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January 1, 2012Frontiers in Neuroscience79 citationsOpen Access

Transcript Diversification in the Nervous System: A to I RNA Editing in CNS Function and Disease Development

ATAamira TariqMJMichael F. Jantsch

Key Result

A to I RNA editing by ADARs diversifies the central nervous system transcriptome by altering receptor and channel properties, and its dysregulation is associated with various neurological diseases.

PICO

P
Population
Neurological and psychiatric disorders associated with RNA editing
I
Intervention / Comparator
A to I RNA editing by ADARs

Limitations

  • Sample sizes in psychiatric disorder studies are typically small and rarely well controlled or matched, giving a heterogeneous picture.
  • The functional implications of editing in several targets, such as non-translated regions and specific proteins like FLNa and CyFIP2, remain unknown or under debate.

Abstract

RNA editing by adenosine deaminases that act on RNA converts adenosines to inosines in coding and non-coding regions of mRNAs. Inosines are interpreted as guanosines and hence, this type of editing can change codons, alter splice patterns, or influence the fate of an RNA. A to I editing is most abundant in the central nervous system (CNS). Here, targets for this type of nucleotide modification frequently encode receptors and channels. In many cases, the editing-induced amino acid exchanges alter the properties of the receptors and channels. Consistently, changes in editing patterns are frequently found associated with diseases of the CNS. In this review we describe the mechanisms of RNA editing and focus on target mRNAs of editing that are functionally relevant to normal and aberrant CNS activity.

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Cite This Study

Tariq et al. (2012) conducted a review in Neurological and psychiatric disorders associated with RNA editing. A to I RNA editing by ADARs was evaluated. A to I RNA editing by ADARs diversifies the central nervous system transcriptome by altering receptor and channel properties, and its dysregulation is associated with various neurological diseases.

synapsesocial.com/papers/6a09ea698f2332546a459906https://doi.org/10.3389/fnins.2012.00099
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