The DEAD-box protein Dbp5p is required to dissociate Mex67p from exported mRNPs at the nuclear rim.
暂无分享,去创建一个
[1] Helena Santos-Rosa,et al. Nuclear mRNA Export Requires Complex Formation between Mex67p and Mtr2p at the Nuclear Pores , 1998, Molecular and Cellular Biology.
[2] 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.
[3] R. Parker,et al. Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts. , 2001, RNA.
[4] 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.
[5] K Strässer,et al. Yra1p, a conserved nuclear RNA‐binding protein, interacts directly with Mex67p and is required for mRNA export , 2000, The EMBO journal.
[6] B. Cullen,et al. Nuclear mRNA export: insights from virology. , 2003, Trends in biochemical sciences.
[7] C. Guthrie,et al. An essential nuclear envelope integral membrane protein, Brr6p, required for nuclear transport , 2001, The EMBO journal.
[8] Jean-Christophe Olivo-Marin,et al. Nuclear pore complexes in the organization of silent telomeric chromatin , 2000, Nature.
[9] C. Cole,et al. Dbp5p/Rat8p is a yeast nuclear pore‐associated DEAD‐box protein essential for RNA export , 1998, The EMBO journal.
[10] M. Rosbash,et al. Quality control of mRNA 3′-end processing is linked to the nuclear exosome , 2001, Nature.
[11] C. Guthrie,et al. Deletion of MUD2, the yeast homolog of U2AF65, can bypass the requirement for sub2, an essential spliceosomal ATPase. , 2001, Genes & development.
[12] Daniel Zenklusen,et al. Perinuclear Mlp proteins downregulate gene expression in response to a defect in mRNA export , 2005, The EMBO journal.
[13] Christine Guthrie,et al. The Glc7p nuclear phosphatase promotes mRNA export by facilitating association of Mex67p with mRNA. , 2004, Molecular cell.
[14] M. Rosbash,et al. Interactions between mRNA Export Commitment, 3′-End Quality Control, and Nuclear Degradation , 2002, Molecular and Cellular Biology.
[15] Tamás Fischer,et al. The mRNA export machinery requires the novel Sac3p–Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores , 2002, The EMBO journal.
[16] Yan Liu,et al. Dbp5p, a cytosolic RNA helicase, is required for poly(A)+ RNA export , 1998, The EMBO journal.
[17] M. Rosbash,et al. A block to mRNA nuclear export in S. cerevisiae leads to hyperadenylation of transcripts that accumulate at the site of transcription. , 2001, Molecular cell.
[18] B. Daneholt,et al. Assembly and transport of a premessenger RNP particle , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[19] Anton J. Enright,et al. References and Notes Materials and Methods Som Text Figs. S1 to S9 Tables S1 to S3 References and Notes Protein Displacement by Dexh/d " Rna Helicases " without Duplex Unwinding , 2022 .
[20] D. Kellogg,et al. Biochemical and genetic characterization of Yra1p in budding yeast , 2005, Yeast.
[21] P. Silver,et al. Messenger RNAs are recruited for nuclear export during transcription. , 2001, Genes & development.
[22] F. Förster,et al. Nuclear Pore Complex Structure and Dynamics Revealed by Cryoelectron Tomography , 2004, Science.
[23] 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.
[24] K. Jeang,et al. Requirement of DDX3 DEAD Box RNA Helicase for HIV-1 Rev-RRE Export Function , 2004, Cell.
[25] W. Gilbert,et al. Phosphorylation by Sky1p promotes Npl3p shuttling and mRNA dissociation. , 2001, RNA.
[26] C. Cole,et al. An early function during transcription for the yeast mRNA export factor Dbp5p/Rat8p suggested by its genetic and physical interactions with transcription factor IIH components. , 2003, Molecular biology of the cell.
[27] B. Chait,et al. The Yeast Nuclear Pore Complex: Composition, Architecture, and Transport Mechanism , 2000 .
[28] E. Izaurralde,et al. TAP binds to the constitutive transport element (CTE) through a novel RNA‐binding motif that is sufficient to promote CTE‐dependent RNA export from the nucleus , 1999, The EMBO journal.
[29] Daniel Zenklusen,et al. The Yeast hnRNP-Like Proteins Yra1p and Yra2p Participate in mRNA Export through Interaction with Mex67p , 2001, Molecular and Cellular Biology.
[30] B. Daneholt,et al. The mRNA export factor Dbp5 is associated with Balbiani ring mRNP from gene to cytoplasm , 2002, The EMBO journal.
[31] E. Izaurralde. A novel family of nuclear transport receptors mediates the export of messenger RNA to the cytoplasm. , 2002, European journal of cell biology.
[32] R. Jackups,et al. Specific alterations of U1-C protein or U1 small nuclear RNA can eliminate the requirement of Prp28p, an essential DEAD box splicing factor. , 2001, Molecular cell.
[33] P. Bork,et al. REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export. , 2000, RNA.
[34] 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.
[35] A. Podtelejnikov,et al. The Mex67p‐mediated nuclear mRNA export pathway is conserved from yeast to human , 1999, The EMBO journal.