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. 1994 Oct;14(10):6419–6432. doi: 10.1128/mcb.14.10.6419

A mitochondrial retroplasmid integrates into mitochondrial DNA by a novel mechanism involving the synthesis of a hybrid cDNA and homologous recombination.

C C Chiang 1, J C Kennell 1, L A Wanner 1, A M Lambowitz 1
PMCID: PMC359172  PMID: 7523850

Abstract

The Mauriceville and Varkud mitochondrial plasmids of Neurospora spp. are closely related, small circular DNAs that propagate via an RNA intermediate and reverse transcription. Although the plasmids ordinarily replicate autonomously, they can also integrate into mitochondrial DNA (mtDNA), yielding defective mtDNAs that in some cases cause senescence. To investigate the integration mechanism, we analyzed four cases in which the Varkud plasmid integrated into the mitochondrial small rRNA gene, three in wild-type subcultures and one in a senescent mutant. Our analysis suggests that the integrations occurred by the plasmid reverse transcriptase template switching between the plasmid transcript and internal sequences in the mitochondrial small rRNA to yield hybrid cDNAs that circularized and recombined homologously with the mtDNA. The integrated plasmid sequences are transcribed, presumably from the mitochondrial small rRNA promoters, resulting in hybrid RNAs containing the 5' segment of the mitochondrial small rRNA linked head-to-tail to the full-length plasmid transcript. Analysis of additional senescent mutants revealed three cases in which the plasmid used the same mechanism to integrate at other locations in the mtDNA. In these cases, circular variant plasmids that had incorporated a mitochondrial tRNA or tRNA-like sequence by template switching integrated by homologous recombination at the site of the corresponding tRNA or tRNA-like sequence in mtDNA. This simple integration mechanism involving template switching to generate a hybrid cDNA that integrates homologously could have been used by primitive retroelements prior to the acquisition of a specialized integration machinery.

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Selected References

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  1. Ahlquist P. Bromovirus RNA replication and transcription. Curr Opin Genet Dev. 1992 Feb;2(1):71–76. doi: 10.1016/s0959-437x(05)80325-9. [DOI] [PubMed] [Google Scholar]
  2. Akins R. A., Grant D. M., Stohl L. L., Bottorff D. A., Nargang F. E., Lambowitz A. M. Nucleotide sequence of the Varkud mitochondrial plasmid of Neurospora and synthesis of a hybrid transcript with a 5' leader derived from mitochondrial RNA. J Mol Biol. 1988 Nov 5;204(1):1–25. doi: 10.1016/0022-2836(88)90594-3. [DOI] [PubMed] [Google Scholar]
  3. Akins R. A., Kelley R. L., Lambowitz A. M. Characterization of mutant mitochondrial plasmids of Neurospora spp. that have incorporated tRNAs by reverse transcription. Mol Cell Biol. 1989 Feb;9(2):678–691. doi: 10.1128/mcb.9.2.678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Akins R. A., Kelley R. L., Lambowitz A. M. Mitochondrial plasmids of Neurospora: integration into mitochondrial DNA and evidence for reverse transcription in mitochondria. Cell. 1986 Nov 21;47(4):505–516. doi: 10.1016/0092-8674(86)90615-x. [DOI] [PubMed] [Google Scholar]
  5. Boer P. H., Gray M. W. Genes encoding a subunit of respiratory NADH dehydrogenase (ND1) and a reverse transcriptase-like protein (RTL) are linked to ribosomal RNA gene pieces in Chlamydomonas reinhardtii mitochondrial DNA. EMBO J. 1988 Nov;7(11):3501–3508. doi: 10.1002/j.1460-2075.1988.tb03226.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Clark J. M. Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases. Nucleic Acids Res. 1988 Oct 25;16(20):9677–9686. doi: 10.1093/nar/16.20.9677. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Collins R. A., Stohl L. L., Cole M. D., Lambowitz A. M. Characterization of a novel plasmid DNA found in mitochondria of N. crassa. Cell. 1981 May;24(2):443–452. doi: 10.1016/0092-8674(81)90335-4. [DOI] [PubMed] [Google Scholar]
  8. Cummings D. J., Domenico J. M., Nelson J., Sogin M. L. DNA sequence, structure, and phylogenetic relationship of the small subunit rRNA coding region of mitochondrial DNA from Podospora anserina. J Mol Evol. 1989 Mar;28(3):232–241. doi: 10.1007/BF02102481. [DOI] [PubMed] [Google Scholar]
  9. Derr L. K., Strathern J. N. A role for reverse transcripts in gene conversion. Nature. 1993 Jan 14;361(6408):170–173. doi: 10.1038/361170a0. [DOI] [PubMed] [Google Scholar]
  10. Derr L. K., Strathern J. N., Garfinkel D. J. RNA-mediated recombination in S. cerevisiae. Cell. 1991 Oct 18;67(2):355–364. doi: 10.1016/0092-8674(91)90187-4. [DOI] [PubMed] [Google Scholar]
  11. Gorbalenya A. E., Koonin E. V., Donchenko A. P., Blinov V. M. A novel superfamily of nucleoside triphosphate-binding motif containing proteins which are probably involved in duplex unwinding in DNA and RNA replication and recombination. FEBS Lett. 1988 Aug 1;235(1-2):16–24. doi: 10.1016/0014-5793(88)81226-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gutell R. R., Weiser B., Woese C. R., Noller H. F. Comparative anatomy of 16-S-like ribosomal RNA. Prog Nucleic Acid Res Mol Biol. 1985;32:155–216. doi: 10.1016/s0079-6603(08)60348-7. [DOI] [PubMed] [Google Scholar]
  13. Heckman J. E., RajBhandary U. L. Organization of tRNA and rRNA genes in N. crassa mitochondria: intervening sequence in the large rRNA gene and strand distribution of the RNA genes. Cell. 1979 Jul;17(3):583–595. doi: 10.1016/0092-8674(79)90266-6. [DOI] [PubMed] [Google Scholar]
  14. Heckman J. E., Sarnoff J., Alzner-DeWeerd B., Yin S., RajBhandary U. L. Novel features in the genetic code and codon reading patterns in Neurospora crassa mitochondria based on sequences of six mitochondrial tRNAs. Proc Natl Acad Sci U S A. 1980 Jun;77(6):3159–3163. doi: 10.1073/pnas.77.6.3159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kennell J. C., Moran J. V., Perlman P. S., Butow R. A., Lambowitz A. M. Reverse transcriptase activity associated with maturase-encoding group II introns in yeast mitochondria. Cell. 1993 Apr 9;73(1):133–146. doi: 10.1016/0092-8674(93)90166-n. [DOI] [PubMed] [Google Scholar]
  16. Kennell J. C., Wang H., Lambowitz A. M. The Mauriceville plasmid of Neurospora spp. uses novel mechanisms for initiating reverse transcription in vivo. Mol Cell Biol. 1994 May;14(5):3094–3107. doi: 10.1128/mcb.14.5.3094. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kroner P. A., Young B. M., Ahlquist P. Analysis of the role of brome mosaic virus 1a protein domains in RNA replication, using linker insertion mutagenesis. J Virol. 1990 Dec;64(12):6110–6120. doi: 10.1128/jvi.64.12.6110-6120.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kubelik A. R., Kennell J. C., Akins R. A., Lambowitz A. M. Identification of Neurospora mitochondrial promoters and analysis of synthesis of the mitochondrial small rRNA in wild-type and the promoter mutant [poky]. J Biol Chem. 1990 Mar 15;265(8):4515–4526. [PubMed] [Google Scholar]
  19. Kuiper M. T., Lambowitz A. M. A novel reverse transcriptase activity associated with mitochondrial plasmids of Neurospora. Cell. 1988 Nov 18;55(4):693–704. doi: 10.1016/0092-8674(88)90228-0. [DOI] [PubMed] [Google Scholar]
  20. Kuiper M. T., Sabourin J. R., Lambowitz A. M. Identification of the reverse transcriptase encoded by the Mauriceville and Varkud mitochondrial plasmids of Neurospora. J Biol Chem. 1990 Apr 25;265(12):6936–6943. [PubMed] [Google Scholar]
  21. Lambowitz A. M., LaPolla R. J., Collins R. A. Mitochondrial ribosome assembly in Neurospora. Two-dimensional gel electrophoretic analysis of mitochondrial ribosomal proteins. J Cell Biol. 1979 Jul;82(1):17–31. doi: 10.1083/jcb.82.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. McClure M. A. Evolution of retroposons by acquisition or deletion of retrovirus-like genes. Mol Biol Evol. 1991 Nov;8(6):835–856. doi: 10.1093/oxfordjournals.molbev.a040686. [DOI] [PubMed] [Google Scholar]
  23. Michel F., Lang B. F. Mitochondrial class II introns encode proteins related to the reverse transcriptases of retroviruses. Nature. 1985 Aug 15;316(6029):641–643. doi: 10.1038/316641a0. [DOI] [PubMed] [Google Scholar]
  24. Miller W. A., Bujarski J. J., Dreher T. W., Hall T. C. Minus-strand initiation by brome mosaic virus replicase within the 3' tRNA-like structure of native and modified RNA templates. J Mol Biol. 1986 Feb 20;187(4):537–546. doi: 10.1016/0022-2836(86)90332-3. [DOI] [PubMed] [Google Scholar]
  25. Nargang F. E., Bell J. B., Stohl L. L., Lambowitz A. M. The DNA sequence and genetic organization of a Neurospora mitochondrial plasmid suggest a relationship to introns and mobile elements. Cell. 1984 Sep;38(2):441–453. doi: 10.1016/0092-8674(84)90499-9. [DOI] [PubMed] [Google Scholar]
  26. Neefs J. M., Van de Peer Y., De Rijk P., Chapelle S., De Wachter R. Compilation of small ribosomal subunit RNA structures. Nucleic Acids Res. 1993 Jul 1;21(13):3025–3049. doi: 10.1093/nar/21.13.3025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. 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]
  28. Wang H., Kennell J. C., Kuiper M. T., Sabourin J. R., Saldanha R., Lambowitz A. M. The Mauriceville plasmid of Neurospora crassa: characterization of a novel reverse transcriptase that begins cDNA synthesis at the 3' end of template RNA. Mol Cell Biol. 1992 Nov;12(11):5131–5144. doi: 10.1128/mcb.12.11.5131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wang H., Lambowitz A. M. Reverse transcription of the Mauriceville plasmid of Neurospora. Lack of ribonuclease H activity associated with the reverse transcriptase and possible use of mitochondrial ribonuclease H. J Biol Chem. 1993 Sep 5;268(25):18951–18959. [PubMed] [Google Scholar]
  30. Wang H., Lambowitz A. M. The Mauriceville plasmid reverse transcriptase can initiate cDNA synthesis de novo and may be related to reverse transcriptase and DNA polymerase progenitor. Cell. 1993 Dec 17;75(6):1071–1081. doi: 10.1016/0092-8674(93)90317-j. [DOI] [PubMed] [Google Scholar]
  31. Xiong Y., Eickbush T. H. Origin and evolution of retroelements based upon their reverse transcriptase sequences. EMBO J. 1990 Oct;9(10):3353–3362. doi: 10.1002/j.1460-2075.1990.tb07536.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Zuker M. On finding all suboptimal foldings of an RNA molecule. Science. 1989 Apr 7;244(4900):48–52. doi: 10.1126/science.2468181. [DOI] [PubMed] [Google Scholar]

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