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1.
玉米抗矮花叶病QTL定位   总被引:14,自引:0,他引:14  
利用玉米自交系X178(抗)和B73(感)组配的F2群体(234个单株),构建了包含249个SSR和AFLP标记位点的遗传连锁图谱,图谱全长1 659.3 cM,平均图距6.58 cM。采用人工接种法对216个F3家系在苗期、拔节期和抽雄期分别进行玉米矮花叶病的抗性鉴定。应用复合区间作图法分析抗病QTL与基因效应。结果表明,在3个发育阶段检测到的  相似文献   

2.
玉米抗丝黑穗病QTL分析   总被引:13,自引:1,他引:12  
以Mo17(抗)×黄早四(感)的F2分离群体(191个单株)为作图群体,构建了含有84个SSR位点和48个AFLP位点的遗传连锁图谱,全长1 542.9 cM,平均图距11.7 cM。在吉林省公主岭和黑龙江省哈尔滨2个地点通过人工接种方法对184个相应的F3家系(缺失7个)进行抗病鉴定。采用复合区间作图法对抗丝黑穗病数量性状位点(QTL)进行定位及遗传效应分析。在吉林公主岭地区检测到5个QTL,分别位于第1、2、3、8、9染色体上,解释的表型方差为10.0%~16.3%。在黑龙江哈尔滨地区也检测到5个QTL,分别位于第1、2、3、4、7染色体上,解释的表型方差为4.6%~13.4%。比较分析发现,两地一致在第2、3染色体上各检测到1个QTL,其中第2染色体上的表现为超显性效应,第3染色体上的表现为加性效应。研究结果为玉米抗丝黑穗病种质改良提供了重要信息。  相似文献   

3.
以玉米遗传连锁图谱IBM2 2008 Neighbors为参考图谱,利用BioMercator 2.1软件,通过映射来自不同实验中的340个玉米抗病QTL,构建出玉米抗病QTL的整合图谱。采用元分析技术,在1、3、6、10号染色体上发掘5个"一致性抗病QTL"区间,图距分别为5.14cM、9.00cM、28.50cM、1.73cM和33.34cM。从MaizeGDB网站下载"一致性抗病QTL"区间内的基因和标记原始序列,采用NCBI网站在线软件BlastX通过同源比对,在5个"一致性抗病QTL"区间内初步确定8个抗病基因同源序列。借助比较基因电子定位策略,将54个水稻和44个玉米抗性基因转定于玉米IBM2 2008 Neighbors遗传连锁图谱上。本文研究结果为玉米抗病QTL精细定位和克隆奠定了基础。  相似文献   

4.
选用感丝裂病的玉米自交系R08与抗丝裂病的自交系Es40组配F2群体共348个单株,构建了包含115个SSR标记的分子遗传连锁图谱,覆盖玉米基因组2 178.6 cM,平均图距为18.9 cM。采用复合区间作图法,对F2:4家系丝裂病数据进行抗性QTL分析,共检测到12个QTL,分别位于第1、2、4、5和7染色体,贡献率为4.22%~37.95%。其中在第1、3染色体上检测到主效QTL,贡献率均大于30%,基因作用方式均为显性,其余10个QTL的作用方式多为加性或部分显性。  相似文献   

5.
玉米种子休眠性的QTL定位   总被引:6,自引:1,他引:5  
选用两个种子休眠性差异较大的普通玉米自交系R08与A318组配的F2群体共331个单株,构建了包含137个SSR标记的分子遗传连锁图谱,覆盖玉米基因组2 076.7 cM,平均图距15.2 cM。采用复合区间作图法对F2:3家系种子休眠性数据进行分析,共检测到7个QTL,分别位于玉米第1、3、5和10染色体上。7个QTL的贡献率在2.45%~26.  相似文献   

6.
玉米抗甘蔗花叶病毒QTL的初步研究   总被引:19,自引:2,他引:17  
以黄早四(抗)×掖107(感)的F2分离群体(184个单株)为作图群体, 构建了具有65个SSR标记位点的遗传连锁图谱, 覆盖玉米基因组1333.3 cM, 标记间平均距离20.5 cM. 通过人工接种鉴定评价184个F3家系对SCMV引起的玉米矮花叶病的抗性反应. 采用复合区间作图法对抗病数量性状位点(QTL)进行定位及遗传效应分析, 结果共检测到3个QTLs,  相似文献   

7.
发掘水稻黑条矮缩病的抗性基因有助于抗病品种的选育,减少黑条矮缩病对水稻生产的危害。本研究构建了包含222个家系的L5494/IR36重组自交系群体。对该群体进行黑条矮缩病的田间诱发鉴定,抗性亲本IR36发病率为28.70%,感病亲本L5494发病率为84.26%,群体发病率范围为11.21%~89.81%。利用134对分子标记构建覆盖12条染色体的遗传连锁图谱,总遗传距离为1475.97 cM,平均标记间距为11.1 cM。利用QTL IciMapping 4.0对抗黑条矮缩病QTL进行分析,共检测到4个QTL,其中第1、第2、第9染色体上QTL的表型贡献率分别为12.64%、16.00%和8.43%,抗病等位基因来自抗病亲本IR36;第6染色体上QTL的表型贡献率为10.82%,抗病等位基因来自感病亲本L5494。在此基础上,利用93-11为供体、日本晴为背景的近等基因系材料,在qRBSDV-1定位区间内检测到来自93-11的抗性QTL。本研究结果为水稻黑条矮缩病抗性基因定位及分子标记辅助选择育种提供借鉴。  相似文献   

8.
水稻抗纹枯病QTL表达的遗传背景及环境效应   总被引:6,自引:4,他引:2  
利用水稻纹枯病菌强致病菌系RH-9人工接种Lemont导入到特青背景的213个近等基因导入系(TQ-ILs)群体和特青导入到Lemont背景的195个近等基因导入系(LT-ILs)群体,定位和分析了水稻抗纹枯病数量性状座位(quantitative trait loci, QTL)及其表达的环境与遗传背景效应。亲本Lemont对RH-9表现为高度感病,特青表现为中等抗病。人工接种后TQ-ILs群体的相对病斑高度(病斑高度与株高比)呈连续正态分布,LT-IL群体则明显偏向感病亲本Lemont。在不同年份和遗传背景下检测到影响纹枯病相对病斑高度的主效QTL 10个和互作QTL 13个,其中2006年在TQ-IL群体定位到的6个主效QTL在2007年均得到验证,表明这些QTL具有较好年度间的重复性。QSh4是唯一在双向导入系背景下表达的QTL,该位点特青等位基因降低相对病斑高度,提高抗性水平。在TQ-ILs群体中定位到位于第10染色体RM216~RM311区间的QSb10a与在LT-IL群体中定位到的位于相邻区间RM222~RM216的QSb10b的基因作用方向不同,推断这两个QTL存在紧密连锁关系。绝大多数在TQ-IL群体中表达的主效及互作QTL在LT-ILs群体中不表达,表明水稻抗纹枯病QTL具有明显的遗传背景效应。通过比较作图,本研究定位到的其中8个QTL在以往不同群体中同样被检测到,这些主效QTL对通过分子标记辅助选择(marker-assisted selection, MAS)培育水稻抗纹枯病育种可能具有应用价值。研究指出,标记辅助选择在不同遗传背景中能稳定表达的QTL或通过聚合不同抗病QTL是进一步提高水稻纹枯病抗性水平的一个有效途径。  相似文献   

9.
玉米SSR连锁图谱构建与株高及穗位高QTL定位   总被引:10,自引:2,他引:8  
用玉米自交系组合R15×掖478的F2群体构建连锁图谱,并通过1年2点随机区组试验设计,考察玉米229个F2:4家系成株期的株高和穗位高。所建连锁图谱上共拟合146个SSR标记位点,覆盖基因组1 666 cM,标记间平均距离为11.4 cM。用复合区间作图法进行QTL分析,共检测到8个控制株高的QTL,分别位于第2、3、4、5和8染色体;3个控制穗位高的QTL位点,位于第4染色体。单个株高QTL的贡献率变幅为6.67%~11.59%,单个穗位高QTL贡献率变幅为10.46%~12.15%。  相似文献   

10.
鲁棉研15号纤维品质性状QTL定位研究   总被引:3,自引:3,他引:0  
 以陆地棉(Gossypium hirsutum L.)杂交种鲁棉研15号的F2群体为作图群体,利用SSR标记和JoinMap3.0软件构建遗传连锁图谱;利用复合区间作图法分别对随机组成的3个鲁棉研15号的F2:3家系亚群体进行纤维品质性状QTL定位。构建的遗传连锁图谱包含116个多态位点,25个连锁群,全长892.25 cM,覆盖棉花总基因组的20.05%,平均每个连锁群4.64个标记,标记间平均距离7.76 cM;根据已有图谱的定位结果,19个连锁群与染色体建立了联系。在3个F2:3家系亚群体中共检测到46个QTL,其中16个为纤维长度(FL)QTL、7个为纤维强度(FS)、12个为麦克隆值(FM)、6个为伸长率(FE),5个为整齐度指数(FU)。发现在Ah05、Ah08、Ah09、Dh02染色体上QTL有成簇分布的现象,并在3个亚群体中检测到一些受环境影响较小、稳定遗传的QTL。这些QTL可以在今后应用于分子标记辅助选择。  相似文献   

11.
大豆种粒斑驳抗性的遗传分析及基因定位   总被引:1,自引:0,他引:1  
运用SSR标记技术及分离群体组群分析法(BSA法), 对大豆品系3C624×东农8143的F2、F3代群体接种SMV1号株系鉴定种粒斑驳抗性, 并进行抗种粒斑驳基因的分子定位。结果表明, 东农8143对SMV1号株系的种粒斑驳抗性受1对显性基因控制。用Mapmaker/Exp 3.0b进行连锁分析, 抗种粒斑驳基因位于大豆染色体组的F连锁群上, 并获得了与抗种粒斑驳基因紧密连锁的5个SSR标记Sat_297、Sat_229、Sat_317、Satt335和Sct_188, 标记与抗病基因间的排列顺序和连锁距离为Sat_297–12.4 cM–Sat_229–3.6 cM–SRSMV1–1.7 cM–Sat_317–2.4 cM– Satt335–13.8 cM–Sct_188。其中近距离标记Sat_229(3.6 cM)、Sat_317(1.7 cM)和Satt335(4.1 cM)可用于标记辅助选择育种和抗源筛选。  相似文献   

12.
陆地棉遗传图谱构建及产量和纤维品质性状QTL定位   总被引:13,自引:0,他引:13  
利用3 458对SSR引物筛选陆地棉中棉所35和渝棉1号间的多态性引物, 获得173对。以多态性引物检测(渝棉1号×中棉所35)F2群体180个单株的标记基因型, 共获得178个标记位点。构建的遗传连锁图谱包括148个标记, 36个连锁群, 总长1 309.2 cM, 标记间平均距离8.8 cM, 覆盖棉花基因组的29.5%。36个连锁群中的28个分别被定位于20条染色体, 8个连锁群未定位于染色体。以渝棉1号×中棉所35的F2、F2:3群体的产量、纤维品质性状鉴定结果, 利用区间作图方法, 检测到4个产量性状QTL, 即2个衣分(LP)、1个铃重(BW)、1个籽指(SD); 5个纤维品质性状QTL, 即1个纤维长度(FL)、2个纤维比强度(FS)和2个纤维细度(FF)。LP1、BW、SD、FL和FS1被定位于第7染色体, LP2、FS2、FF1和FF2被分别位于第15、21、9和20染色体。5个纤维品质QTL的有利等位基因均来源于渝棉1号。  相似文献   

13.
Mapping QTLs for kernel oil content in a tropical maize population   总被引:6,自引:0,他引:6  
Maize cultivars often have low kernel oil content. To increase the oil content, efficient maize breeding programs have to be developed, which require the knowledge of the inheritance of this trait. Thus, the objective of this research was to map quantitative trait locus (QTLs) and estimate their effects for kernel oil content in a tropical maize population. Two maize inbred lines, contrasting for kernel oil content, were used to develop an F2 population. Four hundred and eight F2 plants were self-pollinated, and their kernels (F2:3 progenies) were used for kernel oil evaluation. A genetic map with 75 microsatellites was developed, and the QTLs were mapped using the composite interval map (CIM); also, estimates of genetic and phenotypic variances, and heritability coefficient were computed. The map presented 10 linkage groups, spanned 1,438.6 cM in length with an average interval of 19.18 cM between adjacent markers. The kernel oil content averaged 58.40 g kg–1, and the broad-sense heritability was high (h2= 0.98). Thirteen QTLs were mapped, which were distributed into eight chromosomes, and explained 26.64% of the genetic variation. QTLs in chromosomes 1, 5, and 6 contributed the most for kernel oil content. Nine out of 13 QTLs with favorable alleles were from the parental inbred with the highest kernel oil content. The average level of dominance was partial, but gene action of the QTLs ranged from additive to overdominance. Eight out of 13 mapped QTLs were already reported for temperate maize populations.  相似文献   

14.
一个新的抗玉米矮花叶病基因的发现及初步定位   总被引:3,自引:0,他引:3  
由SCMV引起的矮花叶病是我国的主要玉米病害之一, 鉴定和发掘新的抗病基因对于玉米抗病遗传育种具有重要意义。以抗病自交系海9-21和感病自交系掖478杂交的一个BC2F3群体为试验材料, 通过人工接种矮花叶病毒进行抗病性鉴定, 发现该分离群体中抗病植株与感病植株数符合1∶3的分离比例, 推测其抗病基因是由1对隐性基因控制。抗感池和SSR标记连锁分析表明, 存在一个新的玉米矮花叶病隐性抗病基因(或等位基因), 将该基因命名为scm3。scm3基因来源于抗病玉米自交系海9-21, 位于第3染色体短臂3.04~3.05区域, 在SSR标记umc1965和bnlg420之间, 遗传距离分别为45.7 cM和6.5 cM。连锁的标记还有umc1307、umc2265、bnlg2241和umc2166, 它们与scm3之间的遗传距离分别是8.3、13.3、15.5和19.7 cM, 这些SSR标记与scm3基因在染色体上的排列顺序为umc1965—scm3—bnlg420—umc1307—umc2265—bnlg2241—umc2166。  相似文献   

15.
Exploiting genes and quantitative trait loci (QTLs) related to maize (Zea mays L.) alkaline tolerance is helpful for improving alkaline resistance. To explore the inheritance of maize alkaline tolerance at the seedling stage, a mapping population comprising 151 F2:3 lines derived from the maize cross between Zheng58, tolerant to alkaline, and Chang7-2, sensitive to alkaline, was used to establish a genetic linkage map with 200 SSR loci across the 10 maize linkage groups, with an average interval of 6.5 cM between adjacent markers. QTLs for alkaline resistant traits of alkaline tolerance rating (ATR), germination rate (GR), relative conductivity (RC), weight per plant (WPP) and proline content (PC) were detected. The obtained results were as follows: Five QTLs on chromosomes 2, 5 and 6 (GR and WPP: chr. 2; PC and ATR: chr. 5; and RC: chr. 6) were mapped. For precise mapping of the QTLs related to alkaline resistance, two bulked deoxyribonucleic acid (DNA) pools were constructed using individual DNAs from the most tolerant 30 F2 individuals and the most sensitive 30 F2 individuals according to the ATR and used to establish a high density map of SLAF markers strongly associated with the ATR by specific locus amplified fragment sequencing (SLAF-Seq) combined with super bulked segregant analysis (superBSA). One marker-intensive region involved three SLAFs at 296,000–6,203,000 bp on chromosome 5 that were closely related to the ATR. Combined with preliminary QTL mapping with superBSA, two major QTLs on chromosome 5 associated with alkaline tolerance at the maize seedling stage were mapped to marker intervals of dCap-SLAF31521 and dCap-SLAF31535 and phi024 and dCap-SLAF31521, respectively. These QTL regions involved 9 and 75 annotated genes, respectively. These results will be helpful for improving maize alkaline tolerance at the seedling stage by marker-assisted selection programs and will be useful for fine mapping QTLs for maize breeding.  相似文献   

16.
Sugarcane mosaic virus (SCMV) is one of devastating pathogens in maize (Zea mays L.), and causes serious yield loss in susceptible cultivars. An effective solution to control the virus is utilizing resistant genes to improve the resistance of susceptible materials, whereas the basic work is to analyze the genetic basis of resistance. In this study, maize inbred lines Huangzao4 (resistant) and Mo17 (susceptible) were used to establish an F9 immortal recombinant inbred line (RIL) population containing 239 RILs. Based on this segregation population, a genetic map was constructed with 100 simple sequence repeat (SSR) markers selected from 370 markers, and it covers 1421.5 cM of genetic distance on ten chromosomes, with an average interval length of 14.2 cM. Analysis of the genetic map and resistance by mapping software indicated that a major quantitative trait locus (QTL) was between bin6.00 and bin6.01 on chromosome 6, linked with marker Bnlg1600 (0.1 cM of interval). This QTL could account for 50.0% of phenotypic variation, and could decrease 27.9% of disease index.  相似文献   

17.
大豆对SMV SC-7株系群的抗性遗传与基因定位   总被引:5,自引:0,他引:5  
科丰1号×南农1138-2的P1、P2、F1和180个重组自交家系接种SC-7株系群的鉴定表明,P1与F1全抗,P2全感,说明抗性为显性;重组自交家系抗、感按1∶1分离,说明抗性由一对基因控制。利用王永军等的遗传连锁图对SC-7株系群的抗性基因进行连锁分析,将抗病基因Rsc-7定位于N8-D1b+W连锁群上,并与已定位的5个抗性基因中的3个连锁,还有一个与之相连锁的标记LC5T,其排列顺序和遗传距离为Rsa (30.6 cM) Rsc-7 (22.1 cM) Rn3 (10.3 cM) Rn1 (15.8 cM) LC5T。  相似文献   

18.
Crown rot, caused by Fusarium pseudograminearum, is an important disease of wheat in Australia and elsewhere. In order to identify molecular markers associated with partial seedling resistance to this disease, bulked segregant analysis and quantitative trait loci (QTL) mapping approaches were undertaken using a population of 145 doubled haploid lines constructed from ‘2‐49’ (partially resistant) × ‘Janz’ (susceptible) parents. Phenotypic data indicated that the trait is quantitatively inherited. The largest QTLs were located on chromosomes 1D and 1A, and explained 21% and 9% of the phenotypic variance, respectively. Using the best markers associated with five QTLs identified by composite interval mapping, the combined effect of the QTLs explained 40.6% of the phenotypic variance. All resistance alleles were inherited from ‘2‐49’ with the exception of a QTL on 2B, which was inherited from ‘Janz’. A minor QTL on 4B was loosely linked (19.8 cM) to the Rht1 locus in repulsion. None of the QTLs identified in this study were located in the same region as resistance QTLs identified in other populations segregating for Fusarium head blight, caused by Fusarium graminearum.  相似文献   

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