辣(甜)椒抗黄瓜花叶病毒(CMV)研究进展

黄瓜花叶病毒病(CMV)是为害辣(甜)椒的重要病毒,国内外对其研究较多。通过综述CMV的株系分化、抗性遗传、分子标记、抗CMV基因工程以及抗CMV育种等方面的研究结果和报道,旨在为辣(甜)椒抗CMV育种提供参考依据。     

Molecular assessment of polymorphism among local Jordanian genotypes of the common fig (Ficus carica L.)

This research was conducted to assess polymorphism among local genotypes of common fig available in Jordan (one of countries of origin). Leaf samples were collected in spring for DNA isolation from 20 different local genotypes (5 cultivars and 15 landraces). Two more wild types and one foreign cultivar were included. The genotypes were assessed using the randomly amplified polymorphic DNA (RAPD) technique. Six of the 19 screened primers showed reproducible polymeric profiles. Out of 62 amplified bands, 48 were polymorphic (77%). They generated 1104 data entries (591 for present and 513 for absent bands). After determining Jaccard similarity index, some genotypes showed high genetic similarity (90% between F20 and F22), while other were less similar (3–18% between F11 and all other genotypes). Moreover, the primers were evaluated for their discriminating power, where primer RAPD06 showed the weakest power (0.431), while highest values of 0.989 and 0.996 were achieved for primers RAPD02 and RAPD13, respectively.     

The effect of plant growth regulators on somaclonal variation in Cavendish banana (Musa AAA cv. ‘Zelig’)

The effect of the type and concentration of plant growth regulators and sub-culturing on somaclonal variation were studied in Cavendish banana cv. ‘Zelig’ obtained from African Biotechnologies Ltd., South Africa. In vitro grown plants at the fourth multiplication cycle were used for the investigation. Auxins (IAA, IBA and NAA) and cytokinins (BA and TDZ) were used to multiply shoots for 10 generations. Bands generated through RAPD-PCR were scored according to whether they were present (1) or absent (0) to determine the extent of somaclonal variation. Results were then analyzed using cluster analysis. The relationship between multiplication rate and somaclonal variation was assessed using correlation analysis. Results indicated that treatments with higher multiplication rates produced more variants; sometimes as high as 72%. Dwarf off-types accounted for 88% of the variation. A dwarf-specific band, about 1500 kb in size, was amplified by the primer OPC-15. The band appeared consistently in normal plants but was absent in all dwarf plants.     

Genetic diversity of bitter gourd (Momordica charantia L.) genotypes revealed by RAPD markers and agronomic traits

Bitter gourd or bitter melon (Momordica charantia L.) is considered as minor cucurbitaceous vegetable in spite of having considerable nutritional and medicinal properties. Although some reports on genetic diversity based on morphological characterization are available, no work has been conducted to estimate genetic diversity using molecular markers in this crop. In the present study, 38 genotypes of M. charantia including few commercially cultivars collected from different parts of India based on agro-ecological zones were analysed for diversity study both at morphological and molecular levels. Genomic DNA was extracted from young healthy leaves following the procedure of Doyle and Doyle [Doyle, J.J., Doyle, J.L., 1990. A rapid DNA isolation procedure from small quantity of fresh leaf material. Phytochem. Bull. 119, 11–15]. Pair-wise comparison of genotypes was calculated as per the procedure of Jaccard [Jaccard, P., 1908. Nouvelles recherches sur la distribution florale. Bull. Soc. Vaud. Sci. Nat. 44, 223–270]. Dendrogram was constructed using the unweighted pair group method with arithmetic averages (UPGMA) and the computation for multivariate analysis was done using the computer programme NTSYS-pc Version 2.0 [Rohlf, F.J., 1998. NTSYS-pc Numerical Taxonomy and Multivariate Analysis System, Version 2.01. Exeter Software, Setauket, NY, USA]. Diversity based on yield related traits and molecular analysis was not in consonance with ecological distribution. Among 116 random decamer primers screened 29 were polymorphic and informative enough to analyse these genotypes. A total of 208 markers generated of which 76 (36.50%) were polymorphic and the number of bands per primer was 7.17 out of them 2.62 were polymorphic. Pair-wise genetic distance (GD) based on molecular analysis ranged from 0.07 to 0.50 suggesting a wide genetic base for the genotypes. The clustering pattern based on yield related traits and molecular variation was different.     

Implantation study on the potential of murine epidermal stem cell differentiation

AIM: To investigate the potential of murine epidermal stem cell (ESC) differentiation after seeded in a biodegradable carrier and implanted subcutaneously into syngeneic recipient mice. METHODS: ES cells were induced in vitro to differentiate into ESCs. After stained with a fluorescent dye Hoechst 33342, these ESCs were seeded into a polyglycolic acid (PGA) net containing collagen gel, functioning as a cell carrier, and implanted subcutaneously into 129/J mice, which were syngeneic to these stem cells. RESULTS: The ESCs kept alive in the implant when observed under a fluorescent microscopy 3 weeks or longer after implantation, and could differentiate into hair follicle-like structure, glandular structure, and gave rise to additional structures displaying features resembling native dermis. No apparent rejection or severe side effects were observed at least 10 weeks post-implantation. CONCLUSION: It is feasible to use these ESCs as seed cells in the study to fabricate dermal equivalent having the potential to develop dermal appendages.     

与苹果果皮红色性状相关的RAPD分子标记的筛选

用355条10bp随机引物来筛选与苹果果实红色性状连锁的分子标记。通过分离群体分组分析,在果实红色与非红色2个对比基因池间进行了扩增筛选,初步选出49个多态性引物,进一步对这些多态性引物进行群体上的分析发现S519可以扩增出大约1000bp左右的一条与红色性状相关的DNA特异带。对本研究的73个来自3个不同杂交组合的F1后代个体分析表明,该标记判断果实红色性状的符合率为76.7%。鉴于获得的多态性标记对果皮颜色预测的准确率不高的现状,我们采用了双标记组合分析方案,即用S5191000分别与以往获得的3个与果色性状相关的标记(S12891200、S12351000和S21071200)配对组合进行判断,从而使得标记对目标性状预测的正确性大为提高。另外,对总共获得的4个RAPD标记在9个栽培品种上进行了分析,大多数品种的表现与理论一致。     

DNA标记技术在梨属植物研究中的应用

综述了几种常见的DNA标记如RFLP、RAPD、SSR、AFLP和SCAR在梨属植物研究中的应用以及所取得的进展。DNA标记技术主要在梨属植物的品种鉴别、亲子关系鉴定、分类和系统关系研究、遗传图谱构建与标记辅助育种等研究领域中得到了广泛的应用。还对各种标记的特点和在梨属植物研究中的应用范围做了总结,期望为今后研究中合理选择适宜的标记技术提供参考。     

燕山板栗种质资源遗传多样性的RAPD分析

为研究燕山板栗的遗传多样性,采用随机扩增多态DNA(randomamplifiedpolymorphicDNA,RAPD)技术对36份燕山板栗种质进行了分析。分析了燕山板栗的遗传丰富度,并对包括36个燕山板栗品种和8份外来板栗品种在内的44份板栗种质进行聚类分析。结果表明,RAPD能有效地区分品种间的差异,用16个随机引物经PCR扩增共得到132个片段,其中有83个多态性片段,占62.9%;不同遗传位点之间遗传多样度最大可达0.444,最小值为0.096,平均多样度为0.187;UPGMA法聚类,将44份板栗种质聚成4个大的类群,36份燕山板栗可分为3个大的类群,外来种质聚为一类。燕山板栗明显不同于外来品种。在RAPD图谱中,找到了19个品种(类型)的特异性标记和标记组合,可作为品种(类型)分子鉴别的依据。     

赞皇大枣的群体遗传多样性评价

为了探明三倍体赞皇大枣的遗传基础,利用22个多态性引物对赞皇县及周边县区的50个赞皇大枣类型、26个酸枣类型、8个枣品种等3个群体进行了RAPD扩增,共扩增285个位点。遗传多样性分析表明:赞皇大枣群体的多态性位点百分率为58％,小于枣品种群体(66％)和酸枣群体(89％);赞皇大枣群体共扩增出205种带型,而酸枣群体扩增出416种带型;赞皇大枣群体内平均遗传距离为0．087,小于枣品种群体(0．181)和酸枣群体(0．254)。说明:赞皇大枣的遗传多样性小于枣品种群体,酸枣群体有较丰富的遗传背景。     

甘蓝型油菜―萝卜附加系中萝卜染色体的(dp)RAPD标记

在已掌握甘蓝型油菜―萝卜附加系染色体构成,并构建萝卜分子连锁图谱的基础上,以甘蓝型油菜―萝卜附加系为材料,利用(dp)RAPD分子标记技术,筛选附加系中外源萝卜9条染色体(A～I)的分子标记,为进一步研究萝卜染色体与连锁群对应关系奠定基础.试验筛选了576个随机引物(组合),有413个能从附加系中扩增出萝卜染色体的(dp)RAPD标记,平均有效引物(组合)占71.7%,其中RAPD反应有效引物率67.7%,dpRAPD反应有效引物率73.2%.试验共得到899个萝卜染色体(dp)RAPD标记,包括354个RAPD标记和545个dpRAPD标记,覆盖萝卜整个基因组的全部9条染色体,不同染色体的标记数目变化范围在41～160,其中最多的是染色体C,最少的是染色体I.