Developing super rice varieties resistant to rice blast with enhanced yield and improved quality

IF 10.5 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Plant Biotechnology Journal Pub Date : 2024-10-24 DOI:10.1111/pbi.14492
Naihui Guo, Ruihu An, Zongliang Ren, Jun Jiang, Bonian Cai, Shikai Hu, Gaoneng Shao, Guiai Jiao, Lihong Xie, Ling Wang, Fengli Zhao, Shaoqing Tang, Zhonghua Sheng, Peisong Hu
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So far, more than 70 disease resistance genes and QTLs have been identified, of which at least 25 have been cloned and used in disease resistance breeding (Luo <i>et al</i>., <span>2017</span>). The <i>Pi2</i> gene encodes a protein with a nucleotide-binding site and leucine-rich repeat (LRR) domain (Zhou <i>et al</i>., <span>2006</span>), and is one of the most broad-spectrum and efficient resistance genes to rice blast, exhibiting resistance to 36 out of 43 rice blast strains from 13 countries (Liu <i>et al</i>., <span>2002</span>). However, many elite varieties do not carry <i>Pi2</i> gene, which seriously hinders the widespread and sustainable promotion of these varieties.</p><p>Marker-assisted selection (MAS) is one of the important technologies in modern breeding. It uses molecular markers to quickly detect individual plants carrying target genes, greatly improving breeding efficiency and saving breeding costs. Previously, Jiang <i>et al</i>. (<span>2015</span>) developed blast-resistant thermosensitive genic male sterile (TGMS) lines by employing MAS. High-density whole genome single nucleotide polymorphism (SNP) chips are also a technology that accelerates the breeding process. Therefore, combining MAS and SNP chips can make breeding improvement faster and more accurately. For example, Guo <i>et al</i>. (<span>2024</span>) used MAS and Green Super Rice 40K (GSR40K) detection to screen improved strains with high genetic similarity to the receptor in BC<sub>1</sub>F<sub>2</sub>. In this study, we successfully generated an improved rice germplasm with blast-resistant by integrating MAS and GSR40K detection technology.</p><p>F<sub>1</sub> plants obtained from the cross of Zhonghui261 (ZH261; a good quality restoring line of Huazheyou 261 [HZY261], which was selected as a demonstration and promotion variety of super rice in 2024) and Yuenongsimiao (YNSM; carrying <i>Pi2</i>), were backcross with ZH261 to generate BC<sub>1</sub>F<sub>1</sub>. Among 1025 BC<sub>1</sub>F<sub>1</sub> plants, we selected 70 strains that similar to ZH261 and 26 individual plants were identified to carry <i>Pi2</i> (Heterozygous) using the marker <i>Pi2</i>-CM1. Then, the single plant out of 26 with 89.72% of genetic background reversion was selected by detecting with GSR40K. The single plant was backcrossed again with ZH261 to generate 964 BC<sub>2</sub>F<sub>1</sub> plants. We selected 10 strains that are similar to ZH261 and three individual plants were identified to carry <i>Pi2</i> (Heterozygous) using the marker <i>Pi2</i>-CM1. The single plant out of three with 97.86% of genetic background reversion was selected to selfing and generate BC<sub>2</sub>F<sub>2</sub>. The single plant named ZH261-Pi2 was selected from BC<sub>2</sub>F<sub>2</sub> by employing MAS and detecting with GSR40K (Figure 1a). ZH261-Pi2 exhibited 97.81% genetic similarity to ZH261 and 99.97% purity (Figure 1b). Based on 48 simple sequence repeats (SSR) markers followed by the protocol NY/T 1433-2014, only one pair of SSR marker (RM176) was different between ZH261 and ZH261-<i>Pi2</i> (Figure 1c), indicating that ZH261 and ZH261-<i>Pi2</i> were the same variety. Finally, we hybridised with Huazhe2A using ZH261 and ZH261-<i>Pi2</i>, respectively, to produce HZY261 and HZY261-<i>Pi2</i>, and evaluated their rice blast resistance, yield and quality traits (Figure 1a).</p><p>We found that ZH261-<i>Pi2</i> and HZY261-<i>Pi2</i> significantly increased resistance to blast compared to ZH261 and HZY261 (Figure 1d–g). ZH261-<i>Pi2</i> showed a similar grain numbers per panicle, but higher tiller numbers per plant, 1000 grain weight and grain yield per plant than that of ZH261 (Figure 1h–k). On the other hand, HZY261-<i>Pi2</i> displayed lower 1000 grain weight, but higher grain numbers per panicle, tiller numbers per plant and grain yield per plant compared with HZY261 (Figure 1h–k). 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In particular, the improved varieties can be directly applied to production, providing an important guarantee for food security.</p><p>H.P., T.S. and S.Z. designed the research; G.N., A.R., R.Z., J.J., C.B., H.S., S.G., J.G., X.L., W.L. and Z.F. performed the experiments; S.Z. and G.N. analysed the results and wrote the manuscript.</p><p>The authors declare no conflict of interests.</p>","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":"23 1","pages":"232-234"},"PeriodicalIF":10.5000,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/pbi.14492","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/pbi.14492","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Rice blast, caused by the Magnaporthe oryzae, is the most detrimental disease to rice. Yield losses caused by this disease were from 10% to 30% in rice planting areas (Skamnioti and Gurr, 2009); severe cases may even lead to complete cessation of production (Parker et al., 2008). Cloning rice blast resistant genes and applying them to cultivate resistant varieties is a practical and effective method for controlling rice blast disease. So far, more than 70 disease resistance genes and QTLs have been identified, of which at least 25 have been cloned and used in disease resistance breeding (Luo et al., 2017). The Pi2 gene encodes a protein with a nucleotide-binding site and leucine-rich repeat (LRR) domain (Zhou et al., 2006), and is one of the most broad-spectrum and efficient resistance genes to rice blast, exhibiting resistance to 36 out of 43 rice blast strains from 13 countries (Liu et al., 2002). However, many elite varieties do not carry Pi2 gene, which seriously hinders the widespread and sustainable promotion of these varieties.

Marker-assisted selection (MAS) is one of the important technologies in modern breeding. It uses molecular markers to quickly detect individual plants carrying target genes, greatly improving breeding efficiency and saving breeding costs. Previously, Jiang et al. (2015) developed blast-resistant thermosensitive genic male sterile (TGMS) lines by employing MAS. High-density whole genome single nucleotide polymorphism (SNP) chips are also a technology that accelerates the breeding process. Therefore, combining MAS and SNP chips can make breeding improvement faster and more accurately. For example, Guo et al. (2024) used MAS and Green Super Rice 40K (GSR40K) detection to screen improved strains with high genetic similarity to the receptor in BC1F2. In this study, we successfully generated an improved rice germplasm with blast-resistant by integrating MAS and GSR40K detection technology.

F1 plants obtained from the cross of Zhonghui261 (ZH261; a good quality restoring line of Huazheyou 261 [HZY261], which was selected as a demonstration and promotion variety of super rice in 2024) and Yuenongsimiao (YNSM; carrying Pi2), were backcross with ZH261 to generate BC1F1. Among 1025 BC1F1 plants, we selected 70 strains that similar to ZH261 and 26 individual plants were identified to carry Pi2 (Heterozygous) using the marker Pi2-CM1. Then, the single plant out of 26 with 89.72% of genetic background reversion was selected by detecting with GSR40K. The single plant was backcrossed again with ZH261 to generate 964 BC2F1 plants. We selected 10 strains that are similar to ZH261 and three individual plants were identified to carry Pi2 (Heterozygous) using the marker Pi2-CM1. The single plant out of three with 97.86% of genetic background reversion was selected to selfing and generate BC2F2. The single plant named ZH261-Pi2 was selected from BC2F2 by employing MAS and detecting with GSR40K (Figure 1a). ZH261-Pi2 exhibited 97.81% genetic similarity to ZH261 and 99.97% purity (Figure 1b). Based on 48 simple sequence repeats (SSR) markers followed by the protocol NY/T 1433-2014, only one pair of SSR marker (RM176) was different between ZH261 and ZH261-Pi2 (Figure 1c), indicating that ZH261 and ZH261-Pi2 were the same variety. Finally, we hybridised with Huazhe2A using ZH261 and ZH261-Pi2, respectively, to produce HZY261 and HZY261-Pi2, and evaluated their rice blast resistance, yield and quality traits (Figure 1a).

We found that ZH261-Pi2 and HZY261-Pi2 significantly increased resistance to blast compared to ZH261 and HZY261 (Figure 1d–g). ZH261-Pi2 showed a similar grain numbers per panicle, but higher tiller numbers per plant, 1000 grain weight and grain yield per plant than that of ZH261 (Figure 1h–k). On the other hand, HZY261-Pi2 displayed lower 1000 grain weight, but higher grain numbers per panicle, tiller numbers per plant and grain yield per plant compared with HZY261 (Figure 1h–k). Together, our results indicate that introduction of Pi2 in ZH261 by integrating MAS and GSR40K detection can simultaneously enhance rice blast resistance and yield.

Amylose content is the most critical parameter determining rice eating and cooking quality (Wang et al., 2024). ZH261-Pi2 showed a similar length–width ratio, alkali spreading value and amylose content, but higher gel consistency than that of ZH261 (Figure 1l–o). HZY261-Pi2 had higher length–width ratio, but lower amylose content and gel consistency than that of HZY261 (Figure 1l–n). As for alkali spreading value, no significant difference was observed between HZY261-Pi2 and HZY261 (Figure 1o).

Balancing the yield, quality and resistance to disease is a daunting challenge in crop breeding due to the negative relationship among these traits (Xiao et al., 2021). However, it is feasible to improve the rice blast resistance, yield and quality of existing rice varieties through molecular design breeding (Mao et al., 2021). Our work provides a molecular design strategy to rapidly improve rice blast resistance, yield and quality by integrating MAS and GSR40K detection. In particular, the improved varieties can be directly applied to production, providing an important guarantee for food security.

H.P., T.S. and S.Z. designed the research; G.N., A.R., R.Z., J.J., C.B., H.S., S.G., J.G., X.L., W.L. and Z.F. performed the experiments; S.Z. and G.N. analysed the results and wrote the manuscript.

The authors declare no conflict of interests.

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培育抗稻瘟病的超级稻品种,提高产量和改善品质
稻瘟病是由稻瘟病菌引起的稻瘟病,是对水稻危害最大的病害。在水稻种植区,该病造成的产量损失为10%至30% (Skamnioti和Gurr, 2009年);严重者甚至可能导致完全停产(Parker et al., 2008)。克隆稻瘟病抗性基因,培育稻瘟病抗性品种是防治稻瘟病的一种实用有效的方法。迄今为止,已鉴定出70多个抗病基因和qtl,其中至少有25个已被克隆并用于抗病育种(Luo et al., 2017)。Pi2基因编码一种具有核苷酸结合位点和富含亮氨酸重复序列(LRR)结构域的蛋白(Zhou et al., 2006),是稻瘟病最广谱和最有效的抗性基因之一,对来自13个国家的43种稻瘟病毒株中的36种表现出抗性(Liu et al., 2002)。然而,许多优良品种不携带Pi2基因,这严重阻碍了这些品种的广泛和可持续推广。标记辅助选择(MAS)是现代育种中的重要技术之一。它利用分子标记快速检测携带靶基因的单株植物,大大提高了育种效率,节约了育种成本。此前,Jiang等人(2015)利用MAS开发了抗爆热敏基因雄性不育(TGMS)系。高密度全基因组单核苷酸多态性(SNP)芯片也是一种加速育种过程的技术。因此,结合MAS和SNP芯片,可以使育种改良更快、更准确。如Guo等(2024)利用MAS和绿超级稻40K (GSR40K)检测,筛选了与BC1F2中受体遗传相似性高的改良菌株。在本研究中,我们将MAS和GSR40K检测技术相结合,成功地获得了一种水稻抗病性改良种质。中恢261 (ZH261)杂交获得的F1植株;优质恢复系华浙优261 [HZY261](2024年入选超级稻示范推广品种)和越农四苗(YNSM);携带Pi2),与ZH261回交生成BC1F1。在1025株BC1F1植株中,我们选择了70株与ZH261相似的菌株,通过Pi2- cm1标记鉴定出26株携带Pi2(杂合)。然后,通过GSR40K检测,从26株中筛选出遗传背景还原率为89.72%的单株。将单株与ZH261回交,得到964株BC2F1。我们选择了10株与ZH261相似的菌株,通过Pi2- cm1标记鉴定出3株携带Pi2(杂合)。在遗传背景还原率为97.86%的3株植株中,选择单株自交产生BC2F2。通过MAS和GSR40K检测,从BC2F2中选择单株ZH261-Pi2(图1a)。ZH261- pi2与ZH261的遗传相似性为97.81%,纯度为99.97%(图1b)。基于NY/T 1433-2014协议的48个SSR标记,ZH261与ZH261- pi2之间只有1对SSR标记(RM176)存在差异(图1c),说明ZH261与ZH261- pi2为同一品种。最后,我们将ZH261和ZH261- pi2分别与花泽2a杂交,获得HZY261和HZY261- pi2,并对其稻瘟病抗性、产量和品质性状进行了评价(图1a)。我们发现,与ZH261和HZY261相比,ZH261- pi2和HZY261- pi2对爆炸的抵抗力显著提高(图1d-g)。ZH261- pi2的穗粒数与ZH261相近,但单株分蘖数、千粒重和单株籽粒产量高于ZH261(图1h-k)。另一方面,HZY261- pi2的千粒重低于HZY261,但单穗粒数、单株分蘖数和单株粒产量高于HZY261(图1h-k)。综上所述,通过整合MAS和GSR40K检测,在ZH261中引入Pi2可以同时提高水稻抗稻瘟病能力和产量。直链淀粉含量是决定大米食用和蒸煮质量的最关键参数(Wang et al., 2024)。ZH261- pi2的长宽比、碱扩散值和直链淀粉含量与ZH261相似,但凝胶稠度高于ZH261(图11 - 0)。与HZY261相比,HZY261- pi2具有更高的长宽比,但直链淀粉含量和凝胶浓度较低(图11 - n)。在碱扩散值方面,HZY261- pi2与HZY261无显著差异(图10)。由于这些性状之间存在负相关关系,平衡产量、品质和抗病性是作物育种中的一项艰巨挑战(Xiao et al., 2021)。然而,通过分子设计育种提高现有水稻品种的稻瘟病抗性、产量和品质是可行的(Mao et al., 2021)。 我们的工作提供了通过整合MAS和GSR40K检测来快速提高水稻稻瘟病抗性、产量和品质的分子设计策略。特别是改良品种可直接应用于生产,为粮食安全提供了重要保障。, T.S.和S.Z.设计了研究;R.Z G.N A.R。,j, C.B。,h, S.G, J.G。X.L,柔若Z.F.进行实验;S.Z.和G.N.分析了结果并撰写了手稿。作者声明没有利益冲突。
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来源期刊
Plant Biotechnology Journal
Plant Biotechnology Journal 生物-生物工程与应用微生物
CiteScore
20.50
自引率
2.90%
发文量
201
审稿时长
1 months
期刊介绍: Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.
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