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RNA editing activity is associated with splicing factors in lnRNP particles: The nuclear pre-mRNA processing machinery
Author(s) -
Oleg Raitskin,
DanSung C. Cho,
Joseph M. Sperling,
Kazuko Nishikura,
Ruth Sperling
Publication year - 2001
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.111153798
Subject(s) - adar , rna editing , rna , ribonucleoprotein , rna binding protein , biology , messenger rna , rna splicing , immunoprecipitation , ribonucleoprotein particle , small nuclear rna , small nuclear ribonucleoprotein , microbiology and biotechnology , biochemistry , genetics , non coding rna , gene
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 (lnRNP) particles. The lnRNP 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 lnRNP 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 lnRNP particles. The two ADARs, associated with lnRNP 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 lnRNP particles.

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