一个与马铃薯青枯病抗性连锁的SRAP标记筛选

以两个马铃薯二倍体分离群体ED和CE共105个基因型为材料,利用群分法(BulkedSegregantAnalysis,BSA)筛选与马铃薯青枯病抗性基因连锁的分子标记。在8个正向引物和11个反向引物组成的88对SRAP引物组合中,筛选获得了一个与马铃薯青枯病抗性紧密连锁的SRAP标记M32,遗传连锁分析表明,该标记在ED群体和CE群体中与抗性位点之间的遗传距离分别为10.2cM和17.3cM。     

小麦抗条锈病基因Yr2的SSR标记

为了利用SSR技术寻找与小麦抗务锈病基因Yr2紧密连锁的分子标记,以近等基因系Taichung29*6／HeinesⅦ与感病的背景亲本Taichung29构建F2分离群体,进行了F2单株苗期抗条锈病鉴定。抗性分析表明,近等基因系Taichung29*6／HeinesⅦ中的抗条锈病基因是由单基因控制的。进一步用7B染色体上的45对SSR引物对抗、感亲本及171株F2分离群体进行SSR分析,筛选出一个与小麦抗条锈病基因Yr2紧密连锁的SSR标记WMC364-207 bp／201 bp。通过最大似然法计算,该标记与Yr2基因之间的遗传距离为5.6 cM。     

小麦新种质YW243抗条锈病基因的染色体定位

为鉴定小麦新种质YW243的条锈病抗性基因,用条中31号小种接种,对YW243与中国春的杂种F2群体进行了抗性遗传分析,并利用SSR分子标记技术对抗性基因进行了染色体定位。结果显示,YW243的每锈病抗性在与中国春的杂交组合F1、F2分离群体中呈一对显性基因的遗传模式;经过对264对微卫星引物的筛选,发现位于2BL上的两对引物Xgwm388和Xgwm501能够在双亲和抗、感池之间扩增出特征带,并与抗性基因表现连锁,它们的遗传距离分别为27．9cM和23．5cM,说明抗病基因位于2BL染色体上。从系谱和抗谱分析,推测YW243的抗性基因不同于Yr5,可能是一个新的抗病基因或是Yr5的复等位基因。     

高原粳稻子预44抗稻瘟病基因遗传分析和定位

 以高感稻瘟病的低海拔粳稻江南香糯与高抗稻瘟病的高原粳稻子预44作亲本进行杂交,获得F1、F2、BC1F1和以F2单粒传构建的、由276个株系组成的F7重组自交系群体。分别用稻瘟病菌生理小种ZB13和ZE1对两亲本江南香糯和子预44及其杂交后代群体F1、F2和BC1F1进行抗性接种鉴定和遗传分析。结果表明,子预44对稻瘟病菌生理小种ZB13和ZE1的抗性都表现为单基因控制的显性遗传。进一步利用重组自交系F7群体的266个有效株系作为定位群体,将抗稻瘟病菌生理小种ZE1的基因定位在水稻第11染色体上与SSR标记RM206间遗传距离为0 cM的位置,暂定名为Pi zy（t）。这些结果为进一步将子预44中的抗性基因用于水稻抗病育种及该抗稻瘟病基因的克隆奠定了重要基础。     

大豆灰斑病1号生理小种抗性基因的SSR标记分析

针对中国大豆灰斑病1号生理小种,以抗所有生理小种的品系东农40566为母本,以感1号生理小种的品种东农410为父本配制杂交组合,杂交得到F2代后连续自交3代得到F5代群体.该群体经人工接种灰斑病1号生理小种后,利用BSA法对500个SSR标记进行筛选,其中3个标记Satt565、SOYGPATR和Satt396在抗、感池间表现出稳定的多态性,并且在F2代个体中表现出抗性与多态性协同分离的趋势.这3个标记与抗性基因的连锁顺序为Satt565-SOYGPATR-Hrcs1-Satt396,它们与抗性基因的连锁距离分别为12.7cM、6.5cM、14.7cM.推测抗大豆灰斑病1号生理小种的基因可能位于C1连锁群上.     

波斯小麦Cypa35-3成株期抗白粉病基因定位

源自苏联的波斯小麦Cypa35-3对陕西关中地区白粉菌优势小种表现为成株期高抗白粉病。为明确Cypa35-3抗白粉病基因所在染色体位置及其抗白粉病基因的遗传规律,利用Cypa35-3与高感白粉病的加拿大二粒小麦Flavescens进行杂交,在成株期自然发病条件下对亲本及其杂交F₁、F₂、F_2∶3群体进行白粉病抗性评价与遗传分析;选用分布于A、B染色体组14对染色体上共计601对SSR标记,利用分离群体分组分析法(BSA)对Cypa35-3的F₂群体进行多态性标记筛选。结果表明,Cypa35-3的成株期白粉病抗性受1对显性基因控制,暂命名为PmCypa35-3。通过群体筛选,获得4对位于1B染色体上的SSR标记,分别为Xbarc81、Xcfd48、Xbarc61、Xbarc302,其中Xbarc81、Xcfd48位于PmCypa35-3两侧,遗传距离分别为25.2 cM、8.6 cM。由此将成株期抗白粉病基因PmCypa35-3初步定位于1B染色体。通过与1B染色体上及波斯小麦中正式命名的抗白粉病基因...     

小麦种质资源BJ399抗条锈病基因的分子标记定位

条锈病是影响小麦产量和品质的一种世界性病害。种质资源BJ399对小麦条锈病具有良好的苗期和成株期抗性,为明确其条锈病抗性基因,利用BJ399和高感条锈病品种铭贤169杂交,获得BJ399/铭贤169的F_1、BC_1和F_2代分离群体,并利用我国当前流行的条锈菌生理小种条中34号(CYR34)进行温室苗期抗条锈性鉴定和遗传分析。结果表明,BJ399对CYR34的抗性由1对显性基因控制,暂命名为 YrBJ399。筛选到3个与目的基因连锁的SSR标记Xwmc296、Xgwm425和Xgwm558,且3个标记位于抗病基因的同一侧,距离目的基因最近的标记为Xwmc296,其遗传距离为9.5 cM,标记Xgwm425和Xgwm558与目的基因 YrBJ399的遗传距离分别为14.3 cM和18.0 cM,并初步将抗病基因定位于小麦染色体2AS上。根据抗病基因来源和染色体定位结果推测, YrBJ399可能是一个抗条锈病新基因。     

小麦品系91260抗白粉基因的分子标记定位

白粉病是小麦的重要病害之一,可造成小麦严重减产。小麦品系91260具有优良的成株期白粉病抗性并对白粉菌生理小种E09免疫。为给抗白粉病小麦育种提供参考,本研究对抗病品系91260和感病品种豫麦49的杂交F₂代群体进行遗传分析。结果发现,F₂代群体中抗感植株的分离比为9∶7,表明91260含有两对显性互补的抗白粉基因,暂时命名为Ml91260-1和Ml91260-2。SSR分子标记分析表明,Ml91260-1位于2AL染色体上,侧翼分子标记为Xcfa2263和Xwmc170,遗传距离分别是8.3 cM和4.1 cM;Ml91260-2位于2BL染色体上,侧翼分子标记为Xgpw4103和Xwmc332,遗传距离分别是4.1 cM和6.7 cM。其中,Ml91260-2是2BL上新的抗白粉病基因。     

花生抗北方根结线虫病SSR标记研究

本研究利用抗、感北方根结线虫病的花生品种为亲本配制杂交组合"花育22号×D099",以其F2分离群体为研究材料,采用SSR技术和BSA分析方法,获得了与花生北方根结线虫病抗性基因连锁的2个SSR分子标记S32-380和S89-140,标记与抗病基因间的遗传距离分别为4.421 cM和7.404 cM.该分子标记的建立将为开展花生抗北方根结线虫病的分子标记辅助选择育种奠定基础.     

马铃薯晚疫病抗病基因研究进展

晚疫病是危害马铃薯生产的重要病害,可导致马铃薯的大量减产。多年来研究人员对马铃薯晚疫病进行了大量的研究,取得了一系列的成果。对马铃薯晚疫病防治最有效的方法是使用抗病品种,随着分子生物学技术的发展,从野生资源中分离抗病基因,并将其转入到栽培种马铃薯中可以获得抗病特性。到目前为止,已经有十多个抗晚疫病基因被发现和图谱,且部分基因已被转入到栽培品种中。本文从晚疫病抗病基因的发现、分离、定位及克隆等方面进行了综述。     

Identification of late blight, Colorado potato beetle, and blackleg resistance in three Mexican and two South American wild 2x (1EBN)Solanum species

Wild potatoes are important sources of genes for resistance to disease and insect pests. A collection of wild Mexican and South AmericanSolarium species from the US potato Genebank was evaluated under laboratory and/or field conditions for their reaction to late blight (Phytophthora infestans), Colorado potato beetle (CPB,Leptinotarsa decemlineata Say), and blackleg (Erwinia carotovora subsp.atroseptica (van Hall) Dye) in order to identify individual genotypes with multiple resistance genes. Late blight inoculations using aggressive isolates (US-8/A2 and US-11/A1 mating types) of P.infestans revealed a wide range of variation for resistance between and within the accessions of the wild species tested. For late blight, susceptible as well as moderately to highly resistant genotypes were observed in all the species tested. However, at least one accession from the three Mexican and one South American wild diploid species tested showed a relatively uniform high level of resistance toP. infestans. These includedS. bulbocastanum, S. pinnatisectum, S. cardiophyllum, andS. circaeifolium. Two accessions from South American speciesS. commersonii were highly susceptible to late blight. For the Colorado potato beetle test, only one species,S. pinnatisectum appeared uniformly resistant to CPB under field conditions. Results of screening for blackleg resistance showed that there were major differences between genotypes in the wild species. Accessions ofS. circaeifolium PI 498119 andS. bulbocastanum PI 243504 were identified as having significantly higher blackleg resistance than cultivated potato and the other wild species tested. However, genotypes from these two accessions were more susceptible to late blight and CPB. Characterization of theP. infestans isolate P1801C.16 used for late blight evaluation and multi-locus isolate tests using US-8/A2 and US-11/A1 races revealed that the resistance inS. pinnatisectum genotypes tested corresponded to a race-non-specific genetic system, which was different from any existing R genes.Solanum pin-natisectum genotypes with both high levels of late blight and CPB resistance as well as blackleg resistance genotypes identified in the present study represent a diverse gene pool that may be useful for development of new potato cultivars with multiple disease and insect resistance. The potential utilization of these valuable sources for improvement of cultivated potato is discussed.     

QTL Analysis of Late Blight Resistance in a Diploid Potato Family of Solanum spegazzinii × S. chacoense

Several quantitative trait loci (QTL) for resistance to late blight have been reported in diploid potatoes. The diploid wild potato species Solanum chacoense possesses a high degree of horizontal resistance to late blight. In the present study, we report on QTL mapping for late blight resistance in a diploid mapping population of 126 F₁ of Solanum spegazzinii (susceptible) × S. chacoense (resistant). The area under the disease progress curve (AUDPC) values for late blight resistance using the “whole plant in vitro assay” and the “detached leaf assay” on the mapping population displayed quantitative variation. Out of 64 AFLP primer-pairs combinations and SSR markers, a total of 209 significant AFLP loci were placed onto the 12 linkage group of potato covering a total map length of 6548.1 cM. QTL analysis based on the AUDPC dataset of the “whole plant in vitro assay” using the interval-mapping option identified two QTL (LOD?>?2.5) located on linkage groups IX and X, which explained 14.70 and 3.40% variation, respectively. The present study revealed the presence of potential new genetic loci in the diploid potato family contributing to quantitative resistance against late blight.     

携有抗白叶枯病新基因Xa23水稻近等基因系的构建及应用

 1993～1998年,构建了携有抗稻白叶枯病新基因Xa23的近等基因系,命名为CBB23。以全生育期高度感病并具有改良株型的籼稻品种JG30为轮回亲本，与携有Xa23的抗性供体H-4杂交，JG30/H-4的F1通过回交、自交直至B5F4，各世代均用与目标基因Xa23相对应的专化小种菌系P6人工接种鉴定，同步进行株型和农艺性状选择，直至抗性稳定和农艺性状类似其轮回亲本。比较了CBB23 (携Xa23) 和IRBB21 (携Xa21) 对20个菌系包括10个菲律宾小种、3个日本小种和7个中国病原型代表菌系的抗谱，Xa23抗所有20 个菌系； Xa21 抗19个菌系，对菲律宾10号小种则高度感病。用近等基因系CBB23构建了JG30/CBB23组合的F2分离群体，通过SSR标记筛选，初步将Xa23定位于水稻第11染色体。进一步筛选出3个与Xa23更紧密连锁的AFLP标记。其中的APKj23与Xa23之间的图距约为1.0 cM。并报道了在抗病育种中已有效的应用了携有Xa23的近等基因系 CBB23。     

抗水稻白叶枯病新基因Xa-25(t)的RAPD分析

利用RAPD标记对从体细胞突变体HX-3中鉴定出的抗水稻白叶枯病新基因Xa- 25 (t)进行了研究,在306个随机引物中,两个引物S1269和S1327在亲本和抗感池（均由12个高抗或高感植株组成）之间表现多态性。用这两个引物对龙特甫A和HX-3的F2群体的114个单株进行连锁分析,表明 S1269和 S1327与Xa-25 (t)的连锁距离分别为5.3和23.7 cM,且位于Xa-25 (t)的两侧。     

Marker-assisted Breeding for Disease Resistance in Potato

Sub-project 5 of BIOEXPLOIT aims to design durable disease resistance through marker-assisted breeding by converting existing markers for high-throughput application, developing and validating high-throughput marker technologies and pyramiding major R genes and/or quantitative trait loci into elite material. Activities include (1) the fine mapping of the quantitative trait locus PiXspg which accounts for a large proportion of the variation in late blight resistance, (2) converting SNP-based markers and an AFLP marker to easy-to-use-markers, (3) testing of progenies with combined sources of late blight resistance for presence of R genes and agronomic features, (4) backcrossing new sources of resistance to S. tuberosum and molecular screening of breeding materials with marker GP94 linked with gene Rpi-phu1 conferring late blight resistance, (5) evaluating potato clones with enhanced resistance against Phytophthora infestans under field conditions of Toluca (México), and (6) developing populations and marker-assisted breeding for disease resistance.     

Resistance to late blight (Phytophthora infestans (Mont.) de Bary) of potato plants regenerated fromin vitro selected calli

Summary Cells of seven potato cultivars were selectedin vitro with culture filtrate (CF) ofPhytophthora infestans (Mont.) de Bary. Regenerated plants were tested for late blight resistance. The aim of the study was to check the efficacy of CF in the selection of potatoes for resistance to late blight and to evaluate the effects of additive factors on general resistance. One selection cycle, applied to a cell culture system, selected cells resistant to toxic metabolites of CF.In vivo screening of clones regenerated from selected cells was done in two steps: on whole plants, assessing foliage late blight, and on detached leaves, assessing single factors of horizontal resistance. In general, the frequency of resistant variants selected with CF did not differ from that of resistant somaclonal variants. Nevertheless, high concentrations of CF in the growth medium seemed to induce an improvement of some partial resistance factors as compared with the source plants.     

河北省一季作区马铃薯病虫害发生及综合防控

河北省一季作区马铃薯主要病虫害有晚疫病、早疫病、黑痣病和二十八星瓢虫,此外,病毒引起的品种退化比较普遍,造成不同程度的损失。本文根据河北省一季作区马铃薯病虫害发生特点总结出一套综合防控技术体系,包括将马铃薯与玉米、大白菜等非茄科作物轮作3年减轻黑痣病危害;采用脱毒薯克服病毒引起的品种退化问题;种薯和(或)土壤消毒控制黑痣病和晚疫病;待马铃薯生长至封垄后,遇到适宜晚疫病发生的天气,喷施1～3次保护性杀菌剂预防晚疫病和早疫病;一旦监测到晚疫病中心病株后即拔除并装入塑料袋带出田外,并交替喷施有治疗效果、能兼治早疫病且作用机制不同的内吸性杀菌剂及混剂;田间出现马铃薯二十八星瓢虫成虫,在杀菌剂中混入高效氯氰菊酯或高效氯氟氰菊酯等高效杀虫剂防虫;马铃薯成熟前1～2周将地上部分割掉并运出田外后收获块茎。     

基于近等基因导入系发掘玉米抗甘蔗花叶病毒主效基因

利用玉米自交系掖478与中自01构建近等基因导入系群体(BC4F2),通过田间人工接种甘蔗花叶病毒鉴定获得抗病植株。采用38个SSR标记分析抗病株基因型,通过连锁不平衡分析,在玉米第3和6染色体上发掘3个主效抗病QTL。第3染色体上的QTL置信区间为26.1cM-phi053-5cM;第6染色体上的QTL置信区间分别为1.2cM-bnlg161和5.3cM-bnlg1538-7cM。建立了基于近等基因导入系发掘玉米抗甘蔗花叶病毒主效QTL技术,获得了一批含有抗病毒QTL的近等基因导入系,为抗病育种提供了信息和材料。