Arginine methylation and citrullination of splicing factor proline- and glutamine-rich (SFPQ/PSF) regulates its association with mRNA

RNA

Volumn 21, Issue 3, 2015, Pages 347-359

  Snijders, Ambrosuis P ^a,e   Hautbergue, Guillaume M ^b,e   Bloom, Alex ^a   Williamsom, James C ^a   Minshull, Thomas C ^a   Phillips, Helen L ^a   Mihaylov, Simeon R ^b   Gjerde, Douglas T ^c   Hornby, David P ^a   Wilson, Stuart A ^a   Hurd, Paul J ^d   Dickman, Mark J ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b UNIVERSITY OF SHEFFIELD   (United Kingdom)

^c PHYNEXUS INC   (United States)

^d QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^e IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

Author keywords

Arginine methylation; Citrullination; Mass spectrometry; mRNP binding; Non POU domain containing octamer binding protein; Polypyrimidine tract binding protein associated splicing factor; Splicing factor proline and glutamine rich

Indexed keywords

ARGININE; GLUTAMINE; MESSENGER RNA; PROLINE; PROTEIN ARGININE METHYLTRANSFERASE; MESSENGER RIBONUCLEOPROTEIN; MULTIPROTEIN COMPLEX; NONO PROTEIN, HUMAN; NUCLEAR MATRIX PROTEIN; OCTAMER TRANSCRIPTION FACTOR; PRMT1 PROTEIN, HUMAN; PTB-ASSOCIATED SPLICING FACTOR; REPRESSOR PROTEIN; RIBONUCLEOPROTEIN; RNA BINDING PROTEIN;

ARTICLE; COMPLEX FORMATION; HUMAN; IONIC STRENGTH; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN ASSEMBLY; PROTEIN PURIFICATION; RNA METHYLATION; RNA PROCESSING; RNA SPLICING; TRANSCRIPTION REGULATION; ANIMAL; CHEMISTRY; GENE EXPRESSION REGULATION; GENETIC TRANSCRIPTION; GENETICS; HELA CELL LINE; METABOLISM; METHYLATION; PROTEIN PROCESSING;

MAMMALIA;

ANIMALS; ARGININE; GENE EXPRESSION REGULATION; HELA CELLS; HUMANS; METHYLATION; MULTIPROTEIN COMPLEXES; NUCLEAR MATRIX-ASSOCIATED PROTEINS; OCTAMER TRANSCRIPTION FACTORS; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN-ARGININE N-METHYLTRANSFERASES; REPRESSOR PROTEINS; RIBONUCLEOPROTEINS; RNA SPLICING; RNA, MESSENGER; RNA-BINDING PROTEINS; TRANSCRIPTION, GENETIC;

EID: 84922963164     PISSN: 13558382     EISSN: 14699001     Source Type: Journal    
DOI: 10.1261/rna.045138.114     Document Type: Article

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