中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Identification of Crassostrea ariakensis and related oysters by multiplex species-specific PCR

文献类型:期刊论文

作者Wang, Haiyan1,2; Guo, Ximing1
刊名JOURNAL OF SHELLFISH RESEARCH
出版日期2008-05-01
卷号27期号:3页码:481-487
关键词Oyster Identification Species-specific Pcr Cytochrome Oxidase i 28s Rrna Ostreidae Suminoe Oyster Crassostrea Ariakensis
ISSN号0730-8000
文献子类Article
英文摘要Genetic markers are needed for rapid and reliable identification of oysters. In this study, we developed multiplex genus- and species-specific PCR markers for the identification of oysters from China. We used the mitochondrial cytochrome oxidase I (COI) and nuclear 28S ribosomal RNA genes for marker development. DNA sequences from different species were obtained from GenBank or by direct sequencing. Sequences were aligned, and genus- and species-specific nucleotides were identified. Primers were designed for genus/species-specific amplification to generate fragments of different sizes. A multiplex set of genus- and species-specific primers from the 28S gene was able to separate C. ariakensis and C. hongkongensis from other species and assign oysters to four genera. A set of species-specific COI primers provided positive identification of all five Crassostrea species from China, C. ariakensis, C. hongkongensis, C. angulata, C. gigas, and C. sikamea in a single PCR. The multiplex PCR assays do not require fluorescence-labeling or post-PCR enzyme digestion, providing a simple, fast and reliable method for the identification of oysters from China.; Genetic markers are needed for rapid and reliable identification of oysters. In this study, we developed multiplex genus- and species-specific PCR markers for the identification of oysters from China. We used the mitochondrial cytochrome oxidase I (COI) and nuclear 28S ribosomal RNA genes for marker development. DNA sequences from different species were obtained from GenBank or by direct sequencing. Sequences were aligned, and genus- and species-specific nucleotides were identified. Primers were designed for genus/species-specific amplification to generate fragments of different sizes. A multiplex set of genus- and species-specific primers from the 28S gene was able to separate C. ariakensis and C. hongkongensis from other species and assign oysters to four genera. A set of species-specific COI primers provided positive identification of all five Crassostrea species from China, C. ariakensis, C. hongkongensis, C. angulata, C. gigas, and C. sikamea in a single PCR. The multiplex PCR assays do not require fluorescence-labeling or post-PCR enzyme digestion, providing a simple, fast and reliable method for the identification of oysters from China.
语种英语
WOS记录号WOS:000256117200001
公开日期2010-12-30
源URL[http://ir.qdio.ac.cn/handle/337002/6331]  
专题海洋研究所_海洋生物技术研发中心
作者单位1.Rutgers State Univ, Inst Marine & Coastal Sci, Haskin Shellfish Res Lab, Piscataway, NJ 08349 USA
2.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Shandong, Peoples R China
推荐引用方式
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Wang, Haiyan,Guo, Ximing. Identification of Crassostrea ariakensis and related oysters by multiplex species-specific PCR[J]. JOURNAL OF SHELLFISH RESEARCH,2008,27(3):481-487.
APA Wang, Haiyan,&Guo, Ximing.(2008).Identification of Crassostrea ariakensis and related oysters by multiplex species-specific PCR.JOURNAL OF SHELLFISH RESEARCH,27(3),481-487.
MLA Wang, Haiyan,et al."Identification of Crassostrea ariakensis and related oysters by multiplex species-specific PCR".JOURNAL OF SHELLFISH RESEARCH 27.3(2008):481-487.

入库方式: OAI收割

来源:海洋研究所

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