向日葵品种抗向日葵螟鉴定及抗性评价方法

利用田间自然抗虫鉴定法连续3年在内蒙古巴彦淖尔市对56个向日葵品种进行了抗向日葵螟鉴定,结果表明,17个油葵品种中除P50表现为中抗（籽粒被害率为6.7%）,其余品种全部表现为高抗,籽粒被害率均在0～2.5%;而39个食葵品种中仅新食葵7号表现为高抗（籽粒被害率为1.9%）,其余多表现为感虫或高感,籽粒被害率在5.8%～54.1%。进一步利用黑色素鉴定法对所有品种进行了室内检测,其结果与田间抗虫鉴定结果基本吻合。由此认为：在进行田间自然抗虫鉴定时,宜根据田间向日葵螟成虫种群动态选择适宜的播期,使向日葵的开花期与向日葵螟成虫发生盛期尽量吻合,以提高害虫对向日葵的选择压力和鉴定结果的科学性,同时避免出现播期避害现象,干扰鉴定结果的准确性。     

四川小麦品种高、低分子量麦谷蛋白基因和1B/1R易位的分子标记鉴定

为给四川小麦品质育种提供参考信息,利用7个HMW-GS、17个LMW-GS和1个1B/1R易位的特异分子标记,对105份2000年后育成的四川小麦品种进行上述基因检测。结果表明:(1)针对HMWGS,在Glu-A1位点,含Ax2*的品种有2份,频率为1.9%;在Glu-B1位点,含Bx7、Bx20、Bx17、By8和By9的品种分别有73、26、4、45和30份,频率分别为69.5%、24.8%、3.8%、42.9%和28.6%,未检测到含Bx7OE的品种;在Glu-D1位点,含Dx5的品种有65份,频率为61.9%。(2)针对LMW-GS,在Glu-A3位点,含Glu-A3a、Glu-A3b、Glu-A3c、Glu-A3d和Glu-A3f的品种分别有2、2、63、29和9份,频率分别为1.9%、1.9%、60.0%、27.6%和8.6%,未检测到含Glu-A3e和Glu-A3g的品种;在Glu-B3位点,含Glu-B3b、Glu-B3d、Glu-B3f、GluB3g和Glu-B3i的品种分别有18、10、1、75和1份,频率分别为17.1%、9.5%、1.0%、71.4%和1.0%,未检测到含Glu-B3a、Glu-B3c、Glu-B3e和Glu-B3h的品种。(3)含1B/1R易位的品种有36份,频率为34.3%。(4)组合6种和5种以上优质基因的品种分别有2份(频率为3.8%)和15份(频率为14.3%)。可利用这些品种作为亲本,在四川小麦品质育种中逐步导入优质基因Ax2*、Bx7、By8、Dx5、Glu-A3d、Glu-B3d、Glu-A3b和Glu-B3b,并淘汰1B/1R易位,优化四川小麦面筋优质基因组成。     

马铃薯品种(系)晚疫病抗性鉴定

为提高马铃薯晚疫病抗病育种水平,筛选出适宜于天水地区种植的马铃薯品种和抗晚疫病较强的亲本资源,特此对引自全国的38份马铃薯品种(系)进行晚疫病抗性的田间鉴定。试验采用随机区组设计,对参试材料的植株、块茎晚疫病和产量进行评价与分析。结果表明:植株发病最轻的是‘L0527-4’、‘L9901-10’、‘L0527-7’、‘农天2号’、‘天薯12号’、‘同薯20号’、‘陇薯7号’等;块茎晚疫病未发病的为‘同薯20号’、‘陇薯7号’、‘天薯12号’等17份材料;‘陇薯7号’、‘天薯12号’较对照‘陇薯6号’增产,折合产量依次为26 300 kg/hm2、23 800 kg/hm2;最终筛选出‘陇薯7号’和‘天薯12号’两份晚疫病田间抗性和丰产性较好的材料,可用作马铃薯晚疫病抗病育种的资源,并在天水地区推广种植。     

Introgression of Gene for Non-Pollen Type Thermo-Sensitive Genic Male Sterility to Thai Rice Cultivars

For the two-line hybrid rice system, pol en sterility is regulated by recessive gene that responds to temperature. The recessive gene controlling thermo-sensitive genetic male sterility （TGMS） is expressed when the plants are grown in conditions with higher or lower critical temperatures. To transfer tgms gene（s） control ing TGMS to Thai rice cultivars by backcross breeding method, a male sterile line was used as a donor parent while Thai rice cultivars ChaiNat 1, PathumThani 1, and SuphanBuri 1 were used as recurrent parents. The BC2F2 lines were developed from backcrossing and selfing. Moreover, the simple sequence repeat （SSR） markers were developed for identifying tgms gene and the linked marker was used for assisting selection in backcrossing. The identification lines were confirmed by pol en observation. The results showed the success of introgression of the tgms gene into Thai rice cultivars. These lines will be tested for combining ability and used as female parent in hybrid rice production in Thailand.     

2种受阻酚类防老剂对天然橡胶热氧老化防护效果多尺度分子模拟及实验研究

引入多尺度分子模拟技术对比研究了2种受阻酚类防老剂2,2°-亚甲基双(4-甲基-6-叔丁基苯酚)（防老剂2246）与防老剂2,2°-亚甲基双(4-乙基-6-叔丁基苯酚)（防老剂425）对天然橡胶（natural rubber, NR）的热氧老化防护效果。量子力学模拟（QM）结果表明,2种防老剂的O-H键解离反应自由能（ΔG）均低于NR的C-H键ΔG,且防老剂425在其解离位置h处的O-H键ΔG最低,为250.08 kcal/mol,搜索2种防老剂或NR与过氧自由基CH₃OO·的反应过渡态,发现防老剂425的过渡态能垒（E_barrier）最低,为5.31 kcal/mol,证明其能更快速地捕获过氧自由基,有效延缓NR分子链的氧化反应,表明了其防老剂化学反应防护机制。分子动力学（MD）模拟结果表明,防老剂425与NR之间的溶解度参数（δ）更接近,扩散系数（D）更低,即防老剂425与NR分子链更易相容,迁移性更低。蒙特卡洛（MC）模拟结果表明,氧气在3种体系中的渗透系数（P）大小顺序为P_NR>P_NR/2246>P_NR/425,即防老剂425更容易阻隔氧气渗透,表明了其防老剂物理防护机制。为验证分子模拟结论的准确性,对不同NR复合体系进行0~7 d的热氧老化实验,采用拉力试验机、邵尔A硬度计、傅里叶红外变换光谱仪研究2种防老剂对NR的热氧老化防护效果,发现NR/425体系的力学性能保持率最好,红外图谱结果显示,防老剂425/NR复合体系的氧碳摩尔比增长率最低,表明防老剂425对NR的防护效果更好,与分子模拟结论一致,证明多尺度分子模拟有助于防老剂的选取。     

茶树CsbHLH024和CsbHLH133转录因子功能鉴定

茶树叶片毛状体含有多种次生代谢产物,在茶叶外观质量以及茶树响应生物和非生物胁迫方面起着重要作用。通过双荧光分子互补（BiFC）试验、GUS活性染色试验以及过表达试验对茶树叶片毛状体相关候选基因CsbHLH024和CsbHLH133的功能进行鉴定。结果表明,CsbHLH024/CsbHLH133和CsTTG1蛋白在植物中能够相互作用,并且它们的启动子能够在叶片组织中驱动下游基因的表达。进一步将它们分别过表达到野生型拟南芥Col和对应的拟南芥纯合突变体中,发现它们能够影响拟南芥叶片毛状体的形成,恢复突变体的表型,并引起毛状体相关基因表达水平的变化。本研究为进一步揭示茶树叶片毛状体形成的分子调控机制提供理论依据。     

茶树叶绿体基因组SNP分子标记的初步研究

传统的叶绿体基因分子标记在茶组植物分类系统研究中的应用价值相对有限,为了筛选可用于茶树鉴别与母系溯源的SNP（单核苷酸多态性）位点组合,将18个已报道的茶组植物叶绿体全基因组序列进行比对,通过设计通用引物,在169个茶树品种/品系中进行候选分子标记扩增与一代测序分析,筛选出16对引物,共含25个SNP位点可用于茶树品种母系溯源与鉴别分析。另外,将SNP位点组成的DNA指纹图谱结合茶树品种资源基本信息进行数字编码,最终形成由30位数字组成的茶树品种资源分子身份证,并构建相应的条形码和二维码用于品种识别。本研究数据为茶树品种的母本溯源与鉴别提供新的思路。     

禽呼肠孤病毒分子生物学研究进展

本文就十几年来有关呼肠孤病毒的特性、基因组、基因重组、病毒蛋白、诊断方法等分子生物学的研究进行了综述,并指出了禽呼肠孤病毒分子生物学研究中存在的问题,及进一步研究的方向。     

Genetic mapping of the barley Rrs14 scald resistance gene with RFLP, isozyme and seed storage protein markers

The scald susceptible barley cultivar ‘Clipper’ and a third‐backcross (BC₃) line homozygous for the Rrs14 scald resistance gene that originally came from Hordeum vulgare ssp. spontaneum were grown in replicated field trials. The level of resistance that Rrs14 confers against field populations of the pathogen Rhynchosporium secalis, the causal agent of scald disease, was evaluated. The Rrs14 BC₃ line exhibited 80% and 88% less leaf damage than ‘Clipper’ in 1995 and 1996, respectively. Given this effectiveness of Rrs14, research was undertaken to identify a linked marker locus suitable for indirect selection of Rrs14. Based on linkage to a set of previously mapped loci, Rrs14 was positioned to barley chromosome 1H between the seed storage protein (hordein) loci Hor1 and Hor2, approximately 1.8 cM from the latter locus. The Hor2 locus is thus an ideal codominant molecular marker for Rrs14. The tight linkage between Rrs14 and Hor2 and the availability of alternative biochemical and molecular techniques for scoring Hor2 genotypes, permits simple indirect selection of Rrs14 in barley scald resistance breeding programmes.     

Identification of commercial chicory cultivars for hydroponic forcing and their phenetic relationships revealed by random amplified polymorphic DNAs and amplified fragment length polymorphisms

One‐hundred and twenty‐four amplified fragment length polymorphism (AFLP) and 49 random amplified polymorphic DNA (RAPD) markers have been used to distinguish between 20 and 23 commercial chicory cultivars, respectively. These were all Cichorium intybus var. foliosum F₁ hybrids, currently used in hydroponic forcing. Five‐hundred and twenty RAPD primers (OPERON) were tested, of which 156 resulted in reproducible patterns and 26 yielded polymorphisms. Two‐hundred and fifty‐six AFLP primer‐combinations were tested and six combinations were selected for identification purposes. Similarity indices were measured and clustering has been done using pairwise comparison. Both types of marker provide similar conclusions. Two major clusters are formed, representing late and early cultivars. All cultivars were identified using 10 informative RAPD primers or three AFLP primer combinations. A low degree of polymorphism was detected between some early cultivars, suggesting a narrow genetic base in their breeding strategy.