2006, Número 4
<< Anterior Siguiente >>
Rev Invest Clin 2006; 58 (4)
Grandes alcances de los RNAs pequeños RNA de interferencia y microRNA
Vázquez-Ortiz G, Piña-Sánchez P, Salcedo M
Idioma: Español
Referencias bibliográficas: 139
Paginas: 335-349
Archivo PDF: 160.61 Kb.
RESUMEN
El RNA de doble cadena puede inducir un silenciamiento secuencia-específico en eucarionte. Este proceso de silenciamiento se inicia cuando el RNAdc largo es procesado a RNA pequeño de 21 a 26 nucleótidos mediante la enzima RNAsa III Dicer. Estos RNA pequeños se incorporan a complejos efectores de silenciamiento, que son guiados a secuencias complementarias blanco. Existen diferentes tipos de silenciamiento, cuyas diferencias se basan principalmente en la naturaleza de la secuencia blanco y en la composición proteica de los complejos efectores. La ruta del RNA de interferencia (RNAi) se inicia cuando Dicer genera pequeños RNA de interferencia (siRNA) que se unen por complementariedad al mRNA para su degradación, utilizando el complejo RISC. De manera natural, los siRNA se originan de transposones y virus que producen RNAdc durante su replicación, así como también de otras secuencias repetidas transcritas bidireccionalmente. Algunas de las enzimas que conforman la maquinaria del RNAi como Dicer, entre otras, son codificadas por familias multigénicas en varias especies y también participan en otros mecanismos de silenciamiento mediado por RNA. Los microRNA son otros RNA pequeños que pueden inducir silenciamiento al unirse al mRNA. Éstos se generan de manera general cuando Dicer procesa estructuras de horquilla compuestas de regiones no codificantes, en genomas de plantas y animales. Los miRNA se incorporan a un complejo similar a RISC y, dependiendo de su grado de complementariedad con el mRNA blanco, pueden tener represión traduccional o bien digerir el mRNA. El silenciamiento mediado por miRNA es esencial para el desarrollo de plantas y animales. La inducción artificial del RNAi mediante siRNA o miRNA ha sido adoptada como una herramienta para inactivar la expresión génica, tanto en células en cultivo como en organismos vivos. En esta revisión se muestra el gran progreso en el entendimiento de los mecanismos que participan en la regulación génica mediada por RNA en animales y detalla algunos esfuerzos actuales para encauzar a estos mecanismos como una herramienta en la investigación y como posible terapia en enfermedades.
REFERENCIAS (EN ESTE ARTÍCULO)
Eldering E, Spek CA, Aberson HL, Grummels A, Derks IA, de Vos AF, et al. Expression profiling via novel multiplex assay allows rapid assessment of gene regulation in defined signalling pathways. Nucleic Acids Res 2003; 31: e153.
Cullen BR. Derivation and function of small interfering RNAs and microRNAs. Virus Res 2004; 102: 3-9.
Cullen BR. RNAi the natural way. Nat Genet 2005; 37: 1163-5.
Couzin J. Molecular biology. RNAi shows cracks in its armor. Science 2004; 306: 1124-5.
Novina CD, Sharp PA. The RNAi revolution. Nature 2004; 430: 161-4.
Whither RNAi? Nat.Cell Biol. 2003; 5: 489-90.
Scherr M, Eder M. RNAi in functional genomics. Curr Opin Mol Ther 2004; 6: 129-35.
Tomari Y, Zamore PD. Perspective: machines for RNAi. Genes Dev. 2005; 19: 517-29.
Chalk AM, Warfinge RE, Georgii-Hemming P, Sonnhammer EL. siRNAdb: a database of siRNA sequences. Nucleic Acids Res 2005; 33: D131-D134.
Friedrich I, Ben-Bassat H, Levitzki A. Activation of dsRNA Dependent Protein Kinase PKR in Karpas299 Does Not Lead to Cell Death. Cancer Biol Ther 2005; 4: 734-9.
Piano F, Schetter AJ, Morton DG, Gunsalus KC, Reinke V, Kim SK, et al. Gene clustering based on RNAi phenotypes of ovary-enriched genes in C. elegans. Curr Biol 2002; 12: 1959-64.
Lipardi C, Wei Q, Paterson BM. RNAi as random degradative PCR: siRNA primers convert mRNA into dsRNAs that are degraded to generate new siRNAs. Cell 2001; 107: 297-307.
Grishok A, Pasquinelli AE, Conte D, Li N, Parrish S, Ha I, et al. Genes and mechanisms related to RNA interference regulate expression of the small temporal RNAs that control C. elegans developmental timing. Cell 2001; 106: 23-34.
Parrish S, Fleenor J, Xu S, Mello C, Fire A. Functional anatomy of a dsRNA trigger: differential requirement for the two trigger strands in RNA interference. Mol Cell 2000; 6: 1077-87.
Gao G, Raikar S, Davenport B, Mutapcic L, Montgomery R, Kuzmin E, et al. Cross-species RNAi: Selected Ascaris suum dsRNAs can sterilize Caenorhabditis elegans. Mol Biochem Parasitol 2006; 146: 124-8.
Tabara H, Yigit E, Siomi H, Mello CC. The dsRNA binding protein RDE-4 interacts with RDE-1, DCR-1, and a DExHbox helicase to direct RNAi in C. elegans. Cell 2002; 109: 861-71.
Yang D, Lu H, Erickson JW. Evidence that processed small dsRNAs may mediate sequence-specific mRNA degradation during RNAi in Drosophila embryos. Curr Biol 2000; 10: 1191-200.
Buchon N, Vaury C. RNAi: a defensive RNA-silencing against viruses and transposable elements. Heredity 2006; 96: 195-202.
Hansen KR, Ibarra PT, Thon G. Evolutionary-conserved telomere-linked helicase genes of fission yeast are repressed by silencing factors, RNAi components and the telomere-binding protein Taz1. Nucleic Acids Res 2006; 34: 78-88.
Hutvagner G, Zamore PD. RNAi: nature abhors a doublestrand. Curr Opin Genet Dev 2002; 12: 225-32.
Schwenzer R, Zimmermann G, Fotin M, Wajant H, Grell M. No RISC, no fun: assembly of receptor-induced signalling complexes in the tumor necrosis factor system. Eur Cytokine Netw 2000; 11: 519-20.
Tavernarakis N, Wang SL, Dorovkov M, Ryazanov A, Driscoll M. Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes. Nat Genet 2000; 24: 180-3.
Kato M, Kakutani T. [Control of transposons by DNA methylation and RNAi]. Tanpakushitsu Kakusan Koso 2004; 49: 2097-102.
Kuhlmann M, Borisova BE, Kaller M, Larsson P, Stach D, Na J, et al. Silencing of retrotransposons in Dictyostelium by DNA methylation and RNAi. Nucleic Acids Res. 2005; 33: 6405-17.
Svoboda P, Stein P, Anger M, Bernstein E, Hannon GJ, Schultz RM. RNAi and expression of retrotransposons MuERV-L and IAP in preimplantation mouse embryos. Dev Biol 2004; 269: 276-85.
Dinh A, Mo YY. Alternative approach to generate shRNA from cDNA. Biotechniques 2005; 38: 629-32.
Paddison PJ, Hannon GJ. siRNAs and shRNAs: skeleton keys to the human genome. Curr Opin Mol Ther 2003; 5: 217-24.
Ying SY, Lin SL. Current perspectives in intronic micro RNAs (miRNAs). J Biomed Sci 2006; 13: 5-15.
Filippov V, Solovyev V, Filippova M, Gill SS. A novel type of RNase III family proteins in eukaryotes. Gene 2000; 245: 213-21.
Knight SW, Bass BL. A role for the RNase III enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans. Science 2001; 293: 2269-71.
Zeng Y, Cullen BR. Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences. J Biol Chem 2005; 280: 27595-603.
Han Z, Saam JR, Adams HP, Mango SE, Schumacher JM. The C. elegans Tousled-like kinase (TLK-1) has an essential role in transcription. Curr Biol 2003; 13: 1921-9.
Bohnsack MT, Czaplinski K, Gorlich D. Exportin 5 is a RanGTP-dependent dsRNA-binding protein that mediates nuclear export of pre-miRNAs. RNA 2004; 10: 185-91.
Kim VN. MicroRNA precursors in motion: exportin-5 mediates their nuclear export. Trends Cell Biol 2004; 14: 156-9.
Yi R, Doehle BP, Qin Y, Macara IG, Cullen BR. Overexpression of exportin 5 enhances RNA interference mediated by short hairpin RNAs and microRNAs. RNA 2005; 11: 220-6.
Yi R, Qin Y, Macara IG, Cullen BR. Exportin-5 mediates the nuclear export of pre-microRNAs and short hairpin RNAs. Genes Dev 2003; 17: 3011-6.
Zeng Y, Cullen BR. Structural requirements for pre-microRNA binding and nuclear export by Exportin 5. Nucleic Acids Res 2004; 32: 4776-85.
Hiraguri A, Itoh R, Kondo N, Nomura Y, Aizawa D, Murai Y, et al. Specific interactions between Dicer-like proteins and HYL1/DRB-family dsRNA-binding proteins in Arabidopsis thaliana. Plant Mol Biol 2005; 57: 173-88.
Kim DH, Behlke MA, Rose SD, Chang MS, Choi S, Rossi JJ. Synthetic dsRNA Dicer substrates enhance RNAi potency and efficacy. Nat Biotechnol 2005; 23: 222-6.
Vermeulen A, Behlen L, Reynolds A, Wolfson A, Marshall WS, Karpilow J, et al. The contributions of dsRNA structure to Dicer specificity and efficiency. RNA 2005; 11: 674-82.
Zhang H, Kolb FA, Brondani V, Billy E, Filipowicz W. Human Dicer preferentially cleaves dsRNAs at their termini without a requirement for ATP. EMBO J 2002; 21: 5875-85.
Tahbaz N, Kolb FA, Zhang H, Jaronczyk K, Filipowicz W, Hobman TC. Characterization of the interactions between mammalian PAZ PIWI domain proteins and Dicer. EMBO Rep 2004; 5: 189-94.
Cornejo MF, Maloberti P, Neuman I, Cano F, Castilla R, Castillo F, et al. An arachidonic acid-preferring acyl-CoA synthetase is a hormone-dependent and obligatory protein in the signal transduction pathway of steroidogenic hormones. J Mol Endocrinol 2005; 34: 655-66.
Lingel A, Simon B, Izaurralde E, Sattler M. Structure and nucleic- acid binding of the Drosophila Argonaute 2 PAZ domain. Nature 2003; 426: 465-9.
Tijsterman M, Okihara KL, Thijssen K, Plasterk RH. PPW-1, a PAZ/PIWI protein required for efficient germline RNAi, is defective in a natural isolate of C. elegans. Curr Biol 2002; 12: 1535-40.
Yan KS, Yan S, Farooq A, Han A, Zeng L, Zhou MM. Structure and conserved RNA binding of the PAZ domain. Nature 2003; 426: 468-74.
Jaronczyk K, Carmichael JB, Hobman TC. Exploring the functions of RNA interference pathway proteins: some functions are more RISCy than others? Biochem J 2005; 387: 561-71.
Hutvagner G. Small RNA asymmetry in RNAi: function in RISC assembly and gene regulation. FEBS Lett 2005; 579: 5850-7.
Miyoshi K, Tsukumo H, Nagami T, Siomi H, Siomi MC. Slicer function of Drosophila Argonautes and its involvement in RISC formation. Genes Dev 2005; 19: 2837-48.
Kolb FA, Zhang H, Jaronczyk K, Tahbaz N, Hobman TC, Filipowicz W. Human dicer: purification, properties, and interaction with PAZ PIWI domain proteins. Methods Enzymol 2005; 392: 316-36.
Carthew RW. RNA interference: the fragile X syndrome connection. Curr Biol 2002; 12: R852-R854.
Caudy AA, Myers M, Hannon GJ, Hammond SM. Fragile Xrelated protein and VIG associate with the RNA interference machinery. Genes Dev 2002; 16: 2491-6.
Handa V, Saha T, Usdin K. The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer. Nucleic Acids Res 2003; 31: 6243-8.
Ishizuka A, Siomi MC, Siomi H. A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins. Genes Dev. 2002; 16: 2497-508.
Jin P, Zarnescu DC, Ceman S, Nakamoto M, Mowrey J, Jongens TA, et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nat Neurosci 2004; 7: 113-7.
Scadden AD. The RISC subunit Tudor-SN binds to hyper-edited double-stranded RNA and promotes its cleavage. Nat Struct Mol Biol 2005; 12: 489-96.
Lin SL, Chang D, Ying SY. Asymmetry of intronic pre-miRNA structures in functional RISC assembly. Gene 2005; 356: 32-8.
Maniataki E, Mourelatos Z. A human, ATP-independent, RISC assembly machine fueled by pre-miRNA. Genes Dev 2005; 19: 2979-90.
Schwenzer R, Zimmermann G, Fotin M, Wajant H, Grell M. No RISC, no fun: assembly of receptor-induced signalling complexes in the tumor necrosis factor system. Eur.Cytokine Netw. 2000; 11: 519-20.
Tomari Y, Du T, Haley B, Schwarz DS, Bennett R, Cook HA, et al. RISC assembly defects in the Drosophila RNAi mutant armitage. Cell 2004; 116: 831-41.
Gregory RI, Chendrimada TP, Cooch N, Shiekhattar R. Human RISC couples microRNA biogenesis and posttranscriptional gene silencing. Cell 2005; 123: 631-40.
Chiu YL, Dinesh CU, Chu CY, Ali A, Brown KM, Cao H, et al. Dissecting RNA-interference pathway with small molecules. Chem Biol 2005; 12: 643-8.
Okamura K, Ishizuka A, Siomi H, Siomi MC. Distinct roles for Argonaute proteins in small RNA-directed RNA cleavage pathways. Genes Dev 2004; 18: 1655-66.
Akusjarvi G, Svensson C, Nygard O. A mechanism by which adenovirus virus-associated RNAI controls translation in a transient expression assay. Mol Cell Biol 1987; 7: 549-51.
Mathews MB. Control of translation in adenovirus-infected cells. Enzyme 1990; 44: 250-64.
Sen GL, Wehrman TS, Blau HM. mRNA translation is not a prerequisite for small interfering RNA-mediated mRNA cleavage. Differentiation 2005; 73: 287-93.
Wilson IW, Praszkier J, Pittard AJ. Molecular analysis of RNAI control of repB translation in IncB plasmids. J Bacteriol 1994; 176: 6497-508.
Zhao Z, Fang LL, Johnsen R, Baillie DL. ATP-binding cassette protein E is involved in gene transcription and translation in Caenorhabditis elegans. Biochem Biophys Res Commun 2004; 323: 104-11.
Allshire R. Molecular biology. RNAi and heterochromatin ¯a hushed-up affair. Science 2002; 297: 1818-9.
Martienssen RA, Zaratiegui M, Goto DB. RNA interference and heterochromatin in the fission yeast Schizosaccharomyces pombe. Trends Genet 2005; 21: 450-6.
Matzke M, Matzke AJ. RNAi extends its reach. Science 2003; 301: 1060-1.
Qian Z, Xuan B, Hong J, Hao Z, Wang L, Huang W. Expression and purification of the carboxyl terminus domain of Schizosaccharomyces pombe dicer in Escherichia coli. Protein Pept Lett 2005; 12: 311-4.
Sigova A, Rhind N, Zamore PD. A single Argonaute protein mediates both transcriptional and posttranscriptional silencing in Schizosaccharomyces pombe. Genes Dev 2004; 18: 2359-67.
Yamada T, Fischle W, Sugiyama T, Allis CD, Grewal SI. The nucleation and maintenance of heterochromatin by a histone deacetylase in fission yeast. Mol Cell 2005; 20: 173-85.
Carette JE, Overmeer RM, Schagen FH, Alemany R, Barski OA, Gerritsen WR, et al. Conditionally replicating adenoviruses expressing short hairpin RNAs silence the expression of a target gene in cancer cells. Cancer Res 2004; 64: 2663-7.
Motamedi MR, Verdel A, Colmenares SU, Gerber SA, Gygi SP, Moazed D. Two RNAi complexes, RITS and RDRC, physically interact and localize to noncoding centromeric RNAs. Cell 2004; 119: 789-802.
Noma K, Sugiyama T, Cam H, Verdel A, Zofall M, Jia S, et al. RITS acts in cis to promote RNA interference-mediated transcriptional and post-transcriptional silencing. Nat Genet 2004; 36: 1174-80.
Verdel A, Jia S, Gerber S, Sugiyama T, Gygi S, Grewal SI, et al. RNAi-mediated targeting of heterochromatin by the RITS complex. Science 2004; 303: 672-6.
Verdel A, Moazed D. Labeling and characterization of small RNAs associated with the RNA interference effector complex RITS. Methods Enzymol 2005; 392: 297-307.
Pekarik V. Design of shRNAs for RNAi-A lesson from premiRNA processing: possible clinical applications. Brain Res Bull 2005; 68: 115-20.
An DS, Xie Y, Mao SH, Morizono K, Kung SK, Chen IS. Efficient lentiviral vectors for short hairpin RNA delivery into human cells. Hum Gene Ther 2003; 14: 1207-12.
Bbas-Terki T, Blanco-Bose W, Deglon N, Pralong W, Aebischer P. Lentiviral-mediated RNA interference. Hum Gene Ther 2002; 13: 2197-201.
Ying SY, Lin SL. Current perspectives in intronic micro RNAs (miRNAs). J Biomed Sci 2006; 13: 5-15.
Hayashita Y, Osada H, Tatematsu Y, Yamada H, Yanagisawa K, Tomida S, et al. A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation. Cancer Res 2005; 65: 9628-32.
Bagga S, Bracht J, Hunter S, Massirer K, Holtz J, Eachus R, et al. Regulation by let-7 and lin-4 miRNAs results in target mRNA degradation. Cell 2005; 122: 553-63.
Hsu PW, Huang HD, Hsu SD, Lin LZ, Tsou AP, Tseng CP, et al. miRNAMap: genomic maps of microRNA genes and their target genes in mammalian genomes. Nucleic Acids Res 2006; 34: D135-D139.
Jones-Rhoades MW, Bartel DP. Computational identification of plant microRNAs and their targets, including a stress-induced miRNA. Mol Cell 2004; 14: 787-99.
Zhang Y. miRU: an automated plant miRNA target prediction server. Nucleic Acids Res 2005; 33: W701-W704.
Ma ZL, Yang HY, Tien P. [Progress of miRNA and its functions in eukaryotes]. Yi.Chuan Xue Bao 2003; 30: 693-6.
Abramson J, Rozenblum G, Pecht I. Stable knockdown of MAFA expression in RBL-2H3 cells by siRNA retrovirus-delivery system. Immunol Lett 2004; 92: 179-84.
Agrawal N, Malhotra P, Bhatnagar RK. siRNA-directed silencing of transgene expressed in cultured insect cells. Biochem Biophys Res Commun 2004; 320: 428-34.
Aigner A. Gene silencing through RNA interference (RNAi) in vivo: Strategies based on the direct application of siRNAs. J Biotechnol 2006.
Wu MT, Wu RH, Hung CF, Cheng TL, Tsai WH, Chang WT. Simple and efficient DNA vector-based RNAi systems in mammalian cells. Biochem Biophys Res Commun 2005; 330: 53-9.
Cheng AM, Byrom MW, Shelton J, Ford LP. Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis. Nucleic Acids Res 2005; 33: 1290-7.
Doench JG, Petersen CP, Sharp PA. siRNAs can function as miRNAs. Genes Dev 2003; 17: 438-42.
Kasschau KD, Xie Z, Allen E, Llave C, Chapman EJ, Krizan KA, et al. P1/HC-Pro, a viral suppressor of RNA silencing, interferes with Arabidopsis development and miRNA unction. Dev Cell 2003; 4: 205-17.
Morris JP, McManus MT. Slowing down the Ras lane: miRNAs as tumor suppressors? Sci STKE 2005; 2005: e41.
Xie Z, Allen E, Fahlgren N, Calamar A, Givan SA, Carrington JC. Expression of Arabidopsis MIRNA genes. Plant Physiol 2005; 138: 2145-54.
Arrighi JF, Pion M, Wiznerowicz M, Geijtenbeek TB, Garcia E, Abraham S, et al. Lentivirus-mediated RNA interference of DC-SIGN expression inhibits human immunodeficiency virus transmission from dendritic cells to T cells. J Virol 2004; 78: 10848-55.
Banerjea A, Li MJ, Bauer G, Remling L, Lee NS, Rossi J, et al. Inhibition of HIV-1 by lentiviral vector-transduced siRNAs in T lymphocytes differentiated in SCID-hu mice and CD34+ progenitor cell-derived macrophages. Mol Ther 2003; 8: 62-71.
Bhattacharya S, Ray RM, Johnson LR. Decreased apoptosis in polyamine depleted IEC-6 cells depends on Akt-mediated NF-kappaB activation but not GSK3beta activity. Apoptosis 2005; 10: 759-76.
Brummelkamp TR, Nijman SM, Dirac AM, Bernards R. Loss of the cylindromatosis tumour suppressor inhibits apoptosis by activating NF-kappaB. Nature 2003; 424: 797-801.
Kovalenko A, Chable-Bessia C, Cantarella G, Israel A, Wallach D, Courtois G. The tumour suppressor CYLD negatively regulates NF-kappaB signalling by deubiquitination. Nature 2003; 424: 801-5.
Trompouki E, Hatzivassiliou E, Tsichritzis T, Farmer H, Ashworth A, Mosialos G. CYLD is a deubiquitinating enzyme that negatively regulates NF-kappaB activation by TNFR family members. Nature 2003; 424: 793-6.
Silva JM, Li MZ, Chang K, Ge W, Golding MC, Rickles RJ, et al. Second-generation shRNA libraries covering the mouse and human genomes. Nat Genet 2005; 37: 1281-8.
Lai EC, Wiel C, Rubin GM. Complementary miRNA pairs suggest a regulatory role for miRNA:miRNA duplexes. RNA 2004; 10: 171-5.
Amarzguioui M. Improved siRNA-mediated silencing in refractory adherent cell lines by detachment and transfection in suspension. Biotechniques 2004; 36: 766-8, 770.
Beale G, Hollins AJ, Benboubetra M, Sohail M, Fox SP, Benter I, et al. Gene silencing nucleic acids designed by scanning arrays: anti-EGFR activity of siRNA, ribozyme and DNA enzymes targeting a single hybridization-accessible region using the same delivery system. J Drug Target 2003; 11: 449-56.
Chang HS, Lin CH, Chen YC, Yu WC. Using siRNA technique to generate transgenic animals with spatiotemporal and conditional gene knockdown. Am J Pathol 2004; 165: 1535-41.
Chen S, Wang G, Makrigiorgos GM, Price BD. Stable siRNAmediated silencing of ATM alters the transcriptional profile of HeLa cells. Biochem Biophys Res Commun 2004; 317: 1037-44.
Yoshikawa T, Uchimura E, Kishi M, Funeriu DP, Miyake M, Miyake J. Transfection microarray of human mesenchymal stem cells and on-chip siRNA gene knockdown. J Control Release 2004; 96: 227-32.
Zhelev Z, Bakalova R, Ohba H, Ewis A, Ishikawa M, Shinohara Y, et al. Suppression of bcr-abl synthesis by siRNAs or tyrosine kinase activity by Glivec alters different oncogenes, apoptotic/antiapoptotic genes and cell proliferation factors (microarray study). FEBS Lett 2004; 570: 195-204.
Couturier JP, Root-Bernstein RS. HIV may produce inhibitory microRNAs (miRNAs) that block production of CD28, CD4 and some interleukins. J Theor Biol 2005; 235: 169-84.
Yeung ML, Bennasser Y, Le SY, Jeang KT. siRNA, miRNA and HIV: promises and challenges. Cell Res 2005; 15: 935-46.
Akkina R, Banerjea A, Bai J, Anderson J, Li MJ, Rossi J. siRNAs, ribozymes and RNA decoys in modeling stem cell-based gene therapy for HIV/AIDS. Anticancer Res 2003; 23: 1997-2005.
Andersen JL, Zimmerman ES, DeHart JL, Murala S, Ardon O, Blackett J, et al. ATR and GADD45alpha mediate HIV-1 Vpr-induced apoptosis. Cell Death Differ 2005; 12: 326-34.
Bagasra O, Prilliman KR. RNA interference: the molecular immune system. J Mol Histol 2004; 35: 545-53.
Takaku H. Gene silencing of HIV-1 by RNA interference. Antivir Chem Chemother 2004; 15: 57-65.
Van den HC, Eggermont K, Nuttin B, Debyser Z, Baekelandt V. Lentiviral vector-mediated delivery of short hairpin RNA results in persistent knockdown of gene expression in mouse brain. Hum Gene Ther 2003; 14: 1799-807.
Dave RS, Pomerantz RJ. Antiviral effects of human immunodeficiency virus type 1-specific small interfering RNAs against targets conserved in select neurotropic viral strains. J Virol 2004; 78: 13687-96.
Forstemann K, Tomari Y, Du T, Vagin VV, Denli AM, Bratu DP, et al. Normal microRNA maturation and germ-line stem cell maintenance requires Loquacious, a double-stranded RNA-binding domain protein. P Lo S Biol 2005; 3: e236.
Cai DC, Ren H. [Advance in research of anti-HBV and anti- HCV through RNAi]. Zhonghua Gan Zang Bing Za Zhi 2004; 12: 126-8.
Azkur AK, Kim B, Suvas S, Lee Y, Kumaraguru U, Rouse BT. Blocking mouse MMP-9 production in tumor cells and mouse cornea by short hairpin (sh) RNA encoding plasmids. Oligonucleotides 2005; 15: 72-84.
Bron R, Eickholt BJ, Vermeren M, Fragale N, Cohen J. Functional knockdown of neuropilin-1 in the developing chick nervous system by siRNA hairpins phenocopies genetic ablation in the mouse. Dev Dyn 2004; 230: 299-308.
Calegari F, Haubensak W, Yang D, Huttner WB, Buchholz F. Tissue-specific RNA interference in postimplantation mouse embryos with endoribonuclease-prepared short interfering RNA. Proc Natl Acad Sci USA 2002; 99: 14236-40.
Cui XS, Li XY, Jeong YJ, Jun JH, Kim NH. Gene Expression of Cox 5a, 5b, or 6b1, and their Roles in Preimplantation Mouse Embryos. Biol Reprod 2006.
Davern TJ. Increasing the RISC for HCV. Gastroenterol 2003; 125: 1546-8.
Goh PY, Tan YJ, Lim SP, Tan YH, Lim SG, Fuller-Pace F, et al. Cellular RNA helicase p68 relocalization and interaction with the hepatitis C virus (HCV) NS5B protein and the potential role of p68 in HCV RNA replication. J Virol 2004; 78: 5288-98.
Inglot M, Gladysz A, Rymer W. [Experimental therapy in HCV infection]. Przegl Epidemiol 2005; 59: 525-33.
Albertella MR, Lau A, O’Connor MJ. The overexpression of specialized DNA polymerases in cancer. DNA Repair (Amst) 2005; 4: 583-93.
Fu GF, Lin XH, Han QW, Fan YR, Xu YF, Guo D, et al. RNA Interference Remarkably Suppresses bcl-2 Gene Expression in Cancer Cells in Vitro and in Vivo. Cancer Bio L Ther 2005; 4.
Nishigaki M, Aoyagi K, Danjoh I, Fukaya M, Yanagihara K, Sakamoto H, et al. Discovery of aberrant expression of RRAS by cancer-linked DNA hypomethylation in gastric cancer using microarrays. Cancer Res 2005; 65: 2115-24.
Williams NS, Gaynor RB, Scoggin S, Verma U, Gokaslan T, Simmang C, et al. Identification and validation of genes involved in the pathogenesis of colorectal cancer using cDNA microarrays and RNA interference. Clin Cancer Res 2003; 9: 931-46.
Ota A, Tagawa H, Karnan S, Tsuzuki S, Karpas A, Kira S, et al. Identification and characterization of a novel gene, C13orf25, as a target for 13q31-q32 amplification in malignant lymphoma. Cancer Res 2004; 64: 3087-95.
O’Donnell KA, Wentzel EA, Zeller KI, Dang CV, Mendell JT. c-Myc-regulated microRNAs modulate E2F1 expression. Nature 2005; 435: 839-43.
Finzer P, Krueger A, Stohr M, Brenner D, Soto U, Kuntzen C, et al. HDAC inhibitors trigger apoptosis in HPV-positive cells by inducing the E2F-p73 pathway. Oncogene 2004; 23: 4807-17.
Hougardy BM, Maduro JH, van der Zee AG, de Groot DJ, van den Heuvel FA, de Vries EG, et al. Proteasome inhibitor MG132 sensitizes HPV-positive human cervical cancer cells to rhTRAIL-induced apoptosis. Int J Cancer 2005.
Jiang M, Milner J. Selective silencing of viral gene expression in HPV-positive human cervical carcinoma cells treated with siRNA, a primer of RNA interference. Oncogene 2002; 21: 6041-8.
Tang S, Tao M, McCoy JP, Zheng ZM. Short-term induction and long-term suppression of HPV16 oncogene silencing by RNA interference in cervical cancer cells. Oncogene 2005.