The Landscape of C. elegans 3′UTRs
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Sebastian D. Mackowiak | Emily K. Mis | F. Piano | K. Gunsalus | M. Mangone | M. Vidal | T. Harkins | N. Rajewsky | S. Sugano | Yutaka Suzuki | Y. Kohara | J. Thierry-Mieg | D. Thierry-Mieg | Kevin C. Chen | John K. Kim | M. Gutwein | Vishal Khivansara | P. Bouffard | A. Manoharan | O. Attie | K. Salehi-Ashtiani | Ting-Li Han | Charles Zegar | Marco Mangone
[1] Guoli Ji,et al. Genome-wide landscape of polyadenylation in Arabidopsis provides evidence for extensive alternative polyadenylation , 2011, Proceedings of the National Academy of Sciences.
[2] P. Sternberg,et al. Metazoan Operons Accelerate Recovery from Growth-Arrested States , 2011, Cell.
[3] Chong-Jian Chen,et al. Differential genome-wide profiling of tandem 3' UTRs among human breast cancer and normal cells by high-throughput sequencing. , 2011, Genome research.
[4] A. Aravin,et al. PIWI-interacting small RNAs: the vanguard of genome defence , 2011, Nature Reviews Molecular Cell Biology.
[5] Sylvie Doublié,et al. Crystal structure of a human cleavage factor CFI(m)25/CFI(m)68/RNA complex provides an insight into poly(A) site recognition and RNA looping. , 2011, Structure.
[6] L. Hillier,et al. A global analysis of C. elegans trans-splicing. , 2011, Genome research.
[7] D. Bartel,et al. Formation, Regulation and Evolution of Caenorhabditis elegans 3′UTRs , 2010, Nature.
[8] P. Kapranov,et al. Comprehensive Polyadenylation Site Maps in Yeast and Human Reveal Pervasive Alternative Polyadenylation , 2010, Cell.
[9] Hiroshi Handa,et al. Evidence that cleavage factor Im is a heterotetrameric protein complex controlling alternative polyadenylation , 2010, Genes to cells : devoted to molecular & cellular mechanisms.
[10] Brita Fritsch,et al. Distinct 3′UTRs differentially regulate activity-dependent translation of brain-derived neurotrophic factor (BDNF) , 2010, Proceedings of the National Academy of Sciences.
[11] Pedro J. Batista,et al. Argonautes ALG-3 and ALG-4 are required for spermatogenesis-specific 26G-RNAs and thermotolerant sperm in Caenorhabditis elegans , 2010, Proceedings of the National Academy of Sciences.
[12] O. Hobert,et al. Neuron-type specific regulation of a 3'UTR through redundant and combinatorially acting cis-regulatory elements. , 2010, RNA.
[13] Gene W. Yeo,et al. Comprehensive discovery of endogenous Argonaute binding sites in Caenorhabditis elegans , 2010, Nature Structural &Molecular Biology.
[14] S. Vagner,et al. Molecular mechanisms of eukaryotic pre-mRNA 3′ end processing regulation , 2009, Nucleic acids research.
[15] Kimberly Van Auken,et al. WormBase: a comprehensive resource for nematode research , 2009, Nucleic Acids Res..
[16] B. Tian,et al. Reprogramming of 3′ Untranslated Regions of mRNAs by Alternative Polyadenylation in Generation of Pluripotent Stem Cells from Different Cell Types , 2009, PloS one.
[17] M. Sheets,et al. Deadenylation of maternal mRNAs mediated by miR-427 in Xenopus laevis embryos. , 2009, RNA.
[18] Diana S Chu,et al. 26G endo-siRNAs regulate spermatogenic and zygotic gene expression in Caenorhabditis elegans , 2009, Proceedings of the National Academy of Sciences.
[19] Yan Yan,et al. FLASH, a proapoptotic protein involved in activation of caspase-8, is essential for 3' end processing of histone pre-mRNAs. , 2009, Molecular cell.
[20] Pedro J. Batista,et al. Distinct argonaute-mediated 22G-RNA pathways direct genome surveillance in the C. elegans germline. , 2009, Molecular cell.
[21] Pedro J. Batista,et al. The Argonaute CSR-1 and Its 22G-RNA Cofactors Are Required for Holocentric Chromosome Segregation , 2009, Cell.
[22] A. Riccio,et al. To localize or not to localize: mRNA fate is in 3'UTR ends. , 2009, Trends in cell biology.
[23] R. Duronio,et al. The Drosophila U7 snRNP proteins Lsm10 and Lsm11 are required for histone pre-mRNA processing and play an essential role in development. , 2009, RNA.
[24] C. Mayr,et al. Widespread Shortening of 3′UTRs by Alternative Cleavage and Polyadenylation Activates Oncogenes in Cancer Cells , 2009, Cell.
[25] E. Wahle,et al. Poly(A) Tail Length Is Controlled by the Nuclear Poly(A)-binding Protein Regulating the Interaction between Poly(A) Polymerase and the Cleavage and Polyadenylation Specificity Factor* , 2009, The Journal of Biological Chemistry.
[26] M. Gerstein,et al. Unlocking the secrets of the genome , 2009, Nature.
[27] Zachary Pincus,et al. Dynamic expression of small non-coding RNAs, including novel microRNAs and piRNAs/21U-RNAs, during Caenorhabditis elegans development , 2009, Genome Biology.
[28] J. Pal,et al. Role of 5′‐ and 3′‐untranslated regions of mRNAs in human diseases , 2009, Biology of the cell.
[29] J. Kawai,et al. Tiny RNAs associated with transcription start sites in animals , 2009, Nature Genetics.
[30] B. Tian,et al. Progressive lengthening of 3′ untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development , 2009, Proceedings of the National Academy of Sciences.
[31] P. Green,et al. Massively parallel sequencing of the polyadenylated transcriptome of C. elegans. , 2009, Genome research.
[32] Melissa J. Moore,et al. Pre-mRNA Processing Reaches Back toTranscription and Ahead to Translation , 2009, Cell.
[33] D. Bartel. MicroRNAs: Target Recognition and Regulatory Functions , 2009, Cell.
[34] C. Burge,et al. Most mammalian mRNAs are conserved targets of microRNAs. , 2008, Genome research.
[35] E. Wagner,et al. Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail , 2008, Nature Reviews Genetics.
[36] C. Lutz,et al. Alternative polyadenylation: a twist on mRNA 3' end formation. , 2008, ACS chemical biology.
[37] D. Bartel,et al. The impact of microRNAs on protein output , 2008, Nature.
[38] Steven J. M. Jones,et al. Transcriptome analysis for Caenorhabditis elegans based on novel expressed sequence tags , 2008, BMC Biology.
[39] P. Sharp,et al. Proliferating Cells Express mRNAs with Shortened 3' Untranslated Regions and Fewer MicroRNA Target Sites , 2008, Science.
[40] Taishin Kin,et al. Drosophila endogenous small RNAs bind to Argonaute 2 in somatic cells , 2008, Nature.
[41] N. Perrimon,et al. An endogenous small interfering RNA pathway in Drosophila , 2008, Nature.
[42] Sudha Balla,et al. Two distinct mechanisms generate endogenous siRNAs from bidirectional transcription in Drosophila melanogaster , 2008, Nature Structural &Molecular Biology.
[43] Z. Weng,et al. Endogenous siRNAs Derived from Transposons and mRNAs in Drosophila Somatic Cells , 2008, Science.
[44] Y. Sakaki,et al. Endogenous siRNAs from naturally formed dsRNAs regulate transcripts in mouse oocytes , 2008, Nature.
[45] Oliver H. Tam,et al. Pseudogene-derived small interfering RNAs regulate gene expression in mouse oocytes , 2008, Nature.
[46] D. Bartel,et al. Endogenous siRNA and miRNA Targets Identified by Sequencing of the Arabidopsis Degradome , 2008, Current Biology.
[47] Chun Liang,et al. Unique Features of Nuclear mRNA Poly(A) Signals and Alternative Polyadenylation in Chlamydomonas reinhardtii , 2008, Genetics.
[48] R. Agami,et al. Interplay between microRNAs and RNA-binding proteins determines developmental processes , 2008, Cell cycle.
[49] Hang Wang,et al. Pre-Messenger RNA Cleavage Factor I (CFIm): Potential Role in Alternative Polyadenylation During Spermatogenesis1 , 2008, Biology of reproduction.
[50] M. Hentze,et al. 3′ end mRNA processing: molecular mechanisms and implications for health and disease , 2008, The EMBO journal.
[51] Kristin C. Gunsalus,et al. UTRome.org: a platform for 3′UTR biology in C. elegans , 2007, Nucleic Acids Res..
[52] L. Tong,et al. Protein factors in pre-mRNA 3′-end processing , 2008, Cellular and Molecular Life Sciences.
[53] M. Griswold,et al. Loss of polyadenylation protein τCstF-64 causes spermatogenic defects and male infertility , 2007, Proceedings of the National Academy of Sciences.
[54] S. Schweiger,et al. Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1 , 2007, BMC Molecular Biology.
[55] Manolis Kellis,et al. Evolution, biogenesis, expression, and target predictions of a substantially expanded set of Drosophila microRNAs. , 2007, Genome research.
[56] Z. Dominski,et al. Formation of the 3' end of histone mRNA: getting closer to the end. , 2007, Gene.
[57] L. Lim,et al. MicroRNA targeting specificity in mammals: determinants beyond seed pairing. , 2007, Molecular cell.
[58] D. Bartel,et al. Intronic microRNA precursors that bypass Drosha processing , 2007, Nature.
[59] J. Pettitt,et al. Histone gene expression and histone mRNA 3' end structure in Caenorhabditis elegans , 2007, BMC Molecular Biology.
[60] P. Stadler,et al. RNA Maps Reveal New RNA Classes and a Possible Function for Pervasive Transcription , 2007, Science.
[61] Liang Tong,et al. Crystal structure of murine CstF-77: dimeric association and implications for polyadenylation of mRNA precursors. , 2007, Molecular cell.
[62] Lucie N. Hutchins,et al. Systematic variation in mRNA 3′-processing signals during mouse spermatogenesis , 2006, Nucleic acids research.
[63] A. Fire,et al. Gene silencing by double-stranded RNA. , 2007, Cell death and differentiation.
[64] A. Furger,et al. Two G-Rich Regulatory Elements Located Adjacent to and 440 Nucleotides Downstream of the Core Poly(A) Site of the Intronless Melanocortin Receptor 1 Gene Are Critical for Efficient 3′ End Processing , 2006, Molecular and Cellular Biology.
[65] Christopher M. Player,et al. Large-Scale Sequencing Reveals 21U-RNAs and Additional MicroRNAs and Endogenous siRNAs in C. elegans , 2006, Cell.
[66] H. Handa,et al. Knock-down of 25 kDa subunit of cleavage factor Im in Hela cells alters alternative polyadenylation within 3′-UTRs , 2006, Nucleic acids research.
[67] C. MacDonald,et al. Differences in polyadenylation site choice between somatic and male germ cells , 2006, BMC Molecular Biology.
[68] Piero Carninci,et al. Tagging mammalian transcription complexity. , 2006, Trends in genetics : TIG.
[69] N. Yang,et al. L1 retrotransposition is suppressed by endogenously encoded small interfering RNAs in human cultured cells , 2006, Nature Structural &Molecular Biology.
[70] J. Thierry-Mieg,et al. AceView: a comprehensive cDNA-supported gene and transcripts annotation , 2006, Genome Biology.
[71] D. Gautheret,et al. Conservation of alternative polyadenylation patterns in mammalian genes , 2006, BMC Genomics.
[72] Toshiaki Watanabe,et al. Identification and characterization of two novel classes of small RNAs in the mouse germline: retrotransposon-derived siRNAs in oocytes and germline small RNAs in testes. , 2006, Genes & development.
[73] H. Stark,et al. Cryo-electron microscopy of spliceosomal components. , 2006, Annual review of biophysics and biomolecular structure.
[74] Anton J. Enright,et al. Zebrafish MiR-430 Promotes Deadenylation and Clearance of Maternal mRNAs , 2006, Science.
[75] V. Ambros,et al. Interacting endogenous and exogenous RNAi pathways in Caenorhabditis elegans. , 2006, RNA.
[76] Colin N. Dewey,et al. A Genome-Wide Map of Conserved MicroRNA Targets in C. elegans , 2006, Current Biology.
[77] G. Ruvkun,et al. Functional Proteomics Reveals the Biochemical Niche of C. elegans DCR-1 in Multiple Small-RNA-Mediated Pathways , 2006, Cell.
[78] Haibo Zhang,et al. Biased alternative polyadenylation in human tissues , 2005, Genome Biology.
[79] J. Steitz,et al. Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs. , 2005, Genes & development.
[80] Z. Dominski,et al. The Polyadenylation Factor CPSF-73 Is Involved in Histone-Pre-mRNA Processing , 2005, Cell.
[81] S. Batalov,et al. Antisense Transcription in the Mammalian Transcriptome , 2005, Science.
[82] S. Lowe,et al. A microRNA polycistron as a potential human oncogene , 2005, Nature.
[83] K. Venkataraman,et al. Analysis of a noncanonical poly(A) site reveals a tripartite mechanism for vertebrate poly(A) site recognition. , 2005, Genes & development.
[84] Kristin C. Gunsalus,et al. microRNA Target Predictions across Seven Drosophila Species and Comparison to Mammalian Targets , 2005, PLoS Comput. Biol..
[85] Anton J. Enright,et al. Materials and Methods Figs. S1 to S4 Tables S1 to S5 References and Notes Micrornas Regulate Brain Morphogenesis in Zebrafish , 2022 .
[86] K. Gunsalus,et al. Combinatorial microRNA target predictions , 2005, Nature Genetics.
[87] T. Toda,et al. Inactivation of the Pre-mRNA Cleavage and Polyadenylation Factor Pfs2 in Fission Yeast Causes Lethal Cell Cycle Defects , 2005, Molecular and Cellular Biology.
[88] D. Bartel,et al. Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes. , 2005, RNA.
[89] J. Castle,et al. Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs , 2005, Nature.
[90] N. Sonenberg,et al. Regulation of cap-dependent translation by eIF4E inhibitory proteins , 2005, Nature.
[91] H. Meijer,et al. Mechanisms of translational control by the 3' UTR in development and differentiation. , 2005, Seminars in cell & developmental biology.
[92] C. Burge,et al. Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA Targets , 2005, Cell.
[93] Bin Tian,et al. A large-scale analysis of mRNA polyadenylation of human and mouse genes , 2005, Nucleic acids research.
[94] J. Ecker,et al. Applications of DNA tiling arrays for whole-genome analysis. , 2005, Genomics.
[95] V. Kim,et al. The Drosha-DGCR8 complex in primary microRNA processing. , 2004, Genes & development.
[96] David E Hill,et al. A first version of the Caenorhabditis elegans Promoterome. , 2004, Genome research.
[97] N. Rhind,et al. A single Argonaute protein mediates both transcriptional and posttranscriptional silencing in Schizosaccharomyces pombe. , 2004, Genes & development.
[98] V. Ambros. The functions of animal microRNAs , 2004, Nature.
[99] G. Hannon,et al. Crystal Structure of Argonaute and Its Implications for RISC Slicer Activity , 2004, Science.
[100] D. Bartel,et al. Computational identification of plant microRNAs and their targets, including a stress-induced miRNA. , 2004, Molecular cell.
[101] F. Stutz,et al. mRNA export: an assembly line from genes to nuclear pores. , 2004, Current opinion in cell biology.
[102] E. Sontheimer,et al. Distinct Roles for Drosophila Dicer-1 and Dicer-2 in the siRNA/miRNA Silencing Pathways , 2004, Cell.
[103] K. Ryan,et al. Evidence that polyadenylation factor CPSF-73 is the mRNA 3' processing endonuclease. , 2004, RNA.
[104] W. Keller,et al. Human Fip1 is a subunit of CPSF that binds to U‐rich RNA elements and stimulates poly(A) polymerase , 2004, The EMBO journal.
[105] K. Czaplinski,et al. Exportin 5 is a RanGTP-dependent dsRNA-binding protein that mediates nuclear export of pre-miRNAs. , 2004, RNA.
[106] D. Bartel. MicroRNAs Genomics, Biogenesis, Mechanism, and Function , 2004, Cell.
[107] U. Kutay,et al. Nuclear Export of MicroRNA Precursors , 2004, Science.
[108] Gary Ruvkun,et al. Identification of many microRNAs that copurify with polyribosomes in mammalian neurons , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[109] Oliver Hobert,et al. A microRNA controlling left/right neuronal asymmetry in Caenorhabditis elegans , 2003, Nature.
[110] B. Cullen,et al. Exportin-5 mediates the nuclear export of pre-microRNAs and short hairpin RNAs. , 2003, Genes & development.
[111] Kirk M Brown,et al. A mechanism for the regulation of pre-mRNA 3' processing by human cleavage factor Im. , 2003, Molecular cell.
[112] E. Bertrand,et al. Human let-7 stem-loop precursors harbor features of RNase III cleavage products. , 2003, Nucleic acids research.
[113] Michael Z Michael,et al. Reduced accumulation of specific microRNAs in colorectal neoplasia. , 2003, Molecular cancer research : MCR.
[114] V. Kim,et al. The nuclear RNase III Drosha initiates microRNA processing , 2003, Nature.
[115] P. Sharp,et al. Embryonic stem cell-specific MicroRNAs. , 2003, Developmental cell.
[116] D. Marks,et al. The small RNA profile during Drosophila melanogaster development. , 2003, Developmental cell.
[117] David P. Bartel,et al. MicroRNAs: At the Root of Plant Development?1 , 2003, Plant Physiology.
[118] V. Ambros,et al. MicroRNAs and Other Tiny Endogenous RNAs in C. elegans , 2003, Current Biology.
[119] J. Hudson,et al. C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression , 2003, Nature Genetics.
[120] Bruce A. Hay,et al. The Drosophila MicroRNA Mir-14 Suppresses Cell Death and Is Required for Normal Fat Metabolism , 2003, Current Biology.
[121] R. Russell,et al. bantam Encodes a Developmentally Regulated microRNA that Controls Cell Proliferation and Regulates the Proapoptotic Gene hid in Drosophila , 2003, Cell.
[122] C. Burge,et al. Vertebrate MicroRNA Genes , 2003, Science.
[123] G. Dreyfuss,et al. Numerous microRNPs in neuronal cells containing novel microRNAs. , 2003, RNA.
[124] T. Tuschl,et al. New microRNAs from mouse and human. , 2003, RNA.
[125] Henning Urlaub,et al. Single-Stranded Antisense siRNAs Guide Target RNA Cleavage in RNAi , 2002, Cell.
[126] V. Kim,et al. MicroRNA maturation: stepwise processing and subcellular localization , 2002, The EMBO journal.
[127] Ira M. Hall,et al. Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi , 2002, Science.
[128] G. Hutvagner,et al. A microRNA in a Multiple-Turnover RNAi Enzyme Complex , 2002, Science.
[129] Diana Blank,et al. Yhh1p/Cft1p directly links poly(A) site recognition and RNA polymerase II transcription termination , 2002, The EMBO journal.
[130] B. Reinhart,et al. MicroRNAs in plants. , 2002, Genes & development.
[131] Jean Thierry-Mieg,et al. A global analysis of Caenorhabditis elegans operons , 2002, Nature.
[132] T. Nilsen,et al. New components of the spliced leader RNP required for nematode trans-splicing , 2002, Nature.
[133] Equilibrium studies on the association of the nuclear poly(A) binding protein with poly(A) of different lengths. , 2002, Biochemistry.
[134] D. Licatalosi,et al. Functional interaction of yeast pre-mRNA 3' end processing factors with RNA polymerase II. , 2002, Molecular cell.
[135] T. Tuschl,et al. Identification of Tissue-Specific MicroRNAs from Mouse , 2002, Current Biology.
[136] Jeffrey Wilusz,et al. Downstream sequence elements with different affinities for the hnRNP H/H' protein influence the processing efficiency of mammalian polyadenylation signals. , 2002, Nucleic acids research.
[137] M. Mann,et al. miRNPs: a novel class of ribonucleoproteins containing numerous microRNAs. , 2002, Genes & development.
[138] Marvin Wickens,et al. A PUF family portrait: 3'UTR regulation as a way of life. , 2002, Trends in genetics : TIG.
[139] A. Furger,et al. Integrating mRNA Processing with Transcription , 2002, Cell.
[140] Catriona Crombie,et al. The Caenorhabditis elegans histone hairpin-binding protein is required for core histone gene expression and is essential for embryonic and postembryonic cell division. , 2002, Journal of cell science.
[141] C. Moore,et al. Rna15 Interaction with the A-Rich Yeast Polyadenylation Signal Is an Essential Step in mRNA 3′-End Formation , 2001, Molecular and Cellular Biology.
[142] T. Tuschl,et al. Identification of Novel Genes Coding for Small Expressed RNAs , 2001, Science.
[143] V. Ambros,et al. An Extensive Class of Small RNAs in Caenorhabditis elegans , 2001, Science.
[144] L. Lim,et al. An Abundant Class of Tiny RNAs with Probable Regulatory Roles in Caenorhabditis elegans , 2001, Science.
[145] A. Caudy,et al. Argonaute2, a Link Between Genetic and Biochemical Analyses of RNAi , 2001, Science.
[146] J. Pelletier,et al. Full-length cDNAs: more than just reaching the ends. , 2001, Physiological genomics.
[147] A. Pasquinelli,et al. Genes and Mechanisms Related to RNA Interference Regulate Expression of the Small Temporal RNAs that Control C. elegans Developmental Timing , 2001, Cell.
[148] A. Pasquinelli,et al. A Cellular Function for the RNA-Interference Enzyme Dicer in the Maturation of the let-7 Small Temporal RNA , 2001, Science.
[149] S. Peltz,et al. The cap-to-tail guide to mRNA turnover , 2001, Nature Reviews Molecular Cell Biology.
[150] T. Blumenthal,et al. Interplay between AAUAAA and the trans-splice site in processing of a Caenorhabditis elegans operon pre-mRNA. , 2001, RNA.
[151] A. Caudy,et al. Role for a bidentate ribonuclease in the initiation step of RNA interference , 2001 .
[152] T. Tuschl,et al. RNA interference is mediated by 21- and 22-nucleotide RNAs. , 2001, Genes & development.
[153] S. Shuman,et al. Structure, mechanism, and evolution of the mRNA capping apparatus. , 2001, Progress in nucleic acid research and molecular biology.
[154] G. Carmichael,et al. Nucleocytoplasmic mRNA transport. , 2001, Results and problems in cell differentiation.
[155] Paul W. Sternberg,et al. WormBase: network access to the genome and biology of Caenorhabditis elegans , 2001, Nucleic Acids Res..
[156] B. Reinhart,et al. Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA , 2000, Nature.
[157] W. Keller,et al. Human pre‐mRNA cleavage factor IIm contains homologs of yeast proteins and bridges two other cleavage factors , 2000, The EMBO journal.
[158] M. Simonelig,et al. Tissue-specific autoregulation of Drosophila suppressor of forked by alternative poly(A) site utilization leads to accumulation of the suppressor of forked protein in mitotically active cells. , 2000, RNA.
[159] R. Schultz,et al. Selective reduction of dormant maternal mRNAs in mouse oocytes by RNA interference. , 2000, Development.
[160] D. Gautheret,et al. Patterns of variant polyadenylation signal usage in human genes. , 2000, Genome research.
[161] E. Wahle,et al. The nuclear poly(A) binding protein, PABP2, forms an oligomeric particle covering the length of the poly(A) tail. , 2000, Journal of molecular biology.
[162] P. Sharp,et al. RNAi Double-Stranded RNA Directs the ATP-Dependent Cleavage of mRNA at 21 to 23 Nucleotide Intervals , 2000, Cell.
[163] S. Hammond,et al. An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells , 2000, Nature.
[164] B. Reinhart,et al. The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans , 2000, Nature.
[165] Magdalena Zernicka-Goetz,et al. Specific interference with gene function by double-stranded RNA in early mouse development , 2000, Nature Cell Biology.
[166] M. Carmell,et al. Posttranscriptional Gene Silencing in Plants , 2006 .
[167] J. Birchler,et al. Cosuppression of Nonhomologous Transgenes in Drosophila Involves Mutually Related Endogenous Sequences , 1999, Cell.
[168] A. Wargelius,et al. Double-stranded RNA induces specific developmental defects in zebrafish embryos. , 1999, Biochemical and biophysical research communications.
[169] N. Copeland,et al. Two distinct forms of the 64,000 Mr protein of the cleavage stimulation factor are expressed in mouse male germ cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[170] E. Wahle,et al. 3'-End processing of pre-mRNA in eukaryotes. , 1999, FEMS microbiology reviews.
[171] L Misquitta,et al. Targeted disruption of gene function in Drosophila by RNA interference (RNA-i): a role for nautilus in embryonic somatic muscle formation. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[172] R. Carthew,et al. Use of dsRNA-Mediated Genetic Interference to Demonstrate that frizzled and frizzled 2 Act in the Wingless Pathway , 1998, Cell.
[173] K. Gull,et al. Double-stranded RNA induces mRNA degradation in Trypanosoma brucei. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[174] D. Schümperli,et al. A 5'-3' exonuclease activity involved in forming the 3' products of histone pre-mRNA processing in vitro. , 1998, RNA.
[175] W. G. Kelly,et al. Chromatin silencing and the maintenance of a functional germline in Caenorhabditis elegans. , 1998, Development.
[176] L. Sperling,et al. Homology-dependent gene silencing in Paramecium. , 1998, Molecular biology of the cell.
[177] A. Fire,et al. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans , 1998, Nature.
[178] J. Dantonel,et al. Transcription factor TFIID recruits factor CPSF for formation of 3′ end of mRNA , 1997, Nature.
[179] J. Manley,et al. RNA recognition by the human polyadenylation factor CstF , 1997, Molecular and cellular biology.
[180] G. Edwalds-Gilbert,et al. Alternative poly(A) site selection in complex transcription units: means to an end? , 1997, Nucleic acids research.
[181] D. Baulcombe,et al. A similarity between viral defense and gene silencing in plants. , 1997, Science.
[182] L. Minvielle-Sebastia,et al. A comparison of mammalian and yeast pre-mRNA 3'-end processing. , 1997, Current opinion in cell biology.
[183] M. Wickens,et al. Life and death in the cytoplasm: messages from the 3' end. , 1997, Current opinion in genetics & development.
[184] M. Wickens,et al. The C-terminal domain of RNA polymerase II couples mRNA processing to transcription , 1997, Nature.
[185] Thomas Blumenthal,et al. RNA Processing and Gene Structure , 1997 .
[186] A. Sachs,et al. Association of the yeast poly(A) tail binding protein with translation initiation factor eIF‐4G. , 1996, The EMBO journal.
[187] M. Whitfield,et al. The protein that binds the 3' end of histone mRNA: a novel RNA-binding protein required for histone pre-mRNA processing. , 1996, Genes & development.
[188] J. Spieth,et al. Gene structure and organization in Caenorhabditis elegans. , 1996, Current opinion in genetics & development.
[189] J. Manley,et al. The Polyadenylation Factor CstF-64 Regulates Alternative Processing of IgM Heavy Chain Pre-mRNA during B Cell Differentiation , 1996, Cell.
[190] B. Chabot. Directing alternative splicing: cast and scenarios. , 1996, Trends in genetics : TIG.
[191] M. Wormington,et al. Overexpression of poly(A) binding protein prevents maturation‐specific deadenylation and translational inactivation in Xenopus oocytes. , 1996, The EMBO journal.
[192] S. Peltz,et al. Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells. , 1996, Annual review of biochemistry.
[193] K. Murthy,et al. The 160-kD subunit of human cleavage-polyadenylation specificity factor coordinates pre-mRNA 3'-end formation. , 1995, Genes & development.
[194] J. Wilusz,et al. The G-rich auxiliary downstream element has distinct sequence and position requirements and mediates efficient 3' end pre-mRNA processing through a trans-acting factor. , 1995, Nucleic acids research.
[195] W. Marzluff,et al. The sequence of the stem and flanking sequences at the 3' end of histone mRNA are critical determinants for the binding of the stem-loop binding protein. , 1995, Nucleic acids research.
[196] I. Mattaj,et al. The influence of 5′ and 3′ end structures on pre-mRNA metabolism , 1995, Journal of Cell Science.
[197] Phillip A. Sharp,et al. Split genes and RNA splicing , 1994, Cell.
[198] H. L. Sänger,et al. RNA-directed de novo methylation of genomic sequences in plants , 1994, Cell.
[199] V. Ambros,et al. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14 , 1993, Cell.
[200] G. Ruvkun,et al. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans , 1993, Cell.
[201] W. Dougherty,et al. Induction of a Highly Specific Antiviral State in Transgenic Plants: Implications for Regulation of Gene Expression and Virus Resistance. , 1993, The Plant cell.
[202] C L Hsu,et al. Yeast cells lacking 5'-->3' exoribonuclease 1 contain mRNA species that are poly(A) deficient and partially lack the 5' cap structure , 1993, Molecular and cellular biology.
[203] G. Macino,et al. Quelling: transient inactivation of gene expression in Neurospora crassa by transformation with homologous sequences , 1992, Molecular microbiology.
[204] G. Christofori,et al. Cleavage and polyadenylation factor CPF specifically interacts with the pre‐mRNA 3′ processing signal AAUAAA. , 1991, The EMBO journal.
[205] J. Manley,et al. A multisubunit factor, CstF, is required for polyadenylation of mammalian pre-mRNAs. , 1990, Genes & development.
[206] M. Wickens,et al. Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro. , 1990, Nucleic acids research.
[207] C. Napoli,et al. Introduction of a Chimeric Chalcone Synthase Gene into Petunia Results in Reversible Co-Suppression of Homologous Genes in trans. , 1990, The Plant cell.
[208] C. Moore,et al. Two proteins crosslinked to RNA containing the adenovirus L3 poly(A) site require the AAUAAA sequence for binding. , 1988, The EMBO journal.
[209] J. Manley,et al. Polyadenylation of mRNA precursors. , 1988, Biochimica et biophysica acta.
[210] M. Wickens,et al. Role of the conserved AAUAAA sequence: four AAUAAA point mutants prevent messenger RNA 3' end formation. , 1984, Science.
[211] P. Sharp,et al. Site-specific polyadenylation in a cell-free reaction , 1984, Cell.
[212] A. Levinson,et al. Analysis of processing and polyadenylation signals of the hepatitis B virus surface antigen gene by using simian virus 40-hepatitis B virus chimeric plasmids , 1983, Molecular and cellular biology.
[213] S. Goodbourn,et al. Alpha-thalassaemia caused by a polyadenylation signal mutation. , 1983, Nature.
[214] T. Shenk,et al. THE SITE AT WHICH LATE mRNAs ARE POLYADENYLATED IS ALTERED IN SV40 MUTANT dl882 * , 1980, Annals of the New York Academy of Sciences.
[215] J. Rogers,et al. Two mRNAs can be produced from a single immunoglobulin μ gene by alternative RNA processing pathways , 1980, Cell.
[216] David Baltimore,et al. Synthesis of secreted and membrane-bound immunoglobulin mu heavy chains is directed by mRNAs that differ at their 3′ ends , 1980, Cell.
[217] J. Rogers,et al. Two mRNAs with different 3′ ends encode membrane-bound and secreted forms of immunoglobulin μ chain , 1980, Cell.