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Article

Differential RNA Editing and Intron Splicing in Soybean Mitochondria during Nodulation

1
School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong, China
2
Center for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong, China
3
School of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong, China
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(24), 9378; https://doi.org/10.3390/ijms21249378
Submission received: 8 November 2020 / Revised: 4 December 2020 / Accepted: 7 December 2020 / Published: 9 December 2020
(This article belongs to the Special Issue Organelle Genetics in Plants)

Abstract

:
Nitrogen fixation in soybean consumes a tremendous amount of energy, leading to substantial differences in energy metabolism and mitochondrial activities between nodules and uninoculated roots. While C-to-U RNA editing and intron splicing of mitochondrial transcripts are common in plant species, their roles in relation to nodule functions are still elusive. In this study, we performed RNA-seq to compare transcript profiles and RNA editing of mitochondrial genes in soybean nodules and roots. A total of 631 RNA editing sites were identified on mitochondrial transcripts, with 12% or 74 sites differentially edited among the transcripts isolated from nodules, stripped roots, and uninoculated roots. Eight out of these 74 differentially edited sites are located on the matR transcript, of which the degrees of RNA editing were the highest in the nodule sample. The degree of mitochondrial intron splicing was also examined. The splicing efficiencies of several introns in nodules and stripped roots were higher than in uninoculated roots. These include nad1 introns 2/3/4, nad4 intron 3, nad5 introns 2/3, cox2 intron 1, and ccmFc intron 1. A greater splicing efficiency of nad4 intron 1, a higher NAD4 protein abundance, and a reduction in supercomplex I + III2 were also observed in nodules, although the causal relationship between these observations requires further investigation.

1. Introduction

Soybean is an important cash crop for protein and edible oil. Its ability to perform symbiotic nitrogen fixation in root nodules makes it a nitrogen-rich food source. Root cells obtain photo-assimilates from source tissues and catabolize these chemical compounds through root mitochondria to generate the ATPs required for various physiological and biochemical processes. In eukaryotic cells, cellular respiration mainly takes place inside mitochondria. The tricarboxylic acid (TCA) cycle and mitochondrial electron transport chain (mETC) convert biochemical energy from nutrients into ATP, which is an important energy currency of the cell.
The energy demand in root nodules is much higher than in uninoculated roots, since nitrogen fixation consumes a tremendous amount of energy [1]. Therefore, substantial differences in carbon metabolism and mitochondrial activities between root nodules and uninoculated root cells are expected. Sucrolytic activities (invertase and sucrose synthase) are found to be 3–4-fold higher in root nodules than in uninoculated roots and these enzymatic activities are restricted to the uninoculated cortical tissue and are absent in the infected central tissue of nodules [2]. Bacteroids of the nodules were shown to exhibit a limited capacity to utilize carbohydrates [3], with limited glycolytic activities and no sucrolytic activities. It is reported that sucrose taken up by root nodule cells is converted into malate and succinate as the main energy sources for bacteroids [1]. Hence, to facilitate the carbohydrate supply to bacteroids, the physiology of soybean mitochondria in nodules is significantly different from the uninoculated roots. Mitochondria in nodules were shown to oxidize malate at a rate 2-fold higher than cotyledon mitochondria. However, the activities of TCA cycle enzymes, except malate and succinate dehydrogenases, were lower in nodule mitochondria [4].
The vast majority of mitochondrial proteins from these crucial metabolic pathways are encoded in the nucleus and, after their translation in the cytoplasm, are imported into the mitochondria [5,6]. There are 110 predicted open reading frames in soybean mtDNA and 36 of them can be translated into proteins with known functions [7,8], including some subunits of the respiratory chain: NADH dehydrogenase (complex I), cytochrome oxidase (complex IV), ATP synthase (complex V), and cytochrome C biogenesis. Coordination of the expression and accumulation of mitochondrial proteins derived from the nuclear and mitochondrial genomes are complex, especially in the post-transcriptional regulation of mtDNA expression [9,10].
Some mitochondrial mRNA transcripts are subjected to C-to-U RNA editing, a house-keeping post-transcriptional process in plants [11]. RNA editing is carried out by the editosome complexes, which are composed of pentatricopeptide repeat (PPR) proteins, Multiple Organellar RNA Editing Factors (MORF), organelle RNA Recognition Motif-containing proteins (ORRM), and organelle zinc finger editing factor family (OZ) proteins [12]. RNA editing is complex and energy-consuming. The biological function and evolutionary significance of RNA editing in plants still remain unclear [13,14]. RNA editing may lead to amino acid substitutions and affect the function of the translated proteins [15]. Editing sites, which are edited with different efficiencies in different tissues, have also been identified in the plastids of diverse species [16,17].
RNA editing has been shown to be crucial for nad1 splicing in Oenothera [18] and nad7 splicing in maize [19]. The genomes of plant mitochondria house about 20 group-II introns and their splicing requires maturases [20,21,22]. In Arabidopsis thaliana, there is one maturase gene (matR) in the mitochondrial genome and four nuclear maturase genes (nMat1-4) in the nuclear genome [23]. The four nuclear-encoded maturases are imported into mitochondria after translation [24,25]. It has been experimentally demonstrated that nuclear-encoded maturases [20,23,26] and MatR [27] are required for the splicing of various group-II introns in Arabidopsis mitochondria and the assembly of functional complex I. Here, we compare the degrees of RNA editing and intron splicing on mitochondrial transcripts in soybean nodules and roots.

2. Results

2.1. RNA Sequencing and Differentially Expressed Mitochondrial Genes

To study the differences in mitochondrial transcripts between soybean nodules and uninoculated roots, we collected nodule (N) samples 28 days after rhizobium inoculation. Stripped roots (SR), main roots after the removal of nodules, and uninoculated roots (UR) of the same age were also harvested. We extracted total RNA from N, SR, and UR for RNA sequencing (RNA-seq) analysis (Table 1). The BioProject accession numbers of the RNA-seq data are PRJNA627909 (UR) and PRJNA626514 (N and SR), respectively. Here, we focused on mitochondrial gene expression and identified 93 gene transcripts (Supplementary Table S1). Besides transcripts encoding for hypothetical proteins, we identified 14 transcripts differentially expressed between N and UR, SR and UR, or SR and N (fold change > 1.5, p-value < 0.05 using Student’s t-test). These include transcripts of cytochrome c biogenesis C/FN (ccmC, ccmFN), cytochrome c oxidase subunit III (cox3), NADH dehydrogenase subunit 1/2/4L/5 (nad1, nad2, nad4L, nad5), and some ribosomal proteins (Table 2). Compared to UR, eight transcripts, including six nad transcripts and two ribosomal protein transcripts, were significantly upregulated in SR, while the abundance of six transcripts including cox3, nad1, nad5, and three ribosomal protein transcripts was significantly higher in N. On the contrary, ccmFN was significantly down-regulated in N compared with UR. The abundance of four transcripts, including cytochrome c biogenesis C/FN (ccmC, ccmFN) and ribosomal proteins L5 and S14, was lower in N than in SR, whereas the abundance of cox3 and rps12 transcripts was higher in N when compared with SR and UR.

2.2. Differential RNA Editing in Root Nodules

RNA-seq reads were mapped to the mitochondrial genome. A total of 631 RNA editing sites, with at least 15% edited reads in all three biological replicates of any one of the three samples, were identified (Supplementary Table S2). The average editing degrees of the three groups (N, SR, and UR) were compared, and 74 sites with ≥ 15% differences in the editing degrees between any two of the three tissues were identified (Supplementary Table S3). Out of these 74 editing sites, 12 sites were intronic, 23 sites were synonymous, and 39 sites were non-synonymous. There were a few observations: (i) UR showed higher editing degrees in atp1-1, atp1-2, atp1-3, and atp1-4 than the other two samples, whereas all these sites are synonymous; (ii) There were 29 differentially edited sites in nad transcripts (nad1, nad2, nad4, nad4L, nad5 and nad7). Most of these sites were intronic (11 sites) or synonymous (nine sites). Only six and three sites in nad1 and nad4, respectively, could lead to amino acid substitutions; (iii) There were 18 differentially edited sites in ribosomal protein transcripts (rpl5, rps1, rps4, rps10 and rps12). Only one site was intronic (rps10), but all the other sites could lead to amino acid substitutions. Comparing N to UR, 16 sites in rps 1, 4, 10, and 12 had higher editing degrees, while two sites in rpl5 had lower editing degrees.

2.3. matR Transcripts Underwent Extensive RNA Editing in Root Nodules

We identified 17 editing sites on matR, of which eight sites had been identified in A. thaliana [15] (Table 3) and 11 sites had been reported previously in uninoculated soybean by comparing genomic DNA and cDNA sequences [28]. Out of these 17 editing sites, the degrees of RNA editing of eight sites were higher in the N than UR and SR, of which seven could lead to amino acid substitutions. To confirm that these sites were actually edited, RT-PCR and Sanger sequencing were performed on three biological replicates of each sample (Supplementary Figure S1). In general, the Sanger sequencing data confirmed the next-generation sequencing (NGS) data, and both showed that N had a higher degree of editing than UR and SR in multiple editing sites (Figure 1 and Table 2).

2.4. Identification of Nuclear-Encoded Mitochondrial Intron Maturases in the Soybean Genome

By using the protein sequences of the four Arabidopsis nuclear maturases as baits to search the soybean genome, six homologous nuclear maturases were identified. Among these transcripts, two are likely to have arisen from gene duplication (Figure 2). The expression levels of these six transcripts are presented in Supplementary Table S4. Among these six transcripts, only a transcript homologous to AtnMAT4 had a significantly higher (2X) expression in N than in UR. By contrast, four transcripts homologous to AtnMAT1-4 expressed significantly higher in SR than in UR (Supplementary Table S4).

2.5. Intron Splicing of Mitochondrial Transcripts

Next, the splicing efficiencies of the 20 mitochondrial introns were analyzed among the samples by qRT-PCR (Figure 3). The splicing efficiencies of several introns were higher in both N and SR than UR, such as nad1 introns 2/3/4, nad4 intron 3, nad5 introns 2/3, cox2 intron 1, and ccmFc intron 1. While the nuclear intron maturases responsible for the splicing of some of these introns were identified in A. thaliana [20,23,26], the scenario in soybean is complicated by the presence of six nuclear intron maturases in the soybean genome (Supplementary Table S4). It should be noted that the splicing efficiency of the intron 1 of nad4 was greatly enhanced in N than in UR and SR in the following order (N > UR > SR).

2.6. In-Gel Activity Assay and Western Blotting

Since qRT-PCR showed that there was more splicing of nad4 intron 1 in N, we examined the abundance of NAD4 protein in our samples by Western blotting and in-gel activity assays (Figure 4). In-gel activity assay showed that the activity of protein complex II was similar among the three samples, and the complex I activity assay showed that while the activity of the monomeric complex I was similar among the three samples (Figure 4a,b), the activities of the supercomplex composed of complex I and dimeric complex III were lower in N (Figure 4a). In terms of protein abundance, while the level of NAD9 protein was similar among the three samples, a higher protein level of NAD4 was observed in the N sample in comparison to the other two samples. The N sample also had a higher protein abundance of COXIII, which could be due to a 2× increase in its mRNA abundance (Table 2).

3. Discussion

RNA editing is a common biological process in the plastids and mitochondria of land plants [30]. It is believed to be a post-transcriptional correction mechanism to circumvent mutations in the organellar genomes [11]. Since RNA editing is an energy-consuming and complex process, it must serve important biological functions, or otherwise it should not be maintained in higher plants during evolution. One possible advantage of RNA editing is to provide an additional regulatory mechanism to organelle physiology. RNA editing was shown to play important roles in organellar tRNA maturation [31] and intron splicing [18,19]. Several hundreds of RNA editing sites on mitochondrial transcripts and differential RNA editing were observed in our previous study on A. thaliana [15]. We showed that overexpression of AtPAP2, a phosphatase dually targets the outer membranes of chloroplasts and mitochondria [32,33] and plays a role in the import of pMORF3 into mitochondria [5], might influence cyt c biogenesis by modulating RNA editing of ccm transcripts through its interaction with the MORF proteins [15].
Here, the objective is to examine how nodule formation affects the degrees of RNA editing in soybean mitochondrial transcripts and investigate its possible biological purpose. We identified 631 RNA editing sites with at least 15% of edited transcripts in all three biological replicates of any one of the samples (Supplementary Table S2). Only 12% of these sites were differentially edited between any two of the three samples. One of the mitochondrial transcripts that underwent extensive RNA editing was the matR transcript (Table 3), which encodes an intron maturase that mediates group-II intron splicing. In a previous study, 510 RNA editing sites were identified in Arabidopsis mitochondrial transcripts and 124 sites were differentially edited between the wild-type and a high-energy, fast-growing, transgenic line [15]. There are 12 RNA editing sites in Arabidopsis matR transcripts, but none of them were differentially edited between the two lines [15]. Hence, the differential editing of matR transcripts is specific in our soybean samples and is likely to play a role in nodule function (Table 2). While plant mitochondria have lost most of their intron-encoded ORFs, a single intron maturase gene (matR) is retained in the fourth intron of nad1 in seed plants [21] (Figure 2). In addition to the mitochondrial matR gene, phylogenetic analysis shows that the nuclear maturase genes are also conserved between A. thaliana and soybean, since the homologous sequences of all four Arabidopsis nMat homologs could be found in the soybean genome (Figure 2). Among the six soybean nuclear maturases, only a gene homologous to Arabidopsis nMat4 exhibited a 2X higher expression in N than in UR (Supplementary Table S4).
By suppressing the expression of matR in Arabidopsis, the splicing efficiencies of nad1 introns 3 and 4, nad4 intron 3, cox2 intron 1, and ccmFc intron 1 were downregulated, indicating that AtMatR carries out the splicing of these introns [27]. In soybean, the splicing efficiencies of these introns were higher in N and SR than in UR (Figure 3a). It should be noted that the abundance of matR transcripts were 27% and 38% higher in the SR and the N samples than in the UR sample (p < 0.005), respectively (Supplementary Table S1). Hence, the changes in the splicing efficiencies of these introns could be due to an increase in matR transcript abundance and/or due to the changes in RNA editing. The nad4 intron 1 was not identified as a matR-mediated splicing site in Arabidopsis by matR knockdown experiments. However, it was identified in the MatR-ribonucleoprotein complex in an RNA co-immunoprecipitation experiment [27]. Hence, it is possible that RNA editing of MatR and the subsequent changes in its amino acid sequence might affect the composition of its associated ribonucleoprotein complex, thus affecting the splicing efficiency of nad4 intron 1 by the other maturases. Alternatively, MatR might have an additional splicing activity toward nad4 intron 1 in soybean. A P-type PPR protein, MISF68, was recently shown to be essential for the splicing of nad4 intron 1 in A. thaliana, but the maturase responsible for its splicing has not yet been identified [34]. Nevertheless, several nuclear-encoded splicing factors can independently regulate the intron splicing in plant mitochondria, such as nMat1-4, mitochondrial transcription termination factors (mTERFs), and some PPR proteins. They are responsible for the splicing regulation of multiple introns in the mitochondrial genomes [35,36]. However, the most significant change between SR and N came from nad4 intron 1 in the qRT-PCR results, suggesting that the splicing factor which targets the nad4 intron 1 may play a role in nodule function.
Several nad genes are retained in the mitochondrial genome but are not transferred to the nucleus during evolution, probably because they encode the hydrophobic membrane subunits (NAD1-6) of the complex I [37]. Some nad introns are subjected to RNA editing (Supplementary Table S3). The latest research reveals that some RNA editing sites on the intronic sequences of maize mitochondrial nad7 transcript can affect its intron splicing [19]. For example, in maize, it was previously shown that splicing would be abolished without the C-to-U editing at a specific position in two nad7 introns [19]. In this study, 12 intronic RNA editing sites were identified, 11 of which were situated in nad1/2/4/5/7 introns, including a site located in nad4 intron 1 (base 102195, Supplementary Table S3). RNA editing of these intronic sequences could potentially affect intron splicing in soybean.
We observed the highest splicing efficiency of the nad4 intron 1 in N compared to UR and SR (Figure 3), which might, in turn, affect the NAD4 protein abundance and supercomplex formation (Figure 4). In mammalian cells, spliced mRNA yielded more proteins than identical mRNA not made by splicing, possibly due to an enhanced association of spliced mRNA with polyribosomes [38]. This phenomenon is also observed in viruses [39]. Likewise, a higher splicing efficiency of the first intron of nad4 in nodule (Figure 3a) might enhance the efficiency of translation. Evidentially, we detected a higher NAD4 protein abundance in nodule comparing to roots (Figure 4c) despite a similar nad4 transcript abundance in all samples (Supplementary Table S1). NAD4 is a membrane component of complex I. In a maize nad4 mutant (NCS2), while the missing NAD4 results in the destabilization of the NDH complex, a smaller complex can still exhibit complex I activity in the in-gel enzyme assay [40]. In BN-gel, complex I has two forms, either alone or forming a supercomplex (I + III2) with dimeric complex III, and their ratios are 40%/60% in plants, mammals, and fungi [41]. Our result showed that the mitochondria in nodules contain less I + III2 supercomplex, but contain a similar amount of free complex I to that of the root samples (Figure 4). Factors such as differential intron splicing, differential RNA editing of various nad transcripts and a change in NAD4 abundance could collectively affect the formation of the I + III2 supercomplex during nodulation. It was suggested that the I + III2 supercomplex may enable a more efficient electron transfer from complex I to complex III, as the close proximity of the two complexes enables efficient channeling of reduced quinol [42]. The lower abundance of supercomplex I + III2 in nodule mitochondria might affect electron transport rate in the mETC [41].
In nodules, nitrogen fixation by S. fredii is an extensive energy-consuming process. To fix one molecule of N2, 16 ATP molecules and eight electrons (and eight H+) are required [43]. C4-dicarboxylates (succinate, fumarate, and malate) were suggested to be the primary carbon source provided to the rhizobia by the root cells [1], and a recent study showed that malate, but not succinate or fumarate, is the essential dicarboxylate for bacteroid growth and symbiosis [44]. Normal root mitochondria do not exhibit substantial glycine decarboxylase (GDC) as there is no photorespiration in roots [45]. However, a proteomic study showed that nodule mitochondria contain a significantly higher amount of GDC, but a lower amount of ATP synthase α and β chains than uninoculated roots [46]. A high glycine flux is present in nodule mitochondria due to nitrogen fixation and ureide biosynthesis [47]. The presence of GDC in nodule mitochondria will generate a large amount of NADH. If the electron transport in the mETC is tuned down by the downregulation of the formation of supercomplex I + III2 [42], more NADH generated from GDC can be exported from the nodule mitochondria in the form of malate, which can then be consumed by the bacterioid for energy production. In this study, we reported the changes in RNA editing and intron splicing of the mitochondrial genome in soybean nodules. The relationship among RNA editing, intron splicing, and supercomplex I+III2 formation is complicated and requires further investigation.

4. Materials and Methods

4.1. Plant Materials and Sinorhizobium Fredii Inoculation

Nodules were harvested from a cultivated soybean C08 (Glycine max), which is closely related to Williams 82 from Illinois, USA [48]. Seeds of C08 were surface-sterilized with chlorine gas for 16 h and germinated in the dark in sterilized vermiculite with de-ionized water in the greenhouse. At three days post-germination, seedlings were transferred to individual containers with sterilized vermiculite with 1X low nitrogen nutrient solution (6.35 μM Ca(NO3)2, 133.59 μM CaSO4, 50.30 μM KCl, 12.17 μM MgSO4•7H2O, 39.04 μM K2HPO4, 15.31 μM ferric citrate, 2.31 μM H3BO3, 0.6 μM MnSO4, 0.07 μM ZnSO4, 0.16 μM CuSO4•5H2O, 0.01 μM H2MoO4) in a 16h/8h light/dark cycle at 25–30 °C [49] and inoculated with S. fredii strain CCBAU45436 [50]. A set of uninoculated soybean control was also prepared alongside this. The Rhizobium strain was cultured on TY medium [51] at 28 °C with shaking at 180 rpm for 40 h. The cells were then pelleted and diluted in saline (0.9% w/v NaCl) to a final concentration of 1020 cells mL−1 (OD600 = 0.2) for inoculation. Ten-day-old seedlings were inoculated with 1 mL inoculum per plant. On the 28th day after inoculation, UR, N, and SR samples were collected separately and frozen immediately in liquid nitrogen and stored at −80 °C for RNA extraction. For mitochondria isolation, uninoculated roots, nodules, and the stripped roots were harvested and kept on ice for immediate isolation [5].

4.2. RNA Extraction and Sequencing

RNA was extracted using TRIzol (Life Technologies, Carlsbad, CA, USA) following the manufacturer’s protocol. Three biological replicates were prepared for each of the three conditions to produce a total of nine samples. Nine strand-specific RNA-seq libraries were generated using TruSeq RNA Sample Preparation Kit (Illumina, San Diego, CA, USA). Messenger RNA (mRNA) was enriched by depleting ribosomal protein RNA using Ribo-Zero Plant kit, rather than poly-A enrichment. These libraries were sequenced on Illumina Hiseq series platforms (sequencing service provided by Groken Bioscience, Hong Kong, China).

4.3. Bioinformatics Analysis

G. max Williams 82 v275 reference genome was downloaded from the Phytozome database (v9.0: https://phytozome.jgi.doe.gov/). The complete soybean mitochondrion genome was downloaded from the NCBI database (ID: NC_020455.1) [8]. The sequences were combined into one reference genome for subsequent analysis. Genomic variations (SNPs and Indels) between C08 and the reference genome were identified using the GATK pipeline (version 4.0.5.2) [52] according to GATK best practice workflow for germline short variant discovery (https://software.broadinstitute.org/gatk/best-practices/workflow?id=11145). Briefly, C08 DNA sequencing reads were mapped to the reference genome using BWA-MEM (version 0.7.15) implementation with default parameters. Duplicated reads were marked with GATK MarkDuplicates implementation. Then, base quality score recalibration was performed with known variation sites downloaded from the Phytozome database (v12). Then, SNPs and Indels between C08 and the reference genome were called based on mapped and quality score recalibrated reads using GATK HaplotypeCaller implementation.
RNA-seq reads were mapped to reference genome using Tophat2 (version 2.1.1) [53]. Properly mapped read pairs were assigned to each annotated gene by featureCounts from the subread package [54]. Read pair count of each mitochondrial gene was normalized by transcript length and total read count to calculate FPKM value.
To identify RNA editing sites, RNA-seq reads that could be mapped to the mitochondrial genome were extracted. SNPs were identified, and allele frequency was calculated for each polymorphic site using samtools mpileup (version 1.7) [55] and varScan2 (version 2.4.3) [56]. SNPs that were also identified by GATK with DNA reads were assumed to be germline variations and filtered. The remaining SNPs were considered as candidate RNA-editing sites.

4.4. RT-PCR and Quantitative RT-PCR

cDNAs were synthesized with M-MLV RT (200 U/μL) (Invitrogen, Hong Kong, China) and random hexamers (Invitrogen, Hong Kong, China), according to the manufacturer’s instructions. To verify the differential editing of mitochondrial matR transcript observed in RNA-seq data, specific primers were designed to amplify regions that contain each matR editing site by RT-PCR (Supplementary Table S5). PCR products were sent out to BGI-Shenzhen for Sanger sequencing.
Quantitative reverse transcription PCR (qRT-PCR) analysis was carried out using the same batch of RNA samples. Primers used in qRT-PCR were derived from a previous A. thaliana study in which specific oligonucleotides were designed to target intron-exon and exon-exon regions [23]. New primers were designed based on the homology between A. thaliana and soybean mitochondrial genomes (Supplementary Table S5). SYBR Green Master Mix (ABIsystems, Hong Kong) was used in a 10 μL volume PCR reactions. Tubulin gene (Gene ID: Glyma20g27280) was used as the internal house-keeping control. The assessment of relative expression levels was calculated using the Ct comparative threshold method [15,57]. The expression levels of spliced mRNA and unspliced mRNA were first calculated and the ratio was defined as the splicing efficiency. To compare the splicing efficiencies between samples, the splicing efficiencies of SR and N were divided by that of UR (Figure 3a).

4.5. Isolation of Soybean Mitochondria

Soybean mitochondria were isolated as previously described with modifications [58,59]. All procedures were done at 4 °C including sample harvest and centrifugation. A total of 20 g of the UR, 20 g of SR, and 10 g of the N were sampled and ground in 50 mL grinding buffer (pH 7.5) containing 0.3 M sucrose, 25 mM Tetrasodiumpyrophosphate, 2 mM EDTA, 10 mM KH2PO4, 1.0% (w/v) PVP-40, 1% (w/v) BSA, 20 mM ascorbate and L-cysteine. After 2 min of grinding, the homogenates were filtered through a double layer of Miracloth and rinsed again with 50 mL grinding buffer and centrifuged at 4000 g for 5 min. The supernatant was transferred to a tube and centrifuged at 10,000 g for 15 min. The pellet was resuspended in a wash buffer (0.3 M sucrose, 10 mM TES, 0.1% (w/v) BSA, pH 7.5) and layered on 30 mL of wash buffer containing 45% (v/v) Percoll in a tube and centrifuged at 40,000 g for 30 min. The crude mitochondria located in a tight brown band near the top of the tube were transferred and diluted at least 5-fold with the wash buffer and concentrated by centrifuging at 15,000 g for 10 min. The pellet was resuspended in around 5 mL of wash buffer before loading to a continuous gradient solution containing 0 to 4.4% (v/v) PVP-40 and 28% (v/v) Percoll in the wash buffer. After centrifugation at 40,000 g for 30 min, the mitochondria were concentrated in a pale-yellow band located near the bottom of the tube. This layer was then transferred to a new polycarbonate centrifuge tube with the BSA-free wash buffer and centrifuged at 2450 g for 15 min. After 3-4 wash steps, the mitochondria pellet was resuspended in the wash buffer without BSA. After the protein concentration was determined by the Bradford protein assay (BIO-RAD, Hercules, CA, USA), the mitochondria were stored in aliquots at −80 °C.

4.6. Blue Native-Polyacrylamide Gel Electrophoresis (BN-PAGE) and In-Gel Enzyme Activity Staining

The mitochondrial protein complex extraction and BN-PAGE were carried out as previously published with modifications [60]. An equal amount of mitochondria was collected by centrifugation at 14,300 g for 10 min at 4 °C and resuspended in 5% (w/v) digitonin extraction buffer to a final ratio of 10:1 (w/v) of protein to detergent and incubated on ice for 20 min. The solubilized proteins were then centrifuged at 18,300 g for 20 min at 4 °C. The supernatant (100 µg per sample) was transferred to a new tube supplemented with 5% (v/v) Serva blue G250 solution by a final ratio of 100:1 (w/v) of protein to dye and was loaded to a standard 1.0 mm × 10 well NativePAGETM 3–12% Bis-Tris Gel (Invitrogen, Hong Kong, China). The cathode buffer (50 mM Tricine, 15 mM bis-Tris, 0.02% (w/v) Serva Blue G250, pH 7.0) and the anode buffer (50 mM Bis-Tris, pH 7.0 with HCl) were freshly prepared. The electrophoresis was carried out at 4 °C at 75 V for 30 min, followed by 100 V for 30 min, 125 V for 30 min, 150 V for 1 h, 175 V for 30 min, and then set to a constant voltage 200 V until the sample reached the bottom of the gel.
After electrophoresis, the gels were washed twice with MiliQ water for 10 min. Then, the gels were equilibrated in the appropriate reaction buffer without reagents for 10 min. The gel was then incubated in a fresh reaction buffer of complex I (0.1 M Tris, 0.2 mM NADH, 0.2% (w/v) nitro-blue tetrazolium, pH 7.4) for 30 min. The other gel was incubated in a fresh reaction buffer of complex II (50 mM KH2PO4, 0.1 mM ATP, 0.2 mM Phenazine methosulphate, 10 mM succinate, 0.2% (w/v) nitro-blue tetrazolium) for 2 h. The reactions were terminated by fixing the gels in 40% (v/v) methanol and 10% (v/v) acetic acid for at least 1 h. The gels were destained overnight in 20% (v/v) methanol to remove residual Serva Blue G. For Western blot analysis, 10 µg mitochondrial proteins were run into SDS-PAGE and the proteins were transferred to Hybond-P nitrocellulose membranes (GE Healthcare, Hong Kong, China). The following antibodies were used: anti-beta subunit of ATP synthase (ATP4, PhytoAB PHY0587S, 1:1000; ATPβ, Agrisera AS05 085, 1:4000); anti-cytochrome oxidase subunit II (COXII, Agrisera AS04 053A, 1:2000); anti-cytochrome oxidase subunit III (COXIII, PhytoAB PHY0580S, 1:1000); anti-NAD4 (PhytoAB PHY0511S, 1:1000); anti-NAD9 (from Dr. G. Bonnard, 1:50,000); anti-51kDa (PhytoAB PHY0525S, 1:1000). The signals were developed by the Enhanced Chemiluminescence method (ECL; GE Healthcare, Hong Kong, China).

Supplementary Materials

The following are available online at https://www.mdpi.com/1422-0067/21/24/9378/s1. Figure S1: Sanger sequencing of three biological replicates of each sample. Table S1: Normalized read count for each mitochondrial transcript in the three tissues. Table S2. RNA edited sites in the mitochondrial genome identified in this study. Table S3. Differentially edited RNA editing sites. Table S4: Expression of nuclear intron maturases in the three tissues. Table S5. Primers used in this study.

Author Contributions

B.L.L. and H.-M.L. designed and coordinated the study; Y.S. led the experimental works related to Sanger sequencing intron splicing, isolation of mitochondria, in-gel activity assays, and Western blotting; M.X. performed bioinformatic analysis of the RNA and DNA sequencing data; Z.X. participated in the in-gel activity assays; K.C.C. and J.Y.Z. participated in the isolation of mitochondria and Western blotting; K.F. and J.W.-B. grew the soybean, performed inoculation, and prepared the RNA samples; B.L.L., H.-M.L. and Y.S. wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Hong Kong Research Grants Council Area of Excellence Scheme (AoE/M-403/16), and the Innovation and Technology Fund (Funding Support to State Key Laboratory of Agrobiotechnology) of the HKSAR, China. Any opinions, findings, conclusions, or recommendations expressed in this publication do not reflect the views of the Government of the Hong Kong Special Administrative Region or the Innovation and Technology Commission.

Acknowledgments

We thank Zeta Mui for her help in sample preparation. Man-Wah Li and Qianwen Wang assisted with the analysis of genomic and transcriptome data.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Validation of matR RNA editing by RT-PCR and Sanger sequencing. N, nodule, SR, stripped root, UR, uninoculated root. The numbers (e.g., N11) represented the editing site locates in the 11th amino acid codon of the GlmaxMp73 (matR) transcript. The average percentages (with SD values) of RNA editing of three biological replicates obtained by RNA-seq are shown below the Sanger sequences.
Figure 1. Validation of matR RNA editing by RT-PCR and Sanger sequencing. N, nodule, SR, stripped root, UR, uninoculated root. The numbers (e.g., N11) represented the editing site locates in the 11th amino acid codon of the GlmaxMp73 (matR) transcript. The average percentages (with SD values) of RNA editing of three biological replicates obtained by RNA-seq are shown below the Sanger sequences.
Ijms 21 09378 g001
Figure 2. Phylogenetic tree of soybean intron maturases. Evolutionary analysis was conducted with MEGA X using the Unweighted Pair Group Method with Arithmetic Mean (UPGMA) method [29].
Figure 2. Phylogenetic tree of soybean intron maturases. Evolutionary analysis was conducted with MEGA X using the Unweighted Pair Group Method with Arithmetic Mean (UPGMA) method [29].
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Figure 3. Quantitative RT-PCR analysis of splicing efficiency of mitochondrial transcripts. (a) Splicing efficiencies of mitochondrial transcripts in nodule and stripped root samples were compared with that of the root sample. The ratio of spliced mRNA to unspliced mRNA is designated as the splicing efficiency. The splicing efficiencies of nodules or stripped roots were divided by the splicing efficiency of roots. (b) The relative abundance of spliced mitochondrial mRNAs of nodule and stripped root samples were compared with that of roots. The histogram shows the log2 ratios of spliced transcripts. Values are means SD of three biological replicates.
Figure 3. Quantitative RT-PCR analysis of splicing efficiency of mitochondrial transcripts. (a) Splicing efficiencies of mitochondrial transcripts in nodule and stripped root samples were compared with that of the root sample. The ratio of spliced mRNA to unspliced mRNA is designated as the splicing efficiency. The splicing efficiencies of nodules or stripped roots were divided by the splicing efficiency of roots. (b) The relative abundance of spliced mitochondrial mRNAs of nodule and stripped root samples were compared with that of roots. The histogram shows the log2 ratios of spliced transcripts. Values are means SD of three biological replicates.
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Figure 4. In-gel activity of the mitochondrial respiratory complexes separated by BN-PAGE. Complex I activity (a), Complex II activity (b), and Western blotting (c). UR, uninoculated roots; SR, stripped roots; N, nodules. I, complex I; I + III2, supercomplex composed of complex I and dimeric complex III; II, complex II. For Western blotting, 10 µg mitochondrial proteins were separated by SDS-PAGE and blotted with antibodies. Three biological replicates were run and the results were reproducible. The representative images are shown in (ac).
Figure 4. In-gel activity of the mitochondrial respiratory complexes separated by BN-PAGE. Complex I activity (a), Complex II activity (b), and Western blotting (c). UR, uninoculated roots; SR, stripped roots; N, nodules. I, complex I; I + III2, supercomplex composed of complex I and dimeric complex III; II, complex II. For Western blotting, 10 µg mitochondrial proteins were separated by SDS-PAGE and blotted with antibodies. Three biological replicates were run and the results were reproducible. The representative images are shown in (ac).
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Table 1. Summary of RNA-seq sequencing data.
Table 1. Summary of RNA-seq sequencing data.
SampleRead Length (bp)Read CountTotal Length (bp)
Stripped rootD312566,851,3908,356,423,750
E312575,008,4289,376,053,500
F312570,072,2188,759,027,250
NoduleD412568,175,3008,521,912,500
E412563,858,3367,982,292,000
F412562,615,1367,826,892,000
Control RootC08-Root1150111,230,35416,684,553,100
C08-Root2150106,852,72816,027,909,200
C08-Root3150115,102,33817,265,350,700
Table 2. Differentially expressed mitochondrial transcripts.
Table 2. Differentially expressed mitochondrial transcripts.
Gene IDGeneFunction DescriptionUR FPKMSR FPKMN FPKMN/URp-ValueN/SRp-ValueSR/URp-Value
GlmaxMp01ccmCcytochrome c biogenesis C15,86320,62010,8420.680.0000.530.0001.300.001
GlmaxMp51ccmFncytochrome c biogenesis FN4048298215860.390.0000.530.0000.740.006
GlmaxMp04cox3cytochrome c oxidase subunit III31,64331,48660,5201.910.0001.920.0001.000.943
GlmaxMp20-2nad1NADH dehydrogenase subunit 112,43021,95227,1332.180.0001.240.0021.770.000
GlmaxMp31-1nad2NADH dehydrogenase subunit 212,56519,32416,6261.320.0480.860.0011.540.009
GlmaxMp32nad4L-1NADH dehydrogenase subunit 4L30,65951,84339,5781.290.2570.760.0071.690.035
GlmaxMp46nad4L-2NADH dehydrogenase subunit 4L29,68547,50236,8631.240.3530.780.0091.600.057
GlmaxMp05-1nad5NADH dehydrogenase subunit 517,73926,99425,1701.420.0250.930.0361.520.014
GlmaxMp05-2nad5NADH dehydrogenase subunit 526,30342,02355,6542.120.0001.320.0031.600.004
GlmaxMp07rp15ribosomal protein subunit L515,18119,21710,2400.670.1450.530.0001.270.213
GlmaxMp53rps1ribosomal protein S1969521,17317,8741.840.0130.840.0052.180.004
GlmaxMp16rps12ribosomal protein S1210,42111,11019,8131.900.0011.780.0001.070.572
GlmaxMp08rps14ribosomal protein subunit S1424,48625,45914,7040.600.0770.580.0001.040.826
GlmaxMp52rps4ribosomal protein S4673715,17416,2962.420.0041.070.0122.250.006
Three samples of each tissue were sequenced and the average FPKM is presented in this table. Student’s t-tests were carried out between tissues. Ratios that are significantly increased or decreased (fold change > 1.5 or < 0.067, p-value < 0.05) are shown in bold.
Table 3. RNA editing sites in matR transcripts.
Table 3. RNA editing sites in matR transcripts.
Genome PositionTranscript PositionA.A. PositionCodon ChangeA.A. ChangeNodule Average Editing Degree (%)Stripped Root Average Editing Degree (%)Root Average Editing Degree (%)Changes (N-UR) (%)Changes (N-SR) (%)Changes (SR-UR) (%)Editing Sites in Arabidopsis (Y/N) *Editing Degree (%) *Editing Sites in Soybean (Y/N) #
340,0053211TCC>-<TTCS>-<F88 ± 3 a72 ± 3 b67 ± 4 b21165No-Yes
339,89014749TTC>-<TTTNo (F)26 ± 1 a12 ± 2 b13 ± 4 b1314−1No-No
339,84419365CCA>-<TCAP>-<S92 ± 3 a79 ± 2 b77 ± 3 b15132No-Yes
339,80123679TCC>-<TTTS>-<F93 ± 2 a81 ± 2 b69 ± 2 c241212No-Yes
339,711326109CCA>-<CTAP>-<L75 ± 4 a69 ± 1 b74 ± 2 a06−6Yes87Yes
339,633404135TCG>-<TTGS>-<L84 ± 0 a48 ± 3 b63 ± 2 c2035−15Yes90No
339,126911304GCC>-<GTCA>-<V17 ± 2 a13 ± 0 b19 ± 5 ab−24−6No-No
338,9761061354CCC>-<CTCP>-<77 ± 2 a47 ± 6 b61 ± 2 c1530−15No-Yes
338,4951542514CCC>-<CCTNo (P)42 ± 1 a22 ± 2 b20 ± 4 b22202Yes43No
338,3611676559TCT>-<TTTS>-<F91 ± 1 a79 ± 2 b87 ± 1 c413−9Yes88Yes
338,3401697566CCT>-<CTTP>-<L91 ± 1 a68 ± 2 b84 ± 1 c723−16Yes84Yes
338,3201717573CGC>-<TGTR>-<C80 ± 2 a55 ± 2 b69 ± 2 c1125−14Yes83Yes
338,3061731577TAC>-<TATNo (Y)97 ± 1 a93 ± 1 b95 ± 0 c24−2No-No
338,2841753585CAC>-<TACH>-<Y93 ± 0 a78 ± 2 b88 ± 1 c515−10Yes79Yes
338,2141823608CCC>-<CTCP>-<L83 ± 1 a72 ± 1 b71 ± 1 b12112No-Yes
338,1961841614TCA>-<TTAS>-<L97 ± 1 a91 ± 1 b96 ± 1 a17−5Yes93Yes
338,1861851617GTC>-<GTTNo (V)42 ± 2 a33 ± 1 b39 ± 2a39−6No-No
The MatR gene is located on the negative strand. All the RNA editing sites are C-< U changes. Sites validated by RT-PCR in Figure 1 were underlined. * Editing sites identified in Arabidopsis thaliana (Sun et al., 2017). # Editing sites previously reported in soybean matR (Thomson et al., 1994). abc Sites with significant differences (Student t-test, p < 0.05) in the degree of editing between the samples were labelled by different letters.
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Sun, Y.; Xie, M.; Xu, Z.; Chan, K.C.; Zhong, J.Y.; Fan, K.; Wong-Bajracharya, J.; Lam, H.-M.; Lim, B.L. Differential RNA Editing and Intron Splicing in Soybean Mitochondria during Nodulation. Int. J. Mol. Sci. 2020, 21, 9378. https://doi.org/10.3390/ijms21249378

AMA Style

Sun Y, Xie M, Xu Z, Chan KC, Zhong JY, Fan K, Wong-Bajracharya J, Lam H-M, Lim BL. Differential RNA Editing and Intron Splicing in Soybean Mitochondria during Nodulation. International Journal of Molecular Sciences. 2020; 21(24):9378. https://doi.org/10.3390/ijms21249378

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Sun, Yuzhe, Min Xie, Zhou Xu, Koon Chuen Chan, Jia Yi Zhong, Kejing Fan, Johanna Wong-Bajracharya, Hon-Ming Lam, and Boon Leong Lim. 2020. "Differential RNA Editing and Intron Splicing in Soybean Mitochondria during Nodulation" International Journal of Molecular Sciences 21, no. 24: 9378. https://doi.org/10.3390/ijms21249378

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