81 resultados para Randomly amplified polymorphic DNA


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Mass mortalities of cultured zhikong scallops (Chlamys farreri) have occurred each summer in most culture areas of northern China since 1996. Among the hypothesized causes are high culture density, infectious disease and genetic inbreeding. To investigate these potential agents, C. farreri were deployed at three densities (low, medium and high) at three sites (Jiaonan, Penglai and Yantai) in the summer of 2000. Scallops were sampled for survival, growth and histopathology before, during and after a mortality episode. Most of the mortality occurred in July and August, during and toward the later part of the spawning season, when water temperature reached 23-26 degrees C. Final cumulative mortalities reached 85% to 90% at all three sites. Scallops in the medium and high densities had higher initial death rates than did those at the low density. High densities also inhibited growth. Ciliates from the genus Trichodina, larvae of various organisms and anomalous secretions were observed in sections of the gill cavity, with highest prevalence during and at the end of the mortality period. Prokaryotic inclusion bodies were found in the soft tissues, but their prevalence was low and apparently without correlation with mortalities. Genetic analysis with random amplified polymorphic DNA markers showed slightly lower heterozygosity in the cultured stocks (0.301) than in the wild stocks (0.331). It is possible that the mortalities are caused by a combination of several factors such as stress associated with reproduction, high temperature, overcrowding and poor circulation in the growout cages, opportunistic invaders or pathogens, and possibly inbreeding. (c) 2005 Elsevier B.V. All rights reserved.

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Alien chromosomes of twelve giant spike wheat germplasm lines were identified by C-banding, genomic in situ hybridization (GISH), sequence characterized amplified region (SCAR), and random amplified polymorphic DNA (RAPD). All lines showed a chromosome number of 2n = 42, five of them carried both a pair of wheat-rye (Triticum aestivum-Secale cereal) 1BL/1RS translocation chromosomes and a pair of Agropyron intermedium (Ai) chromosomes, three carried a pair of Ai chromosomes only, three others carried a pair of 1BL/1RS chromosomes only, and one carried neither 1BL/1BS nor Ai chromosome. Further identification revealed that the identical Ai chromosome in these germplasm lines substituted the chromosome 2D of common wheat (Triticum aestivum L.), designated as 2Ai. The genetic implication and further utilization of 2Ai in wheat improvement were also discussed.

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We used random amplified polymorphic DNA markers (RAPDs) to assess genetic variation between- and within-populations of Anisodus tanguticus (Solanaceae), an endangered perennial endemic to the Qinghai-Tibetan Plateau with important medicinal value. We recorded a total of 92 amplified bands, using 12 RAPD primers, 76 of which (P = 82.61%) were polymorphic, and calculated values of H-t and H-sp of 0.3015 and 0.4459, respectively, suggesting a remarkably high rate of genetic variation at the species level. The average within-population diversity also appeared to be high, with P, H-e and H-pop values of 55.11%, 0.1948 and 0.2918, respectively. Analyses of molecular variance (AMOVA) showed that among- and between-population genetic variation accounted for 67.02% and 32.98% of the total genetic variation, respectively. In addition, Nei's coefficient of differentiation (G(ST)) was found to be high (0.35), confirming the relatively high level of genetic differentiation among the populations. These differentiation coefficients are higher than mean corresponding coefficients for outbreeding species, but lower than reported coefficients for some rare species from this region. The genetic structure of A. tanguticus has probably been shaped by its breeding attributes, biogeographic history and human impact due to collection for medicinal purposes. The observed genetic variations suggest that as many populations as possible should be considered in any planned in situ or ex situ conservation programs for this species.

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Random amplified polymorphic DNA ( RAPD) markers were used to measure genetic diversity of Coelonema draboides ( Brassicaceae), a genus endemic to the Qilian Mountains of the Qinghai-Tibet Plateau. We sampled 90 individuals in 30 populations of Coelonema draboides from Datong and Huzhu counties of Qinghai Province in P. R. China. A total of 186 amplified bands were scored from the 14 RAPD primers, with a mean of 13.3 amplified bands per primer, and 87% ( 161 bands) polymorphic bands (PPB) was found. Analysis of molecular variance (AMOVA) shows that a large proportion of genetic variation (84.2%) resides among individuals within populations, while only 15.8% resides among populations. The species shows higher genetic diversity between individuals than other endemic and endangered plants. The RAPDs provide a useful tool for assessing genetic diversity of rare, endemic species and for resolving relationships among populations. The results show that the genetic diversity of this species is high, possibly allowing it to adapt more easily to environmental variations. The main factor responsible for the high level of differentiation within populations and the low level of diversity among populations is probably the outcrossing and long-lived nature of this species. Some long-distance dispersal, even among far separated populations, is also a crucial determinant for the pattern of genetic variation in the species. This distributive pattern of genetic variation of C. draboides populations provides important baseline data for conservation and collection strategies for the species. It is suggested that only populations in different habitats should be studied and protected, not all populations, so as to retain as much genetic diversity as possible.

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Random amplified polymorphism DNA (RAPD) analysis was applied to germplasm characterization in 33 different selected Laminaria male and female gametophytes. The positional homology of the RAPD analysis using sequence characterized applied region (SCAR) method was successfully conducted. A total of 233 polymorphic loci were obtained from 18 selected primers after screening, of which 27 stable and clear bands were selected to construct a fingerprint map for discrimination of each gametophyte. Seven RAPD markers from five primers were finally determined by a computer program to construct the fingerprint map. Three specific markers closely related with gametophytes were obtained and were converted to gametophytic SCAR markers, the first SCAR marker report on Laminaria germplasm and applicable to cultivars identification. These results demonstrated the feasibility of applying RAPD markers to germplasm characterization in selected Laminaria gametophytes, and can provide a molecular basis for breeding new Laminaria strains. (C) 2004 Elsevier B.V. All rights reserved.

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大丽花经兰州重离子加速器提供的80MeV/u12C6+离子束辐照后产生矮化突变体,用随机扩增多态性(Random Amplified Polymorphic,RAPD)DNA技术对野生型和突变体进行检测分析。结果表明,在所用的25条引物中,1.80×108/cm2剂量辐照后有18条引物扩增出现多态性片断,扩增条带多态率19.57%;1.08×108/cm2剂量辐照后仅有6条引物扩增出现多态性片断,扩增条带多态率5.76%。用Jaccard公式对扩增产物进行统计分析,结果表明,两种剂量C6+辐照后与对照相似性系数分别为0.65和0.92。高剂量辐射后DNA易发生突变,在品种改良和诱变育种中相对较高剂量的选择可能更为有效。

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本研究运用RAPD和ISSR两种分子标记技术,对采自山东半岛4个不同地理位置的鼠尾藻(Sargassum thunbergii)和海黍子(S. muticum)种群进行了遗传多样性和遗传结构的研究,从而对其种群间的地理隔离、基因流动水平及其影响因素做出估计和判断,为马尾藻自然资源的保护和开发提供依据。在室内对鼠尾藻有性生殖幼苗的早期发育和生长进行了研究,了解其繁殖生物学特性,为鼠尾藻人工种苗的培育提供依据。主要研究结果如下: 对4个鼠尾藻(S. thunbergii)地理种群的遗传多样性研究中,筛选出了28条RAPD 引物和19条ISSR引物,分别扩增产生了174和125个位点。选用的三种不同指标,即多态位点比率(P%,percentage of polymorphic loci),平均预期杂合度(H,the expected heterozygosity)和 Shannon's 信息多样性指数(I,Shannon's information index),均可反映出鼠尾藻种群内部的遗传多样性呈较低水平。而群体间遗传距离(D,Nei’s unbiased genetic distance)矩阵和固定化指数(FST,the fixation index)矩阵均反映出群体间高度的遗传分化。通过分子变异分析(AMOVA,Analysis of molecular variance)来区分来自种群内部和种群之间的遗传变异,揭示出多数的遗传变异(57.57% 或59.52%)来自于鼠尾藻种群之间。另外,Mantel分析表明,4个鼠尾藻种群间的遗传分化与地理距离呈正相关(r>0.5),遵循传统的IBD(isolation by distance)模式,UPGMA(unweighted pair group method with arithmetic averages)聚类分析也反映出相似的结果。 对4个海黍子(S. muticum)地理种群遗传结构的研究中,筛选出的24条RAPD 引物和19条ISSR引物分别扩增出164和122个位点。遗传多样性评估结果表明,海黍子种群内部存在较低或者中等水平的遗传多样性,而D矩阵和FST 矩阵均显示种群间存在高水平的遗传分化。并且,发现D和FST 矩阵在RAPD和ISSR分析中均具有高且显著的相关性。AMOVA分析显示,种群之间的遗传变异高于种群内部。Mantel分析和UPGMA聚类分析均发现海黍子种群间的遗传分化遵循IBD模式,即与地理隔离呈正相关(r>0.6)。 并且,RAPD和ISSR分析的结果高度一致(r>0.9,P<0.05),均揭示4个海黍子种群之间存在高度的遗传分化。 对鼠尾藻有性生殖幼苗早期生长发育的研究结果表明,其早期发育过程属于马尾藻科(Sargassaceae)中典型的“8核1卵”型。在一定条件下培养两个月后,产生了1~2个小叶,幼苗的长度达2~3毫米。生长实验发现,温度(10, 15, 20, 25℃)和光照强度(9, 18, 44, 88 µEm-2s-1)对培养第一周幼苗的生长均有显著的影响(ANOVA, P<0.01)。在两个月的培养中,幼苗对温度和光强的耐受范围较宽,在10℃~25℃,9~88 µEm-2s-1条件下均可生长,最适温度和光强为25℃,44 µEm-2s-1;低温(10℃)对幼苗的生长有显著抑制。不同光质对幼苗生长的影响显著(P<0.01),相同光强条件下,蓝光和白光相比较,蓝光显然不能满足鼠尾藻幼苗早期生长的需要。

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葡萄属(Vitis.L.)植物隶属于葡萄科(Vitaceae),主要分布于北温带,最南可以分布到南美洲的委内瑞拉和亚洲的越南以及印度北部。本文通过对该属分类研究历史的回顾,认为该属存在的问题主要表现在如下几个方面: 1)葡萄属自1753 年由Carl Linne创立以来,虽经planchon于1887年做了修订,但属的范围仍需进一步界定;2)在Planchon之后的100多年中未见有一全面的分类学修订工作,出现在该属的800多个名称需要考证;3)对一些广布种的变异认识不足,导致了大量可疑种。针对这些问题本文进行了如下几个方面的工作: l、形态学:通过大量的野外工作和标本观察,对该属植物的主要性状做了分析,讨论了这些性状状态在葡萄属中的变异规律及演化趋势,将灌木状习性、退化的卷须以及不裂的叶片视为进化的性状。 2、细胞学:利用前人对葡萄属(Vitis.L.)染色体数目的统计及一些杂交实验分析的结果,结合形态学等方面的特征分析,认为在葡萄科,染色体基数X=10为原始的,而x=19则为衍生的。葡萄属的染色体基数xl9(2n=38),多倍体较少见;麝香葡萄属[Muscadinia (Planch.) Sma11]的染色体基数为x=10 (2n=20).与蛇葡萄属、酸蔹藤属和爬山虎属的一致。葡萄属和麝香葡萄属间的杂种是不育的。 3、孢粉学:对葡萄属32种5变种及麝香葡萄属[Muscadinia (Planch.) Sma11]1种的花粉外壁做扫描电镜观察,结果发现花粉外壁雕纹在这两属间和葡萄属内变异较小,对区分属以及属下种上类群意义不大,但对种的鉴别有重要的价值。 4、植物化学:前人对植物化学的工作表明,植物的一些次生代谢产物如类黄酮化合物在葡萄科各类群中的分布规律较好地反映了各类群间的关系。这些结果较好地支持了Planchon对葡萄属范围的界定。 5、山葡萄复合体(V.amurensis complex)包括山葡萄(V.amurensis Rupr.)、燕山葡萄(V.amuresis Rupr. var. dissecta Skvorts.=var.yanshanensisD.Z.Lu et H.P.Liang)、百花山葡萄(V.baihuashanensis M.S.Kang et D.Z.Lu)、复叶葡萄(V.piasezkii Maxim.)、少毛复叶葡萄[V. piasezkii Maxux1.var. pagnuccii (Planch.) Rehd.]共3个种和2个变种,广泛分布于中国北方,形态变异较大。本文对该复合体做了形态分析,并用RAPD (Random Amplified Polymorphic DNAs)分子标记方法分析了这几个类群的关系。综合这些结果,归并了燕山葡萄和百花山葡萄。 在上述工作的基础上,我们得出了如下的结论: l、葡萄属在葡萄科中是一个进化的类群。整理后的葡萄属包括8系62种、l亚种和15变种,其中有2个新系、1个新组合系、2个新变种、1个新组合种和l3个新异名。 2、本文赞同SmaU在1903年作出的分类学处理,把麝香葡萄作为一个独立的属,比葡萄属原始但与葡萄属有着最近的亲缘关系。 3、依据形态特征和APD分析结果把山葡萄复合体的3个种2变种归并为2种l变种,即山葡萄、复叶葡萄和少毛复叶葡萄,认为分子标记技术在分析属内近缘种闻关系上很有价值。 4、葡萄属具有东亚和北美2个现代分布中心,该属可能起源于北美的东部,在晚白垩纪经白令陆桥散布至欧亚大陆。

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DNA templates were extracted from isolates of Sarcocystis hominis-like cysts collected from cattle and water buffalo, as well as from Sarcocystis fusiformis cysts and Sarcocystis suihominis cysts. The 18S rRNA genes were amplified using DNA from a single

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Six strains of Gram-positive, catalase-negative, non-motile, irregular short rod-shaped Weissella bacteria, with width and length of 0.5-0.6 and 1.2-2.7 mu m were isolated from diseased rainbow trout Oncorhynchus mykiss (Walbaum) in winter of 2007 at a commercial fishery in Jingmen, Hubei province, China. The diseased rainbow trout exhibited hemorrhage in eyes, anal region, intestine and abdomen wall, petechia of liver, some fish with hydrocele in stomach. Six isolates had identical biochemical reactions, phylogenetic analysis of 16S rDNA sequences, amplified ribosomal DNA restriction analysis (ARDRA), enzymatic profile analysis and antimicrobial susceptibility results, indicating as a single clonal outbreak. But all were different from any other validated twelve Weissella species in the term of physiological and biochemical characters. It is indicated that isolates are phylogenetically closer to Weissella halotolerans, Weissella viridescens and Weissella minor on 16S rDNA phylogenetic analysis result, than to W halotolerans and W viridescens on the result of ARDRA study and enzymatic profile analysis. Antimicrobial susceptibility testing was used to scan effective drugs for the therapy of this disease. Experimental infection assays with one isolate were conducted and pathogenicity (by intraperitoneal injection) was demonstrated in rainbow trout O. mykiss (Walbaum) and crucian carp (Carassius auratus gibelio) fingerlings. Because no Weissella was detected in fish feedstuffs and pond water, the source of this pathogen remains unknown, and Weissella isolates were regarded as an opportunistic pathogen for rainbow trout. This is the first report of Weissella strains which can cause disease of cultured fish in the world. (C) 2009 Elsevier B.V. All rights reserved.

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本文以中国科学院成都生物研究所培育的同源四倍体水稻和二倍体水稻为材料,进行遗传差异及产量、品质性状的研究:1、以二倍体水稻为对照,研究了同源四倍体水稻在2004 年和2005 年的结实情况。结果同源四倍体的花粉育性、结实率均不同程度下降,尤其低代材料更是大幅度下降。F 检验表明,同源四倍体不同个体间的各产量性状均差异显著,说明其具有很大的遗传改良潜力。从1996 年到2005 年对部分同源四倍体水稻进行了连续选择改良,T 检验表明经过9 年的选择改良,其结实率显著提高。本文还对同源四倍体水稻各产量性状间的相关性进行了分析,结果结实率与花粉育性、穗着粒数、穗实粒数极显著相关;理论产量与花粉育性、有效穗数、穗着粒数、穗实粒数、结实率及千粒重极显著相关。i2、用(CT)n 微卫星标记和PCR-Acc Ι分子标记对40 份同源四倍体和14 份二倍体水稻Wx 基因进行研究。结果,(CT)n 微卫星标记检测,Wx 基因呈Wx1、Wx2 和Wx3 3 种多态性;PCR-Acc Ι 检测,Wx 基因表现为G-型和T-型。测定稻米直链淀粉含量(AC)、胶稠度(GC)和糊化温度(GT),并探讨其与Wx 基因的关系,结果,二倍体和同源四倍体水稻均存在:Wx 基因型相同,AC 差异较小,Wx 基因型不同时,AC 差异较大,Wx1 基因型品种AC 最高, Wx2 基因型品种AC 次之,Wx3 基因型品种AC 最低;基因型相同时,同源四倍体AC 低于二倍体;同源四倍体与对应二倍体间,Wx 基因型相同时,AC 差异很小;而Wx 基因型发生变异时,AC 差异很大。同时,进行相关性分析,结果二倍体和四倍体水稻均存在AC、GC 与Wx 基因密切相关;而GT 与Wx 基因相关不显著。综合分析,(CT)n微卫星标记与PCR-Acc Ι 分子标记检测的相关系数为0.842,呈极显著正相关,可以将其结合起来进行同源四倍体新品种的选育和改良。3、利用RAPD 技术,对同源四倍体和二倍体水稻的遗传差异进行分析。17条引物在同源四倍体中扩增出178 条带(PPB=81.5%),在二倍体中扩增出173条带(PPB=76.3%);同源四倍体和二倍体的Shannon 遗传多样性指数分别为0.4848 和0.4679,多态信息量分别为0.3301 和0.3216,遗传距离分别为0.3572和0.3460;同源四倍体与其对应二倍体间遗传距离为0.1914-0.4633,平均为0.2914。表明同源四倍体的遗传多样性高于二倍体,且同源四倍体与其二倍体之间存在较大的遗传差异,这些将为水稻品种改良和新品种选育提供科学依据。上述产量、品质性状及遗传差异分析的结果,不仅有利于加快同源四倍体水稻的遗传改良进程,而且为进一步研究、利用同源四倍体水稻奠定了初步基础。 AbstractStudy on genetic diversity, yield characters and quality traitsof autotetraploid and diploid riceLiu Yuhua (Botany)Directed by Associate Prof. Tu ShengbinIn this study, diploid and autotetraploid rice, which were cultivated in ChengduInstitute of Biology were analyzed in genetic diversity, yield characters and qualitytraits.In the study, 2 diploid and 29 autotetraploid rice(2n=4x=48) materials, including4 preliminary and 25 advanced generation, were investigated for yield characters.Compared with diploid check, the pollen fertility and seed set of autotetraploiddeclined dramatically, especially in preliminary generation. F-test indicated that therewere remarkable differences among different varieties, showing that autotetraploidmaterials had strong potential for improvement. From 1996 to 2005, someautotetraploid rice had been selected and improved. T-test showed that seed setincreased obviously. The relationships among yield characters of autotetraploid ricewere analyzed. Seed set was strongly correlated with pollen fertility, total grainnumber per panicle and productive grain number per panicle; theoretical yield wasstrongly correlated with pollen fertility, productive panicle number per plant, totalgrain number per panicle, productive grain number, seed set and 1000-grain weight.Wx genotypes of 40 autotetraploid rice and 14 diploid rice were tested by usingthe (CT)n microsatellite marker and a cleaved amplified polymorphic sequence(CAPS) molecular marker named PCR-Acc Ι. Three microsatellite alleles wereproduced, i.e. Wx1, Wx2 and Wx3 both in autotetraploid and in diploid rice.Comparatively, PCR- Acc Ι molecular marker produced two genotypes, G-type andT-type for both autotetraploid and diploid rice. In this study, amylose content (AC), gel of consistency (GC) and gelatinization temperature (GT) of rice grain weremeasured and their relationships with Wx alleles were analyzed. The results showedthat variation of AC between autotetraploid and diploid rice was small when they hadthe same Wx genotype. However, variation of AC turned to be large when the Wxgenotypes were different. Actually, AC met the maximum value in Wx1 varieties andWx2 varieties the middle and Wx3 varieties the minimum. And AC was lower inautotetraploid than in diploid. Correlation analysis was done in this experiment. ACand GC of rice grain were probably controlled by Wx gene or other gene whoselocation was strictly linked to Wx gene, while GT of rice was not. The correlationcoefficient between Wx genotypes which revealed by (CT)n microsatellite marker andPCR-Acc Ι molecular marker was 0.842 with significant level. That revealed aconsistent result between the two types of markers. So it was possible to utilize boththe two types of markers to select and promote germplasm of autotetraploid rice.RAPD molecular markers were used to analyze the genetic diversity betweendiploid and autotetraploid rice. 178 repeatable bands were detected through 17 RAPDprimers with percentage of polymorphic bands was 81.5% in autotetraploid rice while173 repeatable bands were detected with percentage of polymorphic bands was 76.3%in diploid rice. According to the measurement of Shannon index, polymorphicinformation content and genetic distance, genetic diversity of autotetraploid was on ahigher level, genetic variation between autotetraploid and diploid rice was relativelyhigh. All these contributed to the genetic selection and improvement in rice breeding.As mentioned above, the results are not only helpful to promote the process ofrice improvement, but also to confirm the basic for further study of autotetraploid rice.

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神舟三号飞船搭载带核径迹辐射探测器的水稻种子装置,回收后应用随机扩增多态性DNA(randomamplified polymorphic DNA,RAPD)技术,分析了201粒升空种子长出植株的基因组多态性。在检测的189个基因座位范围内,30.2%的植株中发现与地面对照不同的扩增带,单株的多态性座位数为1 ̄25。特异扩增带的测序及单核苷酸多态性(single-nucleotide polymorphism,SNP)分析进一步证明了空间搭载水稻种子确实可导致当代植株基因组发生变异。同一技术分析个别种子连续世代的基因组多态性,结果显示,当代的部分多态性可遗传至后代。7粒受空间高原子序数、高能粒子轰击的种子,在当代植株均显示不同程度的基因组多态性,从胚受粒子击中的3粒种子后代中,筛选出农艺性状明显变异的突变株系,初步暗示了空间高能重离子辐射对诱导基因组的多态性,乃至遗传性表型变异的有效性。

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Repeated cycles of retreat and recolonization during the Quaternary ice ages are thought to have greatly influenced current species distributions and their genetic diversity. It remains unclear how this climatic oscillation has affected the distribution of genetic diversity between populations of wind-pollinated conifers in the Qinghai-Tibetan region. In this study, we investigated the within-species genetic diversity and phylogenetic relationships of Picea likiangensis, a dominant forest species in this region using polymorphic DNA (RAPD) markers. Our results suggest that this species has high overall genetic diversity, with 85.42% of loci being polymorphic and an average expected heterozygosity (H (E)) of 0.239. However, there were relatively low levels of polymorphism at population levels and the differences between populations were not significant, with percentages of polymorphic bands (PPB) ranging from 46.88 to 69.76%, Nei's gene diversity (H (E)) from 0.179 to 0.289 and Shannon's indices (Hpop) from 0.267 to 0.421. In accordance with our proposed hypothesis, a high level of genetic differentiation among populations was detected based on Nei's genetic diversity (G (ST) = 0.256) and AMOVA analysis (Phi (st) = 0.236). Gene flow between populations was found to be limited (Nm = 1.4532) and far lower than reported for other conifer species with wide distribution ranges from other regions. No clusters corresponding to three morphological varieties found in the south, north and west, respectively, were detected in either UPGMA or PCO analyses. Our results suggest that this species may have had different refugia during the glacial stages in the southern region and that the northern variety may have multiple origins from these different refugia.