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Fine Mapping of qRC10-2, a Quantitative Trait Locus for Cold Tolerance of Rice Roots at Seedling and Mature Stages

  • Ning Xiao ,

    Contributed equally to this work with: Ning Xiao, Wei-nan Huang

    Affiliations College of Bioscience and Biotechnology and Jiangsu Key Laboratory of Crop Genetics and Physiology, Yangzhou University, Yangzhou, Jiangsu Province, China, Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Wei-nan Huang ,

    Contributed equally to this work with: Ning Xiao, Wei-nan Huang

    Affiliation College of Bioscience and Biotechnology and Jiangsu Key Laboratory of Crop Genetics and Physiology, Yangzhou University, Yangzhou, Jiangsu Province, China

  • Xiao-xiang Zhang,

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Yong Gao,

    Affiliation College of Bioscience and Biotechnology and Jiangsu Key Laboratory of Crop Genetics and Physiology, Yangzhou University, Yangzhou, Jiangsu Province, China

  • Ai-hong Li,

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Yi Dai,

    Affiliation College of Bioscience and Biotechnology and Jiangsu Key Laboratory of Crop Genetics and Physiology, Yangzhou University, Yangzhou, Jiangsu Province, China

  • Ling Yu,

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Guang-qing Liu,

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Cun-hong Pan,

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Yu-hong Li,

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Zheng-yuan Dai ,

    yzxiaoning@gmail.com (ZD); jmchen@yzu.edu.cn (JC)

    Affiliation Lixiahe Agricultural Research Institute of Jiangsu Province, National Rice Industry Technology System of Yangzhou Comprehensive Experimental Station, Yangzhou, Jiangsu Province, China

  • Jian-min Chen

    yzxiaoning@gmail.com (ZD); jmchen@yzu.edu.cn (JC)

    Affiliation College of Bioscience and Biotechnology and Jiangsu Key Laboratory of Crop Genetics and Physiology, Yangzhou University, Yangzhou, Jiangsu Province, China

Fine Mapping of qRC10-2, a Quantitative Trait Locus for Cold Tolerance of Rice Roots at Seedling and Mature Stages

  • Ning Xiao, 
  • Wei-nan Huang, 
  • Xiao-xiang Zhang, 
  • Yong Gao, 
  • Ai-hong Li, 
  • Yi Dai, 
  • Ling Yu, 
  • Guang-qing Liu, 
  • Cun-hong Pan, 
  • Yu-hong Li
PLOS
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Abstract

Cold stress causes various injuries to rice seedlings in low-temperature and high-altitude areas and is therefore an important factor affecting rice production in such areas. In this study, root conductivity (RC) was used as an indicator to map quantitative trait loci (QTLs) of cold tolerance in Oryza rufipogon Griff., Dongxiang wild rice (DX), at its two-leaf stage. The correlation coefficients between RC and the plant survival rate (PSR) at the seedling and maturity stages were –0.85 and –0.9 (P = 0.01), respectively, indicating that RC is a reliable index for evaluating cold tolerance of rice. A preliminary mapping group was constructed from 151 BC2F1 plants using DX as a cold-tolerant donor and the indica variety Nanjing 11 (NJ) as a recurrent parent. A total of 113 codominant simple-sequence repeat (SSR) markers were developed, with a parental polymorphism of 17.3%. Two cold-tolerant QTLs, named qRC10-1 and qRC10-2 were detected on chromosome 10 by composite interval mapping. qRC10-1 (LOD = 3.1, RM171-RM1108) was mapped at 148.3 cM, and qRC10-2 (LOD = 6.1, RM25570-RM304) was mapped at 163.3 cM, which accounted for 9.4% and 32.1% of phenotypic variances, respectively. To fine map the major locus qRC10-2, NJ was crossed with a BC4F2 plant (L188-3), which only carried the QTL qRC10-2, to construct a large BC5F2 fine-mapping population with 13,324 progenies. Forty-five molecular markers were designed to evenly cover qRC10-2, and 10 markers showed polymorphisms between DX and NJ. As a result, qRC10-2 was delimited to a 48.5-kb region between markers qc45 and qc48. In this region, Os10g0489500 and Os10g0490100 exhibited different expression patterns between DX and NJ. Our results provide a basis for identifying the gene(s) underlying qRC10-2, and the markers developed here may be used to improve low-temperature tolerance of rice seedling and maturity stages via marker-assisted selection (MAS).

Key Message

With root electrical conductivity used as a cold-tolerance index, the quantitative trait locus qRC10-2 was fine mapped to a 48.5-kb candidate region, and Os10g0489500 and Os10g0490100 were identified as differently expressed genes for qRC10-2.

Introduction

Rice (Oryza sativa L.) is one of the three major food crops in the world and feeds about 21% of the global population in terms of per capita energy [1]. Cold stress is a common problem for rice cultivation and is a crucial factor affecting global food production [2]. A primary objective for rice breeding in low-temperature and high-altitude areas is to improve cold tolerance of rice cultivars. Therefore, mining cold-tolerant germplasms and mapping related genes would provide an opportunity to improve rice yield through marker-assisted selection (MAS) [3][5]. Recently, several quantitative trait loci (QTLs, e.g., Ctb-1, Ctb-2, qCTB3, qCTB7, and qCTB8) related to cold-induced rice damages to aboveground organs–including seedling mortality and growth, leaf wilting, and necrotic yellowing–were mapped [3], [6][11]. To date, however, only Ctb-1, which improves the seed setting rate by enhancing spikelet fertility, has been isolated and cloned and has been proven to be involved primarily in the ubiquitin-proteasome pathway [8]. QTLs contributing to cold tolerance of seedlings are located on several rice chromosomes, accounting for 4–49.3% of phenotypic variations [4], [12][22]. In addition, certain chromosomes also bear germination cold-tolerant QTLs [23], [24]. Cold tolerance of rice is controlled by multiple genes, and different cold-tolerance-related mechanisms take effect during the growth period of rice.

Nevertheless, cold-tolerant QTLs have not been reported in rice roots, an important underground organ that protects rice from cold stress. At low temperatures, the integrity of plant cellular membranes can be compromised by the accumulation of peroxide and oxide radicals, which increasing membrane permeability [25][27]. Rice roots are more sensitive to low temperature than leaves, and cold resistance at the seedling stage can be directly determined by the contribution of roots to cold resistance [28]. Therefore, root conductivity (RC) tests have been used to determine the degree of cold-induced injuries in wheat [29]. However, cold-tolerant QTLs have not been reported in rice roots based on the RC test.

Dongxiang wild rice (DX), a Chinese common wild rice (Oryza rufipogon Griff., AA genome) grown in Jiangxi Province (116°36′ E, 28°14′ N), is the northernmost wild rice known in the world [30]. It possesses extremely high tolerance to cold stress and is able to safely survive winter temperatures as low as –12.8°C [31]. In our present study, we reported fine mapping of a major QTL, qRC10-2, related to root cold tolerance using DX as a cold-tolerant donor and the cold-sensitive indica variety Nanjing 11 (NJ) as a recurrent parent. We also evaluated the effects of qRC10-2 at the seedling and maturity stages. The analysis of the QTL derived from the wild rice will provide novel alleles for improving rice cold tolerance by MAS and also genetic materials for understanding the molecular mechanism of cold tolerance in rice.

Materials and Methods

Plant Materials

The cold-tolerant variety DX was used as a donor parent to cross with the cold-sensitive NJ in the summer of 2006 (Fig. 1). Then, a primary mapping population was constructed by employing the advanced backcross approach described by Thomson et al. [32]. The F1 progeny was first backcrossed to NJ to produce 151 BC1F1 plants, which were then grown in a greenhouse, and subsequently each BC1F1 plant was individually backcrossed to the recurrent parent until BC2F1 was obtained. No cold phenotype was selected for RC during population development because phenotype evaluation is destructive and thus cannot be conducted on individual plants. All BC2F2 seeds from 151 BC2F1 plants were individually harvested, and the resulting population of 151 individual BC2F2 families was used for RC phenotypic characterization in September of 2008.

To eliminate the effect of qRC10-1, a single BC2F2 plant that contained the DX-introgressed segment at the locus qRC10-2 was selected for continuous backcrossing with NJ followed by MAS using the markers RM25570 and RM304. This yielded 14 BC4F2 backcross inbred lines (BILs). Later, 150 simple-sequence repeat (SSR) markers covering the whole genome were used to determine the genetic background recovery rates, which varied from 89.33% to 94.67% (Fig. S1). Among these BILs, L188-3 (hereafter, L188) had a background recovery rate of 94.67%, which was found to have low RC. A large BC5F2 fine-mapping population of 13,324 progenies was constructed by crossing NJ with L188 in the summer of 2012. Then, molecular markers were used to detect recombinant events covering qRC10-2. All needed recombinants were separately harvested and evaluated for RC, and the BC5F4 seeds from the BC5F3 lines were harvested to calculate the plant survival rate (PSR) at the seedling and maturity stages. All plants were grown in the Yangzhou Wantou experimental fields at the Lixiahe Agricultural Research Institute of Jiangsu Province (119°42′ E, 32°39′ N) in summer and in Sanya of Hainan Province (110°02′ E, 18°48′ N) in winter.

Evaluation of Cold Tolerance

The RC phenotypes of the BC2F1 and BC5F2 plants were measured as the average RC of the derived BC2F2 and BC5F3 plants across three replicates, respectively. Twenty seeds were randomly selected and placed in an illuminated incubator for growth to day 9. The seedlings were then given simulated diurnal alternating illumination treatment: 12 h dark at 4±1°C versus 12 h with 25,000 Lx of illumination at 4±1°C with relative humidity of 75–85%. After 48 h treatment, the 2-cm taproot section was immediately cut from each plant, and placed into an Eppendorf centrifuge tube with 2 mL deionized H2O (conductivity of 1.5 µs/cm). After soaking for 1 h, the RC of each plant was measured with a conductivity meter (Mettler Toledo 326) and data were adjusted for RC of deionized H2O.

Approximately 100 BC5F4 seeds were selected from each BC5F3 line with high or low RC to evaluate the PSR using the criteria of RC<10 and RC≥10 for cold tolerance and cold sensitivity, respectively. At day 9, the seedlings were cold-treated as described above and then returned to constant 28°C for recovery under illumination at 25,000 Lx for 72 h. The plants were divided into a sensitive group (with completely-withered leaves) and a tolerant group (normal growth). PSR was estimated as the proportion of the plants showing a tolerant phenotype to all the plants by percentage (0–100%). The PSR of each BC5F3 line was measured in three replicates.

Root cold tolerance at maturity was evaluated as follows: The BC5F4 seedlings obtained from the BC5F3 lines were planted in the field on May 10, 2013. Uniform seedlings were then transplanted into a hydroponic greenhouse on June 10 at Yangzhou University. The hydroponic pool was 880 cm long, 130 cm wide, and 50 cm deep. The cement anchoring the rice plants was 135 cm long, 16.7 cm wide, and 2.5 cm thick, and each had a plate of 14 holes that were 4.0 cm in diameter and away from each other by 10 cm. A single seedling was planted in each hole, which was fixed by cork and sponges. Each group (low RC vs. high RC) contained 126 plants in three replicates. The hydroponic solution (pH 5.8) contained 10 p.p.m. of nitrogen (NH4NO3), phosphorus (NaH2PO4), potassium (K2SO4), calcium (CaCl2), and magnesium (MgSO4) each, 2 p.p.m. of iron (Fe(III)-EDTA), and 0.5 p.p.m. of manganese (MnCl2), and the solution was changed every other day. An oxygen pump was used to provide a steady flow of hydroponic nutrients, which maintained the nutrient concentrations and pH conditions in the pool during plant growth from seedling to maturity. These concentrations were elevated to twice the starting concentrations 60 days later. After 15-day post-heading, the cold hydroponic solution at 5±1°C was circulated around the roots for 24 h. After recovery at 28°C for two days, the PSR was measured.

Linkage Mapping and QTL Analysis

A genetic linkage map was constructed with Mapmaker/Exp 3.0 [33]. The segregation data of each marker were statistically analyzed to measure the segregation distortion from Mendelian expectations. Table S1 lists the SSR markers. QTL analysis was conducted by composite interval mapping using QTL Cartographer 2.5 [34][36]. The logarithm of odds (LOD) threshold of 2.5 was used to identify QTLs while avoiding false positives.

DNA Extraction and Molecular Marker Analysis

DNA was extracted from leaves following the cetyltrimethylammonium bromide (CTAB) method [37]. All leaves were stored at –80°C before extraction. Additional SSR markers between RM25570 and RM304 were chosen from the Gramene database (http://www.gramene.org). The sequences of indica cv. 93-11 and japonica cv. Nipponbare were downloaded from IRGSP1.0 (http://rapdb.dna.affrc.go.jp/) and used to design insertion/deletion (indel) markers and real-time polymerase chain reaction (PCR) markers using Premier 5.0 (Tables S2 and S3).

PCR and electrophoresis were performed following the method of Panaud et al. [38]. PCR was performed in a 20 µL volume containing 20 ng of template DNA, 0.15 µL of 10 mM dNTPs, 2 U of Taq DNA polymerase, 2 µL of 10×PCR buffer (50 mM KCl, 10 mM Tris-HCl pH 8.3, 1.5 mM MgCl2, and 0.01% gelatin), and 1.5 µL of 2 µM forward and reverse primers each. The cycling conditions were 5 min at 94°C, followed by 35 cycles of 94°C for 1 min, 55°C for 1 min, and 72°C for 1 min, with a final extension at 72°C for 10 min. The PCR products were subjected to electrophoresis on 6% denaturing polyacrylamide gels, which were then stained with silver [39].

Data Analysis

Differences between parents and BILs for cold-related measurement were compared via t-test using SPSS 11.0 for Windows (SPSS Inc., 2002). The correlation coefficient between RC and the PSR was calculated using the SAS software (SAS Institute, 2000).

Gene Expression Analysis

At the two-leaf stage after cold treatment for 0, 6, 12, or 24 h, the total RNA was extracted from 100 mg roots and 100 mg leaves using the RNeasy extraction kit (Invitrogen, Carlsbad, CA, USA), and any remaining genomic DNA was removed by DNaseI treatment. Total RNA (3 µg) was used as a template for cDNA synthesis using M-MLV transcriptase (TaKaRa Biotechnology, Dalian, China) with oligo (dT)18 primer. On an ABI PRISM 7500 system (Applied Biosystems, Foster City, CA, USA), real-time PCR was performed in a 20 µL volume containing 2 µL of first-strand cDNA, 10 µL of 2×SYBR Premix Ex Taq (TaKaRa, Shiga, Japan), 0.4 µL of 50×ROX reference dye, and 2 µL of each primer (2.5 µM). The used amplification protocol was 95°C for 30 s, followed by 40 cycles of 95°C for 5 s and 60°C for 30 s. Rice Actin 1 was used as an internal control, and each experiment was repeated at least three times.

Results

RC is a Reliable Indicator of Cold Resistance in Rice Seedlings

RC was significantly different for DX and NJ at day 8 (P = 0.01, Table 1). The stem root was quite long and had excessive root hairs after 9 days, making it difficult to measure RC in an Eppendorf tube. Therefore the cold-treatment period was determined to be 9 days. The difference in RC between cold-sensitive and cold-tolerant plants was apparent for 1 h cold treatment (Fig. 2A). The RC for cold-tolerant seedlings increased to 8.1 at 24 h, but at 48 h the RC for DX decreased to 4.4 whereas that for NJ increased to 12.9. In addition, NJ had high RC of 16.2 at 72 h whereas the cold-tolerant DX had low RC of 5.3. The high RC in NJ can be explained by the observation that more intracellular liquids leak into the environment per unit time (Fig. 2B).

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Figure 2. RC of DX and NJ as the function of the time exposed to cold and soaking.

A. RC measured as a function of cold treatment duration. B. RC measured as a function of soaking time. An asterisk (*) indicates that the RC between NJ and DX was significantly different (P<0.01).

https://doi.org/10.1371/journal.pone.0096046.g002

QTLs for Cold Tolerance

After recovery at 28°C, DX grew normally, whereas NJ showed cold-induced injuries (Fig. 3A). The RC was 2.9 for the cold-tolerant DX and 12.1 for NJ, and the distribution of the RC phenotypes among the BC2F1 population was continuous and skewed towards tolerance (Fig. 3B).

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Figure 3. Cold-induced injury phenotype of parents and frequency distribution of BC2F1 plants after cold treatment.

A. Cold-induced injury phenotype of DX and NJ after exposure to 4°C for 48 h. B. Frequency distribution of the RC values among BC2F1 population. Arrows indicate the mean scores of DX and NJ.

https://doi.org/10.1371/journal.pone.0096046.g003

A total of 653 SSR markers were used to screen polymorphisms between the two parents. Only 113 markers were codominant, with the polymorphism of only 17.3%; all the 113 developed markers were mapped essentially and uniformly to the 12 chromosomes. Based on this, two seedling cold-tolerant QTLs, named qRC10-1 and qRC10-2 (Fig. 4A), were detected on chromosome 10 via composite interval mapping. qRC10-1 (LOD = 3.1) was mapped at 148.3 cM between RM171 and RM1108, and qRC10-2 (LOD = 6.1) was mapped at 163.3 cM between RM25570 and RM304, which accounted for 9.4% and 32.1% of phenotypic variances, respectively (Table 2).

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Figure 4. Genetic and physical map covering qRC10-2.

A. Location of qRC10-2 on rice chromosome 10. B. The linkage map shows six indels and a SSR marker. C. Progeny test of homozygous recombinants delimited qRC10-2 to the region between the markers RM25570 and RM304. The number of recombinants in each group and the phenotypic difference of each group from controls are shown. D. Further fine mapping of qRC10-2. E. Six genes in the candidate region. aSignificantly different from P1 at P = 0.01; bsignificantly different from P2 at P = 0.01. P1: DX; P2: NJ.

https://doi.org/10.1371/journal.pone.0096046.g004

Fine Genetic and Physical Mapping of qRC10-2

To obtain a fine map of qRC10-2, 45 molecular markers were developed between RM25570 and RM304. As shown in Table S3, 10 of these markers showed codominant polymorphisms between DX and NJ, consisting of 2 SSR markers (RM25681 and RM25628) and 8 indel markers (qc8, qc18, qc19, qc25, qc27, qc45, qc48, and qc55). The arrangement of these markers is shown in Fig. 4B and 4D.

Using the markers RM25570 and RM304, a total of 211 BC5F2 BIL recombinants were identified. Among them, 64 showed the homozygous genotype for DX or NJ alleles and were divided into six groups (LR1, LR2, HR1, HR2, R1 and R2) based on the genotypes of qc8, qc18, qc19, qc25, qc27, RM25681 and qc55 (Fig. 4C). Group LR1 (RC = 4.1) had DX alleles to the left of qc55, and group LR2 (RC = 3.5) had DX alleles to the right of RM25681, indicating that qRC10-2 was located upstream of qc55. Groups R1 and R2 had recombinant loci between RM25681 and qc55, and there was a large range in RC for these groups. Based on this, we deduced that qRC10-2 was located between RM25681 and qc55 (Fig. 4C).

Based on the genotypes of the three polymorphic markers qc45, qc48 and RM25628 (Fig. 4D), groups R1 and R2 were further divided into four subgroups: R1-1, R2-1, R1-2 and R2-2. Then, according to the RC data, the candidate region was narrowed to 68.7 kb between qc45 and RM25628, and qc45, qc48 and RM25628 were used to rescreen all mapped plants. Finally, we obtained four BC5F2 plants with high RC of 11.4 (named group R3) heterozygous in the qc48 allele. Therefore, qRC10-2 between qc45 and qc48 was restricted to 48.5 kb based on the Nipponbare sequence, in which a bacterial artificial chromosome clone (AC146481.2) contained six candidate genes, as shown in Fig. 4D and 4E.

Effects of qRC10-2 on Cold Tolerance at the Seedling and Maturity Stages

Subgroups R1-1, R2-1, R1-2 and R2-2 were used to determine PSRs. The PSRs for R1-1 and R2-1 with high RC values were 25–44% in seedlings and 21–35% in mature plants, whereas those for the subgroups R1-2 and R2-2 with low RC values were 52–60% in seedlings and 48–57% in mature plants. The correlation coefficients between RC and the PSR at the seedling and maturity stages were –0.85 and –0.9 (P = 0.01), respectively (Table 3), indicating that a lower RC value was correlated with a higher PSR. Lines with qRC10-2 grew normally after 24 h under 5±1°C treatment, and lines lacking qRC10-2 showed necrosis or death at the maturity stage (Fig. 5). These results indicated that qRC10-2 contributed to rice cold tolerance at both stages.

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Figure 5. Cold-induced phenotype of the BC5F3 lines containing or lacking qRC10-2 after heading at the 15-day stage.

https://doi.org/10.1371/journal.pone.0096046.g005

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Table 3. Correlations between RC and PSR of recombinants at seedling and maturity stages.

https://doi.org/10.1371/journal.pone.0096046.t003

Identification of Cold-inducible Genes in the Candidate Region

O. rufipogon Griff., common wild rice, is the ancestor of cultivated rice [40][42]. The collinearity of cold-tolerant genes between different species and the conservation in the cold-responsive pathway has been reported [30], [43], [44]. Therefore, Nipponbare (japonica) was selected as the reference genome to screen candidate genes. Table 4 lists the predicted functions of the six candidate genes in IRGSP1.0 (http://rapdb.dna.affrc.go.jp/).

To further identify genes related to cold tolerance, real-time PCR was used to assess gene expression in the leaf and root tissues after 0, 6, 12, and 24 h of cold treatment (Fig. 6). The results suggested that Os10g0489448, Os10g0489650, Os10g0489800, and Os10g0489900 shared a similar gene expression profile in DX, L188 and NJ. Os10g0489500 was induced under cold stress and showed high levels of inducible expression in the leaves of NJ at 6 h and 12 h, whereas no significant variation was observed in DX. This pattern was different from that in the roots, as it was highly expressed in the roots of DX at 6 h but not up-regulated in NJ until 24 h. Os10g0490100 in the roots of NJ showed higher expression than in DX before and after cold treatment. Therefore, Os10g0489500 and Os10g0490100 were considered as the genes associated with cold tolerance in the qRC10-2 region.

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Figure 6. Expression of the candidate genes for plants subjected to 4°C cold treatment for 0, 6, 12, or 24 h as assessed by real-time PCR.

https://doi.org/10.1371/journal.pone.0096046.g006

Discussion

Cold stress is one of the major environmental concerns in rice cultivation, especially in low-temperature and high-altitude areas [45]. The rice subspecies indica and japonica showed cold injury symptoms below 18°C and 15°C, respectively [46]. Under low-temperature stress, the root cell plasma membrane might become damaged and less fluid, resulting in functionality loss, which in turn caused increased cell membrane permeability and intracellular material’s extravasation into the external environment [47], [48], [49]. In our present study, RC was used as a cold phenotype indicator reflecting the integrity and permeability of root membrane at low temperatures. With prolonged treatment time, the RC values of DX and NJ increased gradually, indicating cumulative cold injuries in both parents. Besides, more serious damages accumulated in the NJ root membrane. During the recovery period, high-RC plants showed wilting leaves and retarded growth, but low-RC plants maintained green leaves. Such a cold-tolerant phenotype had a consistent effect on plants at the maturity stage with qRC10-2. Moreover, the correlation coefficients (–0.85 and –0.9) between RC and the PSR were significant in seedlings and mature plants (P = 0.01), indicating that RC could be used as a reliable index for evaluating cold tolerance in rice.

In previous studies, most cold-tolerant QTLs at the seedling stage were detected using recombinant inbred lines derived from indica/japonica cultivars [12], [18], [50], [51]. However, QTL analysis on a wider range of variations from wild species could be equally important. Koseki et al. identified the cold-tolerant QTL qCtss10 (LOD = 3.0) from W1943 (O. rufipogon) on chromosome 10, which accounted for 9.8% of phenotypic variations [17]. In our study, two QTLs qRC10-1 and qRC10-2 were identified on the same chromosome in DX. A QTL for cold tolerance (qCTSS-10) was also identified in seedlings by Yang et al. [52]. qCTSS-10 for 7°C cold treatment was mapped by high-throughput sequencing in the F3 mapping population from a cross between a cold-tolerant japonica rice variety (Nipponbare) and a cold-sensitive indica variety. The interval of qCTSS-10 (15.48–21.06 Mb) overlapped that of qRC10-1 and qRC10-2, indicating that these QTLs may be controlled by the same cold-tolerant gene. Liu et al. also identified the same QTL (qCST10, LOD = 2.4) with 12% of the phenotypic contribution from the cold-tolerant line IL112 [53]; all early seedlings of the line IL112 survived normally for 9 days at 4–5°C. A molecular marker tightly linked to qCST10 was OSR33, which was the same marker as RM171 linked to qRC10-1 and qRC10-2 according to the Gramene marker data (http://www.gramene.org/). As described above, the same cold-tolerant QTL was identified on chromosome 10 among different parents and cold-treatment conditions based on a different cold tolerance index, suggesting that qRC10-2 was a stable and reliable cold-tolerant QTL for the rice seedling stage. Further studies on the candidate gene(s) in this region will aid in elucidating the molecular mechanism underlying rice cold tolerance.

In the candidate region, Os10g0489500 and Os10g0490100 were differentially expressed between cold-tolerant and -sensitive plants. Os10g0489500 encoded a terpene synthase that was localized to the cytoplasm. In our study, Os10g0489500 was up-regulated in response to cold stress in the leaves of NJ. In the roots, however, its expression in DX and L188 was ∼18-fold higher than that in NJ, suggesting that the root may be a key organ for the Os10g0489500 activity. Yang et al. also identified Os10g0489500 as a gene up-regulated by low temperatures in a cold-tolerant variety [52]. After analyzing differentially-expressed transcripts in indica (K354) and japonica (C418) under controlled conditions (25°C) and cold stress (4°C) for 48 h, Zhang et al. identified two terpene synthase genes (Os02g36140 and Os08g07100) that were associated with signal transduction cascades from K354 during cold-stress responses in seedlings [44]. Another gene differentially-expressed between cold-tolerant and -sensitive plants was Os10g0490100, which encoded virulence factors that degraded the pectin components of the plant cell wall [54], [55]. Pectin functioned as an adhesive in cell wall formation, and the pectin content directly influenced cell wall integrity, which was related to rice cold tolerance as reported previously [56][58]. Solecka et al. found that cold acclimation induced an increase in the pectin content in the cell wall and increased tolerance to freezing [59]. A mutation in QUASIMODO1, a gene encoding the glycosyl transferase required for pectin synthesis, caused reduced pectin content, leading to less cell adhesion and faster water loss during cold stress in common rice plants compared with the wild type [58]. Using Zhonghua 10 plants, Liu et al. overexpressed OsBURP16, a polygalacturonase 1β that degraded pectin, and showed that an increase in the polygalacturonase activity led to a decrease in the pectin content in the cell wall, resulting in more severely curled leaves in the transgenic plants [53]. When the transgenic seedlings were exposed to 4°C for 72 h and allowed to recover for 7 days under normal conditions, the PSR of Zhonghua 10 plants was 42%, and that of the transgenic plants OE3 and OE4 was only 28% and 4%, respectively [60]. The above studies suggested that pectin degradation in the cell wall affected cell wall integrity and decreased tolerance to cold stress. In our present study, Os10g0490100, a pectin lyase fold family protein that participated in pectin degradation, was more highly expressed in NJ roots than in DX and L188 roots before and after cold treatment, indicating that fewer pectin was maintained in cold-sensitive plants.

In conclusion, our data provided useful information for cultivating cold-tolerant rice varieties by pyramiding qRC10-2 based on other QTLs and also offered a molecular basis for rice cold tolerance mechanisms at the seedling and maturity stages.

Supporting Information

Figure S1.

Genetic background recovery rates determined among the BC4F2 plants.

https://doi.org/10.1371/journal.pone.0096046.s001

(JPG)

Table S1.

Primer sequences for SSR markers.

https://doi.org/10.1371/journal.pone.0096046.s002

(DOCX)

Table S2.

Real-time PCR primer sequences for candidate genes.

https://doi.org/10.1371/journal.pone.0096046.s003

(DOCX)

Table S3.

Primer sequences and sizes of polymorphic markers developed for fine mapping locus qRC10-2.

https://doi.org/10.1371/journal.pone.0096046.s004

(DOCX)

Acknowledgments

The authors thanked Dr. Yan for his critical review of the manuscript.

Author Contributions

Conceived and designed the experiments: NX ZYD JMC. Performed the experiments: YG XXZ YHL. Analyzed the data: WNH LY. Contributed reagents/materials/analysis tools: GQL CHP. Wrote the paper: NX JMC. DNA extraction and molecular marker identification: AHL YD.

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