Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae.
about
Regulon-specific control of transcription elongation across the yeast genomeHuman hHpr1/p84/Thoc1 regulates transcriptional elongation and physically links RNA polymerase II and RNA processing factors.Recruitment of the human TREX complex to mRNA during splicingCancer cells and normal cells differ in their requirements for Thoc1The yeast THO complex and mRNA export factors link RNA metabolism with transcription and genome instability.Stable mRNP formation and export require cotranscriptional recruitment of the mRNA export factors Yra1p and Sub2p by Hpr1pMolecular evidence for a positive role of Spt4 in transcription elongation.Vps factors are required for efficient transcription elongation in budding yeast.Tho1, a novel hnRNP, and Sub2 provide alternative pathways for mRNP biogenesis in yeast THO mutantsAn hpr1 point mutation that impairs transcription and mRNP biogenesis without increasing recombination.Swt1, a novel yeast protein, functions in transcription.The Transcription Factor THO Promotes Transcription Initiation and Elongation by RNA Polymerase I.Evidence that Spt2/Sin1, an HMG-like factor, plays roles in transcription elongation, chromatin structure, and genome stability in Saccharomyces cerevisiaeInteractions between mRNA export commitment, 3'-end quality control, and nuclear degradationAn ataxia-telangiectasia-mutated (ATM) kinase mediated response to DNA damage down-regulates the mRNA-binding potential of THOC5THOC5 controls 3'end-processing of immediate early genes via interaction with polyadenylation specific factor 100 (CPSF100).Protecting exons from deleterious R-loops: a potential advantage of having intronsGenome-wide analysis of factors affecting transcription elongation and DNA repair: a new role for PAF and Ccr4-not in transcription-coupled repair.An allelic series for studying the mouse Thoc1 geneAID induces double-strand breaks at immunoglobulin switch regions and c-MYC causing chromosomal translocations in yeast THO mutants.Intronic L1 retrotransposons and nested genes cause transcriptional interference by inducing intron retention, exonization and cryptic polyadenylation.Genome-wide profiling of yeast DNA:RNA hybrid prone sites with DRIP-chipRole of transcription in plasmid maintenance in the hpr1Delta mutant of Saccharomyces cerevisiaeThe connection between transcription and genomic instability.Activation-induced cytidine deaminase action is strongly stimulated by mutations of the THO complexThoc1/Hpr1/p84 is essential for early embryonic development in the mouse.THOC5, a member of the mRNA export complex, contributes to processing of a subset of wingless/integrated (Wnt) target mRNAs and integrity of the gut epithelial barrier.Genes with internal repeats require the THO complex for transcriptionStructural characterization of the Saccharomyces cerevisiae THO complex by small-angle X-ray scatteringDepleting components of the THO complex causes increased telomere length by reducing the expression of the telomere-associated protein Rif1pUse of an in vivo reporter assay to test for transcriptional and translational fidelity in yeast.Splicing-independent loading of TREX on nascent RNA is required for efficient expression of dual-strand piRNA clusters in Drosophila.New roles for old characters: an educational primer for use with "Vps factors are required for efficient transcription elongation in budding yeast".mRNA journey to the cytoplasm: attire required.Thoc1 deficiency compromises gene expression necessary for normal testis development in the mouseThe yeast THO complex forms a 5-subunit assembly that directly interacts with active chromatin.THOC5, a member of the mRNA export complex: a novel link between mRNA export machinery and signal transduction pathways in cell proliferation and differentiation.Genome-wide function of THO/TREX in active genes prevents R-loop-dependent replication obstacles.Depletion of three combined THOC5 mRNA export protein target genes synergistically induces human hepatocellular carcinoma cell death.Nucleoporin 35 regulates cardiomyocyte pH homeostasis by controlling Na+-H+ exchanger-1 expression.
P2860
Q21144996-AF57A704-D79D-4292-A9EE-2E48BABBE815Q24301347-554D28FA-1275-4FF8-8FEC-39A30F921F70Q24306879-A98E512C-6D7E-4D8B-9917-8414C63B24C2Q24647728-456E7E32-D22A-4169-A894-F92DACBC6669Q27929526-D8648D91-4B46-40C6-A6D2-862652868707Q27929754-9301F743-DE47-418A-B070-B06CCA66C061Q27930449-D34D5E2A-0833-467D-AA15-C1DF1D987025Q27931871-0F45383E-7A63-459C-8A72-E4F52E60F39DQ27931954-AF4AA347-99C5-48F3-860D-9B973640E0C4Q27931955-4C88CA4F-AFD3-4A97-90AC-10F91193C20CQ27932271-9777A038-622A-4E55-A8F9-3CB557B5748CQ27933292-7E3A76A8-D27D-42B4-9EA6-357EC3222BA7Q27938910-76FD1F0C-3F50-4927-9CE4-10F8BD1F5E12Q27938985-818DFE3B-435A-45C4-9196-579F8C254E46Q28392918-F153E341-EE43-4C9B-B45E-315A5C97BA9AQ30425526-7C1EE719-6D46-4470-ABD7-5FFA9BB9E115Q33282780-AA5DC4A0-3376-4330-8715-51E5784D3762Q33406244-0A5D2883-2AC1-4DC1-8491-E09DA2EB6245Q33561995-0802D345-6851-4C61-A30F-E4BC89618321Q33839428-E5BCA4A1-EADE-45C2-9CE8-F9D6A1AADEE9Q34055996-62497514-3221-474C-BD93-9799777E2D5BQ34415765-B6CD8FBC-E05C-4A1F-9E26-B1EB31AD1DDDQ34443697-EE7004FC-B77B-4CE7-80B8-E92F7759EB5CQ34514282-50E71C7E-30F3-405A-9298-DC9346EB2983Q34626621-5CB7E48C-267F-4C51-AEDB-EDC905E7AF64Q34718004-73A65564-FB6E-4045-94C1-F31C9B4ABA60Q35051126-3038C46D-D344-4CEB-A44A-DA2DAB6D51E0Q35080678-D8CB7B3F-9B3D-4ABA-8B05-0FEC9DA3AFA3Q35213228-731CC7F6-1D65-489F-AE2A-3B3DEFE0A110Q35842463-DE102DF0-29C9-4E08-B8BE-1838DA7AD8BBQ36021423-8400A0DD-61FD-4505-B651-A91BD8D8B5EBQ36783025-A3FB637F-879C-42D6-8C10-FC2B495C558DQ36784770-E42F8091-56A3-49BF-8B23-CFCB88F53E3CQ37163404-EBE051C2-E75D-428F-B27D-BAFC3EE90D3DQ37192086-9F7CC728-9A69-42AE-B02F-F6EA6AB275C9Q38042310-53EB9C6D-D3D3-4D20-A807-0D2F1A680D95Q38177381-E24ABC29-6F04-4A31-B408-C805BE677DC0Q38254699-4C990804-9BE2-4B21-ACF4-285CB6A31BF2Q38821041-C1C78BCA-0703-49BC-87BD-9ECC52F4B465Q38844797-D513BAFB-74D7-4510-AED7-122A03C57715
P2860
Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Hpr1 is preferentially require ...... s in Saccharomyces cerevisiae.
@en
Hpr1 is preferentially require ...... s in Saccharomyces cerevisiae.
@nl
type
label
Hpr1 is preferentially require ...... s in Saccharomyces cerevisiae.
@en
Hpr1 is preferentially require ...... s in Saccharomyces cerevisiae.
@nl
prefLabel
Hpr1 is preferentially require ...... s in Saccharomyces cerevisiae.
@en
Hpr1 is preferentially require ...... s in Saccharomyces cerevisiae.
@nl
P2860
P50
P1476
Hpr1 is preferentially require ...... es in Saccharomyces cerevisiae
@en
P2093
M García-Rubio
P2860
P304
P356
10.1128/MCB.21.20.7054-7064.2001
P407
P577
2001-10-01T00:00:00Z