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三地钉螺线粒体DNA两个分子的遗传变异研究 被引量:11

Genetic Variation of Two Mitochondrial DNA Molecules from Three Isolates of Oncomelania hupensis
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摘要 目的分析广西、云南、湖南三地钉螺线粒体DNA细胞色素C氧化酶Ⅰ(CO1)基因和细胞色素氧化酶b(Cytb)基因的遗传变异。方法收集广西靖西、云南洱源和湖南岳阳三地钉螺,提取其基因组DNA,PCR法扩增线粒体CO1和Cytb基因并测序。用ClustalW(1.82)软件对所测基因序列排序,用MEGA(3.1)计算其碱基组成、转换及颠换;用Kimura双参数法计算遗传距离,用非加权组平均法(UPGMA)和最大简约法(MP)构建系统发生树。结果PCR扩增获得CO1和Cytb基因大小分别约为700及600bp(含两侧引物)。三地钉螺CO1基因中共检测到106个多态性位点,约占核苷酸总数的15.9%,Cytb基因中多态性位点为165个,约占核苷酸总数的28.5%。广西靖西与湖南岳阳、广西靖西与云南洱源的钉螺CO1基因和Cytb基因的遗传距离分别为0.051、0.158和0.031、0.405。根据CO1和Cytb的基因序列,用上述两种方法构建的系统发生树结果均一致。广西靖西与湖南岳阳的钉螺同属一个支系,云南洱源钉螺单独形成另一支系。结论广西、湖南和云南的钉螺CO1和Cytb基因总体上具有相对丰富的多态性。 Objective To study the genetic variation of two mitochondrial DNA molecules (CO1 and Cytb gene) of Oncomelania hupensis isolated from different areas. Methods Snails were collected from Jingxi of Guangxi, Yueyang of Hunan and Eryuan of Yunnan. Genomic DNA was extracted from the snails, Col and Cytb gene fragments were amplified by PCR, then purified and sequenced. Sequences of each isolates were edited by using Clustal W (1.82) software, and the nucleotide composition, transition and transversion were accounted by using MEGA (3.1) software. The genetic distances were computed with Kimura method and phylogenetic trees were constructed with UPGMA and MP method respectively. Results CO1 and Cytb gene fragments were about 700 bp and 600 bp (including 2 primers) respectively. A total of 106 mutation spots (15.9%) were tested in CO1 homological nucleotides, and 165 mutation spots (28.5%) were tested in Cytb homological nucleotides. The distance matrix between Guangxi isolate and Hunan isolate was 0.051 and 0.031 for CO1 gene and Cytb gene respectively; while that between Guangxi and Yunnan isolates was 0.158 and 0.405 respectively. Phylogenetic trees constructed by UPGMA and MP took on the similar topo-structure: isolates of Guangxi and Hunan clustered into one group, while the Yunnan isolate exhibited as another group. Conclusion Oncomelania hupensis in Guangxi, Hunan and Yunnan are of relatively rich polymorphism in CO1 and Cytb genes in general.
出处 《中国寄生虫学与寄生虫病杂志》 CAS CSCD 北大核心 2007年第6期474-477,共4页 Chinese Journal of Parasitology and Parasitic Diseases
基金 广西CDC医药卫生科研基金(No.20030005)~~
关键词 钉螺 细胞色素C氧化酶Ⅰ基因 细胞色素氧化酶b基因 遗传变异 Oncomelania hupensis CO1 gene Cytb gene Gene variation
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参考文献8

  • 1Davis GM, Wilke T, Spolsky C, et al. Cytochrome oxidase 1-based phylogenetic relationships among the Pomatiopsidae, Hydrobiidae, Rissoidae and Truncatellidae ( Gastropoda: Caenogastropoda: rissoacea) [J] . Malacologia, 1998, 40 (1-2): 251-266.
  • 2Spolsky C, Davis GM, Zhang Y. Sequencing methodology and phylogenetic analysis: cytochrome b gene sequence reveals significant diversity in Chinese populations of Oncomelania (Ggastropoda: Pomatiopsidae)[J]. Malacologia, 1996, 38 (1-2): 213-221.
  • 3Wilke T, Davis GM, Chen CE, et al. Oncomelania hupensis (Gastropoda: Rissoodiea) in eastern China: molecular phylogeny, population structure, and ecology[J]. Acta Trop, 2000, 77: 215-227.
  • 4韩庆霞,牛安欧,李金木.不同地域株湖北钉螺CO1基因的差异研究[J].中国人兽共患病杂志,2005,21(4):320-322. 被引量:12
  • 5石朝辉,邱持平,夏明仪,冯正,George M.Davis.湖北省庙河地区钉螺细胞色素C氧化酶1基因差异的研究[J].中国寄生虫学与寄生虫病杂志,2001,19(1):41-44. 被引量:29
  • 6许静,郑江.中国大陆不同地区光壳钉螺遗传多样性的RAPD分析[J].中国血吸虫病防治杂志,2003,15(4):251-254. 被引量:10
  • 7Pauplin Y. Direct calculation of a tree length using a distance matrix[J]. J Mol Evol, 2000, 51: 41-47.
  • 8Kimball RT, Braun EL, Zwartjes PW, et al. A molecular phylogeny of the pheasants and partridges suggests that these lineages are not monophyletic[J]. Mol Phylog Evol, 1999, 11: 38-54.

二级参考文献19

  • 1周晓农,孙乐平,洪青标,徐秋,吴中兴,陆安生,ThomasK.Kristensen.中国大陆钉螺种群遗传学研究 Ⅰ.种群遗传变异[J].中国血吸虫病防治杂志,1995,7(2):67-71. 被引量:24
  • 2刘蓉,牛安欧,李莉.用RAPD技术对湖北钉螺遗传变异的研究[J].中国寄生虫病防治杂志,2004,17(3):136-139. 被引量:13
  • 3何毅勋.中国大陆日本血吸虫品系的研究——ⅩⅢ.总结[J].中国寄生虫学与寄生虫病杂志,1993,11(2):93-97. 被引量:23
  • 4William JG, Kubelik AR, Livak KT,et al. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers[J].Nucleic Acids Res, 1990, 18(22) : 6531--6535.
  • 5Welsh J, McCkelland M. Fingerprinting genome using PCR with arbitrary primers[J]. Mol Ecol, 1990, 18(24): 7213--7218.
  • 6Spolsky CM, Davis GM, Zhang Y. Sequencing methodology and phylogenetic analysis: cytochrome b gene sequence reveals significant diversity in Chinese populations of Oncomelania (Gastropoda: Pomatiopsidae) [J]. Malacologia, 1996, 38(1 -- 2) :213--221.
  • 7Nei M. Mathematical model for studying genetic variation in terms of restriction endonucleases [J]. Proc Natl Acad Sci,1979, 76:5269--5273.
  • 8Black Iv WC, Duteau NM, Puterka GJ, et al. Use of the random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) to detect DNA polymorphisms in aphids (Homoptera : Aphididae) [J]. Bull Entomol Res, 1992, 82(2) : 151--159.
  • 9Larson S. E. , Anderson PC, Miller AN, et al. Use of RAPD-PCR to differentiate genetically defined genetics of an intermediate host of Schistosoma mansoni , Biomphalaria glabrata [J]. J Parasitol, 1996, 82(2):237-244.
  • 10Davis GM, Zhang Y, Guo YH, et al. Population genetics and systematic status of Oncomelania hupensis (Gastropoda:Pomatiopsidae) throughout China [J]. Malacologia, 1995, 37(1):133--156.

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