反義RNA:修订间差异
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2015年12月16日 (三) 13:17的版本
此條目目前正依照其他维基百科上的内容进行翻译。 (2015年12月16日) |
反義RNA(Antisense RNA, 常縮寫爲asRNA),是一種與轉錄產物mRNA(信使RNA)互補的單鏈RNA。部分學者亦將這類RNA稱爲「micRNA」(mRNA干擾互補RNA,英語:mRNA-interfering complementary RNA),但此名稱並未得到廣泛使用[1]。
Antisense RNA may be introduced into a cell to inhibit translation of a complementary mRNA by base pairing to it and physically obstructing the translation machinery.[2] This effect is therefore stoichiometric. An example of naturally occurring mRNA antisense mechanism is the hok/sok system of the E. coli R1 plasmid. Antisense RNA has long been thought of as a promising technique for disease therapy; the only such case to have reached the market is the drug fomivirsen. One commentator has characterized antisense RNA as one of "dozens of technologies that are gorgeous in concept, but exasperating in [commercialization]".[3] Generally, antisense RNA still lack effective design, biological activity, and efficient route of administration.[4]
The effects of antisense RNA are related with the effects of RNA interference (RNAi). The RNAi process, found only in eukaryotes, is initiated by double-stranded RNA fragments, which may be created by the expression of an anti-sense RNA followed by the base-pairing of the anti-sense strand to the target transcript.[5] Double-stranded RNA may be created by other mechanisms (including secondary RNA structure). The double-stranded RNA is cleaved into small fragements by DICER, and then a single strand of the fragment is incorporated into the RNA-induced silencing complex (RISC) so that the RISC may bind to and degrade the complementary mRNA target.[6] Some genetically engineered transgenic plants that express antisense RNA do activate the RNAi pathway.[7] This processes resulted in differing magnitudes of gene silencing induced by the expression of antisense RNA. Well-known examples include the Flavr Savr tomato and two cultivars of ringspot-resistant papaya.[8][9]
Transcription of longer cis-antisense transcripts is a common phenomenon in the mammalian transcriptome.[10] Although the function of some cases have been described, such as the Zeb2/Sip1 antisense RNA, no general function has been elucidated. In the case of Zeb2/Sip1,[11] the antisense noncoding RNA is opposite the 5' splice site of an intron in the 5'UTR of the Zeb2 mRNA. Expression of the antisense ncRNA prevents splicing of an intron that contains a ribosome entry site necessary for efficient expression of the Zeb2 protein. Transcription of long antisense ncRNAs is often concordant with the associated protein-coding gene,[12] but more detailed studies have revealed that the relative expression patterns of the mRNA and antisense ncRNA are complex.[13][14]
參見
- 順式自然反義轉錄(Cis-natural antisense transcript)
參考
- ^ Mizuno, T.; Chou, M. Y.; Inouye, M. A unique mechanism regulating gene expression: Translational inhibition by a complementary RNA transcript (micRNA). Proceedings of the National Academy of Sciences of the United States of America. 1984, 81 (7): 1966–1970. PMC 345417
. PMID 6201848. doi:10.1073/pnas.81.7.1966.
- ^ Weiss, B; Davidkova, G; Zhou, LW. Antisense RNA gene therapy for studying and modulating biological processes.. Cellular and molecular life sciences : CMLS. March 1999, 55 (3): 334–58. PMID 10228554. doi:10.1007/s000180050296.
- ^ DePalma, Angelo. Twenty-Five Years of Biotech Trends. Genetic Engineering News 25 (14) (Mary Ann Liebert). August 2005: 1, 14–23 [2008-08-17]. ISSN 1935-472X.
- ^ Antisense Oligonucleotides: Basic Concepts and Mechanisms Nathalie Dias and C. A. Stein. Columbia University, New York, New York 10032
- ^ Ennio Giordano1, Rosaria Rendina, Ivana Peluso and Maria Furia. RNAi Triggered by Symmetrically Transcribed Transgenes in Drosophila melanogaster. Genetics February 1, 2002 vol. 160 no. 2 637-648 http://www.genetics.org/content/160/2/637.short. 缺少或
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为空 (帮助) - ^ Ross C. Wilson and Jennifer A. Doudna (2013) Molecular Mechanisms of RNA Interference.
Annual Review of Biophysics Vol. 42: 217-239 http://www.annualreviews.org/doi/full/10.1146/annurev-biophys-083012-130404. 缺少或
|title=
为空 (帮助) - ^ The Flavr Savr Tomato, an Early Example of RNAi Technology
Elysia K. Krieger, Edwards Allen, Larry A. Gilbertson, James K. Roberts, William Hiatt, and Rick A. Sanders
HortScience June 2008 43:962-964 http://hortsci.ashspublications.org/content/43/3/962.full. 缺少或
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为空 (帮助) - ^ Sanders RA, Hiatt W. Tomato transgene structure and silencing. Nat Biotechnol. 2005, 23 (3): 287–9. PMID 15765076. doi:10.1038/nbt0305-287b.
- ^ Chiang CH, Wang JJ, Jan FJ, Yeh SD, Gonsalves D. Comparative reactions of recombinant papaya ringspot viruses with chimeric coat protein (CP) genes and wild-type viruses on CP-transgenic papaya. J. Gen. Virol. November 2001, 82 (Pt 11): 2827–36. PMID 11602796.
- ^ Katayama S, Tomaru Y, Kasukawa T; et al. Antisense transcription in the mammalian transcriptome. Science. September 2005, 309 (5740): 1564–6. PMID 16141073. doi:10.1126/science.1112009.
- ^ Beltran M, Puig I, Peña C; et al. A natural antisense transcript regulates Zeb2/Sip1 gene expression during Snail1-induced epithelial-mesenchymal transition. Genes & Development. March 2008, 22 (6): 756–69. PMC 2275429
. PMID 18347095. doi:10.1101/gad.455708.
- ^ Engström PG, Suzuki H, Ninomiya N; et al. Complex Loci in human and mouse genomes. PLoS genetics. April 2006, 2 (4): e47. PMC 1449890
. PMID 16683030. doi:10.1371/journal.pgen.0020047.
- ^ Dinger ME, Amaral PP, Mercer TR; et al. Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation. Genome Research. September 2008, 18 (9): 1433–45. PMC 2527704
. PMID 18562676. doi:10.1101/gr.078378.108.
- ^ Mercer TR, Dinger ME, Sunkin SM, Mehler MF, Mattick JS. Specific expression of long noncoding RNAs in the mouse brain. Proceedings of the National Academy of Sciences of the United States of America. January 2008, 105 (2): 716–21. PMC 2206602
. PMID 18184812. doi:10.1073/pnas.0706729105.
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