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7 条 记 录,以下是 1-7
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中药材蛤蚧的特异性PCR鉴定被引量:8
2012年
以线粒体Cytb、COI、12SrRNA、16SrRNA基因序列为基础,探讨特异性PCR技术鉴定蛤蚧及伪品的可行性。本研究以所扩增的16条COI序列为引物设计依据序列设计了1对位点特异性引物COISF,COISR,同时从Gen-Bank上下载30条序列,设计了CytbSF,CytbSR;16S rRNASF,16S rRNASR;12S rRNASF,12S rRNASR另外3对位点特异性引物,因此共用4对位点特异性引物分别扩增蛤蚧及伪品实验样本。结果表明在复性温度为65℃时,4对引物都出现了理想的结果,即蛤蚧正品出现了扩增条带,而伪品没有扩增条带。同时对市售的蛤蚧商品进行了检测,在所供的7号标本中,有4号为蛤蚧正品,其余3号为蛤蚧伪品。本研究所设计的位点特异性引物可快捷、准确的鉴定蛤蚧及伪品,且在药检工作中具有极大的应用前景。
顾海丰夏云徐永莉谷颖乐许尧李力曾晓茂
关键词:特异性引物分子鉴定
蛤蚧及其伪品微型DNA条形码的引物筛选被引量:10
2011年
文章旨在筛选出适合于扩增蛤蚧及伪品微型DNA条形码引物。通过引物设计软件,经过多序列比对,设计了两对引物mini-barcode F2,mini-barcode R2;mini-barcode F3,mini-barcode R3,并用这两对引物和目前已报道的微型条形码引物PCR扩增蛤蚧及伪品61个样本,结果表明mini-barcode F2,mini-barcode R2和mini-barcode F3,mini-barcode R3这两对引物的PCR扩增成功率分别为100%和90%,而目前已报道的微型条形码引物PCR扩增蛤蚧及其伪品得到了长度约500 bp非微型条形码序列片段。因此目前已报道的微型条形码引物不适用于扩增蛤蚧及伪品,该研究筛选出了适合于蛤蚧及伪品的微型条形码引物。
李力顾海丰夏云徐永莉彭锐莫邦辉曾晓茂
关键词:PCR引物
FISH of 5S rDNA and telomeric(TTAGGG)n repeats in normal and translocated populations of the frog Quasipaa boulengeri(Anura,Ranidae)被引量:2
2013年
Quasipaa boulengeri,a spiny frog,is widely distributed in the low mountain regions,around Sichuan Basin.Our previous study revealed five karyotypes,caused by a translocation,that are randomly distributed throughout different populations.5S rDNA and telomere sequence(TTAGGG) n are potential good markers for chromosome identification and karyological evolution.In this study,we examined the sequences of 14 populations using fluorescence in situ hybridization(FISH) to detect if there is any variation between karyologically normal and translocated populations.5S rDNA loci were located at the same position on chromosomes 1 in 7 translocated populations.In two of the seven normal populations,5S rDNA also occurred on chromosome 5 in addition to chromosome 1.Our findings further indicate that the 5S rDNA on No.1 most likely represents the ancestral condition,while the minor loci represent the derived state.Signal density variations of the 5S rDNA were observed beteween homologous chromosomes or sister chromatids of pair 1 in both normal and translocated populations.Telomere sequences were identically located on all ends of the 26 chromosomes in seven rearranged populations,however,no ITSs were observed on the translocated chromosomes 1 and 6.Two of the six normal populations were found to contain ITSs which indicates that populations with translocation events diverged prior to those with ITSs rearrangements.In the KKS and BF populations,the ITSs of chromosome 3 are not always found on both homologues.Inter-chromosomal signal strength of telomeric sequences commonly differs within all populations.
QING LiYanXIA YunZHENG YuChiZENG XiaoMao
关键词:端粒序列无尾目
Catalogue of the Type Specimens of Amphibians and Reptiles in the Herpetological Museum of the Chengdu Institute of Biology,Chinese Academy of Sciences:Ⅱ.Hynobiidae (Amphibia,Urodela)被引量:2
2012年
In order to facilitate herpetological research for herpetologists in and outside of China,we will report all the type specimens of Amphibia and Reptilia deposited in the Herpetological Museum of the Chengdu Institute of Biology(CIB),Chinese Academy of Sciences(CAS) in series. This report focuses on the type specimens of the family Hynobiidae of Urodela in Amphibia,which comprises seven species. Each entry provides the genus name,species name,information of the original description,the catalog number of holotype,sex,type locality,information of allotype(if any) and paratype,number and distribution of deposited specimens,and comments where they are appropriate.
Jianli XIONGYueying CHENXiaomao ZENG
关键词:CATALOGUEMUSEUM
DNA条形码在蛤蚧真伪品鉴定中的前景被引量:10
2010年
蛤蚧作为重要的动物药材,在咳嗽、哮喘、胆结石及性功能障碍上有治疗功效。由于药材蛤蚧原动物大壁虎(Gekkogecko)物种数量逐年减少,不能满足中药市场的需求而出现了众多伪品。文章概述了近二十年来蛤蚧及其伪品的鉴别研究情况,介绍了传统性状、显微、理化和现代分子生物学技术等鉴定方法,并比较总结了各种方法在蛤蚧真伪品鉴定中的特点。在此基础上,引入物种识别学科前沿-DNA条形码(DNABarcoding)技术,并阐述了其在蛤蚧真伪品鉴定中的优势和应用前景。
夏云胡陆军莫帮辉缪剑华徐永莉张月云曾晓茂李力
关键词:蛤蚧DNA条形码中药鉴定
Discovery of an Internasal Bone in Hynobius maoershanensis(Urodela:Hynobiidae)被引量:2
2011年
Internasal bones have generally been recorded in teleostean and tetrapod fossils,being absent in most extant vertebrates.Presently,there has been one case of the internasal bone discovered in a living salamander,Pseudohynobius puxiongensis(Caudata:Hynobiidae).The second case discovered in living salamanders is reported in this article,which is present in one of five specimens of Hynobius maoershanensis,a species endemic to China.This case is again regarded as individual variation.Thus,the presence of an"internasal bone"may represent intraspecific variation and is thus a misleading taxonomic character.
Jianli XIONGXiuying LIUXiaomao ZENG
关键词:小鲵科种内变异蝾螈
棘腹蛙(Quasipaa boulengeri)易位和非易位种群5SrDNA及端粒序列(TTAGGG)_n的荧光原位杂交比较分析被引量:1
2013年
棘腹蛙广泛分布于四川盆地周边及毗邻的低山区.我们前期的研究显示,在棘腹蛙中存在5种由易位引起的核型,这些核型随机分布在不同的种群中.5S rDNA和端粒序列(TTAGGG)n是染色体鉴定和演化研究的良好标记.本研究采用荧光原位杂交的方法,对棘腹蛙的14个种群进行了分析,目的在于了解易位和非易位种群间在这两种序列上是否存在差异.7个易位种群中,5S rDNA杂交信号位于所有核型1号染色体长臂近着丝粒区.7个非易位种群中,除1号染色体上的信号外,在BZ和BFX两个种群的5号染色体的长臂末端也检测到了微弱的信号,推测1号染色体上的5S rDNA位点可能代表祖先状态,而5号染色体上的位点则代表衍生状态.在大部分种群中,1号同源染色体间或是姐妹染色单体间的5S rDNA信号强度有差异.7个易位种群中,端粒序列位于所有染色体的末端,相互易位的1和6号染色体上未见内端粒序列(ITSs).6个核型正常的种群中,除端部端粒信号外,BF和KKS种群的部分个体的3号染色体长臂有微弱的ITSs信号,推测棘腹蛙中发生易位的种群较具ITSs的种群分化更早.在某些种群中,部分大染色体上的端部端粒信号较小染色体上弱.
卿立燕夏云郑渝池曾晓茂
关键词:棘腹蛙RDNA
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