scholarly article | Q13442814 |
P2093 | author name string | D Tollervey | |
E Petfalski | |||
P Mitchell | |||
C Allmang | |||
P2860 | cites work | The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism | Q24322559 |
Functions of the exosome in rRNA, snoRNA and snRNA synthesis | Q24529845 | ||
Comparative sequence analysis of ribonucleases HII, III, II PH and D | Q24545101 | ||
Yeast exosome mutants accumulate 3'-extended polyadenylated forms of U4 small nuclear RNA and small nucleolar RNAs | Q24554352 | ||
The 5' end of yeast 5.8S rRNA is generated by exonucleases from an upstream cleavage site | Q24595513 | ||
The yeast exosome and human PM-Scl are related complexes of 3' --> 5' exonucleases | Q24600315 | ||
The exosome: a conserved eukaryotic RNA processing complex containing multiple 3'-->5' exoribonucleases | Q27930922 | ||
Depletion of yeast ribosomal proteins L16 or rp59 disrupts ribosome assembly | Q27931599 | ||
Rrp6p, the yeast homologue of the human PM-Scl 100-kDa autoantigen, is essential for efficient 5.8 S rRNA 3' end formation | Q27933100 | ||
RRP5 is required for formation of both 18S and 5.8S rRNA in yeast | Q27933500 | ||
A nuclear 3'-5' exonuclease involved in mRNA degradation interacts with Poly(A) polymerase and the hnRNA protein Npl3p | Q27934140 | ||
The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex | Q27934144 | ||
Ribosome synthesis in Saccharomyces cerevisiae | Q27935371 | ||
A novel protein shared by RNase MRP and RNase P. | Q27935679 | ||
The POP1 gene encodes a protein component common to the RNase MRP and RNase P ribonucleoproteins | Q27936503 | ||
Mutations in nucleolar proteins lead to nucleolar accumulation of polyA+ RNA in Saccharomyces cerevisiae | Q27937192 | ||
Pop3p is essential for the activity of the RNase MRP and RNase P ribonucleoproteins in vivo | Q27937799 | ||
Depletion of Saccharomyces cerevisiae ribosomal protein L16 causes a decrease in 60S ribosomal subunits and formation of half-mer polyribosomes | Q27938597 | ||
Dob1p (Mtr4p) is a putative ATP-dependent RNA helicase required for the 3' end formation of 5.8S rRNA in Saccharomyces cerevisiae | Q27939006 | ||
The yeast La protein is required for the 3' endonucleolytic cleavage that matures tRNA precursors | Q27939555 | ||
Saccharomyces cerevisiae Nip7p is required for efficient 60S ribosome subunit biogenesis. | Q27939938 | ||
Protein trans-acting factors involved in ribosome biogenesis in Saccharomyces cerevisiae | Q29620522 | ||
Depletion of U3 small nucleolar RNA inhibits cleavage in the 5′ external transcribed spacer of yeast pre-ribosomal RNA and impairs formation of 18S ribosomal RNA | Q29620875 | ||
Fungal small nuclear ribonucleoproteins share properties with plant and vertebrate U-snRNPs. | Q30403263 | ||
Yeast 18S rRNA dimethylase Dim1p: a quality control mechanism in ribosome synthesis? | Q32075110 | ||
The exosome: a proteasome for RNA? | Q33778598 | ||
Identification and functional analysis of two U3 binding sites on yeast pre-ribosomal RNA | Q33937656 | ||
A new rRNA processing mutant of Saccharomyces cerevisiae | Q35012229 | ||
A temperature sensitive mutant of Saccharomyces cerevisiae defective in pre-rRNA processing | Q35782598 | ||
One-step PCR mediated strategy for the construction of conditionally expressed and epitope tagged yeast proteins | Q39717268 | ||
The exosome subunit Rrp43p is required for the efficient maturation of 5.8S, 18S and 25S rRNA. | Q39727370 | ||
Some characteristics of processing sites in ribosomal precursor RNA of yeast | Q40481736 | ||
Birth of the snoRNPs: the evolution of RNase MRP and the eukaryotic pre-rRNA-processing system | Q40497606 | ||
The nucleotide sequence of the intergenic region between the 5.8S and 26S rRNA genes of the yeast ribosomal RNA operon. Possible implications for the interaction between 5.8S and 26S rRNA and the processing of the primary transcript | Q40499995 | ||
Two distinct recognition signals define the site of endonucleolytic cleavage at the 5′-end of yeast 18S rRNA | Q40789596 | ||
Processing of the yeast pre-rRNA at sites A(2) and A(3) is linked. | Q41965703 | ||
Evolutionarily Conserved Structural Elements are Critical for Processing of Internal Transcribed Spacer 2 fromSaccharomyces cerevisiaePrecursor Ribosomal RNA | Q48072730 | ||
The role of the 3′ external transcribed spacer in yeast pre-rRNA processing | Q64443147 | ||
Internal transcribed spacer 1 of the yeast precursor ribosomal RNA. Higher order structure and common structural motifs | Q68348636 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1684-1691 | |
P577 | publication date | 2000-04-01 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | Degradation of ribosomal RNA precursors by the exosome | |
P478 | volume | 28 |
Q34699786 | 5'-end surveillance by Xrn2 acts as a shared mechanism for mammalian pre-rRNA maturation and decay |
Q27936402 | 5-fluorouracil enhances exosome-dependent accumulation of polyadenylated rRNAs |
Q43940122 | A RAC protein-binding site in the internal transcribed spacer 2 of Pre-rRNA transcripts from Schizosaccharomyces pombe |
Q52542673 | A chaperone for ribosome maturation. |
Q40315347 | A complex pathway for 3' processing of the yeast U3 snoRNA. |
Q35641757 | A novel plasmid-based microarray screen identifies suppressors of rrp6Delta in Saccharomyces cerevisiae |
Q27935552 | A single subunit, Dis3, is essentially responsible for yeast exosome core activity |
Q34133261 | A source of the single-stranded DNA substrate for activation-induced deaminase during somatic hypermutation |
Q33741719 | A tool kit for quantifying eukaryotic rRNA gene sequences from human microbiome samples |
Q24658122 | A yeast exosome cofactor, Mpp6, functions in RNA surveillance and in the degradation of noncoding RNA transcripts |
Q24291926 | AU binding proteins recruit the exosome to degrade ARE-containing mRNAs |
Q37390891 | Active destruction of defective ribosomes by a ubiquitin ligase involved in DNA repair |
Q36246643 | Air proteins control differential TRAMP substrate specificity for nuclear RNA surveillance |
Q27936597 | An NMD pathway in yeast involving accelerated deadenylation and exosome-mediated 3'-->5' degradation |
Q36676485 | Apoptotic signals induce specific degradation of ribosomal RNA in yeast |
Q37288767 | Arabidopsis AtRRP44A is the functional homolog of Rrp44/Dis3, an exosome component, is essential for viability and is required for RNA processing and degradation |
Q38210936 | Assembly and nuclear export of pre-ribosomal particles in budding yeast |
Q50135088 | Assembly and structure of the SSU processome-a nucleolar precursor of the small ribosomal subunit. |
Q27933565 | Assembly factors Rpf2 and Rrs1 recruit 5S rRNA and ribosomal proteins rpL5 and rpL11 into nascent ribosomes |
Q37233841 | Assembly of ribosomes and spliceosomes: complex ribonucleoprotein machines |
Q88523573 | Assembly of the small ribosomal subunit in yeast: mechanism and regulation |
Q27931503 | Bms1p, a novel GTP-binding protein, and the related Tsr1p are required for distinct steps of 40S ribosome biogenesis in yeast |
Q28115038 | Both endonucleolytic and exonucleolytic cleavage mediate ITS1 removal during human ribosomal RNA processing |
Q30673378 | Brix from xenopus laevis and brx1p from yeast define a new family of proteins involved in the biogenesis of large ribosomal subunits. |
Q24301838 | C1D and hMtr4p associate with the human exosome subunit PM/Scl-100 and are involved in pre-rRNA processing |
Q28260762 | Cell and molecular biology of the exosome: how to make or break an RNA |
Q28271596 | Characterization of native and reconstituted exosome complexes from the hyperthermophilic archaeon Sulfolobus solfataricus |
Q41432701 | Characterization of the mammalian RNA exonuclease 5/NEF-sp as a testis-specific nuclear 3' → 5' exoribonuclease |
Q39317738 | Comparison of preribosomal RNA processing pathways in yeast, plant and human cells - focus on coordinated action of endo- and exoribonucleases. |
Q24540216 | Contribution of domain structure to the RNA 3' end processing and degradation functions of the nuclear exosome subunit Rrp6p |
Q34813102 | Conventional and nonconventional roles of the nucleolus |
Q27639469 | Crystal structure of an RNA helix recognized by a zinc-finger protein: an 18-bp duplex at 1.6 A resolution |
Q21562658 | Crystal structure of the S. solfataricus archaeal exosome reveals conformational flexibility in the RNA-binding ring |
Q51440900 | DRN and TRAMP degrade specific and overlapping aberrant mRNAs formed at various stages of mRNP biogenesis in Saccharomyces cerevisiae. |
Q42595526 | Deadenylation of interferon-beta mRNA is mediated by both the AU-rich element in the 3'-untranslated region and an instability sequence in the coding region |
Q38333308 | Deletion of the three distal S1 motifs of Saccharomyces cerevisiae Rrp5p abolishes pre-rRNA processing at site A(2) without reducing the production of functional 40S subunits |
Q83100754 | Determining in vivo activity of the yeast cytoplasmic exosome |
Q27932355 | Dhr1p, a putative DEAH-box RNA helicase, is associated with the box C+D snoRNP U3. |
Q34365638 | Dim2p, a KH-domain protein required for small ribosomal subunit synthesis |
Q28238338 | Discovering modes of action for therapeutic compounds using a genome-wide screen of yeast heterozygotes |
Q40689793 | Distinct 18S rRNA precursors are targets of the exosome complex, the exoribonuclease RRP6L2 and the terminal nucleotidyltransferase TRL in Arabidopsis thaliana |
Q44506953 | Down-regulation of RNA helicase II/Gu results in the depletion of 18 and 28 S rRNAs in Xenopus oocyte |
Q24555249 | ERB1, the yeast homolog of mammalian Bop1, is an essential gene required for maturation of the 25S and 5.8S ribosomal RNAs |
Q47141748 | EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis. |
Q66317406 | Elimination of 01/A'-A0 pre-rRNA processing by-product in human cells involves cooperative action of two nuclear exosome-associated nucleases: RRP6 and DIS3. |
Q27932846 | Evidence for core exosome independent function of the nuclear exoribonuclease Rrp6p |
Q36319804 | Exo- and endoribonucleolytic activities of yeast cytoplasmic and nuclear RNA exosomes are dependent on the noncatalytic core and central channel. |
Q64255778 | Exonuclease domain mutants of yeast DIS3 display genome instability |
Q27939455 | Exosome Cofactors Connect Transcription Termination to RNA Processing by Guiding Terminated Transcripts to the Appropriate Exonuclease within the Nuclear Exosome |
Q47664727 | Feedback regulation of ribosome assembly. |
Q41429445 | Genetic interactions suggest multiple distinct roles of the arch and core helicase domains of Mtr4 in Rrp6 and exosome function |
Q39773502 | Genome-wide analysis reveals distinct substrate specificities of Rrp6, Dis3, and core exosome subunits |
Q47844891 | Heterologous rRNA gene expression: internal fragmentation of Sciara coprophila 28S rRNA within microinjected Xenopus laevis oocytes |
Q42133042 | Human Ribosomal RNA-Derived Resident MicroRNAs as the Transmitter of Information upon the Cytoplasmic Cancer Stress. |
Q27931532 | Identification of a regulated pathway for nuclear pre-mRNA turnover. |
Q36191091 | Immature large ribosomal subunits containing the 7S pre-rRNA can engage in translation in Saccharomyces cerevisiae |
Q64053337 | Impaired autophagic degradation of lncRNA ARHGAP5-AS1 promotes chemoresistance in gastric cancer |
Q27650116 | Insights into the mechanism of progressive RNA degradation by the archaeal exosome |
Q33767816 | Investigating the cellular fate of a DNA-targeted platinum-based anticancer agent by orthogonal double-click chemistry |
Q30414922 | Kinetic analysis demonstrates a requirement for the Rat1 exonuclease in cotranscriptional pre-rRNA cleavage |
Q27932560 | Las1 interacts with Grc3 polynucleotide kinase and is required for ribosome synthesis in Saccharomyces cerevisiae |
Q28215280 | Lsm Proteins are required for normal processing and stability of ribosomal RNAs |
Q24300437 | MPP6 is an exosome-associated RNA-binding protein involved in 5.8S rRNA maturation |
Q34162276 | MRNA stability and the control of gene expression: implications for human disease |
Q42605427 | MTR4, a putative RNA helicase and exosome co-factor, is required for proper rRNA biogenesis and development in Arabidopsis thaliana |
Q37518637 | Multiple myeloma-associated hDIS3 mutations cause perturbations in cellular RNA metabolism and suggest hDIS3 PIN domain as a potential drug target |
Q37685645 | Mutations of EXOSC3/Rrp40p associated with neurological diseases impact ribosomal RNA processing functions of the exosome in S. cerevisiae |
Q24306533 | Nol9 is a novel polynucleotide 5′-kinase involved in ribosomal RNA processing |
Q27930263 | Nop53p is a novel nucleolar 60S ribosomal subunit biogenesis protein |
Q27929870 | Nop53p is required for late 60S ribosome subunit maturation and nuclear export in yeast |
Q27937186 | Nop53p, an essential nucleolar protein that interacts with Nop17p and Nip7p, is required for pre-rRNA processing in Saccharomyces cerevisiae. |
Q27940272 | Nop9 is an RNA binding protein present in pre-40S ribosomes and required for 18S rRNA synthesis in yeast |
Q36626011 | Nuclear RNA surveillance: role of TRAMP in controlling exosome specificity |
Q27937695 | Nuclear export of 60s ribosomal subunits depends on Xpo1p and requires a nuclear export sequence-containing factor, Nmd3p, that associates with the large subunit protein Rpl10p |
Q47373951 | Nuclear mRNA degradation tunes the gain of the unfolded protein response in Saccharomyces cerevisiae. |
Q27931072 | Processing of 20S pre-rRNA to 18S ribosomal RNA in yeast requires Rrp10p, an essential non-ribosomal cytoplasmic protein |
Q44042962 | Processing of 3'-extended read-through transcripts by the exosome can generate functional mRNAs. |
Q26853246 | Processing of preribosomal RNA in Saccharomyces cerevisiae |
Q36008871 | Pronounced and extensive microtubule defects in a Saccharomyces cerevisiae DIS3 mutant. |
Q24292231 | Protein-protein interactions of hCsl4p with other human exosome subunits |
Q74593512 | Purification of yeast exosome |
Q90664437 | R1 retrotransposons in the nucleolar organizers of Drosophila melanogaster are transcribed by RNA polymerase I upon heat shock |
Q38013753 | RNA decay and RNA silencing in plants: competition or collaboration? |
Q38025564 | RNA degradation in Saccharomyces cerevisae |
Q36627371 | RNA recognition by 3'-to-5' exonucleases: the substrate perspective |
Q40956479 | RNA substrate length as an indicator of exosome interactions in vivo |
Q28251052 | RNA-quality control by the exosome |
Q50488241 | RRP41L, a putative core subunit of the exosome, plays an important role in seed germination and early seedling growth in Arabidopsis. |
Q41893438 | Rapid cytoplasmic turnover of yeast ribosomes in response to rapamycin inhibition of TOR. |
Q27938577 | Rat1p and Rai1p function with the nuclear exosome in the processing and degradation of rRNA precursors |
Q27935106 | Regulation of unsaturated fatty acid biosynthesis in Saccharomyces: the endoplasmic reticulum membrane protein, Mga2p, a transcription activator of the OLE1 gene, regulates the stability of the OLE1 mRNA through exosome-mediated mechanisms |
Q41747137 | Relative contributions of the structural and catalytic roles of Rrp6 in exosomal degradation of individual mRNAs |
Q35567494 | Ribosomal RNA processing in Candida albicans. |
Q28587678 | Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute |
Q93360289 | Ribosome assembly coming into focus |
Q39007231 | Ribosome biogenesis in african trypanosomes requires conserved and trypanosome-specific factors |
Q37269766 | Ribosome biogenesis in the yeast Saccharomyces cerevisiae |
Q24321927 | Roles of the HEAT repeat proteins Utp10 and Utp20 in 40S ribosome maturation |
Q34452050 | Rrp12 and the Exportin Crm1 participate in late assembly events in the nucleolus during 40S ribosomal subunit biogenesis |
Q33590679 | Rrp17p is a eukaryotic exonuclease required for 5' end processing of Pre-60S ribosomal RNA |
Q27935348 | Rrp47p is an exosome-associated protein required for the 3' processing of stable RNAs. |
Q26776427 | Rrp6: Integrated roles in nuclear RNA metabolism and transcription termination |
Q42143254 | SETX sumoylation: A link between DNA damage and RNA surveillance disrupted in AOA2. |
Q39963552 | Self-splicing of a group I intron reveals partitioning of native and misfolded RNA populations in yeast |
Q24535685 | Ski7p G protein interacts with the exosome and the Ski complex for 3'-to-5' mRNA decay in yeast |
Q27940354 | Slx9p facilitates efficient ITS1 processing of pre-rRNA in Saccharomyces cerevisiae. |
Q47135435 | Structural insights into the interaction of the nuclear exosome helicase Mtr4 with the preribosomal protein Nop53. |
Q37680380 | Structure and Activities of the Eukaryotic RNA Exosome. |
Q41364737 | Structure and reconstitution of yeast Mpp6-nuclear exosome complexes reveals that Mpp6 stimulates RNA decay and recruits the Mtr4 helicase. |
Q27934309 | Surveillance of nuclear-restricted pre-ribosomes within a subnucleolar region of Saccharomyces cerevisiae |
Q27938215 | Temperature-sensitive mutants of the exosome subunit Rrp43p show a deficiency in mRNA degradation and no longer interact with the exosome. |
Q37339449 | The Evolutionarily-conserved Polyadenosine RNA Binding Protein, Nab2, Cooperates with Splicing Machinery to Regulate the Fate of pre-mRNA. |
Q24644651 | The N-terminal PIN domain of the exosome subunit Rrp44 harbors endonuclease activity and tethers Rrp44 to the yeast core exosome |
Q43207300 | The RNA catabolic enzymes Rex4p, Rnt1p, and Dbr1p show genetic interaction with trans-acting factors involved in processing of ITS1 in Saccharomyces cerevisiae pre-rRNA. |
Q47593634 | The RNA exosome and RNA exosome-linked disease. |
Q37649461 | The Rrp6 C-terminal domain binds RNA and activates the nuclear RNA exosome. |
Q27934229 | The Saccharomyces cerevisiae small GTPase, Gsp1p/Ran, is involved in 3' processing of 7S-to-5.8S rRNA and in degradation of the excised 5'-A0 fragment of 35S pre-rRNA, both of which are carried out by the exosome |
Q27935211 | The budding yeast homolog of the human EBNA1-binding protein 2 (Ebp2p) is an essential nucleolar protein required for pre-rRNA processing |
Q36827121 | The cytoplasmic mRNA degradation factor Pat1 is required for rRNA processing |
Q38660612 | The dhp1(+) gene, encoding a putative nuclear 5'-->3' exoribonuclease, is required for proper chromosome segregation in fission yeast |
Q28478876 | The essential nucleolar yeast protein Nop8p controls the exosome function during 60S ribosomal subunit maturation |
Q37700949 | The eukaryotic RNA exosome |
Q34024670 | The exozyme model: a continuum of functionally distinct complexes. |
Q24805333 | The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma |
Q24292126 | The mammalian exosome mediates the efficient degradation of mRNAs that contain AU-rich elements |
Q27940256 | The nuclear RNA polymerase II surveillance system targets polymerase III transcripts |
Q27930582 | The nuclear exosome is active and important during budding yeast meiosis |
Q30440025 | The nuclear poly(A) polymerase and Exosome cofactor Trf5 is recruited cotranscriptionally to nucleolar surveillance |
Q24321301 | The small-subunit processome is a ribosome assembly intermediate |
Q27938670 | The yeast homolog of human PinX1 is involved in rRNA and small nucleolar RNA maturation, not in telomere elongation inhibition |
Q24292314 | The yin and yang of the exosome |
Q24337846 | The zinc-finger antiviral protein recruits the RNA processing exosome to degrade the target mRNA |
Q24290597 | Three novel components of the human exosome |
Q38508542 | Transcript-based cloning of RRP46, a regulator of rRNA processing and R gene-independent cell death in barley-powdery mildew interactions |
Q30444616 | Transcription elongation by RNA polymerase I is linked to efficient rRNA processing and ribosome assembly. |
Q53427865 | Transcriptome targets of the exosome complex in plants. |
Q36326593 | Transcriptome-wide analysis of alternative routes for RNA substrates into the exosome complex |
Q36231781 | Trashing the genome: the role of nucleases during apoptosis |
Q52685060 | Turnover of aberrant pre-40S pre-ribosomal particles is initiated by a novel endonucleolytic decay pathway. |
Q27937486 | Ultrastructural localization of rRNA shows defective nuclear export of preribosomes in mutants of the Nup82p complex. |
Q37687012 | Visualization of distinct substrate-recruitment pathways in the yeast exosome by EM. |
Q27935269 | Yeast polypeptide exit tunnel ribosomal proteins L17, L35 and L37 are necessary to recruit late-assembling factors required for 27SB pre-rRNA processing. |
Q35011995 | mRNA degradation machines in eukaryotic cells |
Search more.