Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (466K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (29)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Zhou, Y.
Right arrow Articles by Jin, D.-Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhou, Y.
Right arrow Articles by Jin, D.-Y.
Related Collections
Right arrow Monitoring gene expression
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2002, Vol. 30, No. 7 1664-1669
© 2002 Oxford University Press

Post-transcriptional suppression of gene expression in Xenopus embryos by small interfering RNA

Yuan Zhou1, Yick-Pang Ching1, Kin Hang Kok2, Hsiang-fu Kung1 and Dong-Yan Jin1,2,*

1Institute of Molecular Biology and 2Department of Biochemistry, The University of Hong Kong, Pokfulam, Hong Kong SAR, China

Double-stranded RNA (dsRNA) induces gene-specific silencing in organisms from fungi to animals, a phenomenon known as RNA interference (RNAi). RNAi represents an evolutionarily conserved system to protect against aberrant expression of genes and a powerful tool for gene manipulation. Despite reports that RNAi can be induced in vertebrates, severe sequence-non-specific effects of long dsRNA have been documented in various systems. It has recently been shown in cultured mammalian cells that small interfering RNAs (siRNAs) of 21–23 nt can mediate RNAi but bypass the non-specific response induced by longer dsRNAs. However, the effectiveness of siRNAs has not been demonstrated in living vertebrates. In addition, the mechanism of siRNA suppression of gene expression in vertebrate cells remains to be elucidated. Here we show that synthetic 21 nt siRNAs can specifically inhibit the expression of exogenously introduced as well as endogenous genes in the embryos of Xenopus laevis. siRNAs significantly reduced the steady-state amount of both the mRNA and protein of the cognate gene target. Moreover, co-injection of siRNA with the target RNA transcript specifically suppressed the activity of the latter. Taken together, our findings establish siRNA-mediated post-transcriptional suppression of gene expression in Xenopus embryos.

* To whom correspondence should be addressed at: Department of Biochemistry, The University of Hong Kong, 3rd Floor, Li Shu Fan Building, 5 Sassoon Road, Pokfulam, Hong Kong. Tel: +852 28199245; Fax: +852 28551254; Email: dyjin{at}hkucc.hku.hk


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
K. H. Kok, M.-H. J. Ng, Y.-P. Ching, and D.-Y. Jin
Human TRBP and PACT Directly Interact with Each Other and Associate with Dicer to Facilitate the Production of Small Interfering RNA
J. Biol. Chem., June 15, 2007; 282(24): 17649 - 17657.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
K. H. Kok and D.-Y. Jin
Influenza A virus NS1 protein does not suppress RNA interference in mammalian cells
J. Gen. Virol., September 1, 2006; 87(9): 2639 - 2644.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Kuriyama, G. Lupo, K. Ohta, S.-i. Ohnuma, W. A. Harris, and H. Tanaka
Tsukushi controls ectodermal patterning and neural crest specification in Xenopus by direct regulation of BMP4 and X-delta-1 activity
Development, January 1, 2006; 133(1): 75 - 88.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
X. Huang, R. P. Barrett, S. A. McClellan, and L. D. Hazlett
Silencing Toll-like Receptor-9 in Pseudomonas aeruginosa Keratitis
Invest. Ophthalmol. Vis. Sci., November 1, 2005; 46(11): 4209 - 4216.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
A. V. Oleinikov, J. Zhao, and M. D. Gray
RNA interference by mixtures of siRNAs prepared using custom oligonucleotide arrays
Nucleic Acids Res., June 7, 2005; 33(10): e92 - e92.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. Ridgway, K. D. Brown, D. Rangasamy, U. Svensson, and D. J. Tremethick
Unique Residues on the H2A.Z Containing Nucleosome Surface Are Important for Xenopus laevis Development
J. Biol. Chem., October 15, 2004; 279(42): 43815 - 43820.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. L. Lopez, A. R. Paganelli, M. V. R. Siri, O. H. Ocana, P. G. Franco, and A. E. Carrasco
Notch activates sonic hedgehog and both are involved in the specification of dorsal midline cell-fates in Xenopus
Development, May 15, 2003; 130(10): 2225 - 2238.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
M. E. Hase and V. C. Cordes
Direct Interaction with Nup153 Mediates Binding of Tpr to the Periphery of the Nuclear Pore Complex
Mol. Biol. Cell, May 1, 2003; 14(5): 1923 - 1940.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. Sohail, G. Doran, J. Riedemann, V. Macaulay, and E. M. Southern
A simple and cost-effective method for producing small interfering RNAs with high efficacy
Nucleic Acids Res., April 1, 2003; 31(7): e38 - e38.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.