The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
about
Three novel components of the human exosomeAutoantibodies directed to novel components of the PM/Scl complex, the human exosomeMPP6 is an exosome-associated RNA-binding protein involved in 5.8S rRNA maturationDown-regulation of Myc as a potential target for growth arrest induced by human polynucleotide phosphorylase (hPNPaseold-35) in human melanoma cellsC1D and hMtr4p associate with the human exosome subunit PM/Scl-100 and are involved in pre-rRNA processingThe association of the human PM/Scl-75 autoantigen with the exosome is dependent on a newly identified N terminusNucleolar KKE/D repeat proteins Nop56p and Nop58p interact with Nop1p and are required for ribosome biogenesisInteraction between Ski7p and Upf1p is required for nonsense-mediated 3'-to-5' mRNA decay in yeastHuman polynucleotide phosphorylase selectively and preferentially degrades microRNA-221 in human melanoma cellsDegradation of ribosomal RNA precursors by the exosomeThe final step in the formation of 25S rRNA in Saccharomyces cerevisiae is performed by 5'-->3' exonucleasesFunction of the ski4p (Csl4p) and Ski7p proteins in 3'-to-5' degradation of mRNAYeast exosome mutants accumulate 3'-extended polyadenylated forms of U4 small nuclear RNA and small nucleolar RNAsExoribonuclease superfamilies: structural analysis and phylogenetic distributionDiazaborine treatment of yeast cells inhibits maturation of the 60S ribosomal subunitThe yeast exosome and human PM-Scl are related complexes of 3' --> 5' exonucleasesThe human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma.The 3' to 5' Exoribonuclease DIS3: From Structure and Mechanisms to Biological Functions and Role in Human DiseaseProcessing of preribosomal RNA in Saccharomyces cerevisiaeArchitecture of the Rix1-Rea1 checkpoint machinery during pre-60S-ribosome remodelingRNA helicase Prp43 and its co-factor Pfa1 promote 20 to 18 S rRNA processing catalyzed by the endonuclease Nob1.An endoribonuclease functionally linked to perinuclear mRNP quality control associates with the nuclear pore complexesThe yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo.Biogenesis of the signal recognition particle (SRP) involves import of SRP proteins into the nucleolus, assembly with the SRP-RNA, and Xpo1p-mediated export.Three conserved members of the RNase D family have unique and overlapping functions in the processing of 5S, 5.8S, U4, U5, RNase MRP and RNase P RNAs in yeast.Dbp7p, a putative ATP-dependent RNA helicase from Saccharomyces cerevisiae, is required for 60S ribosomal subunit assembly.Dbp3p, a putative RNA helicase in Saccharomyces cerevisiae, is required for efficient pre-rRNA processing predominantly at site A3.Rrp6p, the yeast homologue of the human PM-Scl 100-kDa autoantigen, is essential for efficient 5.8 S rRNA 3' end formation.RRP5 is required for formation of both 18S and 5.8S rRNA in yeast.Rio2p, an evolutionarily conserved, low abundant protein kinase essential for processing of 20 S Pre-rRNA in Saccharomyces cerevisiae.The PMC2NT domain of the catalytic exosome subunit Rrp6p provides the interface for binding with its cofactor Rrp47p, a nucleic acid-binding proteinThe 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.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 exosomeThe box H + ACA snoRNAs carry Cbf5p, the putative rRNA pseudouridine synthase.Synthetic lethal interactions with conditional poly(A) polymerase alleles identify LCP5, a gene involved in 18S rRNA maturationDeletions in the S1 domain of Rrp5p cause processing at a novel site in ITS1 of yeast pre-rRNA that depends on Rex4pNip7p interacts with Nop8p, an essential nucleolar protein required for 60S ribosome biogenesis, and the exosome subunit Rrp43pDbp6p is an essential putative ATP-dependent RNA helicase required for 60S-ribosomal-subunit assembly in Saccharomyces cerevisiaeTemperature-sensitive mutants of the exosome subunit Rrp43p show a deficiency in mRNA degradation and no longer interact with the exosome.Dob1p (Mtr4p) is a putative ATP-dependent RNA helicase required for the 3' end formation of 5.8S rRNA in Saccharomyces cerevisiae.
P2860
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P2860
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
description
1996 nî lūn-bûn
@nan
1996 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@ast
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en-gb
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@nl
type
label
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@ast
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en-gb
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@nl
prefLabel
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@ast
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en-gb
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@nl
P3181
P356
P1433
P1476
The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
@en
P2093
E Petfalski
P Mitchell
P304
P3181
P356
10.1101/GAD.10.4.502
P407
P577
1996-02-15T00:00:00Z