Antisense RNA
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Correspondence: Jonathan B Weitzman jonathanweitzman@hotmail.com
Genome Biology 2002, 3:spotlight-20020125-01 doi:10.1186/gb-spotlight-20020125-01
The electronic version of this article is the complete one and can be found online at:
| Published: | 25 January 2002 |
© 2002 BioMed Central Ltd
Research news
Gene silencing by RNA interference (RNAi) has become a powerful tool for functional genomics. In the January 25 Science, Tijsterman et al. report a gene-silencing method induced by short (25 nucleotide) antisense RNA molecules (Science 2002, 295:694-697). They found that injecting single-stranded, antisense RNA (asRNA) oligomers into the gonadal syncytium of Caenorhabditis elegans resulted in silencing of the maternal pos-1 gene and of germline-expressed genes. Tijsterman et al. found that asRNA silencing requires the mutator/RNAi genes mut-7 and mut-14. They cloned the mut-14 gene and report that it encodes a putative RNA helicase with a DEAD-box motif. The authors propose that asRNA-induced gene-silencing may result from the priming of RNA synthesis on mRNA templates, thereby creating dsRNA for subsequent degradation.
References
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Functional anatomy of a dsRNA trigger: differential requirement for the two trigger strands in RNA interference.
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[http://www.sciencemag.org] webcite
Science