MISC

2009年

Knockdown of Severe Acute Respiratory Syndrome Corona Virus (SARS-CoV) Genes by Small Interfering RNA (siRNA) Using siRNA-expression Vectors and Synthetic Double-stranded RNA (dsRNA) as a Model for siRNA Design

Genes and Environment
  • Shizuyo Sutou
  • ,
  • Miho Kunishi
  • ,
  • Toshiyuki Kudo
  • ,
  • Kenji Kawano
  • ,
  • Yasuomi Takagi
  • ,
  • Malgorzata Sierant
  • ,
  • Masayuki Sano
  • ,
  • Makoto Miyagishi

31
1
開始ページ
15
終了ページ
23
記述言語
英語
掲載種別
DOI
10.3123/jemsge.31.15

While offering the promise of therapeutic use in the future, RNA interference (RNAi) technology is useful to knock down genes posttranscriptionally. We attempted to knock down severe acute respiratory syndrome (SARS)-corona virus (Cov) genes using small interfering RNA (siRNA) employing siRNA-expression vectors and synthetic double-stranded RNA (dsRNA) as a model for effective siRNA design. First, we selected three target sites without mutations among 15 SARS-Cov strains using a prediction algorithm and constructed three siRNA-expression vectors. Using a pGL3 vector, we constructed three corresponding model target vectors to the firefly luciferase gene (Fluc), to which the model targets were connected. Using Renilla luciferase gene (Rluc) as the internal control, the three siRNA vectors knocked down the targets, providing effective target sequences. Almost identical results were obtained when Rluc was integrated into the pGL3-Fluc target vector. Next, effective structures of synthetic doublestranded RNA (dsRNA) were investigated using two targets. In all, six RNAs per target were synthesized: complementary sense and antisense 19-mer core RNAs
sense 21-mer RNAs having a 2-nucleotide (nt) match or unmatch overhang at the 3'-end
and antisense 21-mer RNAs having a 2-nt match or unmatch overhang at the 3'-end. The six RNAs provided nine species of dsRNAs (a blunt 19-mer duplex, a total of 4 19-mer/21-mer duplexes with a match or unmatch 2-nt overhang at the 3'- end of the sense or antisense strand, 4 21-mer/21-mer duplexes with match or unmatch 2-nt overhang at both ends) in combination. Targets were sense or antisense sequences. Generally, 19-mer/21-mer dsRNA with a match 2-nt overhang at the 3'-end of the antisense strand showed the highest activity, irrespective of the thermodynamic stabilities at terminalends, suggesting that the 2-nt overhang is more critical than thermodynamic stabilities to select the antisense strand to the RNA-induced silencing complex (RISC). Key words: SARS-CoV, siRNA, RNAi, thermodynamic stability, 3'-end overhang. © 2009, The Japanese Environmental Mutagen Society. All rights reserved.

リンク情報
DOI
https://doi.org/10.3123/jemsge.31.15
CiNii Articles
http://ci.nii.ac.jp/naid/110007138017
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85024291618&origin=inward 本文へのリンクあり
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85024291618&origin=inward
ID情報
  • DOI : 10.3123/jemsge.31.15
  • ISSN : 1880-7062
  • ISSN : 1880-7046
  • eISSN : 1880-7062
  • CiNii Articles ID : 110007138017
  • SCOPUS ID : 85024291618

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