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Phylogeny of Ptychostomum (Bryaceae,Musci) inferred from sequences of nuclear ribosomal DNA internal transcribed spacer (ITS) and chloroplast rps4 被引量:2
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作者 Chen-Ying WANG Jian-Cheng ZHAO 《Journal of Systematics and Evolution》 SCIE CSCD 北大核心 2009年第4期311-320,共10页
The phylogeny of Ptychostomum was first spacer (ITS) region of the nuclear ribosomal (nr) DNA DNA rps4 sequences. Maximum parsimony, maximum undertaken based on analysis of the internal transcribed and by combinin... The phylogeny of Ptychostomum was first spacer (ITS) region of the nuclear ribosomal (nr) DNA DNA rps4 sequences. Maximum parsimony, maximum undertaken based on analysis of the internal transcribed and by combining data from nrDNA ITS and chloroplast likelihood, and Bayesian analyses all support the conclusion that the reinstated genus Ptychostomum is not monophyletic. Ptychostomum funkii (Schwagr.) J. R. Spence (≡ Bryum funkii Schwaigr.) is placed within a clade containing the type species of Bryum, B. argenteum Hedw. The remaining members of Ptychostomum investigated in the present study constitute another well-supported clade. The results are congruent with previous molecular analyses. On the basis of phylogenetic evidence, we agree with transferring B. amblyodon Mull. Hal. (≡ B. inclinatum (Brid.) Turton≡ Bryum archangelicum Bruch & Schimp.), Bryum lonchocaulon Mull. Hal., Bryum pallescens Schleich. ex Schwaigr., and Bryum pallens Sw. to Ptychostomum. 展开更多
关键词 Bryum molecular phylogeny nuclear ribosomal DNA internal transcribed spacer sequences Ptychostomum rps4 sequences.
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Phylogenetic Relationships of <i>Termitomyces aurantiacus</i>Inferred from Internal Transcribed Spacers DNA Sequences 被引量:1
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作者 Shafiquzzaman Siddiquee Kobun Rovina +2 位作者 Laila Naher Kenneth F. Rodrigues Md Akhter Uzzaman 《Advances in Bioscience and Biotechnology》 2015年第5期358-367,共10页
Fungus-growing termites cultivate species of the mutualistic basidiomycete genus Termitomyces on a substrate called the fungal comb. Identification of fungal species based on morphological features is complicated, ted... Fungus-growing termites cultivate species of the mutualistic basidiomycete genus Termitomyces on a substrate called the fungal comb. Identification of fungal species based on morphological features is complicated, tedious, and prone to errors. As an alternative, nuclear ribosomal DNA sequences consisting of the internal transcribed spacers (ITS1 and ITS2) and 5.8S rDNA were used to identify Malaysian isolates of Termitomyces sp. The morphological characteristics and molecular data indicate that Malaysian Termitomyces isolated is clearly monophyletic and belongs to the Tricholomataceae family. The Malaysian isolates analyzed in this study represent the termite fungus species called T. aurantiacus. 展开更多
关键词 Fungal Comb internal transcribed spacers Morphological Feature Phylogenetic Relationship
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Characterization of Fusarium Oxysporum Isolates Obtained from Wax Gourd and Chieh-qua in China by Pathogenicity, RAMs and Sequence Analysis of the rDNA Internal Transcribed Spacers (ITS1 and ITS2) 被引量:2
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作者 D.S. Xie  X.M. He  Q.W. Peng 《分子植物育种》 CAS CSCD 2007年第2期271-272,共2页
Wax gourd (Benincasa hispida Thumb. Cogn) is called white gourd, winter melon, Chinese preserving melon, Chinese squash, and don kwa. It has been cultivated in China for over 2 300 years. It probably
关键词 镰刀霉 病原 序列分析 白葫芦
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Application of the first internal transcribed spacer(ITS-1)of ribosomal DNA as a molecular marker to population analysis in farrer's scallop Chlamys farreri 被引量:1
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作者 YU Ziniu WEI Xiaohua +1 位作者 KONG Xiaoyu YU Shanshan 《Acta Oceanologica Sinica》 SCIE CAS CSCD 2007年第1期93-100,共8页
Sequence variation of the first internal transcribed spacer of ribosomal DNA ( ITS - 1 ) was examined and its application to the study of genetic variation was explored in four populations of farter' s scallop Chla... Sequence variation of the first internal transcribed spacer of ribosomal DNA ( ITS - 1 ) was examined and its application to the study of genetic variation was explored in four populations of farter' s scallop Chlamys farreri. ITS - 1 fragments, with a length of about 300 bp,of 78 individuals collected from Dalian, Qingdao, Yantai in China and Korea respectively were amplified via PCR, cloned and sequenced. Intra-genomic variation was examined by sequencing several clones of single individuals. Alignment and polymorphism analysis detected 44 haplotypes and 50 polymorphic sites which consist of 30 substitutions and 20 indels, indicating a high level of polymorphisms. Sequence analysis also showed a very low level of intra-individual variation. All these features validated the feasibility of application of ITS - 1 fragment to population analysis. Polymorphism analysis showed that the Korea sample has the richest genetic variation, followed by Yantai and Qingdao samples. AMOVA (analysis of molecular variance) showed that the majority (96.26%) of genetic variation was distributed within populations and 3.74% resulted from among populations, but with P 〈 0.05 ( = 0.042), indicating that the populations in this study have significant divergence. This output was basically concordant with the result arising from RAPD data and different from that from mitochondrial 16S rDNA sequence data. Discussion on this inconsistency was made accordingly. 展开更多
关键词 Chlamys farreri farrer' s scallop internal transcribed spacer its - 1 DNA sequence genetic variation
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Development and evaluation of specific PCR primers targeting the ribosomal DNA-internal transcribed spacer(ITS)region of peritrich ciliates in environmental samples 被引量:1
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作者 SU Lei ZHANG Qianqian GONG Jun 《Journal of Oceanology and Limnology》 SCIE CAS CSCD 2018年第3期818-826,共9页
Peritrich ciliates are highly diverse and can be important bacterial grazers in aquatic ecosystems. Morphological identifi cations of peritrich species and assemblages in the environment are time-consuming and experti... Peritrich ciliates are highly diverse and can be important bacterial grazers in aquatic ecosystems. Morphological identifi cations of peritrich species and assemblages in the environment are time-consuming and expertise-demanding. In this study, two peritrich-specifi c PCR primers were newly designed to amplify a fragment including the internal transcribed spacer(ITS) region of ribosomal rDNA from environmental samples. The primers showed high specifi city in silico, and in tests with peritrich isolates and environmental DNA. Application of these primers in clone library construction and sequencing yielded exclusively sequences of peritrichs for water and sediment samples. We also found the ITS1, ITS2, ITS, D1 region of 28 S rDNA, and ITS+D1 region co-varied with, and generally more variable than, the V9 region of 18 S rDNA in peritrichs. The newly designed specifi c primers thus provide additional tools to study the molecular diversity, community composition, and phylogeography of these ecologically important protists in dif ferent systems. 展开更多
关键词 Ciliophora Peritrichia clone library internal transcribed spacer(its rDNA specific PCR PRIMERS
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基于ITS和ISSR标记的灵芝遗传多样性和群体结构分析
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作者 赵翠敏 赵岑 +3 位作者 张兰迎 吴倩倩 武恩斯 李敏敏 《北方园艺》 CAS 北大核心 2024年第3期103-111,共9页
以来自不同地理区域的48个灵芝种质资源为试材,采用ITS和ISSR分子标记的方法,研究了灵芝遗传多样性,以期利用遗传信息数据较理想地显示出不同灵芝菌株的遗传多样性。结果表明:通过进行ITS序列扩增测序,将48个灵芝菌株分为赤芝(35个)、... 以来自不同地理区域的48个灵芝种质资源为试材,采用ITS和ISSR分子标记的方法,研究了灵芝遗传多样性,以期利用遗传信息数据较理想地显示出不同灵芝菌株的遗传多样性。结果表明:通过进行ITS序列扩增测序,将48个灵芝菌株分为赤芝(35个)、无柄灵芝(11个)、四川灵芝(1个)、古巴栓孔菌(1个)。5条ISSR引物共扩增得到53条条带,多态性条带比率为96.23%,Nei′s基因多样性为0.27,Shannon′s信息指数为0.43。ISSR标记遗传相似系数约为0.70,将48个灵芝菌株分为3组,其中第1组为11个无柄灵芝,第2组为菌株29“盆景1”,其他菌株为第3组,说明2种标记结合分析能够更加准确分析不同菌株间的亲缘关系。菌株16和17同为赤芝,且ISSR分子标记遗传相似系数达0.98,推测可能为同一品种,为生产中出现的同物异名现象。该研究选取的用于PCR扩增的ISSR引物,多态性较好、稳定性较高,能有效鉴别出无柄灵芝与其他灵芝,并揭示种质的遗传多样性和群体遗传结构,可为灵芝种质资源保护及优质种质材料选育提供参考依据,以期更好地推动灵芝产业健康发展。 展开更多
关键词 灵芝 its ISSR 遗传多样性
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DNA Barcoding of <i>Ricinus communis</i>from Different Geographical Origin by Using Chloroplast <i>matK</i>and Internal Transcribed Spacers
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作者 Mohamed Enan Mohammad Al-Deeb +1 位作者 Nael Fawzy Khaled Amiri 《American Journal of Plant Sciences》 2012年第9期1304-1310,共7页
Ricinus communis have attracted considerable attention because of its specific industrial and pharmacological activities. DNA barcodes can be used as reliable tools to facilitate the identification of medicinal plants... Ricinus communis have attracted considerable attention because of its specific industrial and pharmacological activities. DNA barcodes can be used as reliable tools to facilitate the identification of medicinal plants for the safe use, quality control and forensic investigation. In this study, the differential identification of eight accessions of R. com-munis was investigated through DNA sequence analysis of two candidate DNA barcodes. The nucleotide sequence of internal transcribed spacers (ITS2) and chloroplast maturase gene (matK) have been determined to construct the phylogenetic tree. The phylogenetic relationships of accessions based on the nrITS2 region and partial matK region showed that all accessions in this study were related to three geographical origins. Based on sequence align-ment and phylogenetic analyses we concluded that the ITS2 sequences can distinguish R. communis accessions from different geographical distributions. 展开更多
关键词 DNA BARCODING internal transcribed Spacer Maturase K RICINUS communis
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A preliminary analysis of phylogenetic relationships of Arundinaria and related genera based on nucleotide sequences of nrDNA (ITS region) and cpDNA (trnL-F intergenic spacer) 被引量:5
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作者 ZHUGEQiang DINGYu-long +3 位作者 XUChen ZOUHui-yu HUANGMin-ren WANGMing-xiu 《Journal of Forestry Research》 SCIE CAS CSCD 2005年第1期5-8,i001,共5页
Phylogenetic relationships of Arundinaria and related genera (Pleioblastus, Pseudosasa, Oligostachyum, Bashania, Clavinodum, etc.) were assessed by analyzing the sequences of the nrDNA internal transcribed spacer (ITS... Phylogenetic relationships of Arundinaria and related genera (Pleioblastus, Pseudosasa, Oligostachyum, Bashania, Clavinodum, etc.) were assessed by analyzing the sequences of the nrDNA internal transcribed spacer (ITS) and the cpDNA trnL-F intergenic spacer (IGS). Comparison with trnL-F IGS sequence, the ITS region provided the higher number of parsimony informative characters, and the interspecific variation of the ITS sequence was higher than that of the trnL-F IGS sequence.The tree obtained by combining both sets of data showed that the species sampled in Arundinaria and the related genera were monophyletic and divided into two clades. The relationships and positioning of all the taxa surveryed (including A. oleosa, A. hsienchuensis, A. chino, A. amara, A. yixingensis, A. amabilis, A. fortunei, A. pygmaea, A. gramineus, A. fargesii, A. faberi, A. hupehense, Pseudosasa japonica cv. Tsutsumiana, P. japonica and Brachystachyum densiflorum) were also discussed. The results from the sequences were broadly consistent with morphological characters, appearing all these taxa sampled belong to the genus of Arundinaria. The topologies of the trees generated from individual data and the combined data were similar. 展开更多
关键词 Arundinaria internal transcribed spacers (its) sequences trnL-F intergenic spacer (IGS) sequences Phylogenetic relationships
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Phylogenetic relationships within the genus Aspidisca(Protozoa,Ciliophora,Euplotida) revealed by ITS1-5.8S-ITS2 region sequences 被引量:2
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作者 黄洁 伊珍珍 +3 位作者 苗苗 AL-RASHEID KhaledA.S 宋微波 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2011年第2期277-283,共7页
Abstract The internal transcribed spacer regions (ITS1 and ITS2) and 5.8S rRNA genes were sequenced in six populations of four Aspidisca species, namely A. leptaspis, A. orthopogon, A. rnagna and A. aculeata. Phylog... Abstract The internal transcribed spacer regions (ITS1 and ITS2) and 5.8S rRNA genes were sequenced in six populations of four Aspidisca species, namely A. leptaspis, A. orthopogon, A. rnagna and A. aculeata. Phylogenetic trees were constructed by means of Bayesian inference (BI), Maximum Parsimony (MP), Neighbor-Joining (NJ), and Maximum Likelihood (ML) to assess the inter- and intra-species relationships within the genus Aspidisca. All trees show similar topologies with stable supports and indicate that: (1) four well known groups, i.e., Oligotrichia, Stichotrichia, Choreotrichia and Hypotrichia, are distinctly outlined within the class Spirotrichea, and all are monophyletic other than Hypotrichia; (2) members of Aspidisca can be distinguished well, based on the ITSI-5.SS-ITS2 region sequences, and A. leptaspis and A. magna shared a closer relationship than other species; (3) Aspidisca and Euplotes branch early in the subclass Hypotrichia. To compare the phylogenetic relationships based on different genes, SSU rRNA trees were also constructed with nearly the same species inclusion, which revealed different topologies of inter-species, inter-genera and inter-subclasses. 展开更多
关键词 marine ciliates Aspidisca PHYLOGENY internal transcribed spacer 5.8S rRNA
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基于ITS和ISSR的灵芝种质资源遗传多样性分析
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作者 许琳 张瑞 +3 位作者 王胜 李金涛 刘琳玲 闫梅霞 《河南农业科学》 北大核心 2023年第11期66-74,共9页
为明确吉林栽培的灵芝(Ganoderma lucidum)种质资源的遗传多样性,以吉林省18个主栽灵芝菌株为试验材料,通过应用ITS(Internal transcribed spacer)序列分析及拮抗试验,并与ISSR(Inter-simple sequence repeat)分子标记相结合对其进行鉴... 为明确吉林栽培的灵芝(Ganoderma lucidum)种质资源的遗传多样性,以吉林省18个主栽灵芝菌株为试验材料,通过应用ITS(Internal transcribed spacer)序列分析及拮抗试验,并与ISSR(Inter-simple sequence repeat)分子标记相结合对其进行鉴定和遗传多样性分析。基于ITS序列构建的系统发育树表明,18种灵芝菌株均与赤芝(Ganoderma lingzhi)聚为一类,并细分为4个类群;79.7%的灵芝菌株之间存在拮抗现象,基于ITS序列分析及拮抗试验结果,菌株被分为7个类群;ISSR遗传多样性分析结果表明,18种灵芝菌株的遗传相似系数在0.3824~0.9744,平均为0.6529,当相似系数约0.679时,其亦可被分为7个类群。综上,基于ISSR分子标记的分类结果与基于ITS序列分析+拮抗试验结果的分类一致,18种灵芝菌株表现出明显的遗传多样性。 展开更多
关键词 灵芝 拮抗试验 its ISSR 遗传多样性
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内蒙古不同产地小秦艽ITS序列比较研究
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作者 刘倩 黄艺晓 +2 位作者 臧二欢 张明旭 李旻辉 《中医药导报》 2023年第6期55-59,共5页
目的:研究内蒙古不同产地野生小秦艽内转录间隔区(ITS)序列的遗传变异情况并进行聚类分析,为保护及优化小秦艽种质资源提供参考。方法:对野外采集的内蒙古不同产地的62份小秦艽样品进行DNA提取,选取合适引物进行PCR扩增并测序,测序结果... 目的:研究内蒙古不同产地野生小秦艽内转录间隔区(ITS)序列的遗传变异情况并进行聚类分析,为保护及优化小秦艽种质资源提供参考。方法:对野外采集的内蒙古不同产地的62份小秦艽样品进行DNA提取,选取合适引物进行PCR扩增并测序,测序结果使用BioEdit、CLC Sequence Viewer 8及MEGA 11.0软件进行处理后,分析遗传变异并构建系统发育树。结果:聚类分析结果表明,62份小秦艽样品主要分为两支,编号为BT1(采自包头市白云鄂博巴润园区东南1 km处)和BY1(采自巴彦淖尔盟乌拉特前旗阿嘎如泰苏木大桦背)的样品聚为一个小分支,其他60份样品聚为一个大分支,说明各分支内存在较近的亲缘关系,遗传变异过程相似;在相似的遗传变异条件下,样品中龙胆苦苷含量相近,排除环境主要生态因子的影响,推测小秦艽样品的龙胆苦苷含量可能与遗传变异过程相关;样品BT1和HH4(呼和浩特市和林格尔县太平夭),BT1和AL1(阿拉善左旗巴润别立镇贺兰山雪岭子沟)的遗传距离最大,因其地理距离较大,推测地理环境因素在一定程度上影响了小秦艽的生物进化过程;序列中的变异位点为129个;各样品ITS序列的Kimura-2-parameter(K2P)遗传距离范围为0.0000~0.2632,平均值为0.0494。结论:DNA分子技术—ITS序列有助于研究药用植物小秦艽种质资源遗传多样性,了解种内遗传变异的大小及其与环境的关系,从而保护及发展小秦艽种源优势。 展开更多
关键词 小秦艽 内转录间隔区(its) 鉴定 遗传多样性
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新颖栽培丹参材料的rDNA内外转录间隔区(ITS和ETS)分子标记鉴定
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作者 尹艳艳 任瑞花 +3 位作者 冯洁 李海宾 王锐钦 李关荣 《中国科技论文在线精品论文》 2023年第3期289-300,共12页
本研究对前期发现的2个新颖多年生大紫花单株(V-HNYZ-bV-1和W-SXXA-bV-1)和1个二年生白花丹参(Salvia miltiorrhiza)栽培居群(W-SCHY-W-1)材料,进行了基于其rDNA内、外转录间隔区(ITS和ETS)的分子标记鉴定。结果表明:W-SXXA-bV-1和V-HNY... 本研究对前期发现的2个新颖多年生大紫花单株(V-HNYZ-bV-1和W-SXXA-bV-1)和1个二年生白花丹参(Salvia miltiorrhiza)栽培居群(W-SCHY-W-1)材料,进行了基于其rDNA内、外转录间隔区(ITS和ETS)的分子标记鉴定。结果表明:W-SXXA-bV-1和V-HNYZ-bV-1的ITS的GC含量均较高,W-SCHY-W-1的ITS和ETS的GC含量最低;新颖材料W-SXXA-bV-1和V-HNYZ-bV-1的ITS序列变异率较高,均高于W-SCHY-W-1,而对于ETS序列,W-SXXA-bV-1和V-HNYZ-bV-1接近(7.1%~6.5%),但低于W-SCHY-W-1(8.2%);W-SXXA-bV-1与V-HNYZ-bV-1亲缘关系较近,W-SXXA-bV-1、V-HNYZ-bV-1和W-SCHY-W-1均与Q-DZH-V-4亲缘关系较远,V-HNYZ-V-1与Q-DZH-V-4亲缘关系很近。上述结果与栽培形态观察结果都高度一致表明:W-SXXA-V-1和V-HNYZ-V-1是康定或甘西鼠尾草,新颖单株材料W-SXXA-bV-1可能为W-SXXA-V-1的突变体,V-HNYZ-V-1和Q-DZH-V-4同为荔枝草,V-HNYZ-bV-1可能为混杂在V-HNYZ-V-1中的康定或西藏鼠尾草,与W-SXXA-bV-1非常相似。W-SCHY-W-1为粘毛鼠尾草。 展开更多
关键词 分子生物学 栽培丹参 内转录间隔区(its) 外转录间隔区(ETS) 分子标记鉴定 遗传多样性
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The homology analysis of internal transcribed spacer sequence of ribosomal DNA in common dermatophytes
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作者 QIANG WANG ZHAO HUI JI +6 位作者 HOU MIN LI LI JUAN ZHANG WEI LIU ZHE WAN XIAO HONG WANG DUAN LI WANG RUO YU LI 《Journal of Microbiology and Immunology》 2006年第2期110-116,共7页
In order to analyze the sequences of the internal transcribed spacer (ITS) including the 5.8 S ribosomal DNA (rDNA) of common dermatophytes, so as to obtain a rapid and accurate method to identify the species of d... In order to analyze the sequences of the internal transcribed spacer (ITS) including the 5.8 S ribosomal DNA (rDNA) of common dermatophytes, so as to obtain a rapid and accurate method to identify the species of dermatophytes and to establish the phylogenetic tree of these species to understand their relationship, 16 strains of dermatophytes were collected and preliminarily identified by morphological characteristics. General primers for fungi ITS1 and ITS4 were used to amplify the ITS rDNA of each strains with PCR. The PCR products after purification were sequenced directly and were analyzed through internet. In the results, 11 strains were identified by means of morphological features, among which 5 strains were Trichophyton, 5 strains were Microsporum and 1 was Epidermophytoa, which was consistent with the results by molecular biology. In the 5 unidentifiable strains, 1 strain was proved to be Chrysosporium by molecular biology. These strains studied could be divided into 3 different classes as indicated in the analysis of the phylogenetic tree of the sequences in ITS, which were quite different from those of morphological classification. It is evident from the above observations that the molecular method of analysis on the ITS sequences is a rapid, highly sensitive and accurate approach for the detection of dematophyte species, however, it still exhibits some limitations needing the supplementation with morphological identification. 展开更多
关键词 Dermatophyte internal transcribed spacer sequence identification Phylogenetic tree
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基于ISSR-PCR体系鉴别樟芝单核体交配型
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作者 李晓晖 盖舒萍 +5 位作者 汪雯翰 琚建伟 张守兵 丁保安 李燕 贾薇 《中国食用菌》 2024年第2期68-75,共8页
通过原生质体单核化技术获得樟芝单核体,基于内转录间隔区(internal transcribed spacer,ITS)序列进行鉴定,采用14个引物对简单重复序列区间(inter-simple sequence repeats,ISSR)进行多态性扩增,筛选条带清晰、重复性好的引物用于樟芝... 通过原生质体单核化技术获得樟芝单核体,基于内转录间隔区(internal transcribed spacer,ITS)序列进行鉴定,采用14个引物对简单重复序列区间(inter-simple sequence repeats,ISSR)进行多态性扩增,筛选条带清晰、重复性好的引物用于樟芝单核体的交配型鉴定。结果表明,通过原生质体单核化技术获得31个樟芝单核体,经ITS序列分析确定获得的单核体为樟芝。以单核体S2、S10、S14、S27的DNA为模板,对14条ISSR引物进行初步筛选,得到4个条带清晰、重复性好的引物P7、P9、P21、P25用于交配型鉴定。单核体S9和S25为同一交配型,两者与S2为不同交配型,通过镜检进一步验证S9、S25可以与S2形成具有锁状联合的双核菌株。该方法可明显缩短樟芝单核体交配型的鉴定时间。 展开更多
关键词 樟芝 单核体 交配型 ISSR its
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腐烂茎线虫不同地理种群ITS区序列比对及系统发育 被引量:14
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作者 王金成 季镭 +2 位作者 黄国明 杨秀丽 林茂松 《河北农业大学学报》 CAS CSCD 北大核心 2007年第5期79-83,98,共6页
为弄清我国腐烂茎线虫(Ditylenchus destructor)不同地理种群ITS(Internal transcribed spacer)区之间的碱基差异及系统发育关系,本研究通过网络软件Clustalw1.83对腐烂茎线虫的核糖体ITS区核酸序列进行了比对,结果发现腐烂茎线虫的8个... 为弄清我国腐烂茎线虫(Ditylenchus destructor)不同地理种群ITS(Internal transcribed spacer)区之间的碱基差异及系统发育关系,本研究通过网络软件Clustalw1.83对腐烂茎线虫的核糖体ITS区核酸序列进行了比对,结果发现腐烂茎线虫的8个种群中,DEll、DEly、DEAY987007三个种群(I组)内部之间的碱基差异在1%以内,其它的5个种群(II组)之间的差异为0~1%,而I组与II组种群之间的差异达到了15%(根据ITS1+5.8s+ITS2序列)或20%(根据ITS1+ITS2序列)。这说明我国腐烂茎线虫很可能是1个复合种。根据ITS区核酸序列构建的系统发育图同样显示,我国腐烂茎线虫的7个地理种群明显分为2个分支A和B。 展开更多
关键词 腐烂茎线虫 鳞球茎茎线虫 食菌茎线虫 its(internal transcribed spacer) 系统发育关系
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苏皖产大戟属药用植物rDNA的ITS序列分析 被引量:22
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作者 蒋继宏 孟娜 +2 位作者 曹小迎 周守标 戴传超 《中草药》 CAS CSCD 北大核心 2005年第6期900-902,共3页
目的研究苏皖产大戟属内6种药用植物的ITS长度的变异,为探讨大戟属植物的系统演化关系和大戟属植物鉴定提供DNA分子证据.方法利用PCR技术对大戟属植物的rDNA ITS区碱基序列进行测定.结果这6种大戟属植物的ITS1的长度范围为255~262 bp,I... 目的研究苏皖产大戟属内6种药用植物的ITS长度的变异,为探讨大戟属植物的系统演化关系和大戟属植物鉴定提供DNA分子证据.方法利用PCR技术对大戟属植物的rDNA ITS区碱基序列进行测定.结果这6种大戟属植物的ITS1的长度范围为255~262 bp,ITS2的长度范围为214~236 bp.运用Mega2软件进行的系统分析得到大戟属内6种植物的系统进化树.这一分析结果与来自形态学的研究结果相吻合.结论此法可用于大戟属植物种间及真伪品鉴别. 展开更多
关键词 药用植物 its序列分析 rDNAits 大戟属植物 DNA分子 PCR技术 系统进化树 植物鉴定 碱基序列 its1 its2 系统分析 分析结果 伪品鉴别 长度 形态学
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弓形虫ITS及5.8S序列的PCR扩增、克隆及分析 被引量:16
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作者 翁亚彪 谢德华 +4 位作者 林瑞庆 李华文 张德林 吴绍强 朱兴全 《畜牧兽医学报》 CAS CSCD 北大核心 2005年第1期70-73,共4页
通过对国内来源于不同宿主的ZS人株、SH人株、CN猪株、QH绵羊株4个弓形虫虫株,以及国际标准强毒株RH株的核糖体DNA内转录间隔区(ITS)及5 8SDNA序列进行PCR扩增、克隆、测序和序列分析,旨在对国内不同宿主间弓形虫虫株的遗传变异情况进... 通过对国内来源于不同宿主的ZS人株、SH人株、CN猪株、QH绵羊株4个弓形虫虫株,以及国际标准强毒株RH株的核糖体DNA内转录间隔区(ITS)及5 8SDNA序列进行PCR扩增、克隆、测序和序列分析,旨在对国内不同宿主间弓形虫虫株的遗传变异情况进行分析和验证,为分子遗传学和分子诊断学研究提供资料。结果显示:QH绵羊株、ZS人株、SH人株、CN猪株的ITS及5 8S序列完全一致,且与GenBank上注册RH株的ITS及5 8S序列也一致;仅实验室传代保存的RH株的ITS2序列与其它4株的ITS2有2个碱基的差异。结果表明ITS可作为分子标记用于弓形虫与其它原虫的种间鉴定,但不适合用于弓形虫种内遗传变异的研究。 展开更多
关键词 弓形虫 SH 序列 RH 克隆 宿主 CN 绵羊 PCR扩增 强毒株
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根肿病菌核糖体基因ITS区段的克隆测序及其在检测中的应用 被引量:40
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作者 杨佩文 李家瑞 +2 位作者 杨勤忠 曾莉 王群 《云南农业大学学报》 CAS CSCD 2003年第3期228-233,共6页
应用真菌核糖体基因ITS区段通用引物ITS1和ITS4,对十字花科蔬菜根肿病菌(Plasmodiophorabrassicae)rDNA进行PCR扩增,并将扩增到的目的片段克隆到pGEM-T载体上。对重组克隆进行测序和碱基编码结构特点分析,结果表明:十字花科蔬菜根肿病菌... 应用真菌核糖体基因ITS区段通用引物ITS1和ITS4,对十字花科蔬菜根肿病菌(Plasmodiophorabrassicae)rDNA进行PCR扩增,并将扩增到的目的片段克隆到pGEM-T载体上。对重组克隆进行测序和碱基编码结构特点分析,结果表明:十字花科蔬菜根肿病菌ITS1区长141bp,5 8S区长160bp,ITS2区长187bp,rDNA总长为488bp.根据此序列设计一对根肿病菌特异性寡聚核苷酸引物(前引物:5'AGGTGAACCTGCGGAAGGAT3'和后引物:5'TTCAGCGGGTAATCCTACCT3'),应用聚合酶链式反应(polymerasechainreaction,PCR)技术,对分离自十字花科蔬菜(白菜、青菜、甘蓝、芥蓝、花椰菜等)根肿病菌全基因组DNA进行特异性扩增试验。试验结果表明,该对引物能从十字花科根肿病菌全基因组DNA中扩增到约500bp长度的分子片段,而对照菌株和健康对照则无扩增产物。该实验结果对有效追踪根肿病菌在田间的发生动态监测和预测预报提供了重要的信息和手段。 展开更多
关键词 十字花科蔬菜 根肿病菌 核糖体基因its区段 基因克隆 基因测序 基因检测 预测预报 发生动态监测
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中国不同地区蛇床的rDNA ITS序列分析 被引量:47
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作者 蔡金娜 周开亚 +4 位作者 徐珞珊 王峥涛 沈曦 王义权 李晓波 《药学学报》 CAS CSCD 北大核心 2000年第1期56-59,共4页
目的:探讨不同分布区的蛇床Cnidium monnieri 的ITS序列变异与其地理分布和化学成分的相关性。方法:设计2 对引物,Pf+ Pb 及P5-8SITS1+ P5-8SITS2 ,PCR扩增产物纯化后用银染法或A... 目的:探讨不同分布区的蛇床Cnidium monnieri 的ITS序列变异与其地理分布和化学成分的相关性。方法:设计2 对引物,Pf+ Pb 及P5-8SITS1+ P5-8SITS2 ,PCR扩增产物纯化后用银染法或ABI310 测序。结果:得到核糖体DNA中的ITS及5-8SrDNA 完全序列,18S和26SrDNA 部分序列,共约700 bp 。5 个地点样品的ITS1及ITS2 的序列大小分别为210~217 bp 和219 ~224 bp。ITS1 碱基序列的遗传距离0-00 ~1-93% ,ITS2 碱基序列的遗传距离0-46 ~2-34% ,ITS1 较为保守。以NJ法根据ITS2 序列数据重建系统发生树。哈尔滨样品聚为一组,衡水与德州样品和郑州与高淳样品各自聚为一组。结论:ITS2 序列的变异与中国产蛇床的纬度分布相关,而其与蛇床化学型的关系尚需作进一步研究。 展开更多
关键词 蛇床 CDNA 内转录间隔区 序列分析 its
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广西山药炭疽病病原菌的鉴定与ITS序列分析 被引量:41
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作者 朱桂宁 蔡健和 +2 位作者 胡春锦 韦本辉 黄福新 《植物病理学报》 CAS CSCD 北大核心 2007年第6期572-577,共6页
本文对山药炭疽病在广西的危害、症状特点以及病原菌的鉴定进行了研究。2005年从广西5个病区采集的25个标样均分离到类似的分离物,根据病原菌的形态特征和致病性,并结合其rDNA-ITS区域的序列分析,将广西山药炭疽病的病原菌鉴定为胶孢炭... 本文对山药炭疽病在广西的危害、症状特点以及病原菌的鉴定进行了研究。2005年从广西5个病区采集的25个标样均分离到类似的分离物,根据病原菌的形态特征和致病性,并结合其rDNA-ITS区域的序列分析,将广西山药炭疽病的病原菌鉴定为胶孢炭疽菌(Colletotrichum gloeosporioides)。 展开更多
关键词 山药 炭疽病 rDNA—its序列 鉴定
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