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几个四倍体小麦山羊草双二倍体及其部分亲本的抗小麦白粉病基因分析 被引量:12
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作者 朱振东 周荣华 +1 位作者 董玉琛 贾继增 《植物遗传资源学报》 CAS CSCD 2003年第2期137-143,共7页
用离体叶段接种方法鉴定了 11个四倍体小麦 -山羊草双二倍体、波斯小麦PS5、硬粒小麦DR14 7、5份山羊草、杂交高代材料Am9/莱州 95 3 2 F5和 (DR14 7/Ae14 ) //莱州 95 3 2 F4对 2 0个具有不同毒力白粉菌株的抗谱。通过与含有已知抗病... 用离体叶段接种方法鉴定了 11个四倍体小麦 -山羊草双二倍体、波斯小麦PS5、硬粒小麦DR14 7、5份山羊草、杂交高代材料Am9/莱州 95 3 2 F5和 (DR14 7/Ae14 ) //莱州 95 3 2 F4对 2 0个具有不同毒力白粉菌株的抗谱。通过与含有已知抗病基因品种或品系的反应模式比较 ,推测Am9/莱州 95 3 2 F5含有Pm4b ,波斯小麦PS5含有Pm4b与一个未知抗病基因组合 ;(DR14 7/Ae14 ) //莱州 95 3 2 F4和硬粒小麦DR14 7含有Pm4a和一个未知抗病基因组合 ;尾状山羊草Ae14和小伞山羊草Y39抗所有白粉菌株 ,由于迄今还没有在尾状山羊草和小伞山羊草中鉴定出抗白粉病基因 ,推测这 2份山羊草含有新的抗白粉病基因。除Am9外 ,在其它双二倍体中波斯小麦或硬粒小麦的抗性部分受到抑制 ,山羊草的抗性部分或完全受到抑制。 展开更多
关键词 四倍体小麦 山羊草 双二倍体 亲本 抗小麦白粉病基因
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小麦抗白粉病基因pm42的EST连锁图谱构建和比较基因组学分析 被引量:10
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作者 刘子记 朱婕 +3 位作者 华为 杨作民 孙其信 刘志勇 《作物学报》 CAS CSCD 北大核心 2011年第9期1569-1576,共8页
目的基因精细遗传连锁图谱的构建是图位克隆的基础,小麦功能基因精细遗传连锁图谱的构建依赖于比较基因组学分析。水稻和短柄草(Brachypodium distachyon)基因组序列是小麦比较基因组学分析和功能基因精细遗传定位的重要工具。本研究利... 目的基因精细遗传连锁图谱的构建是图位克隆的基础,小麦功能基因精细遗传连锁图谱的构建依赖于比较基因组学分析。水稻和短柄草(Brachypodium distachyon)基因组序列是小麦比较基因组学分析和功能基因精细遗传定位的重要工具。本研究利用小麦、短柄草和水稻的基因组共线性关系对小麦抗白粉病基因pm42进行比较基因组学分析,明确了pm42基因所在2BS基因组区域与短柄草第1染色体和水稻第3染色体直系同源基因组区域的对应关系,开发出与抗白粉病基因pm42连锁的EST-SSCP(expressed sequence tag-single strand conformation polymorphism)标记CD452782和BF201235,以及EST-STS(expressed sequence tag-sequence tagged site)标记CJ674042、EB513371和CV771633,构建了pm42基因EST标记遗传连锁图谱,CJ674042、BF201235、CD452782和CV771633位于pm42近端粒侧,距离pm42的遗传距离分别为1.9、12.0、19.7和25.7cM;EB513371位于pm42近着丝粒侧,与pm42的遗传距离为14.6cM。整合原有的作图数据,构建了pm42基因的高密度比较基因组学遗传连锁图谱,pm42被定位于3.3cM的区间,该区间对应于短柄草66kb的基因组区域及水稻69kb的基因组区域。该结果为抗白粉病基因pm42高密度精细遗传连锁图谱构建、分子辅助选择和基因聚合奠定了基础。 展开更多
关键词 小麦白粉病基因 pm42 比较基因组学 二穗短柄草 共线性 EST-STS EST-SSCP
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小麦白粉病抗性基因的研究与利用 被引量:5
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作者 董进英 《种子》 CSCD 北大核心 1993年第2期35-37,共3页
小麦白粉病是小麦中的一种重要病害,广泛分布于世界各产麦区,造成了小麦产量的重大损失,因此,如何挖掘抗源.提高抗白粉病育种的成效,减轻白粉病的流行、危害,是育种家一直研究的重要问题。本文概述了世界上已鉴定出的19个白粉病抗性基... 小麦白粉病是小麦中的一种重要病害,广泛分布于世界各产麦区,造成了小麦产量的重大损失,因此,如何挖掘抗源.提高抗白粉病育种的成效,减轻白粉病的流行、危害,是育种家一直研究的重要问题。本文概述了世界上已鉴定出的19个白粉病抗性基因的来源,携带该基因的有关品种和部分抗性基因的抗性表现及在育种上的应用。其中,P_(m2)、P_(m4)、P_(m6)等抗性基因在我国为高效抗性基因,特别是含有P_(m2)、p_(m6)基因的CI_(12632)、CI_(12633)、TP_(114)等是良好的抗源,有很高的利用价值。本文还论述了小麦抗白粉病育种中的几个问题。 展开更多
关键词 小麦白粉病基因 育种工作 育种家 种质库 育种学家 性品种 白粉病 白粉病 病品种
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50个小麦生产及后备品种(系)的抗白粉病基因推导 被引量:10
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作者 王振花 刘伟 +3 位作者 徐志 范洁茹 彭云良 周益林 《植物保护》 CAS CSCD 北大核心 2017年第6期152-158,共7页
为明确我国小麦品种(系)中抗白粉病基因的组成,利用25个不同毒性的小麦白粉菌菌株对50个小麦生产及后备品种(系)进行抗白粉病基因推导,结果表明,参试的50个小麦品种(系)中有8个小麦品种(系)对供试的25个菌株全部感病,5个品种含有抗病基... 为明确我国小麦品种(系)中抗白粉病基因的组成,利用25个不同毒性的小麦白粉菌菌株对50个小麦生产及后备品种(系)进行抗白粉病基因推导,结果表明,参试的50个小麦品种(系)中有8个小麦品种(系)对供试的25个菌株全部感病,5个品种含有抗病基因Pm8,2个品种含有Pm4a,9个品种含有Pm2+6,4个品种含有Pm2,22个品种(系)可能含有供试基因之外的其他抗性基因或新基因。此研究结果可为小麦抗病育种以及品种利用提供依据。 展开更多
关键词 小麦 小麦白粉 小麦白粉病基因 基因推导
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山东省小麦白粉病菌群体毒性鉴定和分析 被引量:1
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作者 张眉 郭霞 +4 位作者 辛志梅 王升吉 辛相启 姜珊珊 吴斌 《山东农业科学》 2020年第7期95-100,共6页
为明确山东省小麦白粉病菌群体的毒性结构组成,利用31份已知抗白粉病基因的小麦品种(系)对采自山东省德州、烟台、济南、济宁、聊城、临沂6市共62个小麦白粉病菌株毒性结构进行鉴定,并构建山东省小麦白粉病菌系毒性聚类图。结果表明,山... 为明确山东省小麦白粉病菌群体的毒性结构组成,利用31份已知抗白粉病基因的小麦品种(系)对采自山东省德州、烟台、济南、济宁、聊城、临沂6市共62个小麦白粉病菌株毒性结构进行鉴定,并构建山东省小麦白粉病菌系毒性聚类图。结果表明,山东省小麦白粉病菌群体对抗病基因Pm1a、Pm3b、Pm3c、Pm3d、Pm3e、Pm3f、Pm5a、Pm6、Pm7、Pm8、Pm13、Pm17、Pm19、Pm2+Ta、Pm"Era"和Pm"XBD"的毒性频率均高于70%,对抗病基因Pm21、Pm4b+5b及Pm5+6的毒性频率低于30%,仅对Pm21抗病基因无毒性;德州市、烟台市、济宁市、济南市、聊城市和临沂市白粉病菌群体分别对12、15、22、23、25、28个抗病基因的毒性频率高于70%;对小麦白粉病菌株毒性聚类分析发现,62个小麦白粉病菌株毒性相似系数在0.67~1.00之间,说明6地市的小麦白粉病菌群体间毒性存在一定差异,德州市和烟台市的大部分菌株毒性结构相似度高,其余地市菌株毒性结构相似度高。 展开更多
关键词 山东省 小麦白粉病 小麦白粉病基因 毒性频率
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新疆小麦白粉病菌群体的毒性监测和分析 被引量:11
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作者 王振花 刘伟 +2 位作者 高海峰 范洁茹 周益林 《新疆农业科学》 CAS CSCD 北大核心 2017年第10期1903-1910,共8页
【目的】通过对新疆小麦白粉菌群体的毒性鉴定,研究其病菌群体的毒性结构和组成,为小麦抗白粉病品种的选育及抗病品种的应用和合理布局提供依据。【方法】对采自新疆的小麦白粉菌标样进行分离纯化,采用抖接法接种到35个已知抗病基因的... 【目的】通过对新疆小麦白粉菌群体的毒性鉴定,研究其病菌群体的毒性结构和组成,为小麦抗白粉病品种的选育及抗病品种的应用和合理布局提供依据。【方法】对采自新疆的小麦白粉菌标样进行分离纯化,采用抖接法接种到35个已知抗病基因的小麦鉴别寄主上,调查鉴别寄主对病菌的反应型,明确小麦白粉菌不同菌株的毒性。【结果】新疆小麦白粉菌群体对抗病基因Pm1c、Pm2、Pm4a、Pm4b、Pm4c、Pm5b、Pm12、Pm13、Pm16、Pm21、Pm24、Pm25、Pm30、Pm35、Pm"XBD"、Pm2+Mld、Pm2+6、Pm4+8、Pm4b+5b和Pm5+6的毒性频率低于30%,其中对Pm12、Pm16和Pm21的毒性频率为0;对Pm3b、Pm3d和Pm34的毒性频率在30%~70%;对抗病基因Pm1a、Pm3a、Pm3c、Pm3e、Pm3f、Pm5a、Pm6、Pm7、Pm8、Pm17、Pm19、Pm1+2+9等的毒性频率均高于70%。【结论】抗病基因Pm1c、Pm2、Pm4a、Pm4b、Pm4c、Pm5b、Pm12、Pm13、Pm16、Pm21、Pm24、Pm25、Pm30、Pm35、Pm"XBD"、Pm2+Mld、Pm2+6、Pm4+8、Pm4b+5b和Pm5+6均是当前可用的有效抗病基因,可应用在小麦育种及生产上;Pm1a、Pm3a、Pm3c、Pm3e、Pm3f、Pm5a、Pm6、Pm7、Pm8、Pm17、Pm19、Pm1+2+9这些基因抗小麦白粉病性能较差,已不适合在育种和生产上使用;Pm3d、Pm3b和Pm34在生产上应注意合理使用。 展开更多
关键词 小麦白粉 小麦白粉病基因 毒性频率 病育种
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The Relationship of Methyl Jasmonate Enhanced Powdery Mildew Resistance in Wheat and the Expressions of 9 Disease Resistance Related Genes 被引量:18
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作者 牛吉山 刘靖 +3 位作者 马文斌 李巧云 王正阳 贺德先 《Agricultural Science & Technology》 CAS 2011年第4期504-508,共5页
[Objective] This study was carried out to determine the induction effect of jasmonic acid(JA)on powdery mildew resistance in wheat,the activation effect on the expressions of plant disease resistance related genes,a... [Objective] This study was carried out to determine the induction effect of jasmonic acid(JA)on powdery mildew resistance in wheat,the activation effect on the expressions of plant disease resistance related genes,and to investigate the relationship between the induced resistance and the gene expression patterns.[Method] Three powdery mildew susceptible cultivars of "Chinese Spring","Pumai 9" and "Zhoumai 18" typically representing different phenotypes in the field were employed.The powdery mildew was assessed by detached leaf assay,and real time quantitative RT-PCR was used to determine the expression patterns of 9 disease resistance related genes of PR1(PR1.1),PR2(β,1-3 glucanase),PR3(chitinase),PR4(wheatwin1),PR5(thaumatin-like protein),PR9(TaPERO,peroxidase),PR10,TaGLP2a(germin-like)and Ta-JA2(jasmonate-induced protein)in leaf of the three cultivars.[Result] MeJA application enhanced the powdery mildew resistances of "Chinese Spring","Pumai 9" and "Zhoumai 18".The induced powdery mildew resistance could be detected from 12 h to 96 h after MeJA treatment,and the peak value was at 24 h.Though there were differences between the three cultivars,MeJA significantly effect on the expressions of the 8 disease resistance related genes except TaGLP2a,and the peak values were at 12 h,24 h or 48 h after treatments.The strongest activation of MeJA was on PR9 and PR1 that their expressions could reach more than 100 times of the untreated samples.MeJA strongly activated PR2、PR4、PR5、PR3、PR10 and Ta-JA2,their expression could reach 10 to 70 times,and there was almost no activation effect on TaGLP2a.The induced powdery mildew resistance positively correlated with the induced expressions of the 8 disease related genes.[Conclusion] The induced powdery mildew resistance positively correlated with the induced expressions of the disease related genes.Jasmonate signalling plays a role in defence against Blumeria graminis f.sp.tritici.and future manipulation of this pathway may improve powdery mildew resistance in wheat. 展开更多
关键词 WHEAT Powdery mildew Jasmonic acid(JA) Resistance Gene Expression
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Cloning, Characterization and Chromosome Localization of Two Powdery Mildew Resistance-Related Gene Sequences from Wheat 被引量:4
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作者 于玲 牛吉山 +3 位作者 马正强 陈佩度 齐莉莉 刘大钧 《Acta Botanica Sinica》 CSCD 2002年第12期1438-1444,共7页
Reverse_transcription Polymerase Chain Reaction (RT_PCR) was performed using cDNAs as templates from wheat_ Haynaldia villosa 6VS/6AL translocation line and 'Yangmai 5' induced with fungus Erysiphe gramin... Reverse_transcription Polymerase Chain Reaction (RT_PCR) was performed using cDNAs as templates from wheat_ Haynaldia villosa 6VS/6AL translocation line and 'Yangmai 5' induced with fungus Erysiphe graminis , and degenerate primers designed based on the conserved amino acid sequences of known plant disease_resistance genes. The cDNA sequences encoding cyclophilin_like and H +_ATPase_like genes were first isolated and characterized in wheat. The putative amino acid sequences of the two clones showed that they were highly homologous to those of cyclophilin proteins and H +_ATPases isolated from other plants. Thus they were designated as Ta_Cyp and Ta_MAH . The obvious expression differences could be observed between wheat_ H. villosa 6VS/6AL translocation line and susceptible wheat cultivar 'Yangmai 5', implying that the two genes may be related with the resistance of wheat_ H. villosa 6VS/6AL translocation line to disease. Southern blot indicated that the wheat genome contained 2-3 copies of Ta_Cyp gene and one copy of the Ta_MAH gene. Chinese Spring nulli_tetrasomic line analysis located the Ta_Cyp homologous genes on wheat chromosome 6A, 6B and 6D. Southern blot using Ta_Cyp clone as a probe showed that the polymorphic bands existed among the H. villosa , amphiploid of Triticum durum _ H. villosa , wheat_ H. villosa 6VS/6AL translocation line and 'Yangmai 5', suggesting that Ta_Cyp homologies exist in wheat genome as well as on the short arm of chromosome 6V in H. villosa . 展开更多
关键词 CLONING wheat_ Haynaldia villosa 6VS/6AL translocation line cyclophilin gene H +_ATPase gene
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Molecular and Physical Mapping of Powdery Mildew Resistance Genes and QTLs in Wheat: A Review 被引量:7
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作者 Jun GUO Cheng LIU +8 位作者 Shengnan ZHAI Haosheng LI Aifeng LIU Dungong CHENG Ran HAN Jianjun LIU Lingrang KONG Zhendong ZHAO Jianmin SONG 《Agricultural Science & Technology》 CAS 2017年第6期965-970,共6页
Wheat powdery mildew (Pro) is a major disease of wheat worldwide. During the past years, numerous studies have been published on molecular mapping of Pm resistance gene(s) in wheat. We summarized the relevant find... Wheat powdery mildew (Pro) is a major disease of wheat worldwide. During the past years, numerous studies have been published on molecular mapping of Pm resistance gene(s) in wheat. We summarized the relevant findings of 89 major re- sistance gene mapping studies and 25 quantitative trait loci (QTL) mapping studies. Major Pm resistance genes and QTLs were found on all wheat chromosomes, but the Pm resistance genes/QTLs were not randomly distributed on each chromosome of wheat. The summarized data showed that the A or B genome has more major Pm resistance genes than the D genome and chromosomes 1A, 2A, 2B, 5B, 5D, 6B, 7A and 7B harbor more major Pm resistance genes than the other chromosomes. For adult plant resistance (APR) genes/QTLs, B genome of wheat harbors more APR genes than A and D genomes, and chromo- somes 2A, 4A, 5A, 1B, 2B, 3B, 5B, 6B, 7B, 2D, 5D and 7D harbor more Pm resistance QTLs than the other chromosomes, suggesting that A genome except 1A, 3A and 6A, B genome except 4B, D genome except 1D, 3D, 4D, and 6D play an impor- tant role in wheat combating against powdery mildew. Furthermore, Pm resistance genes are derived from wheat and its rela- tives, which suggested that the resistance sources are diverse and Pm resistance genes are diverse and useful in combating against the powdery mildew isolates. In this review, four APR genes, Pm38/Lr34/Yr18/Sr57, Pm46/Lr67/Yr46/Sr55, Pm?/Lr27/Yr30/ SY2 and Pm39/Lr46/Yr29, are not only resistant to powdery mildew but also effective for rust diseases in the field, indicating that such genes are stable and useful in wheat breeding programmes. The summarized data also provide chromosome locations or linked markers for Pm resistance genes/QTLs. Markers linked to these genes can also be utilized to pyramid diverse Pm resis- tance genes/QTLs more efficiently by marker-assisted selection. 展开更多
关键词 Wheat powdery mildew Molecular mapping Major Pm resistance genes Quantitative trait loci (QTL) Marker-assisted selection
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