文蛤肠、外套膜和肝胰脏组织 cDNA 文库构建及其 ESTs 序列分析
DOI:
CSTR:
作者:
作者单位:

1. 辽宁省海洋水产科学研究院,辽宁省海洋水产分子生物学重点实验室,大连 116023;2. 辽宁师范大学 生命科学学院,大连 116029

作者简介:

通讯作者:

中图分类号:

基金项目:


Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    2.10×106,重组率高于 1 000 bp 3 168 ESTs1 0051 005ContigsSingletons,外套膜:个),占总数

    Abstract:

    mantle and hepatopancreas of hard clam were constructed with SMART cDNA Library Construction Kit. The libraries have a high titer of 2.10×10and 1.60×10respectively. The recombined efficiency of each cDNA library exceeded 95 %. The all insert sizes of intestine library were over 1 kband the insert sizes over 1 kb in the mantle and hepatopancreas libraries were over 87.5%. Atotal of 3 168 clones of the libraries were randomly picked and sequenced from the 5 ′end of the cDNAs using a M13 universal primerand 3 029 raw sequences of the ESTs were processed and then assembled into 1 796 unigene involving 306 contigs and 1 490 singletons. Blastx analysis showed that 696 unigenes235 for mantle and 245 for hepatopancreasEvalueG10 to genes with known or putative functions in GenBank.The sequences containing microsatellite DNA accounted for 3.1% of all ESTs indicating that SSR sequences were rich in the ESTs of hard clam.

    参考文献
    相似文献
    引证文献
引用本文

高祥刚,李云峰,宋文涛,王健,傅立元,刘卫东,鲍相渤,赫崇波.文蛤肠、外套膜和肝胰脏组织 cDNA 文库构建及其 ESTs 序列分析[J].中国水产科学,2010,17(2):0-
.[J]. Journal of Fishery Sciences of China,2010,17(2):0-

复制
相关视频

分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2010-03-30
  • 出版日期:
文章二维码