Abstract
Gene expression in all living organisms is controlled at different steps of information processing: transcription of DNA into premessenger RNAs; splicing of mRNA precursors; post-transcriptional modifications of mRNAs (capping, polyadenylation); transfer of mRNAs from the nucleus to the cytoplasm; translation of mRNA; mRNA stability …. In most cases this regulation is achieved by proteins that bind to specific regions of DNA or RNA and either block or stimulate the enzymatic processes (see Hélène and Lancelot, 1982, for a review). Recently it has been shown that small RNAs could play a role similar to that of regulatory proteins. Upon hybridization with a messenger RNA, these regulatory RNAs may alter the translation process or induce premature termination of transcription (see Green et al., 1986, for a review). These regulatory processes have been originally observed in bacteria (Green et al., 1986) but they might also occur in eukaryotes (Heywood, 1986). The discovery of regulatory RNAs has been the starting point for the design of ‘antisense’ RNAs. By inserting a gene fragment close to a strong promoter in the reverse orientation as compared with that of the gene itself, the non-template strand of the gene fragment is now used as a template by RNA polymerase. As a consequence this ‘antisense’ transcript is fully complementary to the mRNA. This might block mRNA translation or other post-transcriptional processes such as splicing or mRNA migration from the nucleus to the cytoplasm (Kim and Wold, 1985; Green et al., 1986).
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References
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Hélène, C., Toulmé, JJ. (1989). Control of Gene Expression by Oligodeoxynucleotides Covalently Linked to Intercalating Agents and Nucleic Acid-cleaving Reagents. In: Cohen, J.S. (eds) Oligodeoxynucleotides. Topics in Molecular and Structural Biology. Palgrave, London. https://doi.org/10.1007/978-1-349-10869-5_8
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