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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1994 Jan 18;91(2):629–633. doi: 10.1073/pnas.91.2.629

Evidence for RNA editing in mitochondria of all major groups of land plants except the Bryophyta.

R Hiesel 1, B Combettes 1, A Brennicke 1
PMCID: PMC43002  PMID: 8290575

Abstract

RNA editing has been documented in mitochondria of higher plants, notably dicots and monocots. To determine the distribution of mitochondrial RNA editing in the plant kingdom, we have now undertaken a survey of evolutionarily distant plants. RNA editing occurs in all major groups of land plants except the Bryophyta, suggesting that this process is an ancient trait that was established before the radiation of kormophyte plants. No editing is observed in representatives of the green algae, suggesting that editing arose in early land plants after the split of the Bryophyta or has been lost selectively in both algae and mosses. In ferns several U-->C changes are observed, one of which eliminates a genomically encoded UAA termination codon and creates a functional open reading frame.

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Selected References

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  1. Covello P. S., Gray M. W. RNA editing in plant mitochondria. Nature. 1989 Oct 19;341(6243):662–666. doi: 10.1038/341662a0. [DOI] [PubMed] [Google Scholar]
  2. Glaubitz J. C., Carlson J. E. RNA editing in the mitochondria of a conifer. Curr Genet. 1992 Aug;22(2):163–165. doi: 10.1007/BF00351477. [DOI] [PubMed] [Google Scholar]
  3. Gray M. W., Covello P. S. RNA editing in plant mitochondria and chloroplasts. FASEB J. 1993 Jan;7(1):64–71. doi: 10.1096/fasebj.7.1.8422976. [DOI] [PubMed] [Google Scholar]
  4. Gualberto J. M., Lamattina L., Bonnard G., Weil J. H., Grienenberger J. M. RNA editing in wheat mitochondria results in the conservation of protein sequences. Nature. 1989 Oct 19;341(6243):660–662. doi: 10.1038/341660a0. [DOI] [PubMed] [Google Scholar]
  5. Gualberto J. M., Weil J. H., Grienenberger J. M. Editing of the wheat coxIII transcript: evidence for twelve C to U and one U to C conversions and for sequence similarities around editing sites. Nucleic Acids Res. 1990 Jul 11;18(13):3771–3776. doi: 10.1093/nar/18.13.3771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hiesel R., Schobel W., Schuster W., Brennicke A. The cytochrome oxidase subunit I and subunit III genes in Oenothera mitochondria are transcribed from identical promoter sequences. EMBO J. 1987 Jan;6(1):29–34. doi: 10.1002/j.1460-2075.1987.tb04714.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hiesel R., Wissinger B., Schuster W., Brennicke A. RNA editing in plant mitochondria. Science. 1989 Dec 22;246(4937):1632–1634. doi: 10.1126/science.2480644. [DOI] [PubMed] [Google Scholar]
  8. Hiesel R., von Haeseler A., Brennicke A. Plant mitochondrial nucleic acid sequences as a tool for phylogenetic analysis. Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):634–638. doi: 10.1073/pnas.91.2.634. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hoch B., Maier R. M., Appel K., Igloi G. L., Kössel H. Editing of a chloroplast mRNA by creation of an initiation codon. Nature. 1991 Sep 12;353(6340):178–180. doi: 10.1038/353178a0. [DOI] [PubMed] [Google Scholar]
  10. Kudla J., Igloi G. L., Metzlaff M., Hagemann R., Kössel H. RNA editing in tobacco chloroplasts leads to the formation of a translatable psbL mRNA by a C to U substitution within the initiation codon. EMBO J. 1992 Mar;11(3):1099–1103. doi: 10.1002/j.1460-2075.1992.tb05149.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Maier R. M., Neckermann K., Hoch B., Akhmedov N. B., Kössel H. Identification of editing positions in the ndhB transcript from maize chloroplasts reveals sequence similarities between editing sites of chloroplasts and plant mitochondria. Nucleic Acids Res. 1992 Dec 11;20(23):6189–6194. doi: 10.1093/nar/20.23.6189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Marienfeld J. R., Reski R., Abel W. O. The first analysed archegoniate mitochondrial gene (COX3) exhibits extraordinary features. Curr Genet. 1991 Sep;20(4):319–329. doi: 10.1007/BF00318522. [DOI] [PubMed] [Google Scholar]
  13. Oda K., Yamato K., Ohta E., Nakamura Y., Takemura M., Nozato N., Akashi K., Kanegae T., Ogura Y., Kohchi T. Gene organization deduced from the complete sequence of liverwort Marchantia polymorpha mitochondrial DNA. A primitive form of plant mitochondrial genome. J Mol Biol. 1992 Jan 5;223(1):1–7. doi: 10.1016/0022-2836(92)90708-r. [DOI] [PubMed] [Google Scholar]
  14. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Schuster W., Hiesel R., Wissinger B., Brennicke A. RNA editing in the cytochrome b locus of the higher plant Oenothera berteriana includes a U-to-C transition. Mol Cell Biol. 1990 May;10(5):2428–2431. doi: 10.1128/mcb.10.5.2428. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wissinger B., Brennicke A., Schuster W. Regenerating good sense: RNA editing and trans splicing in plant mitochondria. Trends Genet. 1992 Sep;8(9):322–328. doi: 10.1016/0168-9525(92)90265-6. [DOI] [PubMed] [Google Scholar]
  17. Wissinger B., Schuster W., Brennicke A. Species-specific RNA editing patterns in the mitochondrial rps13 transcripts of Oenothera and Daucus. Mol Gen Genet. 1990 Dec;224(3):389–395. doi: 10.1007/BF00262433. [DOI] [PubMed] [Google Scholar]

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