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Comparative transcriptome analysis reveals that tricarboxylic acid cycle-related genes are associated with maize CMS-C fertility restoration

Abstract

Background

C-type cytoplasmic male sterility (CMS-C) is one of the three major types of cytoplasmic male sterility (CMS) in maize. Rf4 is a dominant restorer gene for CMS-C and has great value in hybrid maize breeding, but little information concerning its functional mechanism is known.

Results

To reveal the functional mechanism of Rf4, we developed a pair of maize near-isogenic lines (NILs) for the Rf4 locus, which included a NIL_rf4 male-sterile line and a NIL_Rf4 male fertility-restored line. Genetic analysis and molecular marker detection indicated that the male fertility of NIL_Rf4 was controlled by Rf4. Whole-genome sequencing demonstrated genomic differences between the two NILs was clustered in the Rf4 mapping region. Unmapped reads of NILs were further assembled to uncover Rf4 candidates. RNA-Seq was then performed for the developing anthers of the NILs to identify critical genes and pathways associated with fertility restoration. A total of 7125 differentially expressed genes (DEGs) were identified. These DEGs were significantly enriched in 242 Gene Ontology (GO) categories, wherein 100 DEGs were involved in pollen tube development, pollen tube growth, pollen development, and gametophyte development. Homology analysis revealed 198 male fertility-related DEGs, and pathway enrichment analysis revealed that 58 DEGs were enriched in cell energy metabolism processes involved in glycolysis, the pentose phosphate pathway, and pyruvate metabolism. By querying the Plant Reactome Pathway database, we found that 14 of the DEGs were involved in the mitochondrial tricarboxylic acid (TCA) cycle and that most of them belonged to the isocitrate dehydrogenase (IDH) and oxoglutarate dehydrogenase (OGDH) enzyme complexes. Transcriptome sequencing and real-time quantitative PCR (qPCR) showed that all the above TCA cycle-related genes were up-regulated in NIL_Rf4. The results of our subsequent enzyme-linked immunosorbent assay (ELISA) experiments pointed out that the contents of both the IDH and OGDH enzymes accumulated more in the spikelets of NIL_Rf4 than in those of NIL_rf4.

Conclusion

The present research provides valuable genomic resources for deep insight into the molecular mechanism underlying CMS-C male fertility restoration. Importantly, our results indicated that genes involved in energy metabolism, especially some mitochondrial TCA cycle-related genes, were associated with maize CMS-C male fertility restoration.

Background

Plant cytoplasmic male sterility (CMS) involves the shortage of functional pollen grains while female gametes are still normal. CMS is caused by a chimeric opening reading frame (ORF) resulting from spontaneous mitochondrial genome rearrangement [1]. Some nuclear genes that are referred to as restorer of fertility (Rf) genes can rescue CMS at different levels, such as the genomic, mRNA, protein, and metabolic levels [2,3,4]. The CMS/Rf system not only serves as an ideal model for studying communication between the nucleus and mitochondria but also represents a valuable tool for exploiting heterosis in hybrid seed production [2, 5]. At present, deep insight into plant CMS fertility restoration contributes to its wide utilization in hybrid seed production [6].

In maize, male-sterile cytoplasm can be divided into three categories according to the fertility restoration patterns displayed in the F1 hybrids: Texas (T), USDA (S) and Charrua (C) [7]. Among plants of these categories, C-type cytoplasmic male sterility (CMS-C) presents a stable male sterility and positively affects grain yield, contributing to its great application value in maize hybrid seed production [8, 9]. However, the fertility restoration mechanism of CMS-C appears to be highly complex. Previous studies have indicated that, with the exception of the two dominant Rf4 and Rf5 genes, quantitative trait loci (QTLs) are also involved in maize CMS-C fertility restoration [10,11,12]. These QTLs always partially restore CMS-C male fertility, which makes their use difficult. Moreover, Rf-I on chromosome 7 can inhibit the function of Rf5 but not Rf4 [13]. Furthermore, the genetic background of sterile lines might also affect the function of Rf genes in CMS-C, and the number of functional Rf gene might diverge when facing different male-sterile lines [14]. Overall, the complex mechanism of CMS-C fertility restoration brings about serious challenges to the application of CMS-C in hybrid seed production. Rf4 can completely rescue most of the maize CMS-C lines and has great potential value in maize CMS-C hybrid popularization and utilization. Much work has been undertaken for Rf4, which was preliminarily mapped to the short arm of chromosome 8 [15,16,17]. Rf4 was further mapped to a 1.5 cM interval (520 kb) that contained 12 candidate genes [18]. Rf4 was ultimately narrowed down to a 12 kb region at the tip of chromosome 8; this region contains two nuclear-targeted genes: GRMZM2G021276 and GRMZM2G582028 [19]. However, additional experimental evidence is needed to confirm the Rf4 candidate gene and to elucidate its functional mechanism.

Most restorer genes encode different pentatricopeptide repeat (PPR) proteins, enabling them both to be targeted to mitochondria where CMS genes and products are located and to bind to CMS transcripts [20, 21]. Surprisingly, no PPR-encoded genes were found in the final mapping region of Rf4, suggesting that Rf4 might be a new type of restorer gene [18]. Elucidating the Rf4 functional mechanism would be interesting, which may provide novel insights into plant CMS fertility restoration. However, the probability of Rf4 encoding a PPR protein cannot be excluded because the reference genome of B73 is still incomplete and because B73 might even lack Rf4. In this study, comparative transcriptome sequencing was performed on Rf4 near-isogenic lines (NILs) to reveal the functional mechanism of Rf4.

Methods

Plant materials

In this study, a nearly isogenic line at the Rf4 locus (NIL_Rf4) was developed for comparative genome and transcriptome analyses. NIL_Rf4 was developed from the maize inbred donor line A619 (Rf4Rf4) and the CMS-C male-sterile recipient line C698–3 (rf4rf4) (NIL_rf4). Moreover, the male-fertile plants (> 5 plants) were backcrossed with the plants of maintainer line 698–3 (rf4rf4) to produce the subsequent generation of the backcross population. Briefly, plants from the BC4 and BC5 populations were used for phenotype and genotype characterization, male-fertile plants from both the BC5 population and line C698–3 were used for comparative genome and transcriptome analysis, and male-fertile plants from the BC6 population were used for measurements of isocitrate dehydrogenase (IDH) and oxoglutarate dehydrogenase (OGDH) enzyme abundance. Specifically, fresh leaves from three NIL_Rf4 or NIL_rf4 individuals were separately mixed for genome sequencing. Moreover, spikelets at the pollen maturation stage with a length of 0.7–0.8 cm were collected from three individual fertile plants (NIL_Rf4_r1, NIL_Rf4_r2, and NIL_Rf4_r3) and three individual sterile plants (NIL_rf4_r1, NIL_rf4_r2, and NIL_rf4_r3) for transcriptome sequencing. The samples were frozen directly in liquid nitrogen and then stored at − 70 °C.

Phenotype and genotype characterization

To characterize NIL_Rf4, the male fertility of each individual in backcross populations BC4 and BC5 was investigated. For male fertility, both anther exertion and pollen fertility were rated as we described previously [14]. Moreover, in that report, we developed a tightly linked Rf4 marker (5′-CGCACCTAACCGTCTCC-3′, 5′-GCGCAAGTACGCCGTAC-3′). Here, the marker was used to confirm all plant genotypes in the BC5 backcross population. Genomic DNA from the fresh leaves of each plant was extracted using the modified cetyl-trimethylammonium bromide (CTAB) method [22]. PCR amplification was performed using Tsingke PCR Master Mix (Tsingke, China) in accordance with its specifications.

Genome-Seq mapping, single nucleotide polymorphism (SNP) calling and annotation

Genomic DNA was isolated from the fresh leaves of NIL_Rf4 (BC5) and NIL_rf4 using a Plant Genomic DNA Kit (Tiangen, China). The concentration, purity, and integrity of the DNA samples were examined using 1% agarose gels, a NanoDrop 2000 Spectrophotometer and a Qubit fluorometer (Thermo Fisher Scientific, USA). Afterward, the two DNA composites were sent to Novogene Technology Co., Ltd. (Beijing, China) for library construction and sequencing. Paired-end sequencing libraries were prepared for genome sequencing on an Illumina HiSeq™ 2500 analyser (Illumina, USA). The length of the reads was 150 bp, and paired ends were obtained. Before mapping, we removed the adaptor fragments, low-quality sequences (≥ 50% of the bases with a quality score Q ≤ 5), and impurities (N > 10%). BWA 0.7.8 (parameters: mem -t 4 -k 32 -M -R) was used to map the clean reads against the B73 reference genome sequence (ftp://ftp.ensemblgenomes.org/pub/release-31/plants/fasta/zea_mays/dna/). SNP calling was performed with SAMtools 0.1.19 software [23]. Low-quality SNPs with a base quality value < 20 or with a read depth < 4 or > 1000 from the two composite sequences were excluded. The SNPs were categorized as exonic, intronic, intergenic, and splicing as well as within the untranslated region (UTR) based on their positions. Moreover, an average SNP index [24, 25] was calculated for both samples using a sliding window analysis with a 100 kb window size and a 10 kb increment.

Identification and characterization of non-reference genes

Unmapped reads of NILs were used to assemble contigs by SOAPdenovo with default parameters. Novel gene models were predicted using Genewise and AUGUSTUS. Then, each novel gene putative function was annotated using the InterPro (http://www.ebi.ac.uk/interpro/), KEGG (https://www.kegg.jp/), Swissprot (https://www.uniprot.org/), TrEMBL (https://www.uniprot.org/), and GO (http://www.geneontology.org/) databases. HMMER 3.0 software with the Hidden Markov (HMM) profile of PPR domain (PF01535) was used to identify PPR genes among novel genes. TargetP (http://www.cbs.dtu.dk/services/TargetP/) was used to predict each novel gene subcellular location.

RNA-Seq mapping

The total RNA of six samples, which included three NIL_rf4 samples (NIL_rf4_r1, NIL_rf4_r2, and NIL_rf4_r3) and three NIL_Rf4 (BC5) samples (NIL_Rf4_r1, NIL_Rf4_r2, and NIL_Rf4_r3), was respectively extracted using a Qiagen RNeasy Kit (Qiagen, USA). The concentration, purity, and integrity of the RNA samples were examined using 1% agarose gels, a NanoDrop 2000 Spectrophotometer (Thermo Fisher Scientific, USA), and an Agilent Bioanalyzer 2100 System (Agilent Technologies, USA). DNase I was used to digest the residual genomic DNA. The samples were subsequently sent to Chengdu Basebio Biotechnology Company (China) for library construction and transcriptome sequencing on an Illumina HiSeq™ 2500 platform (Illumina, USA). Raw reads (150 bp paired-end) were filtered in accordance with the same method used for Genome-Seq. Clean reads from the RNA-Seq were mapped via TopHat v2.0.9 to the same version of the B73 reference genome as that used for Genome-Seq. Only reads that uniquely mapped to the reference genome were used for further analysis.

Identification of differentially expressed genes (DEGs) and functional analysis

Transcripts per million (TPM) was used to calculate the expression of each transcript [26]. Based on the normalized transcript expression, the P_values were corrected in accordance with the Benjamini-Hochberg method, and Q_value (corrected P_value) < 0.01 served as the threshold for screening the DEGs. All the DEGs were then subjected to Gene Ontology (GO) analysis (http://bioinfo.cau.edu.cn/agriGO/analysis.php) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis (http://www.genome.jp/kegg/) via hypergeometric tests. In the above enrichment analyses, the P_values were corrected with the default methods on the websites, and Q_value ≤0.05 was used as the threshold for selecting significantly enriched GO terms and KEGG pathways.

To identify the potential genes involved in altering male fertility, all the DEGs with an E_value <1e− 30 were queried in the Plant Male Reproduction Database (PMRD) (http://202.120.45.92/addb/), which contains 548 male fertility-related genes in Arabidopsis. The maize gene sequences were retrieved from MaizeGDB (ftp://ftp.ensemblgenomes.org/pub/plants/release-31/fasta/zea_mays). Afterward, all target gene expression data (fragments per kilobase of exon per million fragments mapped (FPKM)) in various tissues were obtained from qTeller (www.qteller.com). The FPKM values were log2 normalized (FPKM + 1), after which the Z-scores for each gene were calculated to assess their tissue expression specificity. Moreover, the corresponding information on PPR genes in maize was obtained from a recent report [27].

Enzyme-linked immunosorbent assay (ELISA) detection of IDH and OGDH abundance in spikelets

A total of 100 mg of spikelets whose length ranged from 0.7–0.8 cm at the pollen maturation stage (the same stage as that used for transcriptome sequencing) of three individual sterile NIL_rf4 plants and three individual fertile NIL_Rf4 plants (BC6) was collected for IDH and OGDH content measurements. Each sample was fully pelletized in 900 μL of PBS (0.01 mol/L, pH = 7.2–7.4), chilled on ice and ultrasonicated for 30 min with 300 W of power to obtain mitochondrial IDH and OGDH. The homogenates were then centrifuged (5000 g, 10 min, 4°C), after which the supernatants were ultimately used for IDH and OGDH content measurements via ELISA kits (Nanjing SenBeiJia Biological Technological Co., Ltd., China) in accordance with the manufacturer’s protocol. Each sample was tested three times, and statistical differences were tested by independent Student’s t-tests.

Real-time quantitative PCR (qPCR) analysis

To measure the expression levels of the tricarboxylic acid (TCA) cycle-related genes and validate the accuracy of the transcriptome sequencing, 12 and 9 genes were respectively selected to analyse their expression via qPCR (see primer information in Additional file 1). 18S RNA was used as an internal control. The RNA samples were prepared in the same manner as those used for RNA-Seq. One microgram of total RNA from each sample was used to synthesize cDNA via a PrimeScript™ RT Reagent Kit (TaKaRa, China) with RT-Primer Mix. qPCR was conducted on a CFX96™ Real Time system (Bio-Rad, USA) in conjunction with SYBR Green Real-time PCR Master Mix (TaKaRa, China). The comparative threshold cycle (CT) method (2−ΔΔCt) was then used to assess the relative expression level of each gene [28].

Results

Characterization of NIL_Rf4

Only two phenotypes, complete male fertility and complete male sterility, were observed in the BC4 and BC5 populations, and the male-fertile plants could form normal pollen and flowered normally (see Additional file 2). We observed a 1:1 ratio in terms of the number of plants that produced normal pollen and the number of plants that displayed aborted pollen in the BC4 and BC5 populations, indicating that male fertility was controlled by one single nuclear gene (see Additional file 3). In addition, we observed that the male fertility of the BC5 population co-segregated with the tightly linked the Rf4 marker (see Additional file 4). The above results indicated that Rf4 was successfully transferred to NIL_Rf4.

Genomic profiles of NILs

To reveal genomic variations between the NILs, polymorphic SNPs were detected using whole-genome sequencing. Total amounts of 98,331,340 and 83,494,528 short reads were obtained from NIL_Rf4 (7.44× depth coverage) and NIL_rf4 (6.48× depth coverage), respectively. These reads were then aligned to the B73 reference genome. A total of 1,216,260 SNPs between NIL_Rf4 and NIL_rf4 were identified throughout the whole genome, of which 26,383 SNPs were located in exons, 58,671 SNPs were located in introns, 169 SNPs were located at the variable splicing sites, 41,150 SNPs were located in UTRs, and 1,089,887 SNPs were located in intergenic regions (Fig. 1a). The above results showed that these SNPs were located mainly in noncoding regions. The genome sequencing results indicated that GRMZM2G122850 was the unique gene that harboured amino acid changes in the Rf4 mapping region. GRMZM2G122850 encodes a selenium-binding protein that contains 390 amino acid residues; subcellular localization prediction via TargetP showed that this protein might be targeted to the mitochondria. Four SNPs were found to be located in its coding sequence and caused two missense mutations: R316H and D359N. These SNPs were confirmed via the dideoxy chain-termination method (see Additional file 5), and their potential effects need to be studied further.

Fig. 1
figure1

a Distribution of SNPs and DEGs between NIL_Rf4 and NIL_rf4. From inner circle to the outer circle, the first and the second circles indicate the distribution of SNPs within exons and genome, respectively. In the third circle, the green dots represent up-regulated transcripts in NIL_Rf4, while the red dots represent down-regulated transcripts. b SNP index graphs of the NIL_Rf4 (yellow lines) and NIL_rf4 (black lines)

Next, a SNP index was calculated for each identified SNP, and all SNP indexes of the two samples were plotted onto the whole maize genome (Fig. 1b). We found that the NILs shared similar SNP indexes across the majority of the maize genome. However, a series of biased SNP indexes were observed on the short arm of chromosome 8 from 0 to 1 Mb, which is consistent with the Rf4 mapping region [19]. These results demonstrated that the genomic variations between NILs were located mainly near the Rf4 locus.

Putative functions of novel genes

As stated before, the reference genome of B73 may not be complete and it may even miss the sequence of Rf4. In this study, those unmapped reads were further assembled and annotated. We obtained 2890 putative genes in NILs (see Additional file 6) and most of their functions (> 90%) could be annotated (see Additional file 7). Among the novel genes, 645 genes could be targeted to the mitochondria and one PPR protein (Contig.4402.1) was found. These novel genes might help to uncover Rf4 candidates in the future.

Transcriptomic profiles of NILs

Six libraries, which consisted of three biological replicates per line, were prepared for RNA-Seq. A total of 265 million 150 bp paired-end reads were obtained for 6 samples; the reads for each sample ranged from 37 million to 54 million. The read length of all samples combined was > 37 Gb, representing an approximately 15-fold coverage of the maize genome. Approximately 71% of these short reads could be uniquely mapped to the reference genome (Table 1). Pearson correlation coefficient analysis revealed that the r2 value was greater than 0.93 for both groups and revealed both high correlations between and slight variability among biological replicates, showing the reliability of the transcriptome sequencing data (Fig. 2).

Table 1 Summary of RNA-Seq yields and alignments for six samples
Fig. 2
figure2

Pearson correlation coefficient analysis of the transcriptome data for three biological replicates

Validation and functional characterization of DEGs

To detect transcriptomic variation during male fertility conversion, the expression levels of all genes expressed in developing spikelets were compared between NIL_Rf4 and NIL_rf4 (Fig. 1a). In total, 7125 DEGs with 8125 transcripts were identified, the latter of which 91.22% (7740/8125) were up- or down-regulated by ≥2.0-fold. Among the 7125 DEGs, 3873 genes were up-regulated in NIL_Rf4, and 3252 genes were down-regulated. The abundance of DEGs suggested that changes in gene expression were active during the fertility restoration of CMS-C maize. By combining our Genome-Seq data, we identified a total of 1679 DEGs that had exonic SNPs throughout the whole genome (Fig. 1a and Additional file 8). Additional analyses of these DEGs might help to reveal the fertility restoration mechanism of Rf4. To verify the accuracy of the transcriptome changes revealed by RNA-Seq in this study, the transcript levels of nine randomly selected DEGs were subsequently examined via qPCR (Fig. 3). The expression patterns of these nine genes obtained by qPCR were highly consistent with the results of RNA-Seq (r2 = 0.9536), which confirmed the reliability of the transcriptome sequencing results.

Fig. 3
figure3

Correlation of gene expression levels estimated by RNA-Seq and qPCR. The x-axis and y-axis indicate relative expression values from qPCR and RNA-Seq, respectively. Both values are log2 normalized. The r value represents the Pearson correlation coefficient

To determine their putative function, the DEGs were subjected to GO analysis. A total of 5269 DEGs were annotated with 4810 GO terms. Within the biological process category, metabolic process, cellular process, and single-organism process were the top three abundant clusters. Under the cell component category, there were 451 enriched GO terms, and most of those genes were categorized as cell and cell part. With respect to the molecular function category, binding and catalytic activity were the most abundant subcategories. In addition, hypergeometric tests revealed 242 significantly enriched GO terms (see Additional file 9). Among the 242 GO terms, 4 terms were associated with 100 DEGs directly involved in pollen formation: pollen tube development (GO0048868), pollen tube growth (GO0009860), pollen development (GO0009855), and gametophyte development (GO0048229). RNA-Seq revealed that 74 of the 100 genes associated with the four abovementioned GO terms were up-regulated in the male-fertile NIL_Rf4 plants (Fig. 4a), indicating that most of these genes play a positive regulatory role in maize pollen formation. Moreover, Euler diagram analysis revealed that most of these genes have various functions in pollen development (Fig. 4b). Importantly, four of them, GRMZM2G170400 (phosphoethanolamine N-methyltransferase 3), GRMZM2G060886 (S-adenosyl-L-methionine-dependent methyltransferase), GRMZM2G122296 (phosphoethanolamine N-methyltransferase 1-like), and GRMZM2G113506 (galacturonosyltransferase), are associated with all of the GO terms related to pollen development, implying their crucial effect on pollen development.

Fig. 4
figure4

Expression (a) and Euler diagram (b) analyses of DEGs related to pollen development

Identification of male fertility-related DEGs

To identify key genes related to stamen development, the DEGs were aligned with 548 male Arabidopsis reproductive genes retrieved from the PMRD. A total of 198 genes were highly homologous to these Arabidopsis male reproductive genes; the cut-off E_value was <1e− 30 (see Additional file 10). Among these target genes, 63 were preferentially expressed in maize anthers and tassels (see Additional file 11), suggesting that they might play a critical role in maize male reproduction. Most of the Rf proteins are encoded by the PPR gene family. To reveal potential PPR genes involved in maize CMS-C fertility restoration, 56 differentially expressed PPR proteins were observed, among which 16 and 28 are located in the mitochondrion and chloroplast, respectively (see Additional file 12). However, only two differentially expressed PPR genes, ZmPPR432 (GRMZM5G851564) and ZmPPR443 (GRMZM2G050485), were found on chromosome 8, but both were far from the mapping region of Rf4 and could not be the Rf4 candidate gene.

Identification of energy metabolism-related DEGs

Plant male fertility conversion is tightly associated with energy metabolism, and energy deficiency may cause male sterility [2, 29]. To gain a deep insight into the energy mechanism underlying CMS-C maize fertility restoration, 58 DEGs were found via KEGG analysis to participate in cell energy metabolism processes such as glycolysis, the pentose phosphate pathway, and pyruvate metabolism (Table 2). Among the 58 energy metabolism-related genes, 31 and 27 were up-regulated and down-regulated in NIL_Rf4, respectively. GRMZM2G154007, which encodes an alcohol dehydrogenase-like 2 protein, was the most up-regulated gene (fold change = 4096), whereas GRMZM2G345493, which encodes a fructose-bisphosphate aldolase 7 protein, was the most down-regulated gene (fold change = − 2048). Interestingly, two glycolysis-related genes (GRMZM5G824600 and GRMZM2G071630) were not expressed in NIL_Rf4 or NIL_rf4, respectively. The different expression levels of the energy metabolism-related genes indicated the potential different energy levels between NIL_rf4 and NIL_Rf4 and that energy metabolism processes might play a key role in CMS-C fertility restoration.

Table 2 Annotations of energy metabolism-related DEGs

The abundance of IDH and OGDH in the mitochondrial TCA cycle were associated with fertility restoration

Our KEGG analysis results above showed the probable different energy metabolism levels between NIL_Rf4 and NIL_rf4. The mitochondrial TCA cycle plays a crucial role in energy metabolism [30]. As such, all DEGs were queried in the Plant Reactome Pathway database (http://plantreactome.oicr.on.ca/), and fourteen DEGs that participate in the mitochondrial TCA cycle were identified. Among these DEGs, GRMZM2G079538/GRMZM5G807639 and GRMZM2G142863/GRMZM2G151041 are duplicate genes. The RNA-Seq data demonstrated that these genes were all up-regulated in NIL_Rf4 (Fig. 5), and the qPCR results confirmed the changes in their expression between NIL_Rf4 and NIL_rf4 (Fig. 6). Expression profile analysis revealed that these genes were expressed mainly in the anthers and tassels (see Additional file 13). We also used qPCR to explore the expression levels of these genes in developing anthers and leaves (see Additional file 13). For the maintainer line(HZS), the expression levels of these genes were similar between leaves and developing anthers; while for the CMS-C male-sterile line (CHZS), most of them were highly expressed in anthers during meiosis I. Compared with the maintainer line, all of these genes tended to show higher transcription levels at meiosis I in the male-sterile line. Three (GRMZM2G120857, GRMZM2G018566, GRMZM2G025366) and six (GRMZM2G807639, GRMZM2G151041, GRMZM2G142863, GRMZM2G335657, GRMZM2G079538, GRMZM2G151169) genes were found to participate in the IDH and OGDH complexes, respectively, both of which are key enzymes in the TCA cycle. Our additional ELISA experiments showed that the abundance of both IDH and OGDH was significantly higher in NIL_Rf4 than in NIL_rf4 (Fig. 7). The above results indicated that the genes related to the TCA cycle were associated with CMS-C male fertility.

Fig. 5
figure5

Identification of DEGs involved in the mitochondrial TCA cycle. The number indicates the gene expression fold changes that were log2 transformed in NIL_Rf4 compared with NIL_rf4

Fig. 6
figure6

qPCR confirmation of genes associated with the mitochondrial TCA cycle. The data are given as means ± SEMs of three biological replicates. Independent Student’s t-tests were used to calculate the P values. **P < 0.01

Fig. 7
figure7

Comparison of IDH and OGDH enzyme levels between NIL_Rf4 and NIL_rf4. The data are presented as the means ± SEMs of three biological replicates. Each replicate consisted of three technical replicates. The asterisks represent statistically significant differences between NIL_Rf4 and NIL_rf4 at P < 0.05 (*) or P < 0.01 (**) (Independent Student’s t-test)

Discussion

As a dominant restorer gene for CMS-C, Rf4 has great potential value in hybrid maize seed production. Understanding the function approach of Rf4 will also benefit for revealing the abortive mechanism of maize CMS-C. Until now, the Rf4 candidate gene had not been confirmed, and its functional mechanism was unknown. In this study, lines that were nearly isogenic at the Rf4 locus were developed for comparative transcriptome analysis to uncover its function. The results of the genetic analysis and genotype characterization proved that the NIL_Rf4 male fertility was restored just by Rf4. Genome-Seq was used to reveal the genomic variation in the NILs, and the results confirmed that most of the SNPs were crowded near the Rf4 location. However, many SNPs were also gathered near the middle of chromosome 2. Various genomic differences clustering in the non-object area of NILs have also been reported in other studies [31]. In fact, NILs always present extensive residual heterozygosity because of the complexity of genomic composition and recombination [32, 33]. Moreover, previous studies in which SNP chips were used have generally reported the presence of SNPs between NILs [34,35,36]. Compared to SNP chips, next-generation sequencing has a broader and more sensitive detection ability, which might also explain why we detected more SNPs than did previous researchers.

Insufficient energy supplies can impair male gamete development but not vegetative organs, ultimately causing male sterility [2]. Previous studies have also shown that a close relationship exists between pollen dysfunction and energy metabolism in CMS-C. Three ATP-synthesizing chimeric ORFs, i.e., atp9-c, cox2-c, and atp6-c, were first identified in CMS-C plants [37]. Nevertheless, Meyer did not observe any chimeric proteins but did report that the expression of several ATP synthase complex proteins decreased within CMS-C tassels [38]. It can be inferred that pollen abortion in CMS-C plants is caused by inadequate ATP production because of the low atp9-c translation efficiency. Moreover, our group analysed the differences between the male-sterile line (C48–2) and its maintainer line N48–2, and we found that some DEGs and differentially expressed proteins were related to energy metabolism [39, 40]. At the metabolic level, compared to the anthers of the maintainer line, the anthers of the CMS-C line always present lower levels of respiratory intensity, cyanide-resistant respiration, cytochrome oxidase activity and ATP content during microspore development [41, 42]. In the present study, elevated IDH and OGDH enzyme levels were detected in the male fertility-restored line. Both IDH and OGDH are NADH-synthesizing enzymes and play a key role in the mitochondrial TCA cycle, which determines the energy supply in cells [29, 30]. Down-regulation of the mitochondrial citrate synthase enzyme ultimately causes male sterility [43]. Our results provided new evidence for the association between the mitochondrial TCA cycle and plant male fertility. Interestingly, when compared with the CMS-C male-sterile line, these TCA cycle-related genes were up-regulated in anthers of NIL_Rf4 while down-regulated in maintainer line anthers. These results revealed the probable existence of different energy metabolism-related genes expression levels between the maintainer line and NIL_Rf4 although they both were male fertile. This hypothesis needs to be further verified because the difference might also be caused by different pollen developmental stages in comparison.

With the exception of those in maize, many studies about CMS in other species show that, compared with normal lines, CMS lines always appear to have lower energy metabolism levels [44,45,46]. Mitochondria play an essential role in supplying cellular energy. Most mitochondrial proteins are encoded by nuclear genes; these proteins are synthesized in the cytoplasm and then imported into the mitochondria [47]. Recently, increasing amounts of attention have been paid to the connection between these nuclear-encoded mitochondrial proteins and CMS fertility restoration. Rf2 encodes a mitochondrial aldehyde dehydrogenase (ALDH) enzyme, and its expression can rescue maize T-type cytoplasmic male sterility (CMS-T) [48, 49]. Both GRP162 and RFC3 proteins accumulate within mitochondria and can directly interact with Rf5 to rescue HongLian cytoplasmic male sterility (HL-CMS) in rice [50, 51]. Hexokinase 6 is a mitochondrial-localized protein whose interaction with Rf6 is necessary for HL-CMS fertility restoration [52]. This report provided direct evidence that energy metabolism-related genes directly contribute to plant CMS fertility restoration. In our experiments, 14 up-regulated genes involved in the TCA cycle were identified; however, their detailed function in restoring the fertility of maize CMS-C requires further study.

Conclusions

Lines that were nearly isogenic at the Rf4 locus were developed and characterized via genetic analysis, molecular marker detection and whole-genome sequencing. Comparative transcriptome analysis between male-fertile NIL_Rf4 plants and male-sterile NIL_rf4 plants revealed several crucial genes and metabolic pathways during CMS-C male fertility restoration. Interestingly, all of the DEGs involved in the mitochondrial TCA cycle were up-regulated in the male-fertile NIL_Rf4 plants, and most of those DEGs tended to be involved in the IDH and OGDH complexes. Our ELISA results demonstrated that the abundance of both the IDH and OGDH enzymes was higher in NIL_Rf4 than in NIL_rf4, indicating that the IDH and OGDH enzymes might be related to maize CMS-C fertility restoration. These results expand the current understanding of maize CMS-C male fertility restoration.

Abbreviations

ALDH:

aldehyde dehydrogenase

CMS:

cytoplasmic male sterility

CMS-C:

C-type cytoplasmic male sterility

CMS-T:

T-type cytoplasmic male sterility

DEGs:

differentially expressed genes

ELISA:

enzyme-linked immunosorbent assay

FPKM:

fragments per kilobase of exon per million fragments mapped

GO:

Gene Ontology

HL-CMS:

HongLian cytoplasmic male sterility

HMM:

Hidden Markov Motif

IDH:

isocitrate dehydrogenase

KEGG:

Kyoto Encyclopedia of Genes and Genomes

NIL:

near-isogenic line

OGDH:

oxoglutarate dehydrogenase

ORF:

opening reading frame

PMRD:

Plant Male Reproduction Database

PPR:

pentatricopeptide repeat

qPCR:

real-time quantitative PCR

QTL:

quantitative trait locus

Rf:

restorer of fertility

SNP:

Single nucleotide polymorphism

TCA:

tricarboxylic acid

TPM:

transcripts per million

UTR:

untranslated region

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Acknowledgements

We thank colleagues at Novogene (Beijing, China) and Basebio (Chengdu, China) for their help in interpreting the genomic and transcriptomic data.

Funding

The present work was supported by the National Key Research and Development Program of China (2016YFD0101206) and the Science and Technology Department of Sichuan Province (2016NZ0106).

Availability of data and materials

The Genome-Seq and transcriptome sequencing raw data generated and analysed during the current study are available in the Fig SHARE repository (https://doi.org/10.6084/m9.figshare.5709637.v1, https://doi.org/10.6084/m9.figshare.5709646.v1, https://doi.org/10.6084/m9.figshare.5709658.v1).

Author information

YML designed the research, performed most of the experiments, and wrote the paper. GW performed most of the experiments and analysed the results. YYX, XWL, and JT performed part of the experiments. YLL, HL, SZZ, and CL provided advice for the experiment. MJC designed the research and revised the paper. All authors reviewed and approved the final manuscript.

Correspondence to Moju Cao.

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The authors declare that they have no competing interests.

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Additional files

Additional file 1:

List of primers used for qPCR in this study. 18S RNA was used as an internal control. (XLSX 12 kb)

Additional file 2:

Comparisons of male-fertile tassels (a), anthers (b), and pollen (c) between NIL_Rf4 and NIL_rf4. In Fig. (c), the pollen grains were stained with 1% (w/v) KI-I2. (TIF 787 kb)

Additional file 3:

Fertility segregations of the BC4 and BC5 populations. A chi-squared test was used to evaluate the fertility segregation ratios. (XLSX 11 kb)

Additional file 4:

Genotype analysis of the BC5 population via the dominant Rf4 tightly linked marker (5′-CGCACCTAACCGTCTCC-3′, 5′-GCGCAAGTACGCCGTAC-3′). F, fertile individuals; S, sterile individuals. (TIF 129 kb)

Additional file 5:

Validation of SNPs within the coding sequence of GRMZM2G122850. (TIF 191 kb)

Additional file 6:

Coding sequences of novel genes. (TXT 1323 kb)

Additional file 7:

Function annotations of novel genes. (XLSX 315 kb)

Additional file 8:

All DEGs with exonic SNPs. (XLSX 504 kb)

Additional file 9:

Two hundred forty-two significantly enriched GO terms obtained by Fisher’s test (Q ≤ 0.05). (XLSX 20 kb)

Additional file 10:

DEGs homologous to Arabidopsis male sterility (MS)/reproduction (MR) genes. (XLSX 35 kb)

Additional file 11:

Expression patterns of male reproduction-related DEGs. Their expression values (FPKM) were retrieved from the qTeller website (www.qteller.com), and the FPKM values were log2 transformed by (FPKM + 1); a Z-score was then calculated for each gene. (TIF 298 kb)

Additional file 12:

Identification of PPR genes among DEGs. “Direction” means relative to the expression level in NIL_Rf4. (XLSX 13 kb)

Additional file 13:

(a)Tissue expression profile of 14 TCA cycle-related DEGs. The expression data (FPKM values) were obtained from qTeller (www.qteller.com). The FPKM values were log2 transformed (FPKM + 1), and a Z-score was calculated for each gene. (b) Comparison of TCA-related DEGs expression levels between the male-sterile line CHZS and its maintainer line HZS. A1, A2, and A3 denote developing anthers with the length of 1.5~ 2.0 mm (meiosis I), 2.0~ 2.5 mm (meiosis II) and 2.5~ 3.0 mm (uninucleate microspore) respectively. The data are given as means ± SEMs of at least three biological replicates. The relationship between maize pollen development stage and anther lenght can be found in another report [53]. (TIF 466 kb)

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Keywords

  • Maize
  • Cytoplasmic male sterility
  • Fertility restoration
  • Oxoglutarate dehydrogenase
  • Isocitrate dehydrogenase
  • Transcriptome sequencing