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Development of 101 Novel EST-Derived Single Nucleotide Polymorphism Markers for Zhikong Scallop (Chlamys farreri) 被引量:2

Development of 101 Novel EST-Derived Single Nucleotide Polymorphism Markers for Zhikong Scallop (Chlamys farreri)
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摘要 Zhikong scallop(Chlamys farreri) is an important maricultured species in China.Many researches on this species,such as population genetics and QTL fine-mapping,need a large number of molecular markers.In this study,based on the expressed sequence tags(EST),a total of 300 putative single nucleotide polymorphisms(SNPs) were selected and validated using high resolution melting(HRM) technology with unlabeled probe.Of them,101(33.7%) were found to be polymorphic in 48 individuals from 4 populations.Further evaluation with 48 individuals from Qingdao population showed that all the polymorphic loci had two alleles with the minor allele frequency ranged from 0.046 to 0.500.The observed and expected heterozygosities ranged from 0.000 to 0.925 and from 0.089 to 0.505,respectively.Fifteen loci deviated significantly from Hardy-Weinberg equilibrium and significant linkage disequilibrate was detected in one pair of markers.BLASTx gave significant hits for 72 of the 101 polymorphic SNP-containing ESTs.Thirty four polymorphic SNP loci were predicted to be non-synonymous substitutions as they caused either the change of codons(33 SNPs) or pretermination of translation(1 SNP).The markers developed can be used for the population studies and genetic improvement on Zhikong scallop. Zhikong scallop (Chlamys farreri) is an important maricultured species in China. Many researches on this species, such as population genetics and QTL fine-mapping, need a large number of molecular markers. In this study, based on the ex- pressed sequence tags (EST), a total of 300 putative single nucleotide polymorphisms (SNPs) were selected and validated using high resolution melting (HRM) technology with unlabeled probe. Of them, 101 (33.7%) were found to be polymorphic in 48 indi- viduals from 4 populations. Further evaluation with 48 individuals from Qingdao population showed that all the polymorphic loci had two alleles with the minor allele frequency ranged from 0.046 to 0.500. The observed and expected heterozygosities ranged from 0.000 to 0.925 and from 0.089 to 0.505, respectively. Fifteen loci deviated significantly from Hardy-Weinberg equilibrium and significant linkage disequilibrate was detected in one pair of markers. BLASTx gave significant hits for 72 of the 101 poly- morphic SNP- containing ESTs. Thirty four polymorphic SNP loci were predicted to be non-synonymous substitutions as they caused either the change of codons (33 SNPs) or pretermination of translation (1 SNP). The markers developed can be used for the population studies and genetic improvement on Zhikong scallop.
出处 《Journal of Ocean University of China》 SCIE CAS 2013年第3期403-412,共10页 中国海洋大学学报(英文版)
基金 the National Natural Science Foundation of China(No.31130054) the National Basic Research Program of China(973 Program,2010CB126406 and 2010CB126402) the National High-Tech R&D Program(863 Program,2012AA10A402 and 2012AA10A405) the National Key Technology R&D Program(2011BAD13B06) the Earmarked Fund for Modern Agro-Industry Technology Research
关键词 Zhikong scallop Chlamysfarreri SNP EST HRM 单核苷酸多态性 多态性标记 栉孔扇贝 EST序列 衍生 海水养殖品种 等位基因 SNP
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  • 1Choi, Y. S., Lee, K. S., and Park, D. H., 2005. Single nucleo- tide polymorphism (SNP) detection using microelectrode biochip array. Journal of Micromechanics and Microengi- neering, 15 (10): 1938.
  • 2Dames, S., Margraf, R. L., Pattison, D. C., Wittwer, C. T., and Voelkerding, K. V., 2007. Characterization of aberrant melt- ing peaks in unlabeled probe assays. Journal of Molecular Diagnostics, 9 (3): 290-296.
  • 3Garvin, M. R., Saitoh, K., and Gharrett, A. J., 2010. Applica- tion of single nucleotide polymorphisms to non-model spe-cies: a technical review. Molecular Ecology Resources, 10: 915-934.
  • 4Guo, X., Ford, S. E., and Zhang, F., 1999. Molluscan auqacul- ture in China. Journal of Shellfish Research, 18 ( 1 ): 19-31.
  • 5Jiang, G. D., Li, J. Q., Li, L., Zhang, L. L., and Bao, Z. M., 2011. Development of 44 gene-based SNP markers in Zhikong scallop, Chlamys farreri. Conservation Genetic Re- sources, 3: 659-663.
  • 6Li, H., Zhu, D., Gao, X., Li, Y., Wang, J., and He, C., 2010. Mining single nueleotide polymorphisms from EST data of hard clam Meretrix meretrix. Conservation Genetic Re- sources, 2: 69-72.
  • 7Liew, M., Seipp, M., Durtschi, J., Margraf, R. L., Dames, S., Erali, M., Voelkerding, K., and Wittwer, C., 2007. Closed- tube SNP genotyping without labeled probes/a comparison between unlabeled probe and amplicon melting. American Jounal of Clinical Pathology, 127: 341-348.
  • 8Liu, W. D., Li, H. J., Bao, X. B., He, C. B., Li, W. J., and Shan, Z. G., 2011. The first set of EST-derived single nucleotide polymorphism markers for Japanese scallop, Patinopecten yessonsis. Journal of the Worm Aquaculture Society, 42 (3): 456-461.
  • 9Liu, Z., Karsi, A., and Dunham, R. A., 1999. Development of polymorphic EST markers suitable for genetic linkage map- ping of Catfish. Marine Biotechnology, 1 (5): 437-447.
  • 10Moen, T., Hayes, B., Nilsen, F., Delghandi, M., Fjalestad, K. T., Fevolden, S. E., Berg, P. R., and Lien, S., 2008. Identification and characterization of novel SNP markers in Atlantic cod: Evidence for directional selection. BMC Genetics, 9:18.

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