Abstract
Genome evolution is commonly viewed as a gradual process that is driven by random mutations that accumulate over time. However, DNA- and RNA-editing enzymes have been identified that can accelerate evolution by actively modifying the genomically encoded information. The apolipoprotein B mRNA editing enzymes, catalytic polypeptide-like (APOBECs) are potent restriction factors that can inhibit retroelements by cytosine-to-uridine editing of retroelement DNA after reverse transcription. In some cases, a retroelement may successfully integrate into the genome despite being hypermutated. Such events introduce unique sequences into the genome and are thus a source of genomic innovation. adenosine deaminases that act on RNA (ADARs) catalyze adenosine-to-inosine editing in double-stranded RNA, commonly formed by oppositely oriented retroelements. The RNA editing confers plasticity to the transcriptome by generating many transcript variants from a single genomic locus. If the editing produces a beneficial variant, the genome may maintain the locus that produces the RNA-edited transcript for its novel function. Here, we discuss how these two powerful editing mechanisms, which both target inserted retroelements, facilitate expedited genome evolution.
Original language | English |
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Pages (from-to) | 115-125 |
Number of pages | 11 |
Journal | Annals of the New York Academy of Sciences |
Volume | 1341 |
Issue number | 1 |
DOIs | |
State | Published - 1 Apr 2015 |
Bibliographical note
Publisher Copyright:© 2015 New York Academy of Sciences.
Funding
Funders | Funder number |
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European Commission | 311257 |
Keywords
- ADAR
- APOBEC
- DNA editing
- Genome evolution
- RNA editing
- Retrotransposons