4.8 Article

Loss of Two Introns from the Magnolia tripetala Mitochondrial cox2 Gene Implicates Horizontal Gene Transfer and Gene Conversion as a Novel Mechanism of Intron Loss

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 29, Issue 10, Pages 3111-3120

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/mss130

Keywords

intron loss; horizontal gene transfer; gene conversion; retroprocessing; Magnolia tripetala; cytochrome oxidase subunit 2

Funding

  1. National Science Foundation [IOS-1027529, MCB-1125386]
  2. University of Nebraska-Lincoln
  3. Division Of Integrative Organismal Systems
  4. Direct For Biological Sciences [1027529] Funding Source: National Science Foundation

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Intron loss is often thought to occur through retroprocessing, which is the reverse transcription and genomic integration of a spliced transcript. In plant mitochondria, several unambiguous examples of retroprocessing are supported by the parallel loss of an intron and numerous adjacent RNA edit sites, but in most cases, the evidence for intron loss via retroprocessing is weak or lacking entirely. To evaluate mechanisms of intron loss, we designed a polymerase chain reaction (PCR)-based assay to detect recent intron losses from the mitochondrial cox2 gene within genus Magnolia, which was previously suggested to have variability in cox2 intron content. Our assay showed that all 22 examined species have a cox2 gene with two introns. However, one species, Magnolia tripetala, contains an additional cox2 gene that lacks both introns. Quantitative PCR showed that both M. tripetala cox2 genes are present in the mitochondrial genome. Although the intronless gene has lost several ancestral RNA edit sites, their distribution is inconsistent with retroprocessing models. Instead, phylogenetic and gene conversion analyses indicate that the intronless gene was horizontally acquired from a eudicot and then underwent gene conversion with the native intron-containing gene. The models are presented to summarize the roles of horizontal gene transfer and gene conversion as a novel mechanism of intron loss.

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