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分子遗传标记技术及其在昆虫科学中的应用 总被引:16,自引:3,他引:16
分子遗传标记是随着聚合酶链式反应 (PCR)和Southern杂交等分子生物学技术的飞速发展而出现的遗传学标记技术 ,它突破了以往形态标记 ,细胞学标记和同工酶标记等表达型标记的局限性 ,在揭示物种的遗传变异性研究中发挥着独特的优势。分子遗传标记目前已出现了几十种 ,可依其涉及的位点和反映的多态性的基础分为多位点分子标记和单位点分子标记 ,多位点分子标记反映核苷酸序列的多态性 ,单位点分子标记反映基因座上等位基因的多态性。本文对一些常用的分子标记技术的特点和它们在昆虫系统进化、昆虫分类、昆虫生态、生物防治和特定基因标记等研究中的应用作了介绍。 相似文献
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本文参考了国内外近年来最新研究进展,对分子标记概念和类型作了简要介绍;论述了分子标记技术在植物改良中的主要用途:遗传图谱的构建,基因定位,物种间基因组比较,分子标记辅助育种;较详细地介绍了芸苔属植物在分子标记方面的研究进展。 相似文献
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目的:采用6份卡瓦胡椒材料、21份栽培胡椒和野生胡椒材料、1份不同属的草胡椒材料共计28份试验材料,开发1对特异SCAR引物。方法:在对它们进行了RAPD研究的基础上,通过克隆、测序和引物设计进行了SCAR分子标记研究。结果:本研究开发了1对特异SCAR引物P10.1和P10.2,用这对特异引物对本次试验的28份材料进行PCR扩增,结果显示,6份卡瓦胡椒材料扩增出了三条带,三条带离的较近,中间一条为预期494bp特异片段。其它胡椒属材料均扩增出一条494bp的特异带,而不同属的草胡椒无任何扩增。结论:这说明引物P10.1和P10.2适用于卡瓦胡椒的分子鉴定(三条带),也可用于胡椒属植物的分子鉴定(一条带),这对卡瓦胡椒种质资源的真伪鉴定及胡椒属植物的分子分类有一定帮助。 相似文献
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Molecular markers derived from polymerase chain reaction (PCR) amplification of genomic DNA are an important part of the toolkit of evolutionary geneticists. Random amplified polymorphic DNA markers (RAPDs), amplified fragment length polymorphisms (AFLPs) and intersimple sequence repeat (ISSR) polymorphisms allow analysis of species for which previous DNA sequence information is lacking, but dominance makes it impossible to apply standard techniques to calculate F-statistics. We describe a Bayesian method that allows direct estimates of FST from dominant markers. In contrast to existing alternatives, we do not assume previous knowledge of the degree of within-population inbreeding. In particular, we do not assume that genotypes within populations are in Hardy-Weinberg proportions. Our estimate of FST incorporates uncertainty about the magnitude of within-population inbreeding. Simulations show that samples from even a relatively small number of loci and populations produce reliable estimates of FST. Moreover, some information about the degree of within-population inbreeding (FIS) is available from data sets with a large number of loci and populations. We illustrate the method with a reanalysis of RAPD data from 14 populations of a North American orchid, Platanthera leucophaea. 相似文献
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非损伤性取样在朱?种群遗传研究中的应用 总被引:9,自引:3,他引:9
采用非损伤性取样方法提取DNA,利用20条10bp的随机引物对陕西朱?保护观察站的16只朱?个体间遗传距离进行分析研究。获得的DNA可进行RAPD研究分析,18条引物扩增结果稳定,遗传距离指数介于30.52%~10.18%之间;揭示16只朱?间亲缘关系较近。尝试在朱?种群遗传学研究中应用非损伤性方法抽提基因组DNA,以方便对朱?等小种群珍稀濒危生物进行相关研究。
Abstract:Genetic distance of sixteen crested ibises (Nipponia nippon) was analyzed at the DNA level by polymerase chain reaction (PCR) using random primers after DNA was sampled with non-invasive sampling. The amount of DNA was enough to apply t o genetic analysis by RAPD. Eighteen primers had stable effect. The genetic dist ances are between 30.52% and 10.18%,which showed that the relationship between 16 crested ibises was similar. This study tried to apply a non-invasive method to obtain DNA, which is helpful to research on the genetic background of creste d ibises and other tiny population based on DNA level. 相似文献
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A total of 90 isolates of Mycosphaerella graminicola, the cause of septoria tritici leaf blotch of wheat, were tested for DNA polymorphism using 15 decamer random primers. There was a high level of genetic variability among isolates. In 131 random amplified polymorphic DNA (RAPD) fragments, which were produced, 96% were polymorphic. Based on multilocus analysis, 40 different molecular phenotypes were detected. These molecular phenotypes were randomly distributed among sampling sites, suggesting that no clonal structure existed in the population. Cluster analysis showed that the maximum similarity value among isolates was approximately 81% and no identical isolates were detected, indicating that every isolate was a unique genotype. The high degree of DNA polymorphism, the large number of different molecular phenotypes, their random distribution and the results of the cluster analysis all suggested that sexual reproduction has a major role in the genetic structure of M. graminicola in western Canada. The presence of sexual reproduction provides the opportunity for development of new virulent genotypes in the population and suggests that the pathogen may adapt rapidly to any race‐specific sources of resistance. Therefore, when breeding for resistance to M. graminicola, emphasis should be placed on use of non‐race‐specific resistance. 相似文献
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Long Zhang He-Chun Ye Guo-Feng Li 《植物学报(英文版)》2006,48(9):1054-1062
The effects of development states on the artemisinin content of clone S1 of Artemisia anuua L. grown in a greenhouse were investigated in the present study. The artemisinin content increased gradually during the phase of vegetative growth and reached its highest level at 8-9 mg/g dry weight (DW) when the S1 was 6 months old on a long day (LD) photoperiod. Treatment with 9-18 d of short day (SD) photoperiod resulted in the artemisinin content reaching and being maintained at a higher level (2.059-2.289 mg/g DW), twofold that of control plants and plants of S1 presented at the pro-flower budding and flower-budding stages. The artemisinin content varied in different parts of the plant. The artemisinin content of leaves was higher than that of florets and branches. The artemisinin content in middle leaves was higher than that of bottom leaves, and then top leaves. Different densities of capitate glands (the storage organ of artemisinin) located on the surface of leaves, florets, and branches explained the variations in artemisinin content in these parts of the plant. The correlation coefficient between artemisinin content and density of capitate glands on the surface of different organs was 0.987. The genetic marker for artemisinin content was screened using random amplified polymorphic DNA (RAPD) and sequence characterized amplified region (SCAR) techniques. The random primer OPAl5 (5'-TTCCGAACCC-3') could amplify a specific band of approximately 1 000 bp that was present in all high-artemisinin yielding strains, but absent in all low-yielding strains in three independent replications. This specific band was cloned and its sequence was analyzed. This RAPD marker was converted into a SCAR marker to obtain a more stable marker. 相似文献
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Xia in 1986 combined Gracilaria salicornia, G. canaliculata (G. crassa), G. cacalia and G. minor into one species: G.salicornia. Two morphological variants of G. salicornia were collectedfrom different localities in Malaysia. Variant A collected from Morib,Selangor grew on the roots of Avicennia. The samples showed absenceof main axis; segmented constrictions throughout; cylindrical or slightlycompressed thalli. Variant B was collected from the mudflats of TanjungTuan, growing on rocks, coral or forming mats on the mud. Plants showedabsence of main axis; segments were not constricted throughout the plant(if present only slightly articulated at the upper part), branching wasdichotomous or irregular; cylindrical or slightly compressed thalli. Thetechnique of Random Amplified Polymorphic DNA analysis (RAPD) wasused to investigate molecular characteristics of the two variants. Out ofsixty Operon primers that were screened, four primers, OPA 1, OPA 10,OPA 11 and OPK 7 were able to give polymorphism. The fingerprintsgenerated were stable and reproducible on repeated analysis. The DNAfingerprints generated were visually analysed and clustering analysis wascarried out using GelCompar 4.0. The matrix of similarities was based onthe Dice coefficients (SD) and the cluster analysis was carried outusing the unweighted pair group method using arithmetic averages(UPGMA). DNA analysis showed that two primers (OPA 01, CAGGCCCTTC and OPK 07, AGCGAGCAAG) were able to differentiate the two variants. 相似文献
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A total of 10 non-repetitive multi-drug-resist-ant Acinetobacter strains were collected. With reference to A. calcoaceticus (ATCC23055), A. baumannii (ATCC19606), A. lwoffii (ATCC17986), and A. junii (NCTC5866), DNA fingerprint technique, amplified ribo-somal DNA restriction analysis (ARDRA), and random amplified polymorphism DNA (RAPD) were carried out to identify the genomic species of Acinetobacter spp. The distances between them were calculated by the unweighted pair group method with arithmetic (UPGMA). Genotypes ofAcinetobacter spp. were effectively classified and an A. junii together with nine A. baumannii isolates was genomically identified. The combination of ARDRA and RAPD DNA-fingerprint technique shows high com-plementarity, and could be a useful tool in Acinetobacter genomic species identification. 相似文献