Literature DB >> 17018572

RNA editing in Drosophila melanogaster: New targets and functional consequences.

Mark Stapleton1, Joseph W Carlson, Susan E Celniker.   

Abstract

Adenosine deaminases that act on RNA [adenosine deaminase, RNA specific (ADAR)] catalyze the site-specific conversion of adenosine to inosine in primary mRNA transcripts. These re-coding events affect coding potential, splice sites, and stability of mature mRNAs. ADAR is an essential gene, and studies in mouse, Caenorhabditis elegans, and Drosophila suggest that its primary function is to modify adult behavior by altering signaling components in the nervous system. By comparing the sequence of isogenic cDNAs to genomic DNA, we have identified and experimentally verified 27 new targets of Drosophila ADAR. Our analyses led us to identify new classes of genes whose transcripts are targets of ADAR, including components of the actin cytoskeleton and genes involved in ion homeostasis and signal transduction. Our results indicate that editing in Drosophila increases the diversity of the proteome, and does so in a manner that has direct functional consequences on protein function.

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Year:  2006        PMID: 17018572      PMCID: PMC1624909          DOI: 10.1261/rna.254306

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  81 in total

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4.  Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2.

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  31 in total

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6.  Auto-regulatory RNA editing fine-tunes mRNA re-coding and complex behaviour in Drosophila.

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8.  Assessing the validity and reproducibility of genome-scale predictions.

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