig. 4a). In contrast, the expression of matK was the lowest, with RPKM < 2 in leaf and the expression of petL and petN is extremely low in flower, since the RPKM is barely detectable. Most plastid genes expressed in higher level in leaf than that in flower with the exception of psbK. The differential level of gene expression between leaf and floral tissues could range from 0.8-fold (psbK) to 80-fold (psbT) (Fig. 4b). According to functional categories, the plastid protein-coding genes were classified into seven groups, including CO2 carboxylation (CO), photosystem I (PSI), photosystem II (PSII), cytochrome b6/f complex (PET), ATP synthase, gene expression machinery, and miscellaneous (Fig. 4). The rbcL and genes coding for subunits of electron transport chain complexes had significantly higher (10.6 folds in average) expression level in leaf than floral tissue, although genes involved in other groups such as expression apparatus, ATP synthase and miscellaneous function also had higher (4.6, 3.4 and 2.5 folds, respectively) expression level in leaf than flower (Fig. 4b).
Previously, 44 edits were identified from 24 plastid protein-coding transcripts in leaves of P. aphrodite subsp. formosana by conventional Sanger sequencing (Zeng et al. 2007). In addition, bioinformatic analysis revealed high conservation (43 of 44) of plastid RNA editing sites between P. equestris and P. aphrodite (Jheng et al. 2012). Recently, RNA-Seq approaches were found to be more rapid, sensitive, extensive and cost-effective for investigating organellar RNA editing events than previously developed methods (Bentolila et al. 2013; Wang et al. 2015). For example, with NGS, 13, 133 and 119 new mitochondrial edits were identified from floral and leaf tissue of Arabidopsis and tobacco leaves, respectively (Bentolila et al. 2013; Grimes et al. 2014; Picardi et al. 2010). As well, up to nine new plastid edits were discovered in Arabidopsis (Bentolila et al. 2013), and many more partial edits could be detected in mitochondria of cotton than with the traditional approach (Suzuki et al. 2013). In this study, we investigated the whole plastid RNA editing status from leaf and floral tissues of P. aphrodite by RNA-Seq approaches. We identified 137 plastid RNA edits, including 93 newly discovered edits, which represented an average of 0.09% of the nucleotides examined in the plastid genome (Table 1; Additional file 1: Table S2). Furthermore, comparative cpDNA analysis potentially revealed high conservation (128 of 137) of plastid RNA edits between two endemic moth orchids, P. aphrodite and P. equestris (Additional file 1: Table S2). In addition, we also conducted a comparative analysis for those edits from flower tissue between two different approaches, CLC Genomics Workbench and RES-scanner (Additional file 1: Table S5). The results showed that both approaches can simultaneously identify the same 84 edits which most edits have similar editing ratio. Five or nine edits with the most of editing ratio <8.7% are specifically identified by either CLC Genomics Workbench or RES-scanner, respectively, which it is probably due to the difference for the parameters used and the algorithms of software.
Plant mitochondrial RNA editing sites are abundant and highly variable, with approximately 189–635 edits in angiosperms (Bentolila et al. 2013; Grimes et al. 2014; Sloan et al. 2010), whereas plastid RNA edits are relatively limited, with 21–44 nucleotide conversions in seed plants (Chen et al. 2011; Lin et al. 2015a, b; Sasaki et al. 2003, 2006; Tsudzuki et al. 2001; Zeng et al. 2007). All plastid edits in seed plants are the C-to-U conversion type with the exception of the oil palm Elaeis guineensis Jacq. (Uthaipaisanwong et al. 2012) and Antarctic hairgrass Deschampsia antarctica Desv. (Lee et al. 2014). However, recent reports have revealed more plastid edits in some taxa of seed plants (Additional file 1: Table S3). For example, in the gymnosperm, Cycas taitungensis (Chen et al. 2011) and Ginkgo biloba (He et al. 2016), 85 and 255 edits were identified from protein-coding transcripts, respectively. In dicot, cotton Gossypium hirsutum, 54 edits were identified in 27 transcripts (Jiang et al. 2012). In monocot, coconut Cocos nucifera L., duckweed Spirodela polyrhiza and Tausch’s goatgrass Aegilops tauschii L., 75, 66 and 60 plastid RNA edits were identified, respectively (Huang et al. 2013; Wang et al. 2015, 2017). In the early-branching angiosperm Amborella trichopoda, 138 edits were revealed (Hein et al. 2016). Here we identified 137 edits with 126 C-to-U and 11 U-to-C conversion from moth orchid, the highest number so far reported in monocot (Table 1), though nearly 57% of edits showed poor-level (5–20%) editing (Additional file 1: Figure S1, Table S2). However, chloroplast RNA editing is highly variable, with more edits in lower taxa of land plants. For instance, in hornwort Anthoceros formosae, at least 943 had 509 (54%) C-to-U and 433 (46%) U-to-C conversions (Kugita et al. 2003). Lycophyte showed a large number of plastid RNA editing sites, up to 3415 edits with only C-to-U conversion in the spike moss Selaginella uncinata (Oldenkott et al. 2014). In the fern Adiantum capillus-veneris, 350 RNA editing sites with 90% C-to-U edits and 10% U-to-C edits were identified (Wolf et al. 2004). Additionally, the plastid transcriptomes analysis from two early diverging species of fern, Ophioglossum californicum and Psilotum nudum, identified 297 C-to-U and three U-to-C edits in the former plastid transcripts, but only 27 C-to-U and no U-to-C edits in the latter plastid transcripts (Guo et al. 2015). These analyses suggest an independent gain or loss of RNA edits across the taxa of land plants during evolution.
RNA editing occurs most frequently in the ndh transcripts, accounting for >40% of the edits in the chloroplast transcripts of most higher plants with the exception of Pinus thunbergii and Phalaenopsis aphrodite (Chen et al. 2011; Huang et al. 2013; Lin et al. 2015a, b; Wakasugi et al. 1996; Wang et al. 2015; Zeng et al. 2007) because the functional ndh genes were lost from the plastids of these two species (Chang et al. 2006; Wakasugi et al. 1994). In Arabidopsis, those ndh edits are differentially regulated in distinct tissue types (Tseng et al. 2013). In this study, only a small fraction (5 of 137) of RNA edits were contributed from ndh transcripts in moth orchid, and they also showed poor editing efficiency (3–14%), with the exception of the previously identified ndhB-1977 edit (Additional file 1: Table S2). In addition, two sites (ndhD-528 and -740) in ndhD transcript were completely undetectable in floral tissue (Additional file 1: Table S2), which suggested that some tissue-specific factors may regulate the editing process of ndh transcripts in moth orchid. Additionally, the remaining five partial edits in ndh transcripts are likely an evolutionary remnant from before the complete loss of plastid RNA edits for non-functional ndh pseudogenes in moth orchid.
Previous study showed that the rpo (rpoA, rpoB, rpoC1 and rpoC2) transcripts were the most extensively edited (15 sites, up to 34%) among the functional gene groups in moth orchid (Zeng et al. 2007). We discovered two new edits (rpoB-55; rpoC1-1638) from rpo transcripts, although their editing level was poor (~10%) (Additional file 1: Tables S2, S4). In addition, five edits (rpoB-55, -614, -629, -686 and rpoC1-1638) were preferentially occurred in floral tissues. Furthermore, three edits (rpoB-55, rpoC1-203 and rpoC1-1638) were unique to moth orchid as compared with 17 other seed plants (Additional file 1: Table S4), although their editing level was poor with the exception of rpoC1-203. In contrast, the four nucleotides (rpoA-527, rpoB-1241, rpoC1-243, -656) of rpo transcripts were edited or T is present in the corresponding DNA in most of seed plants but are not edited in moth orchid, which caused the divergence of amino acid residues between moth orchid and other seed plants (Additional file 1: Table S4), though the significance is unknown.
Previous study has demonstrated that the pattern and efficiency of some editing sites in organellar transcripts significantly differed among ecotypes, tissue types, developmental stages and environmental conditions (Bentolila et al. 2005; Chateigner-Boutin and Hanson 2003; Howad and Kempken 1997; Ruf and Kossel 1997; Tillich et al. 2005; Tseng et al. 2013). For instance, in Arabidopsis, the editing of ndhB-149, ndhB-1255, and ndhD-2 occurs in leaf but is completely lost in roots and in lincomycin-treated seedlings (Tseng et al. 2013). In this study, at least 32 sites showed significantly differential (≧20%) RNA editing between leaf and floral tissues in moth orchid (Fig. 3; Additional file 1: Table S2). In addition, 19 and 14 edits are unique for leaf and floral tissues, respectively, which RNA editing is completely undetectable in floral tissue or vice versa (Additional file 1: Table S2). This analysis suggested tissue-specific factors might involve in RNA editing process in moth orchid.
Previously, a C-to-U conversion at the −10 position of the ndhG 5′UTR in monocot plants was predicted to modify the RNA secondary (stem/loop) structure (Drescher et al. 2002), but was not observed in moth orchid. Instead, a C-to-U substitution at the −30 position of the psbH 5′UTR that can form an energetically less stable secondary structure was reported in moth orchid (Zeng et al. 2007). Therefore, edits that occurred in the UTR regions might play an important role in the regulation of gene expression. We found very high efficiency editing (>81%) at the psbH 5′UTR (−30) in both leaf and floral tissues (Additional file 1: Table S2). In addition, at least 50% editing efficiency was observed for the edits of IGSs such as psaI-ycf4 (60,764), psbM-rpoB (27,736), trnD-psbM (31,129), rps16-matK (3095), clpP-rpl20 (70,142) and psbB-psbT (75,495) located in the 3′ or 5′UTR of genes such as psaI (27, 27 nt downstream of stop codon), rpoB (−160, 160 nt upstream of start codon), psbM (−85), matK (−35), rpl20 (−134), psbB (29), respectively. In comparing the structure of edited and unedited transcripts, significant change in free energy was predicted for the former five (Additional file 1: Figure S5D–H), which suggested that some edits occurring at the 3′ or 5′UTR might play a role in the regulation of gene expression in moth orchid.
Previous study reported that some sites of intron editing are a prerequisite for RNA splicing in plant organelles (Borner et al. 1995; Farre et al. 2012; Vogel et al. 1997), and unspliced RNA is often only partially edited (Yang and Mulligan 1991). In this study, 8 RNA edits were identified in seven introns (Additional file 1: Table S2), in particular, edits in rps12 (100,611) and ycf3 (45,108) introns showed high level (>73%) of editing. In addition, leaf-specific editing was found in the clpP intron (71,815) and flower-specific editing in the clpP intron (72,384), though the editing level is poor. Furthermore, the edit ycf3 (44,389) in intron showed significantly (>43%) differential editing between leaf and floral tissues (Fig. 3; Additional file 1: Table S2). These analyses suggested that editing in some cis-elements of primary transcripts might be important for splicing, and unidentified tissue-specific factors might be required for regulating intron editing in moth orchid. Additionally, RNA editing occurs in tRNA in plant organelles and plays an important role in tRNA processing and maturation (Binder et al. 1994; Kunzmann et al. 1998; Marechal-Drouard et al. 1996). The editing of the tRNA precursor might occur in the anticodon stem, acceptor stem, D stem or even anticodon (Janke and Paabo 1993; Marechal-Drouard et al. 1996). In this study, we observed nearly full RNA editing at the D stem of trnM transcripts (52,826 position) in leaf, with significant (>29%) differential editing between leaf and floral tissues (Fig. 3; Additional file 1: Table S2), which suggested that tissue-specific tRNA editing factors might be involved. After being edited in moth orchid, the trnM sequence conservation among plant phylogeny was increased, with the exception of Amborella species, then the standard clover-leaf tRNA structure could be formed (Fig. 2). The corresponding edit might also occur in Amborella, although this has not been reported (Hein et al. 2016).
The Arabidopsis editosome consists of at least four nucleus-encoded protein families, PPR, RIPs, ORRM1 and OZ1, required for plant organelle RNA editing (Sun et al. 2015, 2016). The PPR protein family with more than 400 members in angiosperms is involved in RNA metabolism including RNA editing in plant organelles (Grennan 2011). Although no PPR proteins involved in RNA metabolism have been reported in orchids, approximately 254 expressed sequence tags (EST) potentially encoding PPR proteins in moth orchid were annotated in the Orchidbase database (http://orchidbase.itps.ncku.edu.tw/est/home2012.aspx). In addition, at least three RIP homologues, five OZ1 homologues and two ORRM1-like proteins are available in Orchidbase. Our analysis suggests that the editosome of moth orchids might resemble that of Arabidopsis.
Chloroplast transcription change in large-scale in response to environmental or developmental signals (Barkan 2011). In Arabidopsis, the steady state levels of most plastid gene expression were high in green tissues, while low or undetectable in non-green tissues (Tseng et al. 2013). However, appreciable levels of some plastid transcripts such as clpP and rps14 mRNAs could be detected in non-photosynthetic tissue (Tseng et al. 2013). In this study, the differential steady state level of plastid transcripts between leaf and floral tissues could range from 0.8 to 80 fold (Fig. 4b), with most plastid genes having higher expression level in leaf than floral tissue, with the exception of psbK. In addition, genes located in the inverted repeat regions did not show higher expression level than those in single copy regions (Fig. 4). Chloroplast gene expression is regulated at multiple steps such as transcription, splicing, editing, processing, stability, translation, and post-translational modification, and no single step is the primary regulated step (Barkan 2011). Rather, each step might contribute to distinct patterns of plastid gene expression under different environmental and developmental conditions. Therefore, the variation of gene copy number and steady state transcript level probably did not reflect to the protein level in the plastids of distinctive tissues in moth orchid. Further studies are required to clarify how plastid gene expression is regulated in moth orchid.
We have identified 137 edits including 93 newly discovered edits in plastid transcripts of moth orchid by RNA-Seq. It is the highest number reported so far in monocots. Overall, 79 edits were involved in protein-coding transcripts, and the consequence of 58 nucleotide conversions caused the non-synonymous substitution which tend to increase the amino acid hydrophobicity as well as conservation among plant phylogeny. RNA editing occurred in non-protein-coding transcripts such as tRNA, introns and untranslated regulatory regions could affect the formation and stability of secondary structure, which might play a regulatory role in gene expression. For instance, RNA editing in trnM is required for the formation of a standard clover-leaf structure. The nearest-neighbor bias towards a U_A context immediately before and after RNA edits occurred in both protein-coding and non-protein-coding transcripts in moth orchid. At least 32 edits showed significant (≧20%) differential editing between leaf and floral tissues, which suggested that some unidentified tissue-specific factors might be responsible for the regulation of RNA editing in moth orchid. Furthermore, most plastid genes expressed in higher level in leaf than that in flower, but it might not reflect to the protein level in the plastids of distinctive tissues in moth orchid.
depth of coverage
multiple organellar RNA editing factor
next generation sequencing
pentatricopeptide repeat protein
Royal Horticultural Society
RNA editing-interacting protein
untranslated regulatory region
Barkan A (2011) Expression of plastid genes: organelle-specific elaborations on a prokaryotic scaffold. Plant Physiol 155(4):1520–1532. doi:10.1104/pp.110.171231
Barkan A, Small I (2014) Pentatricopeptide repeat proteins in plants. Annu Rev Plant Biol 65:415–442. doi:10.1146/annurev-arplant-050213-040159
Bentolila S, Chateigner-Boutin AL, Hanson MR (2005) Ecotype allelic variation in C-to-U editing extent of a mitochondrial transcript identifies RNA-editing quantitative trait loci in Arabidopsis. Plant Physiol 139(4):2006–2016. doi:10.1104/pp.105.069013
Bentolila S, Heller WP, Sun T, Babina AM, Friso G, van Wijk KJ, Hanson MR (2012) RIP1, a member of an Arabidopsis protein family, interacts with the protein RARE1 and broadly affects RNA editing. Proc Natl Acad Sci USA 109(22):E1453–1461. doi:10.1073/pnas.1121465109
Bentolila S, Oh J, Hanson MR, Bukowski R (2013) Comprehensive high-resolution analysis of the role of an Arabidopsis gene family in RNA editing. PLoS Genet 9(6):e1003584. doi:10.1371/journal.pgen.1003584
Binder S, Marchfelder A, Brennicke A (1994) RNA editing of tRNA(Phe) and tRNA(Cys) in mitochondria of Oenothera berteriana is initiated in precursor molecules. Mol Gen Genet 244(1):67–74
Bock R (2000) Sense from nonsense: how the genetic information of chloroplasts is altered by RNA editing. Biochimie 82(6–7):549–557
Bolger A, Lohse M, Usadel B (2014) Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120
Borner GV, Morl M, Wissinger B, Brennicke A, Schmelzer C (1995) RNA editing of a group II intron in Oenothera as a prerequisite for splicing. Mol Gen Genet 246(6):739–744
Boussardon C, Avon A, Kindgren P, Bond CS, Challenor M, Lurin C, Small I (2014) The cytidine deaminase signature HxE(x)n CxxC of DYW1 binds zinc and is necessary for RNA editing of ndhD-1. New Phytol 203(4):1090–1095. doi:10.1111/nph.12928
Chang CC, Lin HC, Lin IP, Chow TY, Chen HH, Chen WH, Cheng CH, Lin CY, Liu SM, Chang CC, Chaw SM (2006) The chloroplast genome of Phalaenopsis aphrodite (Orchidaceae): comparative analysis of evolutionary rate with that of grasses and its phylogenetic implications. Mol Biol Evol 23(2):279–291. doi:10.1093/molbev/msj029
Chateigner-Boutin AL, Hanson MR (2003) Developmental co-variation of RNA editing extent of plastid editing sites exhibiting similar cis-elements. Nucleic Acids Res 31(10):2586–2594
Chen H, Deng L, Jiang Y, Lu P, Yu J (2011) RNA editing sites exist in protein-coding genes in the chloroplast genome of Cycas taitungensis. J Integr Plant Biol 53(12):961–970. doi:10.1111/j.1744-7909.2011.01082.x
Christenson EA (2001) Phalaenopsis: a monograph. Timber Press, Portland
Drescher A, Hupfer H, Nickel C, Albertazzi F, Hohmann U, Herrmann RG, Maier RM (2002) C-to-U conversion in the intercistronic ndhI/ndhG RNA of plastids from monocot plants: conventional editing in an unconventional small reading frame? Mol Genet Genom 267(2):262–269. doi:10.1007/s00438-002-0662-9
Dressler RL (2005) How many orchid species? Selbyana 26(1/2):155–158
Farre JC, Aknin C, Araya A, Castandet B (2012) RNA editing in mitochondrial trans-introns is required for splicing. PLoS ONE 7(12):e52644. doi:10.1371/journal.pone.0052644
Fiebig A, Stegemann S, Bock R (2004) Rapid evolution of RNA editing sites in a small non-essential plastid gene. Nucleic Acids Res 32(12):3615–3622. doi:10.1093/nar/gkh695
Grennan AK (2011) To thy proteins be true: RNA editing in plants. Plant Physiol 156(2):453–454. doi:10.1104/pp.111.900412
Grimes BT, Sisay AK, Carroll HD, Cahoon AB (2014) Deep sequencing of the tobacco mitochondrial transcriptome reveals expressed ORFs and numerous editing sites outside coding regions. BMC Genom 15:31. doi:10.1186/1471-2164-15-31
Guo W, Grewe F, Mower JP (2015) Variable frequency of plastid RNA editing among ferns and repeated loss of uridine-to-cytidine editing from vascular plants. PLoS ONE 10(1):e0117075. doi:10.1371/journal.pone.0117075
Hammani K, Giege P (2014) RNA metabolism in plant mitochondria. Trends Plant Sci 19(6):380–389. doi:10.1016/j.tplants.2013.12.008
He P, Huang S, Xiao G, Zhang Y, Yu J (2016) Abundant RNA editing sites of chloroplast protein-coding genes in Ginkgo biloba and an evolutionary pattern analysis. BMC Plant Biol 16:257
Hein A, Polsakiewicz M, Knoop V (2016) Frequent chloroplast RNA editing in early-branching flowering plants: pilot studies on angiosperm-wide coexistence of editing sites and their nuclear specificity factors. BMC Evol Biol 16:23. doi:10.1186/s12862-016-0589-0
Hirose T, Sugiura M (2001) Involvement of a site-specific trans-acting factor and a common RNA-binding protein in the editing of chloroplast mRNAs: development of a chloroplast in vitro RNA editing system. EMBO J 20(5):1144–1152. doi:10.1093/emboj/20.5.1144
Howad W, Kempken F (1997) Cell type-specific loss of atp6 RNA editing in cytoplasmic male sterile Sorghum bicolor. Proc Natl Acad Sci USA 94(20):11090–11095
Hrubec TC, Robinson JM, Donaldson RP (1985) Isolation of mitochondria from soybean leaves on discontinuous percoll gradients. Plant Physiol 77(4):1010–1012
Huang YY, Matzke AJ, Matzke M (2013) Complete sequence and comparative analysis of the chloroplast genome of coconut palm (Cocos nucifera). PLoS ONE 8(8):e74736. doi:10.1371/journal.pone.0074736
Janke A, Paabo S (1993) Editing of a tRNA anticodon in marsupial mitochondria changes its codon recognition. Nucleic Acids Res 21(7):1523–1525
Jheng CF, Chen TC, Lin JY, Chen TC, Wu WL, Chang CC (2012) The comparative chloroplast genomic analysis of photosynthetic orchids and developing DNA markers to distinguish Phalaenopsis orchids. Plant Sci 190:62–73. doi:10.1016/j.plantsci.2012.04.001
Jiang Y, Fan SL, Song MZ, Yu JN, Yu SX (2012) Identification of RNA editing sites in cotton (Gossypium hirsutum) chloroplasts and editing events that affect secondary and three-dimensional protein structures. Genet Mol Res 11(2):987–1001. doi:10.4238/2012.April.19.4
Kotera E, Tasaka M, Shikanai T (2005) A pentatricopeptide repeat protein is essential for RNA editing in chloroplasts. Nature 433(7023):326–330. doi:10.1038/nature03229
Kugita M, Yamamoto Y, Fujikawa T, Matsumoto T, Yoshinaga K (2003) RNA editing in hornwort chloroplasts makes more than half the genes functional. Nucleic Acids Res 31(9):2417–2423
Kunzmann A, Brennicke A, Marchfelder A (1998) 5′ end maturation and RNA editing have to precede tRNA 3′ processing in plant mitochondria. Proc Natl Acad Sci USA 95(1):108–113
Lee J, Kang Y, Shin SC, Park H, Lee H (2014) Combined analysis of the chloroplast genome and transcriptome of the Antarctic vascular plant Deschampsia antarctica Desv. PLoS ONE 9(3):e92501. doi:10.1371/journal.pone.0092501
Lin CP, Ko CY, Kuo CI, Liu MS, Schafleitner R, Chen LF (2015a) Transcriptional Slippage and RNA editing increase the diversity of transcripts in chloroplasts: insight from deep sequencing of Vigna radiata genome and transcriptome. PLoS ONE 10(6):e0129396. doi:10.1371/journal.pone.0129396
Lin JY, Lin BY, Chang CD, Liao SC, Liu YC, Wu WL, Chang CC (2015b) Evaluation of chloroplast DNA markers for distinguishing Phalaenopsis species. Sci Hortic 192:302–310. doi:10.1016/j.scienta.2015.06.019
Lin BY, Chang CD, Huang LLH, Liu YC, Su YY, Chen TC, Lee RH, Huang HJ, Wu WL, Chang CC (2016) The mitochondrial DNA markers for distinguishing Phalaenopsis species and revealing maternal phylogeny. Biol Plant 60(1):68–78. doi:10.1007/s10535-015-0566-2
Liu YC, Lin BY, Lin JY, Wu WL, Chang CC (2016) Evaluation of chloroplast DNA markers for intraspecific identification of Phalaenopsis equestris cultivars. Sci Hortic 203:86–94. doi:10.1016/j.scienta.2016.03.021
Marechal-Drouard L, Kumar R, Remacle C, Small I (1996) RNA editing of larch mitochondrial tRNA(His) precursors is a prerequisite for processing. Nucleic Acids Res 24(16):3229–3234
Mortazavi A, Williams BA, McCue K, Schaeffer L, Wold B (2008) Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods 5(7):621–628. doi:10.1038/nmeth.1226
Oldenkott B, Yamaguchi K, Tsuji-Tsukinoki S, Knie N, Knoop V (2014) Chloroplast RNA editing going extreme: more than 3400 events of C-to-U editing in the chloroplast transcriptome of the lycophyte Selaginella uncinata. RNA 20(10):1499–1506. doi:10.1261/rna.045575.114
Picardi E, Horner DS, Chiara M, Schiavon R, Valle G, Pesole G (2010) Large-scale detection and analysis of RNA editing in grape mtDNA by RNA deep-sequencing. Nucleic Acids Res 38(14):4755–4767. doi:10.1093/nar/gkq202
Ruf S, Kossel H (1997) Tissue-specific and differential editing of the two ycf3 editing sites in maize plastids. Curr Genet 32(1):19–23
Ruwe H, Castandet B, Schmitz-Linneweber C, Stern DB (2013) Arabidopsis chloroplast quantitative editotype. FEBS Lett 587(9):1429–1433. doi:10.1016/j.febslet.2013.03.022
Sasaki T, Yukawa Y, Miyamoto T, Obokata J, Sugiura M (2003) Identification of RNA editing sites in chloroplast transcripts from the maternal and paternal progenitors of tobacco (Nicotiana tabacum): comparative analysis shows the involvement of distinct trans-factors for ndhB editing. Mol Biol Evol 20(7):1028–1035. doi:10.1093/molbev/msg098
Sasaki T, Yukawa Y, Wakasugi T, Yamada K, Sugiura M (2006) A simple in vitro RNA editing assay for chloroplast transcripts using fluorescent dideoxynucleotides: distinct types of sequence elements required for editing of ndh transcripts. Plant J 47(5):802–810. doi:10.1111/j.1365-313X.2006.02825.x
Schattner P, Brooks AN, Lowe TM (2005) The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res 33 (Web Server issue):W686–689. doi:10.1093/nar/gki366
Schwitzguebel JP, Siegenthaler PA (1984) Purification of peroxisomes and mitochondria from spinach leaf by percoll gradient centrifugation. Plant Physiol 75(3):670–674
Sloan DB, MacQueen AH, Alverson AJ, Palmer JD, Taylor DR (2010) Extensive loss of RNA editing sites in rapidly evolving Silene mitochondrial genomes: selection vs. retroprocessing as the driving force. Genetics 185(4):1369–1380. doi:10.1534/genetics.110.118000
Sun T, Germain A, Giloteaux L, Hammani K, Barkan A, Hanson MR, Bentolila S (2013) An RNA recognition motif-containing protein is required for plastid RNA editing in Arabidopsis and maize. Proc Natl Acad Sci USA 110(12):E1169–1178. doi:10.1073/pnas.1220162110
Sun T, Shi X, Friso G, Van Wijk K, Bentolila S, Hanson MR (2015) A zinc finger motif-containing protein is essential for chloroplast RNA editing. PLoS Genet 11(3):e1005028. doi:10.1371/journal.pgen.1005028
Sun T, Bentolila S, Hanson MR (2016) The unexpected diversity of plant organelle RNA editosomes. Trends Plant Sci 21:962–973
Suzuki H, Yu J, Ness SA, O’Connell MA, Zhang J (2013) RNA editing events in mitochondrial genes by ultra-deep sequencing methods: a comparison of cytoplasmic male sterile, fertile and restored genotypes in cotton. Mol Genet Genom 288(9):445–457. doi:10.1007/s00438-013-0764-6
Takenaka M, Zehrmann A, Verbitskiy D, Kugelmann M, Hartel B, Brennicke A (2012) Multiple organellar RNA editing factor (MORF) family proteins are required for RNA editing in mitochondria and plastids of plants. Proc Natl Acad Sci USA 109(13):5104–5109. doi:10.1073/pnas.1202452109
Takenaka M, Zehrmann A, Verbitskiy D, Hartel B, Brennicke A (2013) RNA editing in plants and its evolution. Annu Rev Genet 47:335–352. doi:10.1146/annurev-genet-111212-133519
Takenaka M, Verbitskiy D, Zehrmann A, Hartel B, Bayer-Csaszar E, Glass F, Brennicke A (2014) RNA editing in plant mitochondria-connecting RNA target sequences and acting proteins. Mitochondrion 19(Pt B):191–197. doi:10.1016/j.mito.2014.04.005
Tillich M, Funk HT, Schmitz-Linneweber C, Poltnigg P, Sabater B, Martin M, Maier RM (2005) Editing of plastid RNA in Arabidopsis thaliana ecotypes. Plant J 43(5):708–715. doi:10.1111/j.1365-313X.2005.02484.x
Tseng CC, Lee CJ, Chung YT, Sung TY, Hsieh MH (2013) Differential regulation of Arabidopsis plastid gene expression and RNA editing in non-photosynthetic tissues. Plant Mol Biol 82(4–5):375–392. doi:10.1007/s11103-013-0069-5
Tsudzuki T, Wakasugi T, Sugiura M (2001) Comparative analysis of RNA editing sites in higher plant chloroplasts. J Mol Evol 53(4–5):327–332. doi:10.1007/s002390010222
Uthaipaisanwong P, Chanprasert J, Shearman JR, Sangsrakru D, Yoocha T, Jomchai N, Jantasuriyarat C, Tragoonrung S, Tangphatsornruang S (2012) Characterization of the chloroplast genome sequence of oil palm (Elaeis guineensis Jacq). Gene 500(2):172–180. doi:10.1016/j.gene.2012.03.061
Vogel J, Hubschmann T, Borner T, Hess WR (1997) Splicing and intron-internal RNA editing of trnK-matK transcripts in barley plastids: support for MatK as an essential splice factor. J Mol Biol 270(2):179–187. doi:10.1006/jmbi.1997.1115
Wagoner JA, Sun T, Lin L, Hanson MR (2015) Cytidine deaminase motifs within the DYW domain of two pentatricopeptide repeat-containing proteins are required for site-specific chloroplast RNA editing. J Biol Chem 290(5):2957–2968. doi:10.1074/jbc.M114.622084
Wakasugi T, Tsudzuki J, Ito S, Nakashima K, Tsudzuki T, Sugiura M (1994) Loss of all ndh genes as determined by sequencing the entire chloroplast genome of the black pine Pinus thunbergii. Proc Natl Acad Sci USA 91(21):9794–9798. doi:10.1073/pnas.91.21.9794
Wakasugi T, Hirose T, Horihata M, Tsudzuki T, Kossel H, Sugiura M (1996) Creation of a novel protein-coding region at the RNA level in black pine chloroplasts: the pattern of RNA editing in the gymnosperm chloroplast is different from that in angiosperms. Proc Natl Acad Sci USA 93(16):8766–8770
Wang M, Cui L, Feng K, Deng P, Du X, Wan F, Weining S, Nie X (2015) Comparative analysis of Asteraceae chloroplast genomes: structural organization, RNA editing and evolution. Plant Mol Biol Rep 33(5):1526–1538. doi:10.1007/s11105-015-0853-2
Wang Z, Lian J, Li Q, Zhang P, Zhou Y, Zhan X, Zhang G (2016) RES-Scanner: a software package for genome-wide identification of RNA-editing sites. GigaScience 5:37
Wang M, Liu H, Ge L, Xing G, Wang M, Weining S, Nie X (2017) Identification and analysis of RNA editing sites in the chloroplast transcripts of Aegilops tauschii L. Genes 8(1):13. doi:10.3390/genes8010013
Wolf PG, Rowe CA, Hasebe M (2004) High levels of RNA editing in a vascular plant chloroplast genome: analysis of transcripts from the fern Adiantum capillus-veneris. Gene 339:89–97. doi:10.1016/j.gene.2004.06.018
Yagi Y, Hayashi S, Kobayashi K, Hirayama T, Nakamura T (2013) Elucidation of the RNA recognition code for pentatricopeptide repeat proteins involved in organelle RNA editing in plants. PLoS ONE 8(3):e57286. doi:10.1371/journal.pone.0057286
Yang AJ, Mulligan RM (1991) RNA editing intermediates of cox2 transcripts in maize mitochondria. Mol Cell Biol 11(8):4278–4281. doi:10.1128/MCB.11.8.4278
Zeng WH, Liao SC, Chang CC (2007) Identification of RNA editing sites in chloroplast transcripts of Phalaenopsis aphrodite and comparative analysis with those of other seed plants. Plant Cell Physiol 48(2):362–368. doi:10.1093/pcp/pcl058
The presented research work was carried out in collaboration between authors. TCC and CCC designed the experiments; TCC, CHW and YCL performed the experiments; TCC, YCL, XW, CHH and CCC analyzed the data; TCC, XW and CCC wrote the paper. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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This work was financially supported in part by the Grants (MOST 104-2321-B-006-001, MOST 105-2313-B-006-001 and MOST 106-2313-B-006-003-MY3) to C.-C. Chang from the Ministry of Science and Technology, Taiwan.
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Additional file 1: Table S1. Statistics of NGS libraries mapped to reference genome. Table S2. Plastid RNA edits in Phalaenopsis orchid. Table S3. Plastid RNA edits in protein-coding transcripts among land plants. Table S4. Plastid RNA edits in rpo transcripts among 18 species of higher plants. Table S5. Comparative analysis of plastid RNA edits from flower tissue by two different bioinformatic approaches. Figure S1. The editing efficiency of plastid RNA edits in leaf and floral tissues. Figure S2. The density of RNA editing sites in protein-coding transcripts. Figure S3. RNA editing in protein-coding transcripts. Figure S4. Nearest-neighbor bias toward a U_A context immediately before and after plastid RNA edits in moth orchid. Figure S5. The prediction of RNA secondary structures formed by the unedited and edited plastid transcripts in moth orchid.
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Chen, T., Liu, Y., Wang, X. et al. Whole plastid transcriptomes reveal abundant RNA editing sites and differential editing status in Phalaenopsis aphrodite subsp. formosana . Bot Stud 58, 38 (2017). https://doi.org/10.1186/s40529-017-0193-7
- Plastid gene expression
- RNA editing
- Moth orchids
- Phalaenopsis aphrodite