ISSR标记技术及其在遗传多样性研究中的应用

ISSR(Inter-Simple Sequence Repeat)技术是在PCR中直接使用微卫星序列进行DNA扩增的一种DNA分子标记。章主要介绍了ISSR标记的原理、方法、特点及其在遗传多样性研究中的应用。ISSR标记方法具有无需知道任何靶标序列的微卫星背景信息、遗传多态性高、检测快速等特点,在遗传多样性研究中具有广泛的应用前景。     

栽培沉香遗传多样性的ISSR和AFLP分析比较

探讨2种分子标记技术在沉香属药用植物遗传多样性研究中的应用。用ISSR和AFLP分子标记分析了海南、云南、广东、广西等地17份沉香属植物的遗传多样性。14个ISSR引物、8对AFLP引物分别检测到119、919个位点,多态位点百分率分别为73.95%、86.94%。由于AFLP标记具有较高的多态性位点检测效率,AFLP标记分析的遗传多样性参数高于ISSR。虽然基于Nei’s遗传距离的聚类分析结果存在着一定的差异,但用Mantel检测对两种方法检测的遗传一致度进行相关性分析表明,它们之间存在着明显的相关性（r=0.7705,P=0.0003）。ISSR标记与AFLP标记均能应用于沉香属植物的遗传多样性研究。两种标记的研究结果均揭示出沉香属植物具有较高的遗传多样水平。     

ISSR分子标记技术及其在植物遗传多样性分析中的应用

ISSR分子标记技术是近年发展而来的一种DNA多态性分子标记,具有简单、经济、信息量大、稳定性高等特点。本文论述了ISSR的反应原理及ISSR实验过程中的技术要点．并总结了ISSR在植物品种鉴定、亲缘关系分析,群体遗传结构、遗传多样性检测,以及植物育种研究中的应用。     

烟粉虱生物型的监测及其遗传结构研究

烟粉虱Bemisia tabaci(Gennadius)是一种重要的农业害虫并包括许多生物型,其中B型和Q型是入侵性较强的2种生物型。文章着重介绍近年来在烟粉虱生物型的监测及其遗传结构方面的研究进展。B型烟粉虱和Q型烟粉虱这2个生物型均已入侵我国,其中多数地区烟粉虱是B型烟粉虱,局部地区有Q型烟粉虱并呈现不断蔓延趋势。微卫星(SSR)分子标记分析结果表明我国B型烟粉虱的入侵来源具有多元化,而云南地区Q型烟粉虱来源比较单一。化学农药的使用能够影响室内种群的遗传结构,降低种群的遗传多样性。基于RAPD、ISSR分子标记的分析结果表明,Q型烟粉虱种群各项遗传多样性指数均比B型烟粉虱的高。今后加强烟粉虱入侵生物型的遗传结构及其种群动态关系等方面的研究,对于揭示烟粉虱的灾变机制及其控制具有重要的意义。     

简单重复序列间扩增分子标记技术及其应用

简单重复序列间扩增(ISSR)技术是在PCR基础上发展起来的一种新型的分子标记技术,因其标记通常为显性标记,呈孟德尔遗传,且在进行PCR反应时,稳定性和多态性均很好,而成为是非常理想的分子标记技术.将从ISSR分子标记技术的原理及其在绘制DNA指纹图谱、遗传多样性分析、种质鉴定等领域的应用进行综述.     

ISSR分子标记在棉花遗传育种上的应用

ISSR是一种近些年发展起来的基于微卫星序列的新型分子标记。阐述了ISSR的基本原理、特点及其在棉花遗传多样性与亲缘关系分析、种质鉴定、遗传图谱构建、基因定位及标记辅助选择育种等方面的应用和进展。     

外来植物入侵对生物多样性的影响及本地生物的进化响应

越来越多的证据表明,入侵植物能通过杂交和基冈渐渗等对本地种造成遗传侵蚀,甚至产生新的"基因型"来影响本地种的遗传多样性;通过生境片断化,改变本地种种群内和种群间的基因交流,造成近亲繁殖和遗传漂变,间接影响本地种的遗传多样性.另一方面,本地种能对入侵植物做出适应性进化响应,以减小或消除入侵植物的危害.本地种在与入侵植物的互作过程中产生了一系列的适应进化、物种形成以及灭绝事件,且这些事件不仅局限于地上生态系统,土壤牛物多样性同样受到影响,甚至也能发生进化响应.为更全面地了解外来植物入侵的生态后果和本地生物的适应潜力,本文综述了外来植物入侵对本地(地上和地下)生物(遗传)多样性的影响以及本地生物的进化响应.讨论了外来植物入侵导致的遗传和进化变化与其入侵性的关系,并提出了一些值得研究的课题.如土著种与外来种的协同进化、植物一土壤反馈调节途径和全球变化其他组分与生物入侵的关系等.     

几种基于PCR的分子标记在甘薯遗传多样性研究中的应用

遗传多样性是甘薯品种遗传改良的基础。由于分子标记具有数量极大、不受环境及基因表达与否的限制、多为共显性、不影响生物性状表现等优点,现已在甘薯遗传多样性研究中得到广泛应用。本文比较了RAPD、AFLP、SSR、ISSR和SRAP等几种基于PCR的分子标记方法,分别从遗传差异和亲缘聚类分析两方面,对它们在甘薯遗传多样性研究中的应用进行了综述。对比分析表明ISSR是一种共显性、成本较低、重复性好、多态性较高且非常有发展前途的分子标记,并已经被广泛应用到甘薯遗传多样性、物种亲缘关系、系统分类和辅助育种研究中。     

入侵植物对根际土壤微生物群落影响的研究进展

入侵植物根际土壤微生物是地下生态系统的重要组成部分。外来植物入侵到新的栖息地后能够促进其根际土壤微生物群落结构的演替、改变土壤理化性质, 强化微生物群落功能的发挥, 进而创造更适合外来植物生长的土壤微环境, 促进外来种的入侵进程。从外来入侵植物根际土壤微生物的研究方法、外来入侵植物对根际土壤微生物群落影响以及从地下生态学对外来植物入侵的影响等方面进行了综述。土壤微生物研究方法主要包括微生物计数法、微生物生理生化指标方法及分子技术 3 类; 入侵植物对根际土壤微生物的影响主要体现在对其生物量、多样性以及功能微生物菌群等方面。在今后的研究中, 应当注重对同一区域外来入侵植物和近缘本土种、及其伴生种的根际土壤微生物进行比较研究; 加强入侵植物根际微生物功能机理、环境因子与微生物间关联性的研究; 同时在研究方法上应注重传统方法与生物标记法及其与分子技术的结合。     

共显性分子标记基因型数据转换为二元型数据的处理软件及其在研究种质资源遗传多样性中的意义

遗传多样性研究是植物种质资源有效利用和保护的重要基础.遗传多样性研究所采用的分子标记工具主要有显性和共显性两种,两种不同类型的分子标记将产生不同的数据类型.显性分子标记产生二元型数据,共显性分子标记产生基因型数据.数据形式不同给遗传多样性的分析和研究带来多方面的困难,不同类型数据之间的互相比较也需要将基因型数据进行二元型转换.本研究基于Excel平台,设计开发了将基因型数据转换成二元型数据的处理软件.该软件按照基因型数据向二元型数据转换的原理,可以将庞大的分子标记基因型数据矩阵,迅速、高效、准确地转换成二元型(0、1)数据矩阵.利用显性分子标记ISSR和共显性分子标记SSR对野生大豆居群遗传多样性的案例分析表明,将共显性分子标记的基因型数据转换为二元型数据,有利于种质资源遗传多样性研究中不同分子标记获取的遗传多样性结果之间的比较和综合分析.     

Genetic diversity analysis of Rhododendron aureum Georgi (Ericaceae) located on Changbai Mountain using ISSR and RAPD markers

Rhododendron aureum Georgi (Ericaceae) is a perennial alpine shrub endemic to Changbai Mountain in China. We used ISSR and RAPD markers to describe the diversity and genetic structure within and among four natural populations located at different altitudes. DNA from 66 individuals was amplified with ten ISSR markers and seven RAPD markers. High genetic diversity was observed by these two techniques at the species level. The genetic diversity of populations increased with altitudinal gradients from low to high. The coefficient of gene differentiation (G_ST 0.3652 in ISSR and 0.2511 in RAPD) and AMOVA analysis revealed that most genetic diversity was distributed within populations (61.96% in ISSR and 70.23% in RAPD). The estimate of gene flow based on G_ST was 0.8690 in ISSR and 1.4910 in RAPD. The UPGMA clustering results using ISSR and RAPD showed that all individuals from the same altitude were gathered together, and the two populations (TYD2a and YHLa) from middle altitudes always clustered together. Compared with populations from different altitudes, similar genetic diversity and low genetic differentiation were obtained from populations at the same altitudes, as revealed by ISSR markers. In addition to the reproductive strategy of R. aureum, these data highlight that local environmental conditions may play an important role in shaping the diversity and genetic structure of this species.     

Genetic variation and cultivar identification in Cymbidium ensifolium

As a popular flowering species with many cultivars, Cymbidium ensifolium (L.) is commercially important in horticulture. However, so far little has been known about genetic diversity and conservation genetics of this species. Understanding of the genetic variation and relationships in cultivars of C.?ensifolium is a prerequisite for development of future germplasm conservation and cultivar improvement. Here we report assessment of genetic variations in C.?ensifolium cultivars using the DNA fingerprinting technique of inter-simple sequence repeats (ISSR). A total of 239 ISSR loci were identified and used for evaluation of genetic variation with a selection of 19 ISSR primers. Among these ISSR loci, 99.16% were polymorphic with wide genetic variation as shown by Nei??s gene diversity (H?=?0.2431) among 85 tested cultivars. ISSR fingerprinting profiles showed that each cultivar had its characteristic DNA pattern, indicating unequivocal cultivar identification at molecular level. Eighteen cultivar-specific ISSR markers were identified in seven cultivars. The cultivar Sijiwenhan was confirmed as hybrid by four ISSR primers. Several cultivars with same name but different geographical origins were distinguished based on their ISSR profiles. A dendrogram generated with ISSR markers could group 73 of 85 cultivars into four major clusters. Further analysis of ISSR variation revealed that about 69% of total genetic variation in this species is due to genetic divergence inside geographical groups. Our results suggest that both germplasm collection and in?situ conservation are important for future planning of C.?ensifolium species conservation.     

Molecular diversity and relationships among <Emphasis Type="Italic">Cymbidium goeringii</Emphasis> cultivars based on inter-simple sequence repeat (ISSR) markers

Spring orchid (Cymbidium goeringii) is a popular flowering plant species. There have been few molecular studies of the genetic diversity and conservation genetics on this species. An assessment of the level of genetic diversity in cultivated spring orchid would facilitate development of the future germplasm conservation for cultivar improvement. In the present study, DNA markers of intersimple sequence repeats (ISSR) were identified and the ISSR fingerprinting technique was used to evaluate genetic diversity in C. goeringii cultivars. Twenty-five ISSR primers were selected to produce a total of 224 ISSR loci for evaluation of the genetic diversity. A wide genetic variation was found in the 50 tested cultivars with Nei’s gene diversity (H = 0.2241) and 93.75% of polymorphic loci. Fifty cultivars were unequivocally distinguished based on ISSR fingerprinting. Cultivar-specific ISSR markers were identified in seven of 50 tested cultivars. Unweighted pair-group mean analysis (UPGMA) and principal coordinates analysis (PCA) grouped them into two clusters: one composed the cultivars mainly from Japan, and the other contained three major subclusters mainly from China. Two Chinese subclusters were generally consistent with horticultural classification, and the third Chinese subcluster contained cultivars from various horticultural groups. Our results suggest that the ISSR technique provides a powerful tool for cultivar identification and establishment of genetic relationships of cultivars in C. goeringii.     

Genetic diversity and structure in fragmented populations of the endangered species Ranunculus cabrerensis (Ranunculaceae): implications for conservation

Ranunculus cabrerensis is an endemic and endangered species of the Northwestern Iberian Peninsula. The molecular markers AFLP and ISSR were used to investigate the genetic diversity and population structure of four populations across its known distribution. Fifteen selective primer combinations of AFLP and seventeen ISSR primer combinations produced a total of 2830 and 103 unambiguously repeatable fragments respectively, of which 97.57 and 81.38% were polymorphic for both markers. The genetic diversity of R. cabrerensis at species level was high (H _E = 0.294 by ISSR and H _E = 0.191 by AFLP) and differentiation between sampled locations was also relatively high (G _ST = 0.316 and 0.158 by ISSR and AFLP analysis respectively) compared to other studies of endangered and rare species using the same techniques. The analysis of molecular variance (AMOVA) indicated that the main genetic variation was within sampled locations (73% by AFLP; 52% by ISSR), even though the variation among locations was also significant. Principal Coordinates, NeighborNet and Bayesian analyses revealed a weak but significant relationship between the genetic structures of different populations in R. cabrerensis, with gene flow acting as a homogenizing force that prevents stronger differentiation of populations. Finally, suggestions for conservation strategies to preserve the genetic resources of this species are outlined.     

A comparison of genetic variation among wild and cultivated Morus Species (Moraceae: Morus) as revealed by ISSR and SSR markers

In this study, inter-simple sequence repeats (ISSR) ans simple sequence repeat (SSR) markers were used to investigate genetic diversity of 27 mulberry accessions including 19 cultivated accessions (six M. multicaulis, three M. alba, two M. atropurpurea, two M. bombycis, one M. australis, two M. rotundiloba, one M. alba var. pendula, one M. alba var. macrophylla, and one M. alba var. venose) and 8 wild accessions (two M. cathayana, two M. laevigata, two M. wittiorum, one M. nigra and one M. mongolica). ISSRs and SSRs were compared in terms of their informativeness and efficiency in a study of genetic diversity and relationships among 27 mulberry genotypes. SSRs presented a higher level of polymorphism and greater information content. All index values of genetic diversity both markers analyzed using Popgene 32 software indicated that within wild species had higher genetic diversity than within cultivated species. Cultivation may caused the lose of genetic diversity of mulberry compared with wild species revealed by ISSR and SSR markers. The mean genetic similarity coefficients among all mulberry genotypes ascribed by ISSR and SSR matrices were 0.7677 and 0.6131, respectively. For all markers a high similarity in dendrogram topologies was obtained although some differences were observed. Cluster analysis of ISSR and SSR using UPGMA method revealed that the wild species are genetically distant from the domesticated species studied here. The correlation coefficients of similarity were statistically significant for both marker systems used. Principal coordinates analysis (PCA) for ISSR and SSR data also supports their UPGMA clustering. These results have an important implication for mulberry germplasm characterization, improvement, molecular systematics and conservation.     

Characterization of the Genetic Diversity of Trachemys dorbigni and Phrynops hilarii

The utilization of RAPD and ISSR molecular markers is proposed to initiate studies of genetic variability in Phrynops hilarii(Chelidae) and Trachemys dorbigni(Emydidae), two species of fresh water turtles distributed in South America. Three primers of RAPD and four of ISSR were selected and the amplified products of these markers were evaluated by electrophoretic runs in agarose and polyacrylamide gels. The levels of heterozygosity, Shannon index and different allele numbers were slightly higher in P. hilarii for both types of markers. Levels of polymorphism were also higher in P. hilarii than T. dorbigni and both were elevated compared to those recorded for other species. The fact that similar results were obtained with both types of markers for all estimates of diversity highlights the usefulness and validity of the RAPD technique. The molecular markers used were found potentially useful for analysing future temporal and spatial distribution of genetic diversity in both species, expanding scales work.     

串珠藻目分子系统学研究进展

串珠藻目(Batrachospermales)是淡水红藻中最主要的类群。近年来, 应用DNA序列分析探讨串珠藻目的系统发育, 并与传统的形态学和生态学特征相结合, 为串珠藻目系统学研究拓展了新的思路。本文回顾了串珠藻目的建立及其所含类群的研究历史, 归纳了目前在串珠藻目系统发育与进化研究中常用的分子标记方法, 其中包括核基因组的18S rDNA、26S rDNA和ITS序列, 叶绿体基因组的rbcL序列, 线粒体基因组的cox2-3序列, 以及新兴的ISSR技术, 并对各种分子标记的特点及适用范围做了评述。结果表明, ITS序列多适用于种群分化及相近种间遗传分析, ISSR标记适用于种下分类群间及同一种群不同个体间基因多态性分析, cox2-3序列在一定程度上也可用于同一种群不同个体间的基因多态性分析, 而18S rDNA 与rbcL序列既可用于种间关系分析, 又可用于更高水平分析的构建系统树。这些分子标记已被证明在研究串珠藻目系统地理、物种起源和散布机制方面有着广泛的应用前景。同时, 本文对串珠藻目分子系统学研究的最新进展也进行了概述,并对今后的研究方向做了展望。     

串珠藻目分子系统学研究进展

串珠藻目（Batrachospermales）是淡水红藻中最主要的类群。近年来,应用DNA序列分析探讨串珠藻目的系统发育,并与传统的形态学和生态学特征相结合,为串珠藻目系统学研究拓展了新的思路。本文回顾了串珠藻目的建立及其所含类群的研究历史,归纳了目前在串珠藻目系统发育与进化研究中常用的分子标记方法,其中包括核基因组的18SrDNA、26SrDNA和ITS序列,叶绿体基因组的rbcL序列,线粒体基因组的cox9．-3序列,以及新兴的ISSR技术,并对各种分子标记的特点及适用范围做了评述。结果表明,ITS序列多适用于种群分化及相近种间遗传分析,ISSR标记适用于种下分类群间及同一种群不同个体间基因多态性分析,cox2-3序列在一定程度上也可用于同一种群不同个体间的基因多态性分析,而18SrDNA与rbcLFF列既可用于种问关系分析,又可用于更高水平分析的构建系统树。这些分子枥对己已被证明在研究串珠藻目系统地理、物种起源和散布机制方面有着广泛的应用前景。同时,本文对串珠藻目分子系统学研究的最新进展也进行了概述,并对今后的研究方向做了展望。     

水松自然种群和人工种群遗传多样性比较

采用ISSR分子标记技术分析水松不同起源种群的遗传多样性.结果表明:10条引物共检测出95个扩增位点,多态位点数占39.0%.与其他濒危裸子植物相比,水松的遗传多样性较低,遗传分化系数Gst为0.3982,基因流Nm仅0.3778,种群间存在一定程度的遗传分化,但种群内变异占主导地位;遗传距离与地理距离呈正相关关系.自然种群的多态位点百分率(P)、Nei的条带多样度(He)和Shannon信息指数(Ⅰ)平均值(39.3%、0.1499和0.2202)分别高于人工种群(30.7%、0.1265和0.1759).自然种群的遗传分化系数(Gst0.4513)和平均遗传距离(D=0.0301)也高于人工种群(Gst=0.3025,D=0.0192).