RNA editing activity is associated with splicing factors in InRNP particles: The nuclear pre-mRNA processing machinery

被引:73
作者
Raitskin, O
Cho, DSC
Sperling, J [1 ]
Nishikura, K
Sperling, R
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[2] Hebrew Univ Jerusalem, Dept Genet, IL-91904 Jerusalem, Israel
[3] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
关键词
adenosine deaminases acting on RNA; double-stranded RNA adenosine deaminase nucleic acid-protein interactions; large nuclear ribonucleoprotein;
D O I
10.1073/pnas.111153798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple members of the ADAR (adenosine deaminases acting on RNA) gene family are involved in A-to-I RNA editing. It has been speculated that they may form a large multicomponent protein complex. Possible candidates for such complexes are large nuclear ribonucleoprotein (InRNP) particles, The InRNP particles consist mainly of four spliceosomal subunits that assemble together with the pre-mRNA to form a large particle and thus are viewed as the naturally assembled pre-mRNA processing machinery. Here we investigated the presence of ADARs in InRNP particles by Western blot analysis using anti-ADAR antibodies and by indirect immunoprecipitation. Both ADAR1 and ADAR2 were found associated with the spliceosomal components Sm and SR proteins within the InRNP particles. The two ADARs, associated with InRNP particles, were enzymatically active in site-selective A-to-I RNA editing. We demonstrate the association of ADAR RNA editing enzymes with physiological supramolecular complexes, the InRNP particles.
引用
收藏
页码:6571 / 6576
页数:6
相关论文
共 45 条
[1]  
Bass BL, 1997, RNA, V3, P947
[2]  
Burge CB, 1999, RNA WORLD, P525
[3]   Regulation of serotonin-2C receptor G-protein coupling by RNA editing [J].
Burns, CM ;
Chu, H ;
Rueter, SM ;
Hutchinson, LK ;
Canton, H ;
SandersBush, E ;
Emeson, RB .
NATURE, 1997, 387 (6630) :303-308
[4]   A third member of the RNA-specific adenosine deaminase gene family, ADAR3, contains both single- and double-stranded RNA binding domains [J].
Chen, CX ;
Cho, DSC ;
Wang, QD ;
Lai, F ;
Carter, KC ;
Nishikura, K .
RNA, 2000, 6 (05) :755-767
[5]   Editing of the GluR-B ion channel RNA in vitro by recombinant double-stranded RNA adenosine deaminase [J].
Dabiri, GA ;
Lai, F ;
Drakas, RA ;
Nishikura, K .
EMBO JOURNAL, 1996, 15 (01) :34-45
[6]   The RNA-editing enzyme ADAR1 is localized to the nascent ribonucleoprotein matrix on Xenopus lampbrush chromosomes but specifically associates with an atypical loop [J].
Eckmann, CR ;
Jantsch, MF .
JOURNAL OF CELL BIOLOGY, 1999, 144 (04) :603-615
[7]  
Gerber A, 1997, RNA, V3, P453
[8]   EUKARYOTIC PROTEINS EXPRESSED IN ESCHERICHIA-COLI - AN IMPROVED THROMBIN CLEAVAGE AND PURIFICATION PROCEDURE OF FUSION PROTEINS WITH GLUTATHIONE-S-TRANSFERASE [J].
GUAN, KL ;
DIXON, JE .
ANALYTICAL BIOCHEMISTRY, 1991, 192 (02) :262-267
[9]   Q/R site editing in kainate receptor GluR5 and GluRG pre-mRNAs requires distant intronic sequences [J].
Herb, A ;
Higuchi, M ;
Sprengel, R ;
Seeburg, PH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (05) :1875-1880
[10]   RNA EDITING OF AMPA RECEPTOR SUBUNIT GLUR-B - A BASE-PAIRED INTRON-EXON STRUCTURE DETERMINES POSITION AND EFFICIENCY [J].
HIGUCHI, M ;
SINGLE, FN ;
KOHLER, M ;
SOMMER, B ;
SPRENGEL, R ;
SEEBURG, PH .
CELL, 1993, 75 (07) :1361-1370