采用RAPD标记探讨瓣蕊唐松草(毛茛科唐松草属)的遗传多样性及其地理分布格局(英文)

Random amplified polymerphic DNA(RAPD)method was applied to assessg enetic variation and population structure of Thahctrum petalotdeum L(Ranunoulaceae),Two hundred and forty-six individuals from 11 populations of the species were investigated by RAPD profiles Twenty selected RAPD primers generated 125 bands．in which 120 were polymorphic Ther esults revealed a high level of genetic variation(ercentage of polymorphIc bands(PPB was 96％．Nei’s gene diversity(りwas 03502 and shannon’s information index(I) was 0．5199 at the species level) The differentiation among the populations was high(Gst=0．3511)in this species．Result of analyzing of molecularvariance(AMOVA)showedthat38．88％of genetic variance was found among the populations Positive correlation withr r=01945(P=00002)was found between genetic distance and geographic distance amongpo pulations Two populations distributed in the drainage basin of YanELz River affined genedcally and formed one clada and the rest nine populations formed the other clade in both unweighted pair-group method using arithmetic average(UPGMA)trees made by two different method different methods. It was yen/clear that these two populations were very special, andmust be closely related in history, despite the fact that they now share quite weak link to the restpopulations through gene communication.     

无藻萍的RAPD分析及其在三膘组满江红种间关系研究中的应用

从满江红Azolla Lam.萍-藻共生体中提取DNA进行的RAPD系统分析通常忽视了满江红样品的异质性。本研究通过获得无藻的满江红,比较有藻萍、无藻萍和离体藻之间的RAPD指纹图谱。发现从有藻萍中提取DNA的扩增反应来源于萍藻双方DNA的共同影响。依引物和植物样本的不同,共生双方对扩增产物的贡献结果不同,说明了用无藻萍进行RAPD检测的重要性。对满江红三膘组5个种的11个无藻萍样本进行了RAPD分析,由9个引物产生的127个DNA多态片段用于计算样本间的Jaccard相似系数和UPGMA树状聚类图。结果     

满江红鱼腥藻遗传多样性的RAPD分析

共生在水生蕨类植物满江红(又称“红萍”:Azolla)叶腔中的固氮兰细菌曾被认为是一个种满江红鱼腥藻(Anabaena azollae Strasb.).但由于现存的满江红在分类学上有2个亚属,7个种1,对不同满江红叶腔中鱼腥藻的鉴别,多年来引起人们的重视.80年代,鱼腥藻的单克隆抗体和RFLP的研究,发现了它与宿主分类上一定程度的对应关系2,3.90年代以后,Van Coppenolle和Eskew分别以RAPD-PCR和DAF-PCR对从满江红共生体中提取的DNA进行了分析4,5,但后者发现了共生体中藻的DNA对整个PCR产物的干扰作用会影响满江红属本身系统分类.       

RAPD diversity of Stipa grandis populations and its relationship with some ecological factors

The genetic diversity of Stipa grandis P.Smirn and its relationship with the climatic variables were studied using the RAPD technique for 90 genes from five natural populations sampled in the Xilingol steppe, China. Sixteen oligonucleotides screened from 100 random primers were used to amplify 310 trackable RAPD loci, which were all polymorphic. By analyzing the RAPD data using POPGENE software, different geographic S. grandis populations were studied, which indicated a high level of genetic diversity, and the maximum variation was observed within the populations with a 28% variation observed among the populations. Using Pearson correlation analysis, significant (P < 0.05) or highly significant (P < 0.01) relationships were found between gene diversity indexes and temperature factors (≥10°C cumulative temperature in a year, annual mean temperature and mean temperature in January). Mantel's tests showed that there was no significant correlation between Nei's unbiased genetic distance and the geographic distance of S. grandis populations (r = 0.184, P = 0.261). However, there were significant or highly significant correlations between Nei's genetic distance and the several climatic divergences in pairwise S. grandis populations. All results indicated that natural selection resulting from variations in water and temperature was responsible for the adaptive eco-geographical differentiation indicated by the RAPD markers of different S. grandis populations, and that immigration and gene drift did not play an important role in affecting the differentiation of S. grandis populations.     

结合态氮对满江红内生细菌群落组成和结构的影响

研究从超微结构和分子水平上探讨结合态氮对满江红(Azolla)叶腔中以共生藻占优势的微生物群落的影响。为排除外源污染并保留其内生菌的多样性,采用茎尖组织培养并添加结合态氮等方法,取得了表面无菌的含藻满江红(AmA)和无藻满江红(AmB)。电镜观察揭示, AmB较AmA的萍体表型有某种程度的修饰。AmA的微生物群落结构以共生藻、内生菌和宿主腺毛及其分泌物组成的生物被膜和藻囊为主要特征,而AmB的叶腔几乎中空。基于16S rRNA基因和nif H基因的高通量测序结果显示,生长于无氮培养液的AmA样品的微生物群落有相当高的多样性,共有17个可操作分类单元(OTU),分属4个细菌门,并有一个以Nostoc azollae为优势的固氮微生物亚群包括草螺菌、根瘤菌和Niveispirillum等。而生长于富含结合态氮培养液的AmB样品的群落多样性明显降低,仅有8个OTU,且以Nostoc azollae为优势的上述固氮微生物亚群全部消失。研究结果表明,通过调整氮素营养,可改变宿主植物的微生物群落组成与结构,进而改良植物的生长发育。     

RAPD diversity of Stipa grandis populations and its relationship with some ecological factors

The genetic diversity of Stipa grandis P.Smirn and its relationship with the climatic variables were studied using the RAPD technique for 90 genes from five natural populations sampled in the Xilingol steppe, China. Sixteen oligonucleotides screened from 100 random primers were used to amplify 310 trackable RAPD loci, which were all polymorphic. By analyzing the RAPD data using POPGENE software, different geographic S. grandis populations were studied, which indicated a high level of genetic diversity, and the maximum variation was observed within the populations with a 28% variation observed among the populations. Using Pearson correlation analysis, significant (P < 0.05) or highly significant (P < 0.01) relationships were found between gene diversity indexes and temperature factors (≥10C cumulative temperature in a year, annual mean temperature and mean temperature in January). Mantel's tests showed that there was no significant correlation between Nei's unbiased genetic distance and the geographic distance of S. grandis populations (r = 0.184, P = 0.261). However, there were significant or highly significant correlations between Nei's genetic distance and the several climatic divergences in pairwise S. grandis populations. All results indicated that natural selection resulting from variations in water and temperature was responsible for the adaptive eco-geographical differentiation indicated by the RAPD markers of different S. grandis populations, and that immigration and gene drift did not play an important role in affecting the differentiation of S. grandis populations.     

Correlations between the ages of Alnus host species and the genetic diversity of associated endosymbiotic Frankia strains from nodules

Nodule samples were collected from four alder species: Alnus nepalensis, A. si-birica, A. tinctoria and A. mandshurica growing in different environments on Gaoligong Mountains, Yunnan Province of Southwest China and on Changbai Mountains, Jilin Province of Northeast China. PCR-RFLP analysis of the IGS between nifD and nifK genes was directly applied to uncultured Frankia strains in the nodules. A total of 21 restriction patterns were obtained. The Frankia population in the nodules of A. nepalensis had the highest genetic diversity among all four Frankia populations; by contrast, the population in the nodules of A. mandshurica had the lowest degree of divergence; the ones in the nodules of A. sibirica and A. tinctoria were intermediate. A dendrogram, which was constructed based on the genetic distance between the restriction patterns, indicated that Frankia strains from A. sibirica and A. tinctoria had a close genetic relationship. Frankia strains from A. nepalensis might be the ancestor of Frankia strain     

RAPD analysis of natural populations of Acanthopanax brachypus

Random amplified Polymorphic DNA(RAPD) analysis is a new technology of molecular marking which has proved very powerful in detecting genetic diversity at the level of population.The genomic DNAs used in our experiment were extracted from fresh leaves taken from 59 individuals sampled from three natural populations in Yan an,Shanxi Province.Through more than 2,000 PCRs,deep-going RAPD analysis was carried out on DNA samples from 49 inviduals.The percentage of polymorphic RAPD loci found in these three populations were respectively 27.2%,18.6% and 5.4%;the average genetic distances within population,0.055,0.026 and 0.008;the average genetic distances between populations (I-II),(I-III) and (II-III),0.105,0.096 and 0.060.The genetic diversity of A.brachypus within and between populations was found,for the first time,to be rather poor,thus revealing innate factors as the cause contributing to its endangered status.In addition,our work also provides basic materials for elucidating the underlying cause of its endangerment and for its protection biology.     

蓖麻蚕DNA导入家蚕引起遗传变异的研究-基因组DNA的RAPD检测

借助于精子介导,在家蚕受精的过程中将蓖麻蚕DNA转入家蚕卵内,从它们后代获得了新的变异品系。本文采用RAPD技术对这些品系基因组DNA进行了分析。结果表明,所用50种10mer随机引物中有49个检测出DNA的多态性,统计分析图谱中各类扩增带,其中变异品系与其相应受体的差异带占其总带数的26-37%,提示外源DNA导入受体后引起后代基因组的显著变异,并对这些变异的意义了讨论。 Abstract:With the aid of domesticated silkworm sperms,eri silkworm DNA was transferred into domesticated silkworm eggs during insemination,and variant strains were obtained from the progenies.Genomes of three new strains were analyzed using RAPD assay.Polymorphic fingerprints were obtained from 49 out of 50 primers.Different kinds of amplified bands in RAPD patterns were calculated and analyzed,the variant bands between variants and their recipients counted for 26~37% of the total bands of each variant.The results indicated that exogenous DNA introduced into recipients induced remarkable variation in progeny genomes.The significance of the variation was discussed.     

JL-02多位点探针DNA指纹在近交系小鼠遗传监测中的应用

以公安部二所研制的JL-02多位点探针进行了BALB/C、C57、DBA/2、615和ICR5个品系近交系小鼠DNA指纹分析。结果表明,不同近交系小鼠的DNA指纹图差异很大,而同一品系DNA指纹图基本一致,从而证明这一新探针适用于利用DNA指纹技术对近交系小鼠进行遗传监测并具有高度多态性。 Abstract：To explore the possibility of using the probe JL-02 by the Public Safety Bureau of China in monitoring genetic quality of inbred mic e. Fingerprinting of 5 strains of the inbred mice (BALB/c、C57、DBA/2、615、ICR) was conducted using a nonisotopically HRP labeled JL-02 and southern blot hybri dization. The patterns were completely different among the 5 strains of the mice and those of the samples from the same strains were completely identical and th e probe has the high polymorphism.     

Biodiversity of Anabaena azollae isolates from different Azolla cultures

The random amplified polymorphic DNA (RAPD) profile of A. azollae strains isolated from four different Azolla cultures was studied by using different primers. The objective of this study was to determine whether polymerase chain reaction (PCR) with different primers could differentiate the isolated A. azollae strains from one another. The primers amplified specific sequences of the isolates and generated fingerprinting pattern characteristic of each isolate. Clear polymorphism was noticed among all the strains which depends on the primer sequence.     

Use of DNA/DNA hybridization techniques to authenticate the production of new Azolla-Anabaena symbiotic associations

Abstract The establishment of Azolla-Anabaena 'recombination' symbioses by grafting the Anabaena -containing indusium (cap) from the donor megasporocarp onto a decapitated megasporocarp from an Anabaena -free recipient has been recently reported. We have generated strain- and species-specific DNA probes for unequivocally establishing the identity of Anabaena azollae strains isolated from Azolla-Anabaena symbioses (whether new, i.e. heterosymbioses or natural i.e. homosymbioses). Eight out of nine heterosymbioses tested proved to contain the expected heterosymbiont while one recombined association was shown to contain both its own homosymbiont and a heterosymbiotic Anabaena strain. In addition, a species-specific plant probe was isolated from the total DNA of Azolla microphylla roots and used to establish the identity of a host plant used for recombination experiments.     

An Autoradiographic Study of the Azolla-Anabaena azollae Relationship

The symbiotic relationships between Azolla and Anabaena azollae were studied by means of autoradiography after the Azolla was administered by 3H-thymidine, 3H-uridine, 3H-leucine and 3H-glucose. The experimental results showed that the four labeled compounds mentioned above were transfered from Azolla to Anabaena azollae through cavity hairs. This indicated that there was a transfer way of substances from fern to algae. It is suggested that the symbiotic relationship between Azolla and Anabaena azollae is more complicated than we have known up to now. The fern not only get the NH3 which was formed by symbiont-blue alga, but also supplied some nitrogen-containing substances, such as amino acids (or proteins), ribonucleotides for symbiotic algae. Although the symbiont still retained photosynthetic ability, the ability of nitrogen fixation might be developed and the photosynthetic autotrophic ability might be dropped gradually in the long symbiotic life and the Anabaena azolla needed take a portion of substances from the Azolla as replenishment.     

Azolla: Botany,physiology, and use as a green manure

This is a comprehensive review of literature pertaining to the aquatic fern Azolla and its nitrogen-fixing algal symbiont, Anabaena azollae. The preceding decade has witnessed an explosive growth in research on Azolla, and hopefully this paper will facilitate those efforts. The paper is broken into three major categories: botany, physiology and biochemistry, and agriculture. The botany section includes a world distribution map and reference tables for the 6 Azolla species, and includes the first review of literature on Anabaena azollae. The physiology and biochemistry section covers the range of topics from environmental factors to life processes and nitrogen fixation. Tables on the effect of growth regulators and on the rate of nitrogen fixation measured by acetylene reduction are presented. The agriculture section draws extensively from literature published in the People’s Republic of China and in the Democratic Republic of Vietnam. The major focus of this section is on the history and management practices for Azolla cultivation as a green manure for rice. The effect of weed suppression, use as a fish food and animal fodder, and the insects and diseases of Azolla are also discussed.     

The pore of the leaf cavity of Azolla species: teat cell differentiation and cell wall projections

The differentiation of the specialized secretory teat cells of the leaf cavity pore of Azolla species was investigated at the ultrastructural level with emphasis on their peculiar cell wall projections. The results indicated that the projections are formed as soon as the teat cells complete their differentiation and that their production is principally associated with changes in endoplasmic reticulum profiles. The number of projections increases with the teat cell age and is stimulated under salt and P deficiency stresses. Salt stress also promotes their emergence on Azolla species that under normal conditions do not produce projections. Cytochemical tests on different Azolla species showed that the projection composition is almost identical: proteins, acidic polysaccharides, and pectin are always detected. This study revealed that Azolla teat cell projections differ fundamentally from other types of hitherto described cell wall projections that are considered as remnant structures from cell separation. In contrast, in Azolla teat cells projections are actively produced and compounds are excreted by an exocytotic mechanism. The possible role of the projections in the symbiosis of Azolla spp. with Anabaena azollae is discussed.     

DIVERSITY AND HOST SPECIFICITY OF AZOLLA CYANOBIONTS1

A unique, hereditary symbiosis exists between the water fern Azolla and cyanobacteria that reside within a cavity in the dorsal leaf‐lobe of the plant. This association has been studied extensively, and questions have frequently been raised regarding the number and diversity of cyanobionts (cyanobacterial symbionts) among the different Azolla strains and species. In this work, denaturating gradient gel electrophoresis (DGGE) and a clone library based on the 16S rRNA gene were used to study the genetic diversity and host specificity of the cyanobionts in 35 Azolla strains covering a wide taxonomic and geographic range. DNA was extracted directly from the cyanobacterial packets, isolated after enzymatic digestion of the Azolla leaves. Our results indicated the existence of different cyanobiont strains among Azolla species, and diversity within a single Azolla species, independent of the geographic origin of the host. Furthermore, the cyanobiont exhibited host‐species specificity and showed most divergence between the two sections of genus Azolla, Azolla and Rhizosperma. These findings are in agreement with the recent redefinition of the taxon Azolla cristata within the section Azolla. With regard to the taxonomic status of the cyanobiont, the genus Anabaena of the Nostocaceae family was identified as the closest relative by this work.     

DNA Probes Show Genetic Variation in Cyanobacterial Symbionts of the Azolla Fern and a Closer Relationship to Free-Living Nostoc Strains than to Free-Living Anabaena Strains

Twenty-two isolates of Anabaena azollae derived from seven Azolla species from various geographic and ecological sources were characterized by DNA-DNA hybridization. Cloned DNA fragments derived from the genomic sequences of three different A. azollae isolates were used to detect restriction fragment length polymorphism among all symbiotic anabaenas. DNA clones were radiolabeled and hybridized against southern blot transfers of genomic DNAs of different isolates of A. azollae digested with restriction endonucleases. Eight DNA probes were selected to identify the Anabaena strains tested. Two were strain specific and hybridized only to A. azollae strains isolated from Azolla microphylla or Azolla caroliniana. One DNA probe was section specific (hybridized only to anabaenas isolated from Azolla ferns representing the section Euazolla), and five other probes gave finer discrimination among anabaenas representing various ecotypes of Azolla species. These cloned genomic DNA probes identified 11 different genotypes of A. azollae isolates. These included three endosymbiotic genotypes within Azolla filiculoides species and two genotypes within both A. caroliniana and Azolla pinnata endosymbionts. Although we were not able to discriminate among anabaenas extracted from different ecotypes of Azolla nilotica, Azolla mexicina, Azolla rubra and Azolla microphylla species, each of the endosymbionts was easily identified as a unique genotype. When total DNA isolated from free-living Anabaena sp. strain PCC7120 was screened, none of the genomic DNA probes gave detectable positive hybridization. Total DNA of Nostoc cycas PCC7422 hybridized with six of eight genomic DNA fragments. These data imply that the dominant symbiotic organism in association with Azolla spp. is more closely related to Nostoc spp. than to free-living Anabaena spp.     

Genetic diversity among and within cultured cyanobionts of diverse species of <Emphasis Type="Italic">Azolla</Emphasis>

The cyanobionts isolated from 10 Azolla accessions belonging to 6 species (Azolla mexicana, A. microphylla, A. rubra, A. caroliniana, A. filiculoides, A. pinnata) were cultured under laboratory conditions and analyzed on the basis of whole cell protein profiles and molecular marker dataset generated using repeat sequence primers (STRR(mod) and HipTG). The biochemical and molecular marker profiles of the cyanobionts were compared with those of the free-living cyanobacteria and symbiotic Nostoc strains from Anthoceros sp., Cycas sp. and Gunnera monoika. Cluster analysis revealed the genetic diversity among the selected strains, and identified 3 distinct clusters. Group 1 included cyanobionts from all the 10 accessions of Azolla, group 2 comprised all the symbiotic Nostoc strains, while group 3 included the free-living cyanobacteria belonging to the genera Nostoc and Anabaena. The interrelationships among the Azolla cyanobionts were further revealed by principal component analysis. Cyanobionts from A. caroliniana-A. microphylla grouped together while cyanobionts associated with A. mexicana-A. filiculoides along with A. pinnata formed another group. A. rubra cyanobionts had intermediate relationship with both the subgroups. This is the first study analyzing the diversity existing among the cultured cyanobionts of diverse Azolla species through the use of biochemical and molecular profiles and also the genetic distinctness of these free-living cyanobionts as compared to cyanobacterial strains of the genera Anabaena and Nostoc.