首 页网站地图RSS订阅高级搜索保留
生物实验网
设为首页
加入收藏
站长信箱
主页|bio资讯 |DNA实验 |PCR实验 |RNA实验 |蛋白实验 |基本实验技术 |生化与免疫技术 |生物信息学 |细胞生物学 |杂交实验 |学科相关 |交叉领域 |
当前位置: 主页>RNA实验>RNAi> 查看文章详细内容
站内资料搜索
热门关键字: dna  EST  r DNA  pcr  抗体  rt pcr  t dna  tail pcr  PCR sscp  cDNA

相关文章
>什么是RNA interfere
>How do you&nbs
>RNAi载体pSIREN-DNR 
>siRNA用户指南
>哺乳动物细胞中进行RNA干
>RNA interference&nb
>The Easiest Ro
>通过RNAi使基因特异性沉默
>siRNAs结合生物芯片的实验
>siRNAs结合生物芯片的实验
热点文章
RNAi模式图
siRNA用户手册
RNAi在细胞培养中的应用
果蝇RNAi的实验中双链短RN
RNAi实验中双链短RNA(dsR
siRNA实验方法详解
目前已发表文章中RNAi设计
哺乳动物细胞中进行RNA干
MicroRNA and s
The Easiest Ro
siRNA Design
[ 文章来源: | 文章作者: | 发布时间:2006-09-23|  字体: [ ]  

siRNA Design

RNAi target selection rules:

  1. Targeted regions on the cDNA sequence of a targeted gene should be located 50-100 nt downstream of the start codon (ATG).
  2. Search for sequence motif AA(N19)TT or NA(N21), or NAR(N17)YNN, where N is any nucleotide, R is purine (A, G) and Y is pyrimidine (C, U).
  3. Avoid targeting introns, since RNAi only works in the cytoplasm and not within the nucleus.
  4. Avoid sequences with > 50% G+C content.
  5. Avoid stretches of 4 or more nucleotide repeats.
  6. Avoid 5URT and 3UTR, although siRNAs targeting UTRs have successfully induced gene inhibition.
  7. Avoid sequences that share a certain degree of homology with other related or unrelated genes.

How to obtain a cDNA sequence for target selection

Before finding a RNAi target on the gene of your interest, first you have to get its mRNA sequence or sequence accession number as some siRNA design tools can take accession number as input. It is recommended to use the gene's RefSeq from NCBI, since the RefSeq represents non-redundant, curated and validated sequences. RefSeq mRNA sequences have unique accession numbers which start with NM or XM, followed by 6 digits. For example, NM_123456 (curated mRNA sequence) or XM_0123456 (model mRNA sequence predicted by genome sequence analysis). There are several ways of querying RefSeq.

  1. Search LocusLink by gene name or symbol at http://www.ncbi.nlm.nih.gov/LocusLink/. Once the locus of your gene is found, scroll down to the "NCBI Reference Sequence (RefSeq)" section and look for mRNA.  
  2. Search Entrez Gene at http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene, and select the right gene of desired organism. Once the page for the gene is shown, scroll down to the "NCBI Reference Sequence (RefSeq)" and look for mRNA.
  3. Search Nucleotide database using Entrez query tool at  http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Nucleotide and use Entrez Limits settings to restrict your query to the RefSeq database only
    • select "RefSeq" from the "Only from" menu, this restricts the query to the RefSeq collection
    • select "mRNA" from the "Molecule" menu, this restricts the query to mRNA RefSeq records
Homology search
The RNAi targeted region on the mRNA sequence of a gene should not share significant homology with other genes or sequences in the genome, therefore, homology search is essential to minimize off-target effects. Although most siRNA design tools provide BLAST option, some simply use NCBI BLAST tools which sometimes are quite slow. Here are some BLAST tools for homology search.

Examples of RNAi target selection

References

1. Elbashir SM, Harborth J, Lendeckel W, Yalcin A, Weber K, Tuschl T. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature. 2001 May 24;411(6836):494-8.
2. Elbashir SM, Lendeckel W, Tuschl T. RNA interference is mediated by 21- and 22-nucleotide RNAs. Genes Dev. 2001 Jan 15;15(2):188-200.


上一篇:什么是RNA interference(RNAi)   下一篇:How do you synthesize your dsRN
设为首页 - 加入收藏 - 关于我们 - 版权申明 - 程序支持 - 联系方式 - 留言薄 - 会员中心
Power by DedeCms