Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
about
The role of the ribosome in the regulation of longevity and lifespan extensionIdentification of novel methyltransferases, Bmt5 and Bmt6, responsible for the m3U methylations of 25S rRNA in Saccharomyces cerevisiaeEukaryotic rRNA Modification by Yeast 5-Methylcytosine-Methyltransferases and Human Proliferation-Associated Antigen p120.Translational roles of elongation factor 2 protein lysine methylationRibosome biogenesis factor Tsr3 is the aminocarboxypropyl transferase responsible for 18S rRNA hypermodification in yeast and humans.Yeast Kre33 and human NAT10 are conserved 18S rRNA cytosine acetyltransferases that modify tRNAs assisted by the adaptor Tan1/THUMPD1NSUN6 is a human RNA methyltransferase that catalyzes formation of m5C72 in specific tRNAsNSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNA(Met)The complete chemical structure of Saccharomyces cerevisiae rRNA: partial pseudouridylation of U2345 in 25S rRNA by snoRNA snR9Structural and functional studies of Bud23-Trm112 reveal 18S rRNA N7-G1575 methylation occurs on late 40S precursor ribosomesA network of assembly factors is involved in remodeling rRNA elements during preribosome maturation.Transcriptome-Wide Mapping of RNA 5-Methylcytosine in Arabidopsis mRNAs and Noncoding RNAs.Stepwise assembly of the earliest precursors of large ribosomal subunits in yeastRole of RNA methyltransferases in tissue renewal and pathologyMethylation of ribosomal RNA by NSUN5 is a conserved mechanism modulating organismal lifespan.Partial methylation at Am100 in 18S rRNA of baker's yeast reveals ribosome heterogeneity on the level of eukaryotic rRNA modification.An overview of pre-ribosomal RNA processing in eukaryotesConservation of tRNA and rRNA 5-methylcytosine in the kingdom Plantae.Posttranscriptional methylation of transfer and ribosomal RNA in stress response pathways, cell differentiation, and cancerAdaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts.Deciphering the epitranscriptome: A green perspective.Trm112, a Protein Activator of Methyltransferases Modifying Actors of the Eukaryotic Translational Apparatus.The K⁺-dependent GTPase Nug1 is implicated in the association of the helicase Dbp10 to the immature peptidyl transferase centre during ribosome maturationStatistically robust methylation calling for whole-transcriptome bisulfite sequencing reveals distinct methylation patterns for mouse RNAs.Principles of 60S ribosomal subunit assembly emerging from recent studies in yeast.Placeholder factors in ribosome biogenesis: please, pave my way.Links between nucleolar activity, rDNA stability, aneuploidy and chronological aging in the yeast Saccharomyces cerevisiae.WBSCR22/Merm1 is required for late nuclear pre-ribosomal RNA processing and mediates N7-methylation of G1639 in human 18S rRNAA cluster of methylations in the domain IV of 25S rRNA is required for ribosome stability.The association of late-acting snoRNPs with human pre-ribosomal complexes requires the RNA helicase DDX21Cytosine DNA methylation is found in Drosophila melanogaster but absent in Saccharomyces cerevisiae, Schizosaccharomyces pombe, and other yeast species.Absolute and relative quantification of RNA modifications via biosynthetic isotopomers.Identification of a new ribose methylation in the 18S rRNA of S. cerevisiae.Tuning the ribosome: The influence of rRNA modification on eukaryotic ribosome biogenesis and function.The Dark Side of the Epitranscriptome: Chemical Modifications in Long Non-Coding RNAs.Visualizing the Assembly Pathway of Nucleolar Pre-60S Ribosomes.Visualization of chemical modifications in the human 80S ribosome structure.Two Nucleolar Proteins, GDP1 and OLI2, Function As Ribosome Biogenesis Factors and Are Preferentially Involved in Promotion of Leaf Cell Proliferation without Strongly Affecting Leaf Adaxial-Abaxial Patterning in Arabidopsis thaliana.Sequence-specific and Shape-selective RNA Recognition by the Human RNA 5-Methylcytosine Methyltransferase NSun6.The Emerging Field of Epitranscriptomics in Neurodevelopmental and Neuronal Disorders.
P2860
058602d062a158d2be295044956c17ef3c3fa4510c46be1654dc1a36b0497e5bcbe4a51270a2daca0c783c88f92ed9487e4170cc8fc821f959623247381b85e17647731e611d50bee2357ae0b401e5308467dcc8afe4b47b7f582c9ed4d8405f186620bf87579831579573a8aae32f58b0c4874e58c557faa7757a2c65388dc4e7202472ff842adabd4701c7bc5c37765a9dcc55c2cdd925df3ebda25f2d20c8d12cf52a2170b833c1d22be46e717989d7b44685d9039092346448218b12a673f1416fdfb03db951e2fd37997c577e0388644813f431ce8f18ba456af1f7d90f06abb90a4bc4520ed213f920bf798c5a
P248
Q26770848-807D68D9-E10B-4400-B2BB-133DA266A0BFQ27930970-F8EFE28E-8724-417A-BA36-85D9B5137068Q27931427-EADA0BB1-E81C-4ECF-83FD-BBA62EB69FCBQ27933550-CBC9ED8A-0E21-43C3-8F84-9311AD3689B3Q27935236-70A29989-9397-4035-8146-31D4A291F710Q28115864-5CDDFA26-BC56-4198-A6D4-2E474126D254Q28118217-BFA4668D-3634-49B7-9355-CB0077ABFA59Q28596596-4D5B6A76-126F-459A-82EF-23714FBE4918Q28822098-4223A399-FD51-48E9-B7A0-F1099260F681Q29568202-84131E14-C06F-4AFD-9B96-2B1DBC5919F3Q30601541-BA434495-2167-4F4B-B7EE-DFC96D7E2DEAQ33364540-89149D7A-ACBD-4118-8D09-E2763840BE7AQ33878864-9E75BE36-9AAC-40B5-BA65-AC42A0D48F63Q34549119-8458C9C7-BC5D-47B8-BB12-CAD58F86D205Q35050458-2F45BC17-EB6B-4B73-A2DB-9AAE5BF6F32EQ35107791-C843EEAA-3E94-418A-8B98-B53100F48932Q35180630-EAAA2A24-8DFC-42C3-B71D-1E02B116BEB3Q35744276-4EDC4C2D-2201-4CE3-B4DD-807830D7F542Q36722453-F0F1B66C-4DE1-423A-B9A3-02BCF779B8FCQ37327393-0E8ED156-269D-4319-ADE4-925BFBE44E8BQ37391796-8926965C-8A5A-4882-8AEC-A9BD4FA6E8F8Q37729408-0AD51843-8630-4C59-B783-EA85107C91E6Q38667919-CC1A33E1-11CC-4EF3-9CD1-0E05F50E7CCBQ38690337-51226821-2DB8-4D55-9708-DF6A09D807ADQ39071877-CAC1565F-E9E5-4BF3-8D72-215F300ABE0CQ39419851-1644AC36-426B-4F6E-A9C9-4344CD564C01Q39573387-9258F8C3-B07F-46E9-80BB-9047232231D8Q41668545-CFA621FD-0CE8-4548-BA01-DD80173F8F5FQ41768865-F5ECF1B7-F7CA-4CDD-8670-790D464B1953Q41812618-9EC28076-2F48-4752-8C07-BD6C42A8C945Q42549712-A74F4C39-A06C-44A0-B570-E9A52268CB04Q42937335-0F4A8167-21F1-4AD5-870A-F7678C6EC14DQ43167393-22B6FCDB-0C07-4ACB-AABD-82EDACF5F176Q46904858-A275AF94-0DD2-4A7C-B3EC-7490C3AA7364Q47101298-AF4A4AB2-2819-4C9F-B18C-E402FE6E87ADQ47169623-78E00FE3-1CAC-46FA-9DF7-1F18F35F8F6EQ47397005-C186DC29-A9D9-4F03-851B-CD7095F21301Q49630500-C5DDE07E-C815-404F-BE70-2DAA51EA89EBQ50297032-46026DFD-5C90-4B14-BE18-8AC2B1C7F951Q55071218-45BE470D-0DC0-4928-B610-D0E5F52ECFB7
P2860
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
description
2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@ast
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@en
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@nl
type
label
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@ast
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@en
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@nl
prefLabel
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@ast
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@en
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@nl
P2093
P2860
P3181
P356
P1476
Yeast Nop2 and Rcm1 methylate C2870 and C2278 of the 25S rRNA, respectively.
@en
P2093
Peter Watzinger
Sunny Sharma
P2860
P304
P3181
P356
10.1093/NAR/GKT679
P407
P577
2013-10-01T00:00:00Z