RNA Targets and Specificity of Staufen, a Double-stranded RNA-binding Protein in Caenorhabditis elegans*
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Marvin Wickens | M. Wickens | P. Anderson | J. Kimble | Judith Kimble | Jacqueline Baca LeGendre | Zachary T Campbell | Peggy Kroll-Conner | Phil Anderson | Z. Campbell | P. Kroll-Conner | J. Legendre | Peggy L. Kroll-Conner
[1] D. St Johnston,et al. A conserved double-stranded RNA-binding domain. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[2] Michael Zuker,et al. Mfold web server for nucleic acid folding and hybridization prediction , 2003, Nucleic Acids Res..
[3] Scott Kennedy,et al. Requirement for the ERI/DICER Complex in Endogenous RNA Interference and Sperm Development in Caenorhabditis elegans , 2009, Genetics.
[4] Kuniaki Saito,et al. Endo‐siRNAs depend on a new isoform of loquacious and target artificially introduced, high‐copy sequences , 2009, The EMBO journal.
[5] R. Lehmann,et al. The maternal gene nanos has a central role in posterior pattern formation of the Drosophila embryo. , 1991, Development.
[6] G. Dreyfuss,et al. Messenger-RNA-binding proteins and the messages they carry , 2002, Nature Reviews Molecular Cell Biology.
[7] J. Steitz,et al. Evidence for reassociation of RNA-binding proteins after cell lysis: implications for the interpretation of immunoprecipitation analyses. , 2004, RNA.
[8] B. Bass,et al. dsRNA binding properties of RDE-4 and TRBP reflect their distinct roles in RNAi. , 2008, Journal of molecular biology.
[9] Ayelet T. Lamm,et al. Competition between ADAR and RNAi pathways for an extensive class of RNA targets , 2011, Nature Structural &Molecular Biology.
[10] L. Maquat,et al. lncRNAs transactivate Staufen1-mediated mRNA decay by duplexing with 3'UTRs via Alu elements , 2010, Nature.
[11] D. Johnston,et al. THE POLARISATION OF THE ANTERIOR-POSTERIOR AND DORSAL-VENTRAL AXES DURING DROSOPHILA OOGENESIS , 1999 .
[12] K. Kok,et al. Human TRBP and PACT Directly Interact with Each Other and Associate with Dicer to Facilitate the Production of Small Interfering RNA* , 2007, Journal of Biological Chemistry.
[13] M. Kiebler,et al. The Mammalian Staufen Protein Localizes to the Somatodendritic Domain of Cultured Hippocampal Neurons: Implications for Its Involvement in mRNA Transport , 1999, The Journal of Neuroscience.
[14] V. Ambros,et al. Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences. , 1991, The EMBO journal.
[15] S. Fields,et al. The two-hybrid system: a method to identify and clone genes for proteins that interact with a protein of interest. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[16] Peng Li,et al. Inscuteable and Staufen Mediate Asymmetric Localization and Segregation of prospero RNA during Drosophila Neuroblast Cell Divisions , 1997, Cell.
[17] Min Han,et al. Diverse Chromatin Remodeling Genes Antagonize the Rb-Involved SynMuv Pathways in C. elegans , 2006, PLoS genetics.
[18] Xiaodong Wang,et al. R2D2, a Bridge Between the Initiation and Effector Steps of the Drosophila RNAi Pathway , 2003, Science.
[19] Louise Wickham,et al. Mammalian Staufen Is a Double-Stranded-RNA- and Tubulin-Binding Protein Which Localizes to the Rough Endoplasmic Reticulum , 1999, Molecular and Cellular Biology.
[20] M. O’Connell,et al. RNA editing by mammalian ADARs. , 2011, Advances in genetics.
[21] M. Kiebler,et al. Microtubule-dependent recruitment of Staufen-green fluorescent protein into large RNA-containing granules and subsequent dendritic transport in living hippocampal neurons. , 1999, Molecular biology of the cell.
[22] I. Kerr,et al. Molecular cloning and characterization of the human double-stranded RNA-activated protein kinase induced by interferon , 1990, Cell.
[23] Y. Jan,et al. Staufen: a common component of mRNA transport in oocytes and neurons? , 2000, Trends in cell biology.
[24] R. Carthew,et al. Methods and Materials , 1956, Eco-Art Therapy in Practice.
[25] Ronald H. A. Plasterk,et al. Transposon silencing in the Caenorhabditis elegans germ line by natural RNAi , 2003, Nature.
[26] S C Schultz,et al. Molecular basis of double‐stranded RNA‐protein interactions: structure of a dsRNA‐binding domain complexed with dsRNA , 1998, The EMBO journal.
[27] A. Caudy,et al. Role for a bidentate ribonuclease in the initiation step of RNA interference , 2001 .
[28] Luc DesGroseillers,et al. Mammalian Staufen1 Recruits Upf1 to Specific mRNA 3′UTRs so as to Elicit mRNA Decay , 2005, Cell.
[29] G. Barber,et al. The dsRNA binding protein family: critical roles, diverse cellular functions , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[30] Gabriele Varani,et al. RNA recognition by a Staufen double‐stranded RNA‐binding domain , 2000, The EMBO journal.
[31] Noah C. Welker,et al. Dicer's helicase domain is required for accumulation of some, but not all, C. elegans endogenous siRNAs. , 2010, RNA.
[32] R. Tibshirani,et al. Significance analysis of microarrays applied to the ionizing radiation response , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[33] L. Maquat,et al. Staufen1 regulates diverse classes of mammalian transcripts , 2007, The EMBO journal.
[34] Gary Ruvkun,et al. A conserved siRNA-degrading RNase negatively regulates RNA interference in C. elegans , 2004, Nature.
[35] C. Mello,et al. The dsRNA Binding Protein RDE-4 Interacts with RDE-1, DCR-1, and a DExH-Box Helicase to Direct RNAi in C. elegans , 2002, Cell.
[36] M. Mathews,et al. Proteins binding to duplexed RNA: one motif, multiple functions. , 2000, Trends in biochemical sciences.
[37] D. St Johnston,et al. Distinct roles of two conserved Staufen domains in oskar mRNA localization and translation , 2000, The EMBO journal.
[38] Thomas D. Schmittgen,et al. Analyzing real-time PCR data by the comparative CT method , 2008, Nature Protocols.
[39] M. Ghosh,et al. Solution structure of the Drosha double-stranded RNA-binding domain , 2010, Silence.
[40] Marvin Wickens,et al. Cooperativity in RNA-protein interactions: global analysis of RNA binding specificity. , 2012, Cell reports.
[41] E. Schuman,et al. A Role for a Rat Homolog of Staufen in the Transport of RNA to Neuronal Dendrites , 2001, Neuron.
[42] N. Buchon,et al. RNAi: a defensive RNA-silencing against viruses and transposable elements , 2006, Heredity.
[43] B. Williams,et al. PKR; a sentinel kinase for cellular stress , 1999, Oncogene.
[44] Marvin Wickens,et al. RNA-protein interactions in the yeast three-hybrid system: affinity, sensitivity, and enhanced library screening. , 2005, RNA.
[45] Gabriele Varani,et al. RNA is rarely at a loss for companions; as soon as RNA , 2008 .
[46] L. Furic,et al. A genome-wide approach identifies distinct but overlapping subsets of cellular mRNAs associated with Staufen1- and Staufen2-containing ribonucleoprotein complexes. , 2007, RNA.
[47] C. Doe,et al. Staufen-dependent localization of prospero mRNA contributes to neuroblast daughter-cell fate , 1998, Nature.
[48] D L Riddle,et al. Gene expression profiling of cells, tissues, and developmental stages of the nematode C. elegans. , 2003, Cold Spring Harbor symposia on quantitative biology.
[49] M. Chalfie,et al. Enhanced neuronal RNAi in C. elegans using SID-1 , 2010, Nature Methods.
[50] D. Silhavy,et al. Double-Stranded RNA Binding May Be a General Plant RNA Viral Strategy To Suppress RNA Silencing , 2006, Journal of Virology.
[51] Marvin Wickens,et al. Binding specificity and mRNA targets of a C. elegans PUF protein, FBF-1. , 2005, RNA.
[52] C. Mello,et al. Revealing the world of RNA interference , 2004, Nature.
[53] E. Wieschaus,et al. Germline autonomy of maternal-effect mutations altering the embryonic body pattern of Drosophila. , 1986, Developmental biology.
[54] E Westhof,et al. RNA–RNA interaction is required for the formation of specific bicoid mRNA 3′ UTR–STAUFEN ribonucleoprotein particles , 1997, The EMBO journal.
[55] Daniel St Johnston,et al. staufen, a gene required to localize maternal RNAs in the Drosophila egg , 1991, Cell.
[56] Ivo L. Hofacker,et al. Vienna RNA secondary structure server , 2003, Nucleic Acids Res..
[57] Kimihito Ito,et al. Tobacco calmodulin-like protein provides secondary defense by binding to and directing degradation of virus RNA silencing suppressors , 2012, Proceedings of the National Academy of Sciences.
[58] B. Bass,et al. RNA hairpins in noncoding regions of human brain and Caenorhabditis elegans mRNA are edited by adenosine deaminases that act on RNA , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[59] M. Krause,et al. Proteomic analysis uncovers a metabolic phenotype in C. elegans after nhr-40 reduction of function. , 2008, Biochemical and biophysical research communications.
[60] D. Court,et al. Noncatalytic assembly of ribonuclease III with double-stranded RNA. , 2004, Structure.
[61] Brad T. Sherman,et al. DAVID: Database for Annotation, Visualization, and Integrated Discovery , 2003, Genome Biology.
[62] Dominique Ferrandon,et al. Staufen protein associates with the 3′UTR of bicoid mRNA to form particles that move in a microtubule-dependent manner , 1994, Cell.
[63] B. Bass,et al. Adar Editing in Double-stranded Utrs and Other Noncoding Rna Sequences , 2022 .
[64] A. Fire,et al. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans , 1998, Nature.
[65] Andres Ramos,et al. The double‐stranded RNA‐binding motif, a versatile macromolecular docking platform , 2005, The FEBS journal.
[66] Ayelet T. Lamm,et al. Distinct phases of siRNA synthesis in an endogenous RNAi pathway in C. elegans soma. , 2010, Molecular cell.
[67] M. Kiebler,et al. Isolation and characterization of Staufen-containing ribonucleoprotein particles from rat brain , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[68] Harrison W. Gabel,et al. mut-16 and other mutator class genes modulate 22G and 26G siRNA pathways in Caenorhabditis elegans , 2011, Proceedings of the National Academy of Sciences.
[69] A. Fire,et al. Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans. , 2001, Gene.
[70] Sandhya P Koushika,et al. Loss of the Putative RNA-Directed RNA Polymerase RRF-3 Makes C. elegans Hypersensitive to RNAi , 2002, Current Biology.
[71] D. St Johnston,et al. Miranda mediates asymmetric protein and RNA localization in the developing nervous system. , 1998, Genes & development.
[72] M. Kiebler,et al. Staufen2 isoforms localize to the somatodendritic domain of neurons and interact with different organelles. , 2002, Journal of cell science.