苦荞重组自交系群体F_5代SSR遗传图谱的构建

以"小米荞×晋荞2号"杂交组合,通过单粒传获得的245个F_5代重组自交系(命名为SJ-RILs)群体为作图材料,构建SSR遗传连锁图谱。结果显示:350对SSR引物在亲本间有多态性的为59对,多态率为16.9%;多态性引物在SJ-RILs群体共扩增出80个等位变异位点;来自小米荞和晋荞2号等位基因分别占群体总基因型的51.5%和48.5%;采用作图Jionmap4.0软件构建的遗传连锁图总长度为1 106.74cm,含11个连锁群,80个分子标记,其中偏分离标记27个,相邻标记的平均间距为13.83cm。结论:该图谱可为苦荞遗传图谱构建、重要性状QTL的定位和基因组学研究隆奠定基础。     

优质早籼稻新品种佳辐占的选育及应用

经过20多年的研究,采用自创的优质早籼稻新品种选育新途径,选育出大粒(千粒重30 g)优质、高产、稳产、抗病虫、适应性广的早籼稻新品种佳辐占.其品质基本上达到了部颁一级优质食用米标准,千粒重、长宽比、垩白度都是当前国内优质早籼稻品种中最好的品种之一.产量水平400～450kg/667m2,高产的超过500kg/667 m2.广西、江西、广东等省、区已引种成功.2003～2004年在福建省推广11.4×104hm2,为农民增收2亿多元.该品种的育成,解决了水稻育种中长期存在的大粒不优质,早籼稻难优质,优质不高产,优质不抗病等难题.     

吉林省主推中晚熟期玉米品种DNA指纹库的构建

以吉林省中晚熟期的43个玉米品种为材料, 从玉米胚中提取基因组DNA并利用10对简单重复序列(SSR)引物进行扩增, 扩增产物经质量分数为8%的聚丙烯凝胶电泳检测, 获得了清晰稳定的图谱, 初步建立了吉林省中晚熟期玉米43个品种的DNA指纹库.     

春小麦重组自交系及多种SSR标记构建遗传图谱

 以春小麦重组自交系(RIL)宁春4 号×宁春27 号为作图群体,利用SSR 标记构建小麦遗传连锁图谱。结果表明,用1001对SSR 引物选出亲本间表现多态性的引物307 对,多态性频率为30.7%。利用307 对多态性引物对RIL 群体进行分析,共检测到266 个多态性标记位点。通过χ²检测(P<0.05),有147 个SSR 标记表现为偏分离,偏分离率为55.3%,129 个偏向母本宁春4号,其偏分离位点主要分布在B 和D 基因组上。用Mapmaker 3.0 和Mapdraw 2.1 软件将266 个SSR 位点绘制在小麦遗传连锁图上,该图谱覆盖小麦基因组全长2187.79 cM,标记间的平均遗传距离为8.22 cM。     

佳辐占和广陆矮4号水稻叶片蛋白质的双向电泳比较研究

应用双向电泳技术研究比较两种不同品质水稻(佳辐占和广陆矮4号)叶片的蛋白质组分的差异.两种水稻叶片提取的蛋白质的双向电泳图谱斑点清晰,形态规则.采用考马斯亮蓝染色获得约400个斑点,银染图谱约800个斑点.两种水稻的蛋白质图谱考马斯亮蓝染色图谱存在5个显著差异点,银染图谱存在11个显著差异点.     

水稻佳辐占成熟种胚培养及其悬浮细胞系的建立

以优质早籼稻佳辐占成熟种胚为材料．研究外植体大小、激素对成熟种胚愈伤组织诱导率的影响，并高频快速建立起水稻胚性悬浮系．结果表明：在外植体较大并只添加2，4-D-种激素时，就可获得较高的愈伤组织诱导率，2，4-D浓度为1．5mg／L时，诱导率达95％；浓度为2mg／L时．诱导率可达100％．佳辐占成熟种胚组织培养最佳的条件为适当大小的外植体和添加浓度为2mg／L2，4-D．以4周龄的胚性愈伤组织为材料可高频快速建立起均质、分散性好的水稻胚性悬浮系，5周龄以上的胚性愈伤组织较难建立起水稻胚性悬浮系．     

萼花臂尾轮虫(Brachionus calyciflorus)的ISSR引物筛选及其多态性检验

采用简单重复序列区间(ISSR:一种基于微卫星的分子标记,无需预知遗传背景即可研究基因组中微卫星序列的变异,适合大规模的种群遗传研究)的方法对萼花臂尾轮虫(Brachionus calyci florus)进行PCR扩增,优化出适宜的ISSR-PCR反应体系,并从100条引物中筛选出16条具有良好多态性和重复性的ISSR引物.研究结果显示,萼花臂尾轮虫简单重复序列以(AC)和(AG)的两碱基重复为主,筛选出的ISSR引物扩增共得到114个位点,66个多态位点,多态性高达57.89%,高于常用于该物种分子生态学研究的线粒体COI基因的多态性.     

水稻佳辐占成熟种胚培养及其悬浮细胞系的建立

以优质早籼稻佳辐占成熟种胚为材料,研究外植体大小、激素对成熟种胚愈伤组织诱导率的影响,并高频快速建立起水稻胚性悬浮系.结果表明在外植体较大并只添加2,4-D一种激素时,就可获得较高的愈伤组织诱导率,2,4-D浓度为1.5 mg/L时,诱导率达95%;浓度为2 mg/L时,诱导率可达100%.佳辐占成熟种胚组织培养最佳的条件为适当大小的外植体和添加浓度为2 mg/L 2,4-D.以4周龄的胚性愈伤组织为材料可高频快速建立起均质、分散性好的水稻胚性悬浮系,5周龄以上的胚性愈伤组织较难建立起水稻胚性悬浮系.     

长筒石蒜种质资源的ISSR研究

借助ISSR分子标记对长筒石蒜变异类型进行了研究,结果表明:ISSR扩增得到的67个位点中,其中62个位点具有遗传多态性,约占总数的92.5%.因此,长筒石蒜遗传多样性是十分丰富的,可以作为育种材料储备种质资源.从UPGMA聚类图来看,依据花色区分的3种类型,被聚在一起,表明亲缘关系较近.在未来的长筒石蒜种质资源利用中,不同花色的长筒石蒜可以作为品系进行开发.     

通用型奶牛多位点基因打靶载体系统的构建

以奶牛为研究对象,以其重复的rRNA基因间的间隔序列为靶位点,基于BAC重组酶系统构建多位点基因打靶载体,为建立体内多位点基因打靶技术获得关键材料.首先构建BAC-TDN筛选载体,然后构建pYLVS-GD表达载体.将BAC-TDN筛选载体和pYLVS-GD表达载体共转化至大肠杆菌NS3529中,通过Cre重组酶的作用形成BAC-TDN-VS-GD质粒,采用归位内切酶I-SceI切除pYLVS载体骨架,构建奶牛多位点基因打靶载体BAC-TDN-GD,利用接头LS使之环化.BAC-TDN-GD打靶载体与pYLSV质粒组成了通用型奶牛多位点打靶载体系统.以重复序列为靶位点的多位点基因打靶技术,将部分解决目前存在的打靶效率低、安全性差等问题.     

SSR标记对籼稻品种的遗传多样性分析

利用500多对SSR标记对广陆矮4号、珍汕97B、佳辐占、明恢86和明恢63 5个籼稻亲本品种进行遗传多样性分析.结果表明,佳辐占与明恢63、明恢86、珍汕97B和广陆矮4号之间的相似系数分别为78.1%、76.1%、72.8%和71.7%.相对而言,其相似系数越小,遗传距离越大,因此利用佳辐占与这些品种组配较有希望选育出品质优良、综合优势明显的新品系.同时研究表明,标记间平均距离为10 cM或小于10 cM时,分析所得结果较为可靠.     

Genetic analysis and gene fine mapping for a rice novel mutant （rl9〈t）） with rolling leaf character

Much attention has been paid to leaf shape of rice in the process of ideotype breeding[1]. Several authors have reported that the rolling of leaf in some degree helps keep it erect, consequently optimizing canopy light transmission condition, which is good for dry matter accumulation and for high yield[2―6]. Rice as a polymorphic crop has many types of vari- ety with different morphologies. In terms of leaf shape, different cultivars with rolling leaf have been identifiedin rice germplasm. Le…     

一个新的水稻矮秆突变体sd-sl的遗传与基因定位研究

新的矮秆基因的发掘、研究和利用对水稻育种和植物生长发育机制研究有重要的作用.用60Coγ射线辐照粳稻9522,获得一个能稳定遗传的突变体.该突变体表型为株高较野生型矮,叶片短而微卷.将该突变体与籼稻广陆矮杂交,F2代呈3∶1分离,说明该突变体受隐性单基因控制.通过InDel分子标记对F2代分离群体进行遗传定位,将该基因定位于第6染色体InDel标记OS604附近.随后又发展了多对有多态性的InDel分子标记,将该基因座位精细定位在InDel标记XL6-6和XL6-1之间,AP003490和AP005619上,两个引物之间的物理距离为118 kb.本研究为该克隆基因及其作用机理的探究奠定了基础.     

Identification of salt-tolerance QTL in rice (Oryza sativa L.)

Quantitative trait loci (QTLs) controlling salt-tolerance at the seedling stage in rice (Oryza sativa L.) were identified by interval mapping (SIM) and composite interval mapping (CIM) using a doubled haploid population ZJDH and its high resolution genetic linkage map. The population was derived from an inter-subspecific cross between an indica variety Zhaiyeqing8 (ZYQ8) and a japonica variety Jingxi17 (JX17). Analysis of survival days of seedlings treated with 0.7% NaCI revealed that a major salt-tolerance quantitative trait locus (QTL), Std, was present between markers RG612 and C131 on chromosome 1 when using both MAPMAKER/QTL 1.1 and PLABQTL 1.0 (SIM). Its allele which contributes to salt-tolerance was from ZYQ8. In addition, seven more QTLs which give additive effect on salt-tolerance are identified when using PLABQTL (CIM), and most of them were from JX17.     

Genetic dissection of a thousand-grain weight quantitative trait locus on rice chromosome 1

Thousand-grain weight （TGWT） is an important factor affecting grain yield as well as grain quality in rice. A quantitative trait locus （QTL） qTGWTI-1 for TGWT was detected previously near DNA marker RG532 on the short arm of chromosome 1 in a recombinant inbred line （RIL） population derived from the indlca-indica rice cross Zhengshan97B （ZS97B）/Milyang46 （MY46）. In this study, two residual heterozygous lines （RHLs）, Chl and Ch2, derived from the ZS97B/MY46 RIL F7 population, were used to develop two Fe populations, RIL-1 and RIL-2. The genome of Chl and Ch2 contains a heterozygous region flanked by RM1--RM3746 and RM151--RM243 on the short arm of chromosome 1, respectively, but is homozygous in other regions. Two tightly linked QTLs, Gwl-1 and Gwl-2, with the same additive direction and similar effect on TGWT, were detected in the region of QTL qTGWTI-1 in population RIL-2. No QTL was detected in the population RIL-1. Four individual RHLs from the population RIL-2 carrying heterozygous segments flanked by RM151--RM10404, RM10381--RM243, RM10435--RM259 and RM10398--RM5359, respectively, were chosen to develop four F= populations. Ten maternal homozygotes and 10 paternal homozygotes were selected from each of the four F2 populations derived from the four RHLs. The four sets of near isogenic lines （NILs） were grown for phenotyping of TGWT and delimitation of Gwl-1 and Gw1-2. Results showed that Gwl-1 and Gw1-2 were located in the intervals RM10376--RM 10398 and RM10404--RM 1344 which cover 392.9 and 308.5 kb regions, respectively. The enhancing alleles were from ZS97B at both loci, and no significant interactions were detected. Genetic dissection of Gwl-1 and Gwl-2 has laid a foundation for their cloning and molecular breeding of grain yield and quality in rice.     

Genetic diversity of rice cultivars （Oryza sativa L.） in China and the temporal trends in recent fifty years

Public concern is often expressed at cultivars because the domestication and modern plant breeding have led to a reduction in the genetic diversity of crops and loss of genes, which could result in crops' genetic vulnerability to changes in the spectrum of pestssity of varieties in this zone is very important to the whole rice production in China. REZV, a important japonica rice production areas with more than 278 thousands ha rice which was about 71% of rice area in north China, accounted fo…     

一个水稻抗纹枯病突变体的遗传分析及其基因的初步定位

高水平抗纹枯病突变体和高感纹枯病品种蜀恢881杂交构建分离群体,经F2分离世代的遗传分析,抗、感单株比例符合3 1(χc2=0.563,χ12,0.05=3.84),初步确定该突变体对纹枯病的抗性由一对显性主效基因所控制,命名为Rsb-2(t)。利用已合成的530对微卫星引物,对抗纹枯病突变体和蜀恢881进行多态性引物筛选,用多态性引物对上述F2分离群体的全部感病单株和部分抗病单株的DNA进行PCR分析,借助MAPERMAKER/EXP3.0软件,对其微卫星标记实验数据进行连锁分析,将Rsb-2(t)定位于第3染色体的p臂,发现RM218、RM251、RM4321和RM5748与Rsb-2(t)连锁,它们均位于着丝粒端,连锁距离分别为32.1 cM,41.1 cM,42.4 cM和49.7 cM。研究结果为进一步对该基因的精细定位奠定了基础。     

水稻表观遗传的研究进展

从DNA甲基化、组蛋白修饰的形成条件及其作用机制等方面,对表观遗传学的一些常见的发生机制进行了简要综述,并对表观遗传在水稻中研究的前景作了展望．     

高空气球搭载诱导水稻育性降低突变体RAPD分析

选用300对引物，对经高空气球30km搭载飞行8h后返地种植筛选获得的水稻育性降低突变体基因组进行DNA多态性分析，结果发现：育性降低突变体与原种之间存在多态性．     

Genetic structure and diversity of Oryza sativa L. in Guizhou, China

Preserving many kinds of rice resources and rich variations, Guizhou Province is one of the districts with the highest genetic diversity of cultivated rice （Oryza sativa L.） in China. In the current research, genetic diversity and structure of 537 accessions of cultivated rice from Guizhou were studied using 36 microsetellite markers and 39 phenotypic characters. The results showed that the model-based genetic structure was the same as genetic-distance-based one using SSRs but somewhat different from the documented classification （mainly based on phenotype） of two subspecies. The accessions being classified into indica by phenotype but japonica by genetic structure were much more than that being classified into japonica by phenotype but indica by genetic structure. Like Ding Ying＇s taxonomic system of cultivated rice, the subspecific differentiation was the most distinct differentiation within cultivated rice. But the differentiation within indica or japonica population was different： japonica presented clearer differentiation between soil-watery ecotypes than indica, and indica presented clearer differentiation between seasonal ecotypes than japonica. Cultivated rices in Guizhou revealed high genetic diversity at both DNA and phenotypic levels. Possessing the highest genetic diversity and all the necessary conditions as a center of genetic diversity, region Southwestern of Guizhou was suggested as the center of genetic diversity of O. sativa L. from Guizhou.