Dynamic evolution of plant mitochondrial genomes: Mobile genes and introns and highly variable mutation rates

  1. Jeffrey D. Palmer*,
  2. Keith L. Adams,
  3. Yangrae Cho,
  4. Christopher L. Parkinson,
  5. Yin-Long Qiu§, and
  6. Keming Song
  1. Department of Biology, Indiana University, Bloomington, IN 47405

Abstract

We summarize our recent studies showing that angiosperm mitochondrial (mt) genomes have experienced remarkably high rates of gene loss and concomitant transfer to the nucleus and of intron acquisition by horizontal transfer. Moreover, we find substantial lineage-specific variation in rates of these structural mutations and also point mutations. These findings mostly arise from a Southern blot survey of gene and intron distribution in 281 diverse angiosperms. These blots reveal numerous losses of mt ribosomal protein genes but, with one exception, only rare loss of respiratory genes. Some lineages of angiosperms have kept all of their mt ribosomal protein genes whereas others have lost most of them. These many losses appear to reflect remarkably high (and variable) rates of functional transfer of mt ribosomal protein genes to the nucleus in angiosperms. The recent transfer of cox2 to the nucleus in legumes provides both an example of interorganellar gene transfer in action and a starting point for discussion of the roles of mechanistic and selective forces in determining the distribution of genetic labor between organellar and nuclear genomes. Plant mt genomes also acquire sequences by horizontal transfer. A striking example of this is a homing group I intron in the mt cox1 gene. This extraordinarily invasive mobile element has probably been acquired over 1,000 times separately during angiosperm evolution via a recent wave of cross-species horizontal transfers. Finally, whereas all previously examined angiosperm mtDNAs have low rates of synonymous substitutions, mtDNAs of two distantly related angiosperms have highly accelerated substitution rates.

Footnotes

  • * To whom reprint requests should be addressed at: Department of Biology, 1001 East Third Street, Indiana University, Bloomington, IN 47405. E-mail: jpalmer{at}bio.indiana.edu.

  • Present address: Stanford Genome Center, 855 California Avenue, Palo Alto, CA 94304.

  • Present address: Department of Biology, University of Central Florida, Orlando, FL 32816-2368.

  • § Present address: Department of Biology, University of Massachusetts, Amherst, MA 01003-5810.

  • Present Address: Sigma Chemical Company, 3300 South Second Street, St. Louis, MO 63118.

  • This paper was presented at the National Academy of Sciences colloquium “Variation and Evolution in Plants and Microorganisms: Toward a New Synthesis 50 Years After Stebbins,” held January 27–29, 2000, at the Arnold and Mabel Beckman Center in Irvine, CA.

  • Abbreviation:
    mt,
    mitochondrial
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