The mRNA Export Factor Gle1 and Inositol Hexakisphosphate Regulate Distinct Stages of Translation
暂无分享,去创建一个
[1] L. Peltonen,et al. Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease , 2008, Nature Genetics.
[2] S. R. Wente,et al. The DEAD-box protein Dbp5 controls mRNA export by triggering specific RNA:protein remodeling events. , 2007, Molecular cell.
[3] C. Hellen,et al. Recycling of Eukaryotic Posttermination Ribosomal Complexes , 2007, Cell.
[4] Ed Hurt,et al. Exporting RNA from the nucleus to the cytoplasm , 2007, Nature Reviews Molecular Cell Biology.
[5] Masatoshi Hagiwara,et al. Cross-talks between transcription and post-transcriptional events within a 'mRNA factory'. , 2007, Journal of biochemistry.
[6] J. Otto,et al. A Conserved Family of Enzymes That Phosphorylate Inositol Hexakisphosphate , 2007, Science.
[7] C. Cole,et al. The DEAD-Box RNA Helicase Dbp5 Functions in Translation Termination , 2007, Science.
[8] W. Sossin,et al. Intracellular Trafficking of RNA in Neurons , 2006, Traffic.
[9] K. Borden,et al. eIF4E is a central node of an RNA regulon that governs cellular proliferation , 2006, The Journal of cell biology.
[10] Alan G Hinnebusch,et al. eIF3: a versatile scaffold for translation initiation complexes. , 2006, Trends in biochemical sciences.
[11] J. Hershey,et al. Decreased expression of eukaryotic initiation factor 3f deregulates translation and apoptosis in tumor cells , 2006, Oncogene.
[12] J. Berger,et al. Activation of the DExD/H-box protein Dbp5 by the nuclear-pore protein Gle1 and its coactivator InsP6 is required for mRNA export , 2006, Nature Cell Biology.
[13] Susan R. Wente,et al. Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export , 2006, Nature Cell Biology.
[14] A. Hinnebusch. Translational regulation of GCN4 and the general amino acid control of yeast. , 2005, Annual review of microbiology.
[15] M. Moore. From Birth to Death: The Complex Lives of Eukaryotic mRNAs , 2005, Science.
[16] Abel R. Alcázar-Román,et al. Interaction between the shuttling mRNA export factor Gle1 and the nucleoporin hCG1: a conserved mechanism in the export of Hsp70 mRNA. , 2005, Molecular biology of the cell.
[17] B. Armbruster,et al. Inositol Diphosphate Signaling Regulates Telomere Length* , 2005, Journal of Biological Chemistry.
[18] S. Emr,et al. Cytoplasmic Inositol Hexakisphosphate Production Is Sufficient for Mediating the Gle1-mRNA Export Pathway* , 2004, Journal of Biological Chemistry.
[19] H. Krebber,et al. Yeast Shuttling SR Proteins Npl3p, Gbp2p, and Hrb1p Are Part of the Translating mRNPs, and Npl3p Can Function as a Translational Repressor , 2004, Molecular and Cellular Biology.
[20] A. Hinnebusch,et al. Functions of eIF3 downstream of 48S assembly impact AUG recognition and GCN4 translational control , 2004, The EMBO journal.
[21] H. Rayala,et al. The mRNA Export Factor Human Gle1 Interacts with the Nuclear Pore Complex Protein Nup155* , 2004, Molecular & Cellular Proteomics.
[22] Jon R Lorsch,et al. The molecular mechanics of eukaryotic translation. , 2003, Annual review of biochemistry.
[23] M. Hammarskjöld,et al. Tap and NXT promote translation of unspliced mRNA. , 2003, Genes & development.
[24] E. O’Shea,et al. Global analysis of protein expression in yeast , 2003, Nature.
[25] E. Griffis,et al. An essential role for hGle1 nucleocytoplasmic shuttling in mRNA export , 2003, The Journal of cell biology.
[26] A. Corbett,et al. Domain analysis of the Saccharomyces cerevisiae heterogeneous nuclear ribonucleoprotein, Nab2p. Dissecting the requirements for Nab2p-facilitated poly(A) RNA export. , 2003, The Journal of biological chemistry.
[27] A. Hinnebusch,et al. A subcomplex of three eIF3 subunits binds eIF1 and eIF5 and stimulates ribosome binding of mRNA and tRNAiMet , 2001, The EMBO journal.
[28] A. Hinnebusch,et al. Related eIF3 subunits TIF32 and HCR1 interact with an RNA recognition motif in PRT1 required for eIF3 integrity and ribosome binding , 2001, The EMBO journal.
[29] P. Silver,et al. Factors affecting nuclear export of the 60S ribosomal subunit in vivo. , 2000, Molecular biology of the cell.
[30] J. York,et al. A role for nuclear inositol 1,4,5-trisphosphate kinase in transcriptional control. , 2000, Science.
[31] S. Snyder,et al. Synthesis of diphosphoinositol pentakisphosphate by a newly identified family of higher inositol polyphosphate kinases , 1999, Current Biology.
[32] C. Cole,et al. Rat8p/Dbp5p is a shuttling transport factor that interacts with Rat7p/Nup159p and Gle1p and suppresses the mRNA export defect of xpo1‐1 cells , 1999, The EMBO journal.
[33] B. Séraphin,et al. Dbp5, a DEAD‐box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p , 1999, The EMBO journal.
[34] J. York,et al. A phospholipase C-dependent inositol polyphosphate kinase pathway required for efficient messenger RNA export. , 1999, Science.
[35] S. Hoshino,et al. The Eukaryotic Polypeptide Chain Releasing Factor (eRF3/GSPT) Carrying the Translation Termination Signal to the 3′-Poly(A) Tail of mRNA , 1999, The Journal of Biological Chemistry.
[36] A. Podtelejnikov,et al. The Mex67p‐mediated nuclear mRNA export pathway is conserved from yeast to human , 1999, The EMBO journal.
[37] M. Kladde,et al. Sth1p, a Saccharomyces cerevisiae Snf2p/Swi2p homolog, is an essential ATPase in RSC and differs from Snf/Swi in its interactions with histones and chromatin-associated proteins. , 1998, Genetics.
[38] A. Hinnebusch,et al. Nip1p Associates with 40 S Ribosomes and the Prt1p Subunit of Eukaryotic Initiation Factor 3 and Is Required for Efficient Translation Initiation* , 1998, The Journal of Biological Chemistry.
[39] J. L. Watkins,et al. The human homologue of Saccharomyces cerevisiae Gle1p is required for poly(A)+ RNA export. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[40] C. Cole,et al. Dbp5p/Rat8p is a yeast nuclear pore‐associated DEAD‐box protein essential for RNA export , 1998, The EMBO journal.
[41] M. Wilm,et al. TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus. , 1998, Molecular cell.
[42] A. Podtelejnikov,et al. Nup116p and Nup100p are interchangeable through a conserved motif which constitutes a docking site for the mRNA transport factor Gle2p , 1998, The EMBO journal.
[43] R. Lührmann,et al. Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)+ RNA and nuclear pores , 1997, The EMBO journal.
[44] J. L. Watkins,et al. GLE2, a Saccharomyces cerevisiae homologue of the Schizosaccharomyces pombe export factor RAE1, is required for nuclear pore complex structure and function. , 1996, Molecular biology of the cell.
[45] C. Cole,et al. The product of the Saccharomyces cerevisiae RSS1 gene, identified as a high-copy suppressor of the rat7-1 temperature-sensitive allele of the RAT7/NUP159 nucleoporin, is required for efficient mRNA export. , 1996, Molecular biology of the cell.
[46] S. Wente,et al. An RNA-export mediator with an essential nuclear export signal , 1996, Nature.
[47] N. Sonenberg,et al. Eukaryotic Translation Initiation Factor 4E Regulates Expression of Cyclin D1 at Transcriptional and Post-transcriptional Levels (*) , 1995, The Journal of Biological Chemistry.
[48] L. Kisselev,et al. Termination of translation in eukaryotes is governed by two interacting polypeptide chain release factors, eRF1 and eRF3. , 1995, The EMBO journal.
[49] J. Rousset,et al. Versatile vectors to study recoding: conservation of rules between yeast and mammalian cells. , 1995, Nucleic acids research.
[50] C. Cole,et al. A conditional allele of the novel repeat-containing yeast nucleoporin RAT7/NUP159 causes both rapid cessation of mRNA export and reversible clustering of nuclear pore complexes , 1995, The Journal of cell biology.
[51] I. Stansfield,et al. A mutant allele of the SUP45 (SAL4) gene of Saccharomyces cerevisiae shows temperature-dependent allosuppressor and omnipotent suppressor phenotypes , 1995, Current Genetics.
[52] G. Blobel,et al. A temperature-sensitive NUP116 null mutant forms a nuclear envelope seal over the yeast nuclear pore complex thereby blocking nucleocytoplasmic traffic , 1993, The Journal of cell biology.
[53] G. Blobel,et al. A new family of yeast nuclear pore complex proteins , 1992, The Journal of cell biology.
[54] D. Goldfarb,et al. NIP1, a gene required for nuclear transport in yeast. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[55] A. Hinnebusch,et al. Association of RAP1 binding sites with stringent control of ribosomal protein gene transcription in Saccharomyces cerevisiae , 1991, Molecular and cellular biology.
[56] F. Sherman,et al. Isolation and characterization of omnipotent suppressors in the yeast Saccharomyces cerevisiae. , 1990, Genetics.
[57] R. Sikorski,et al. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. , 1989, Genetics.
[58] A. Hinnebusch. A hierarchy of trans-acting factors modulates translation of an activator of amino acid biosynthetic genes in Saccharomyces cerevisiae , 1985, Molecular and cellular biology.
[59] B. Cox,et al. Ψ, A cytoplasmic suppressor of super-suppressor in yeast , 1965, Heredity.
[60] B. Séraphin,et al. Dbp 5 , a DEAD-box protein required for mRNA export , is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN / Nup 159 p , 1999 .