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水稻籼粳交DH群体中影响白背飞虱抗虫性QTL的检测 总被引：1，自引：1，他引：1
分析了水稻籼粳交加倍单倍体(DH)群体中影响白背飞虱抗虫性和感虫性的QTL.虽然DH株系的亲本窄叶青8号和京系17没有拒取食抗性,但是白背飞虱在6个DH株系中的取食受到了强烈的抑制,可能属超亲分离.在第3染色体的粳型片段中检测到1个影响蜜露分泌的微效QTL.粳稻亲本京系17具有杀卵抗性.DH株系中的杀卵特性是通过叶鞘上杀卵反应产生的坏死症状表现的.在DH株系分蘖早期和中期,将4个杀卵作用的QTL定位在第1、2、6和8染色体的粳型片段上.出现在分蘖中期的另一个QTL被定位在第9染色体的籼型片段上.在分蘖盛期至孕穗期,杀卵位点减少至2个.整个试验期间对每个DH株系的最高杀卵级别的分析显示,在染色体2、6和9上共有4个QTL.两个主效QTL位于近邻第6染色体的粳型片段.在第1、3和5染色体上检测到3个影响第2代白背飞虱若虫密度的QTL.第3染色体上起主要作用的QTL源自粳稻亲本;第5染色体上的微效QTL源自籼稻亲本.两个白背飞虱为害的QTL位于第8和第10染色体的籼型片段,另一个QTL位于第3染色体的粳型片段.这些QTL被认为与水稻品种对白背飞虱田间抗性表达有关. 相似文献
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【目的】为了创制兼抗白背飞虱和褐飞虱的水稻恢复系,【方法】分别以抗褐飞虱材料B5(携带褐飞虱抗性基因Bph14和Bph15)及携带白背飞虱抗性位点qsI-4的籼型恢复系福恢7011为供体亲本,以骨干恢复系福恢676为轮回亲本,应用低世代分离群体田间表型结合单株鉴定与高世代稳定株系室内筛选和分子标记辅助选择相结合的方法,并对抗虫株系及其测交后代进行考查和农艺性状分析。【结果】选育出聚合Bph14、Bph15和qsI-4的恢复系材料3份,携带2个抗虫基因的恢复系材料3份。其中6份恢复系的褐飞虱抗性鉴定结果均表现中抗以上。通过抗性鉴定和杂交后代农艺性状分析筛选出具有生产应用潜力的恢复系材料2份。【结论】为褐飞虱和白背飞虱抗性聚合新种质的创制和应用提供了基础材料。 相似文献
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聚合白背飞虱和褐飞虱抗性基因创制杂交水稻恢复系 总被引：1，自引：1，他引：1
【目的】为了创制兼抗白背飞虱和褐飞虱的水稻恢复系，【方法】分别以抗褐飞虱材料B5（携带褐飞虱抗性基因Bph14和Bph15）及携带白背飞虱抗性位点qsI-4的籼型恢复系福恢7011为供体亲本，以骨干恢复系福恢676为轮回亲本，应用低世代分离群体田间表型结合单株鉴定与高世代稳定株系室内筛选和分子标记辅助选择相结合的方法，并对抗虫株系及其测交后代进行考查和农艺性状分析。【结果】选育出聚合Bph14、Bph15 和qsI-4的恢复系材料3份，携带2个抗虫基因的恢复系材料3份。其中6份恢复系的褐飞虱抗性鉴定结果均表现中抗以上。通过抗性鉴定和杂交后代农艺性状分析筛选出具有生产应用潜力的恢复系材料2份。【结论】为褐飞虱和白背飞虱抗性聚合新种质的创制和应用提供了基础材料。 相似文献
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水稻抗褐飞虱基因Bph18(t)的STS标记开发及有效性验证 总被引：2，自引：0，他引：2
利用携有Bph18(t)基因抗褐飞虱材料与感虫材料之间在抗虫位点上的单核苷酸差异,成功开发出1个STS标记KC1。该标记可以准确区分含或不含抗虫基因Bph18(t)的基因型。进一步构建扬稻6号(9311)[不含Bph18(t)基因,感褐飞虱]/C4064[携有Bph18(t)基因]的F2群体进行抗虫鉴定,同时使用KC1标记检测F2群体单株的基因型。根据分子标记检测结果与抗虫表现之间的符合程度推算出标记的选择效果达到了82.6%。研究结果表明,KC1标记有较高的目的基因选择效率,可以应用于扬稻6号遗传背景下Bph18(t)基因的分子标记辅助选择。 相似文献
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《杂交水稻》1986,(2)
白背飞虱(Sogatella FurciferaHorvath)是危害热带和亚热带水稻的一种主要害虫。稻飞虱的防治措施,过去主要依靠化学药剂,但由此造成残毒、环境污染、害虫抗药性、杀伤天敌和增加成本等问题。因此,国际水稻所提出防治的战略是开发具有抗虫害基因的种质。目前该所种质库已筛选出抗白背飞虱的水稻品种400多个,并于1976年率先开展水稻栽培品种抗白背飞虱的遗传研究。迄今已发现4个抗性基因,其中有3个为显国基性,命名为Wbphl, Wbph2和Wbph3;第4个为隐性基因,命名为Wbph4。最近又鉴定出一个新的抗白背飞虱的显性基因,被命名为Wbph5。 自背飞… 相似文献
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中国水稻品种对白背飞虱的抗性 总被引：2，自引：0，他引：2
评价了来自中国的13个粳稻品种、11个籼稻品种、13个杂交稻组合,以及11个热带粳稻品种的杀卵作用和拒食抗性.具有杀卵作用的品种仅见于粳稻品种.测试的13个粳稻品种中,4个表现出明显的杀卵作用.重新评价了来自中国不同省份的42份粳稻和43份籼稻对白背飞虱的抗性.10个粳稻(约占24%)具有杀卵抗性,卵死亡率为53%～100%;95%以上的籼稻品种中,白背飞虱的卵死亡率低于30%;来自浙江的4个粳稻品种明显地抑制白背飞虱的取食.浙江的21个粳稻地方品种对白背飞虱拒取食和杀卵作用表现出独立性和连续变化.三千黄、长红稻和矮秆稻具有杀卵抗性,鸡脚黄和麻雀青具有拒取食抗性.这些发现表明抗白背飞虱基因在中国存在于同一生态区的粳稻地方品种中. 相似文献
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《中国水稻科学》2019,(5)
【目的】为了创制兼抗白背飞虱和褐飞虱的水稻恢复系,【方法】分别以抗褐飞虱材料B5(携带褐飞虱抗性基因Bph14和Bph15)及携带白背飞虱抗性位点qsI-4的籼型恢复系福恢7011为供体亲本,以骨干恢复系福恢676为轮回亲本,应用低世代分离群体田间表型结合单株鉴定与高世代稳定株系室内筛选和分子标记辅助选择相结合的方法,并对抗虫株系及其测交后代进行考查和农艺性状分析。【结果】选育出聚合Bph14、Bph15和qsI-4的恢复系材料3份,携带2个抗虫基因的恢复系材料3份。其中6份恢复系的褐飞虱抗性鉴定结果均表现中抗以上。通过抗性鉴定和杂交后代农艺性状分析筛选出具有生产应用潜力的恢复系材料2份。【结论】为褐飞虱和白背飞虱抗性聚合新种质的创制和应用提供了基础材料。 相似文献
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【目的】水稻品系75-1-127携带广谱抗稻瘟病基因Pi9,已被广泛应用于抗稻瘟病水稻品种改良。笔者育种实践发现75-1-127表现出较强的褐飞虱抗性,因此鉴定该品系中的褐飞虱抗性基因并进行分子辅助选择育种。【方法】根据水稻品系B5中褐飞虱抗性基因Bph14和Bph15的序列,设计引物扩增75-1-127的基因组DNA,并对PCR产物进行测序分析。采用苗期集团法鉴定了75-1-127和B5的褐飞虱抗性表型。利用与Bph14与Bph15连锁的分子标记筛查了75-1-127为稻瘟病抗源回交转育的两系不育系后代,并鉴定了这些后代的稻瘟病抗性、褐飞虱抗性和主要农艺性状。【结果】75-1-127中含有与B5完全一致的Bph14和Bph15序列。75-1-127和B5苗期褐飞虱抗性均为1级。在以75-1-127为抗源改良的两系不育系中,携带Bph14、Bph15的单基因系或双基因系的褐飞虱抗性均得以改良,其中双基因聚合系的死苗率为8.5%,与供体亲本75-1-127以及阳性对照B5差异不显著,进一步证实75-1-127含有褐飞虱抗性基因。【结论】水稻品系75-1-127携带褐飞虱抗性基因Bph14和Bph15,可以作为抗源应用于水稻褐飞虱抗性育种。 相似文献
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Nine brown planthopper(BPH) resistance genes have been registered so far, but of them only Bph1, bph2, Bph3, bph4, Bph9,and other three unregistered genes Bph10(t), Bph(t), bph(t) were located on chromosome 3, 4, 10, and 12, respectively, by using traditional and molecular mapping methods. To use the genes for BPH resistance in rice breeding and production, interspecific hybrids between cultivated rice and accessions of O. eichingeri (2n=24, CC), a wild rice species from Africa, with strong resistance to BPH and whitebacked planthopper were produced. 相似文献
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Among the planthoppers of rice, the brown planthopper (BPH) is a major threat to rice production and causes significant yield loss annually. Host-plant resistance is an important strategy to reduce the damage caused by BPH and increase rice productivity. Twenty-one major genes for BPH resistance have been identified by using standard evaluation methods developed at the International Rice Research Institute (IRRI) to distinguish resistance or susceptibility of rice genotypes to BPH biotypes/populations. These genes are from diverse genetic resources such as land race cultivars and wild species of Oryza. Of the 21 resistance genes, 18 genes have been localized on specific region of six rice chromosomes using molecular genetic analysis and genomics tools. Some of these resistance genes are clustered together such as Bph1, bph2, Bph9, Bph10, Bph18, and Bph21 on the long arm of chromosome 12; Bph12, Bph15, Bph17 and Bph20 on the short arm of chromosome 4; bph11 and Bph14 on the long arm of chromosome 3 and Bph13(t) and bph19 on the short arm of chromosome 3. Six genes (Bph11, bph11, Bph12, bph12, Bph13 and Bph13) originated from wild Oryza species have either duplicate chromosome locations or wrong nomenclature. The discrepancy should be confirmed by allelism tests. Besides identification of major resistance genes, some quantitative trait loci (QTLs) associated with BPH resistance have also been identified on eight chromosomes. Most of the rice cultivars developed at IRRI possess one or two of the major resistance genes and the variety IR64 has many QTLs and confers strong resistance to BPH. More BPH resistance genes need to be identified from the wealth of gene pool available in the wild species of Oryza. Two BPH resistance genes (Bph14 and Bph18) have been cloned, and a snow drop lectin gene (GNA) has been identified and used in the development of BPH-resistant transgenic plants. Efficient introgression of resistance genes (Bph1, bph2, Bph3, Bph14, Bph15, Bph18, Bph20, and Bph21) into elite rice cultivars by marker-assisted selection together with strategic deployment of these genes can be an important approach to develop stable resistance to BPH and sustain rice production in the tropical and temperate rice growing regions. 相似文献
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中国杂交稻的"超感虫性"研究概况 总被引：8，自引：1，他引：8
介绍了高度感虫的中国杂交稻推广带来水稻害虫生态地位发生的变化.褐飞虱和白背飞虱上升为杂交稻上最突出的极易爆发成灾的重要害虫.20世纪70年代以前,白背飞虱只是水稻上的次要害虫,但80年代以来其种群大大增加.由于它从中国南部杂交稻种植区大范围迁飞,白背飞虱也成为中国中部地区粳稻上的重要害虫.由于种植具有抗褐飞虱基因Bph1的杂交稻组合,褐飞虱种群曾得到暂时的控制.然而,抗虫性的杂交稻在中国中部和南部稻飞虱迁飞区推广以后,褐飞虱生物型发生了改变,对抗虫品种产生了适应性.1990年以后,以前表现抗虫的杂交稻变得高感褐飞虱.缺乏抗虫性主基因不是中国杂交稻对稻飞虱超感性的充分理由,杂交稻旺盛生长的杂种优势可能是稻飞虱生殖力提高的部分原因.中国杂交稻对稻飞虱的超感虫性是从不育系遗传而来的.因此,杂交稻抗虫性的提高有赖于不育系的改良.利用持久抗性和多抗性的IR品种如IR64作为恢复系是改善中国杂交稻的超感虫性的一种有效方法.杂交稻上二化螟和三化螟为害也有所增加.与常规稻相比,杂交稻是一种更有利的食料植物且耐虫性更强.进行水稻产量损失的估计,尤其是水稻本身对螟虫为害的补偿能力,以及螟虫和杂交稻之间的生态学关系的研究有助于评价杂交稻对螟虫田间抗性的实际影响. 相似文献
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Muduli Lakesh Kumar Pradhan Sukanta Mishra Abinash Nath Bastia Debendra Chandra Samal Kailash Kumar Agrawal Pawan Dash Manasi 《水稻科学》2021,28(6):532-546
Brown planthopper (BPH, Nilaparvata lugens Stål) is the most devastating pest of rice in Asia and causes significant yield loss annually. Around 37 BPH resistance genes have been identified so far in indica, African rice varieties along with wild germplasms such as Oryza officinalis, O. minuta, O. nivara, O. punctata, O. rufipogon and O. latifolia. Genes/QTLs involved in BPH resistance, including Bph1, bph2/BPH26, Bph3, Bph6, bph7, BPH9, Bph12, Bph14, Bph15, Bph17, BPH18, bph19, Bph20, Bph21(t), Bph27, Bph27(t), Bph28(t), BPH29, QBph3, QBph4, QBph4.2, Bph30, Bph32, Bph33, Bph35 and Bph36, have been fine-mapped by different researchers across the globe. The majority of genes/QTLs are located on rice chromosomes 1, 3, 4, 6, 11 and 12. Rice plants respond to BPH attack by releasing various endogenous metabolites like proteinase inhibitors, callose, secondary metabolites (terpenes, alkaloids, flavonoid, etc.) and volatile compounds. Besides that, hormonal signal pathways mediating (antagonistic/synergistic) resistance responses in rice have been well studied. Marker-assisted breeding and genome editing techniques can also be adopted for improving resistance to novel BPH biotypes. 相似文献
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Kazushige SOGAWA 《水稻科学》2005,12(1):63
Whitebacked planthopper (WBPH) -resistance in a japonica / indica doubled haploid (DH) rice population established from a cross between WBPH-resistant japonica Chun]iang 06 and susceptible indica TN1, was comparatively evaluated through a field experiment based on the WBPH immigrant density and standardized seedbox screening test (SSST). All the susceptible DH lines in the field experiment behaved accordingly in SSST. However, 35 of resistant 66 lines (53%) in the field, were categorized to susceptible groups in SSST. Likewise, there were no significant differences in WBPH immigrant densities among 70 DH lines that were highly resistant to susceptible in SSST. The results revealed that SSST could not evaluate properly WBPH resistance in the DH lines. Four QTLs for WBPH-resistance phenotyped by the immigrant density were detected on chromosomes 2, 3, 4, and 11. Of them, the QTL on chromosome 4 was the most effective (LOD 21.8, variance 78%). Five QTLs associated with seedling mortality were mapped on chromosomes 2, 3, 4, 5 and 6. In addition to the QTL (LOD 10.5, variance 68%) on chromosome 4, there was another major QTL (LOD 12.7, variance 71%) located on chromosome 5, which was SSST-specific but might be irrespective of the WBPH resistance traits. 相似文献
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【目的】近年来由白背飞虱传播的南方水稻黑条矮缩病给水稻生产造成了巨大损失,开展该病的抗性遗传分析和基因精细定位,将为抗性育种提供材料和理论依据。【方法】分析了抗性材料D4对南方水稻黑条矮缩病的抗性特征,并通过广恢998/D4F2群体分析该病抗性的遗传规律,利用QTL-seq技术联合遗传连锁分析定位主效抗性QTL。【结果】D4对南方水稻黑条矮缩病的抗性表现为抗病毒性而非抗虫性,且受主效基因和微效基因共同控制。QTL-seq和连锁分析将南方水稻黑条矮缩病主效抗性QTL定位于第9染色体上,命名为qSRBSDV9。利用代换作图法进一步将qSRBSDV9定位在102.3kb的区间内,该区间包含21个预测基因,其中9个基因与赤霉素信号传导相关。【结论】揭示了D4对南方水稻黑条矮缩病的抗性特征及遗传规律,精细定位了南方水稻黑条矮缩病主效抗性QTL qSRBSDV9。这为该QTL的图位克隆及育种利用奠定了基础。 相似文献
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Yuexiong Zhang Gang Qin Qianqian Ma Minyi Wei Xinghai Yang Zengfeng Ma Haifu Liang Chi Liu Zhenjing Li Fang Liu Dahui Huang Rongbai Li 《水稻科学》2020,27(3):237-245
An introgression line RBPH660, derived from wild rice Oryza rufipogon, showed stable resistance to brown planthopper(BPH). Segregation analysis indicated BPH resistance of RBPH660 was controlled by multiple genes/QTLs. By using the bulked segregant analysis(BSA)-seq method, two genomic regions harboring QTLs resistance to BPH were identified from 1.20 to 16.70 Mb on chromosome 4 and from 10.20 to 12.60 Mb on chromosome 9 in RBPH660, respectively. A major resistance locus, designated as Bph35 accounting for 51.27% of the phenotypic variation with a LOD score of 42.51, was mapped to the candidate region of chromosome 4 between In Del(insertion-deletion) markers PSM16 and R4 M13. For fine mapping of Bph35, one simple sequence repeat and three newly developed In Del markers were used to screen the recombinants. Finally, the Bph35 locus was delimited in the region from 6.28 to 6.93 Mb and there were 18 predicted protein-encoding genes with a total of 114 non-synonymous single nucleotide polymorphism(SNP) variant sites between the resistant and susceptible parents. Out of these genes, Os04 g0193950, encoding a putative NB-ARC(nucleotidebinding adaptor shared by APAF-1, R proteins and CED-4) and LRR(leucine-rich repeat) domain protein with nine non-synonymous SNP substitutions in its coding sequence regions, might be the candidate gene for Bph35. These findings would facilitate the map-based cloning of the Bph35 gene and development of resistant varieties against BPH in rice. 相似文献