Skip to main content
RNA logoLink to RNA
. 2000 Jul;6(7):937–951. doi: 10.1017/s1355838200991726

Pentamidine inhibits mitochondrial intron splicing and translation in Saccharomyces cerevisiae.

Y Zhang 1, A Bell 1, P S Perlman 1, M J Leibowitz 1
PMCID: PMC1369971  PMID: 10917591

Abstract

Pentamidine inhibits in vitro splicing of nuclear group I introns from rRNA genes of some pathogenic fungi and is known to inhibit mitochondrial function in yeast. Here we report that pentamidine inhibits the self-splicing of three group I and two group II introns of yeast mitochondria. Comparison of yeast strains with different configurations of mitochondrial introns (12, 5, 4, or 0 introns) revealed that strains with the most introns were the most sensitive to growth inhibition by pentamidine on glycerol medium. Analysis of blots of RNA from yeast strains grown in raffinose medium in the presence or absence of pentamidine revealed that the splicing of seven group I and two group II introns that have intron reading frames was inhibited by the drug to varying extents. Three introns without reading frames were unaffected by the drug in vivo, and two of these were inhibited in vitro, implying that the drug affects splicing by acting directly on RNA in vitro, but on another target in vivo. Because the most sensitive introns in vivo are the ones whose splicing depends on a maturase encoded by the intron reading frames, we tested pentamidine for effects on mitochondrial translation. We found that the drug inhibits mitochondrial but not cytoplasmic translation in cells at concentrations that inhibit mitochondrial intron splicing. Therefore, pentamidine is a potent and specific inhibitor of mitochondrial translation, and this effect explains most or all of its effects on respiratory growth and on in vivo splicing of mitochondrial introns.

Full Text

The Full Text of this article is available as a PDF (1.1 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bonitz S. G., Coruzzi G., Thalenfeld B. E., Tzagoloff A., Macino G. Assembly of the mitochondrial membrane system. Structure and nucleotide sequence of the gene coding for subunit 1 of yeast cytochrme oxidase. J Biol Chem. 1980 Dec 25;255(24):11927–11941. [PubMed] [Google Scholar]
  2. Carr-Schmid A., Durko N., Cavallius J., Merrick W. C., Kinzy T. G. Mutations in a GTP-binding motif of eukaryotic elongation factor 1A reduce both translational fidelity and the requirement for nucleotide exchange. J Biol Chem. 1999 Oct 15;274(42):30297–30302. doi: 10.1074/jbc.274.42.30297. [DOI] [PubMed] [Google Scholar]
  3. Cech T. R. Self-splicing of group I introns. Annu Rev Biochem. 1990;59:543–568. doi: 10.1146/annurev.bi.59.070190.002551. [DOI] [PubMed] [Google Scholar]
  4. Cech T. R., Zaug A. J., Grabowski P. J. In vitro splicing of the ribosomal RNA precursor of Tetrahymena: involvement of a guanosine nucleotide in the excision of the intervening sequence. Cell. 1981 Dec;27(3 Pt 2):487–496. doi: 10.1016/0092-8674(81)90390-1. [DOI] [PubMed] [Google Scholar]
  5. Conrad-Webb H., Butow R. A. A polymerase switch in the synthesis of rRNA in Saccharomyces cerevisiae. Mol Cell Biol. 1995 May;15(5):2420–2428. doi: 10.1128/mcb.15.5.2420. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Conrad-Webb H., Perlman P. S., Zhu H., Butow R. A. The nuclear SUV3-1 mutation affects a variety of post-transcriptional processes in yeast mitochondria. Nucleic Acids Res. 1990 Mar 25;18(6):1369–1376. doi: 10.1093/nar/18.6.1369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cory M., Tidwell R. R., Fairley T. A. Structure and DNA binding activity of analogues of 1,5-bis(4-amidinophenoxy)pentane (pentamidine) J Med Chem. 1992 Feb 7;35(3):431–438. doi: 10.1021/jm00081a003. [DOI] [PubMed] [Google Scholar]
  8. Dykstra C. C., Tidwell R. R. Inhibition of topoisomerases from Pneumocystis carinii by aromatic dicationic molecules. J Protozool. 1991 Nov-Dec;38(6):78S–81S. [PubMed] [Google Scholar]
  9. Edman J. C., Kovacs J. A., Masur H., Santi D. V., Elwood H. J., Sogin M. L. Ribosomal RNA sequence shows Pneumocystis carinii to be a member of the fungi. Nature. 1988 Aug 11;334(6182):519–522. doi: 10.1038/334519a0. [DOI] [PubMed] [Google Scholar]
  10. Franzen J. S., Zhang M., Chay T. R., Peebles C. L. Thermal activation of a group II intron ribozyme reveals multiple conformational states. Biochemistry. 1994 Sep 20;33(37):11315–11326. doi: 10.1021/bi00203a029. [DOI] [PubMed] [Google Scholar]
  11. Gampel A., Tzagoloff A. In vitro splicing of the terminal intervening sequence of Saccharomyces cerevisiae cytochrome b pre-mRNA. Mol Cell Biol. 1987 Jul;7(7):2545–2551. doi: 10.1128/mcb.7.7.2545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Guo W. W., Moran J. V., Hoffman P. W., Henke R. M., Butow R. A., Perlman P. S. The mobile group I intron 3 alpha of the yeast mitochondrial COXI gene encodes a 35-kDa processed protein that is an endonuclease but not a maturase. J Biol Chem. 1995 Jun 30;270(26):15563–15570. doi: 10.1074/jbc.270.26.15563. [DOI] [PubMed] [Google Scholar]
  13. Hagan K. W., Ruiz-Echevarria M. J., Quan Y., Peltz S. W. Characterization of cis-acting sequences and decay intermediates involved in nonsense-mediated mRNA turnover. Mol Cell Biol. 1995 Feb;15(2):809–823. doi: 10.1128/mcb.15.2.809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hefta L. J., Lewin A. S., Daignan-Fornier B., Bolotin-Fukuhara M. Nuclear and mitochondrial revertants of a mitochondrial mutant with a defect in the ATP synthetase complex. Mol Gen Genet. 1987 Apr;207(1):106–113. doi: 10.1007/BF00331497. [DOI] [PubMed] [Google Scholar]
  15. Hensgens L. A., Bonen L., de Haan M., van der Horst G., Grivell L. A. Two intron sequences in yeast mitochondrial COX1 gene: homology among URF-containing introns and strain-dependent variation in flanking exons. Cell. 1983 Feb;32(2):379–389. doi: 10.1016/0092-8674(83)90457-9. [DOI] [PubMed] [Google Scholar]
  16. Hughes W. T. Prevention and treatment of Pneumocystis carinii pneumonia. Annu Rev Med. 1991;42:287–295. doi: 10.1146/annurev.me.42.020191.001443. [DOI] [PubMed] [Google Scholar]
  17. IVADY G., PALDY L. Ein neues Behandlungsverfahren der interstitiellen plasmazelligen Pneumonie Frühgeborener mit fünfwertigem Stibium und aromatischen Diamidinen. Monatsschr Kinderheilkd. 1958 Jan;106(1):10–14. [PubMed] [Google Scholar]
  18. Jarrell K. A., Dietrich R. C., Perlman P. S. Group II intron domain 5 facilitates a trans-splicing reaction. Mol Cell Biol. 1988 Jun;8(6):2361–2366. doi: 10.1128/mcb.8.6.2361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Johnson C. H., McEwen J. E. Mitochondrial protein synthesis is not required for efficient excision of intron aI5 beta from COX1 pre-mRNA in Saccharomyces cerevisiae. Mol Gen Genet. 1997 Sep;256(1):88–91. doi: 10.1007/s004380050549. [DOI] [PubMed] [Google Scholar]
  20. Lamb M. R., Anziano P. Q., Glaus K. R., Hanson D. K., Klapper H. J., Perlman P. S., Mahler H. R. Functional domains in introns. RNA processing intermediates in cis- and trans-acting mutants in the penultimate intron of the mitochondrial gene for cytochrome b. J Biol Chem. 1983 Feb 10;258(3):1991–1999. [PubMed] [Google Scholar]
  21. Lazowska J., Claisse M., Gargouri A., Kotylak Z., Spyridakis A., Slonimski P. P. Protein encoded by the third intron of cytochrome b gene in Saccharomyces cerevisiae is an mRNA maturase. Analysis of mitochondrial mutants, RNA transcripts proteins and evolutionary relationships. J Mol Biol. 1989 Jan 20;205(2):275–289. doi: 10.1016/0022-2836(89)90341-0. [DOI] [PubMed] [Google Scholar]
  22. Lazowska J., Jacq C., Slonimski P. P. Sequence of introns and flanking exons in wild-type and box3 mutants of cytochrome b reveals an interlaced splicing protein coded by an intron. Cell. 1980 Nov;22(2 Pt 2):333–348. doi: 10.1016/0092-8674(80)90344-x. [DOI] [PubMed] [Google Scholar]
  23. Lin H., Niu M. T., Yoganathan T., Buck G. A. Characterization of the rRNA-encoding genes and transcripts, and a group-I self-splicing intron in Pneumocystis carinii. Gene. 1992 Oct 1;119(2):163–173. doi: 10.1016/0378-1119(92)90268-t. [DOI] [PubMed] [Google Scholar]
  24. Liu Y., Leibowitz M. J. Bidirectional effectors of a group I intron ribozyme. Nucleic Acids Res. 1995 Apr 25;23(8):1284–1291. doi: 10.1093/nar/23.8.1284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Liu Y., Leibowitz M. J. Variation and in vitro splicing of group I introns in rRNA genes of Pneumocystis carinii. Nucleic Acids Res. 1993 May 25;21(10):2415–2421. doi: 10.1093/nar/21.10.2415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Liu Y., Rocourt M., Pan S., Liu C., Leibowitz M. J. Sequence and variability of the 5.8S and 26S rRNA genes of Pneumocystis carinii. Nucleic Acids Res. 1992 Jul 25;20(14):3763–3772. doi: 10.1093/nar/20.14.3763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Liu Y., Tidwell R. R., Leibowitz M. J. Inhibition of in vitro splicing of a group I intron of Pneumocystis carinii. J Eukaryot Microbiol. 1994 Jan-Feb;41(1):31–38. doi: 10.1111/j.1550-7408.1994.tb05931.x. [DOI] [PubMed] [Google Scholar]
  28. Ludewig G., Williams J. M., Li Y., Staben C. Effects of pentamidine isethionate on Saccharomyces cerevisiae. Antimicrob Agents Chemother. 1994 May;38(5):1123–1128. doi: 10.1128/aac.38.5.1123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Macino G., Tzagoloff A. Assembly of the mitochondrial membrane system: sequence analysis of a yeast mitochondrial ATPase gene containing the oli-2 and oli-4 loci. Cell. 1980 Jun;20(2):507–517. doi: 10.1016/0092-8674(80)90637-6. [DOI] [PubMed] [Google Scholar]
  30. Manthey G. M., McEwen J. E. The product of the nuclear gene PET309 is required for translation of mature mRNA and stability or production of intron-containing RNAs derived from the mitochondrial COX1 locus of Saccharomyces cerevisiae. EMBO J. 1995 Aug 15;14(16):4031–4043. doi: 10.1002/j.1460-2075.1995.tb00074.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Margossian S. P., Li H., Zassenhaus H. P., Butow R. A. The DExH box protein Suv3p is a component of a yeast mitochondrial 3'-to-5' exoribonuclease that suppresses group I intron toxicity. Cell. 1996 Jan 26;84(2):199–209. doi: 10.1016/s0092-8674(00)80975-7. [DOI] [PubMed] [Google Scholar]
  32. McKee E. E., McEwen J. E., Poyton R. O. Mitochondrial gene expression in saccharomyces cerevisiae. II. Fidelity of translation in isolated mitochondria from wild type and respiratory-deficient mutant cells. J Biol Chem. 1984 Jul 25;259(14):9332–9338. [PubMed] [Google Scholar]
  33. Michel F., Westhof E. Modelling of the three-dimensional architecture of group I catalytic introns based on comparative sequence analysis. J Mol Biol. 1990 Dec 5;216(3):585–610. doi: 10.1016/0022-2836(90)90386-Z. [DOI] [PubMed] [Google Scholar]
  34. Miletti K. E., Leibowitz M. J. Pentamidine inhibition of group I intron splicing in Candida albicans correlates with growth inhibition. Antimicrob Agents Chemother. 2000 Apr;44(4):958–966. doi: 10.1128/aac.44.4.958-966.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Moran J. V., Mecklenburg K. L., Sass P., Belcher S. M., Mahnke D., Lewin A., Perlman P. Splicing defective mutants of the COXI gene of yeast mitochondrial DNA: initial definition of the maturase domain of the group II intron aI2. Nucleic Acids Res. 1994 Jun 11;22(11):2057–2064. doi: 10.1093/nar/22.11.2057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Moran J. V., Wernette C. M., Mecklenburg K. L., Butow R. A., Perlman P. S. Intron 5 alpha of the COXI gene of yeast mitochondrial DNA is a mobile group I intron. Nucleic Acids Res. 1992 Aug 11;20(15):4069–4076. doi: 10.1093/nar/20.15.4069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Moreno S. N. Pentamidine is an uncoupler of oxidative phosphorylation in rat liver mitochondria. Arch Biochem Biophys. 1996 Feb 1;326(1):15–20. doi: 10.1006/abbi.1996.0041. [DOI] [PubMed] [Google Scholar]
  38. Nobrega F. G., Tzagoloff A. Assembly of the mitochondrial membrane system. DNA sequence and organization of the cytochrome b gene in Saccharomyces cerevisiae D273-10B. J Biol Chem. 1980 Oct 25;255(20):9828–9837. [PubMed] [Google Scholar]
  39. Nunn C. M., Jenkins T. C., Neidle S. Crystal structure of gamma-oxapentamidine complexed with d(CGCGAATTCGCG)2. The effects of drug structural change on DNA minor-groove recognition. Eur J Biochem. 1994 Dec 15;226(3):953–961. doi: 10.1111/j.1432-1033.1994.00953.x. [DOI] [PubMed] [Google Scholar]
  40. Partono S., Lewin A. S. Autocatalytic activities of intron 5 of the cob gene of yeast mitochondria. Mol Cell Biol. 1988 Jun;8(6):2562–2571. doi: 10.1128/mcb.8.6.2562. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Peebles C. L., Belcher S. M., Zhang M., Dietrich R. C., Perlman P. S. Mutation of the conserved first nucleotide of a group II intron from yeast mitochondrial DNA reduces the rate but allows accurate splicing. J Biol Chem. 1993 Jun 5;268(16):11929–11938. [PubMed] [Google Scholar]
  42. Pelissier P. P., Camougrand N. M., Manon S. T., Velours G. M., Guerin M. G. Regulation by nuclear genes of the mitochondrial synthesis of subunits 6 and 8 of the ATP synthase of Saccharomyces cerevisiae. J Biol Chem. 1992 Feb 5;267(4):2467–2473. [PubMed] [Google Scholar]
  43. Podar M., Chu V. T., Pyle A. M., Perlman P. S. Group II intron splicing in vivo by first-step hydrolysis. Nature. 1998 Feb 26;391(6670):915–918. doi: 10.1038/36142. [DOI] [PubMed] [Google Scholar]
  44. Queener S. F. New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii. J Med Chem. 1995 Nov 24;38(24):4739–4759. doi: 10.1021/jm00024a001. [DOI] [PubMed] [Google Scholar]
  45. Semrad K., Schroeder R. A ribosomal function is necessary for efficient splicing of the T4 phage thymidylate synthase intron in vivo. Genes Dev. 1998 May 1;12(9):1327–1337. doi: 10.1101/gad.12.9.1327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Sloand E., Laughon B., Armstrong M., Bartlett M. S., Blumenfeld W., Cushion M., Kalica A., Kovacs J. A., Martin W., Pitt E. The challenge of Pneumocystis carinii culture. J Eukaryot Microbiol. 1993 Mar-Apr;40(2):188–195. doi: 10.1111/j.1550-7408.1993.tb04902.x. [DOI] [PubMed] [Google Scholar]
  47. Sogin M. L., Edman J. C. A self-splicing intron in the small subunit rRNA gene of Pneumocystis carinii. Nucleic Acids Res. 1989 Jul 11;17(13):5349–5359. doi: 10.1093/nar/17.13.5349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Sor F., Fukuhara H. Complete DNA sequence coding for the large ribosomal RNA of yeast mitochondria. Nucleic Acids Res. 1983 Jan 25;11(2):339–348. doi: 10.1093/nar/11.2.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Stepien P. P., Margossian S. P., Landsman D., Butow R. A. The yeast nuclear gene suv3 affecting mitochondrial post-transcriptional processes encodes a putative ATP-dependent RNA helicase. Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):6813–6817. doi: 10.1073/pnas.89.15.6813. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Séraphin B., Boulet A., Simon M., Faye G. Construction of a yeast strain devoid of mitochondrial introns and its use to screen nuclear genes involved in mitochondrial splicing. Proc Natl Acad Sci U S A. 1987 Oct;84(19):6810–6814. doi: 10.1073/pnas.84.19.6810. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Tabak H. F., Van der Horst G., Kamps A. M., Arnberg A. C. Interlocked RNA circle formation by a self-splicing yeast mitochondrial group I intron. Cell. 1987 Jan 16;48(1):101–110. doi: 10.1016/0092-8674(87)90360-6. [DOI] [PubMed] [Google Scholar]
  52. Thalenfeld B. E., Tzagoloff A. Assembly of the mitochondrial membrane system. Sequence of the oxi 2 gene of yeast mitochondrial DNA. J Biol Chem. 1980 Jul 10;255(13):6173–6180. [PubMed] [Google Scholar]
  53. Thomas P. S. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5201–5205. doi: 10.1073/pnas.77.9.5201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Vilardell J., Warner J. R. Ribosomal protein L32 of Saccharomyces cerevisiae influences both the splicing of its own transcript and the processing of rRNA. Mol Cell Biol. 1997 Apr;17(4):1959–1965. doi: 10.1128/mcb.17.4.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Waldsich C., Semrad K., Schroeder R. Neomycin B inhibits splicing of the td intron indirectly by interfering with translation and enhances missplicing in vivo. RNA. 1998 Dec;4(12):1653–1663. doi: 10.1017/s1355838298981444. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Wank H., Rogers J., Davies J., Schroeder R. Peptide antibiotics of the tuberactinomycin family as inhibitors of group I intron RNA splicing. J Mol Biol. 1994 Mar 4;236(4):1001–1010. doi: 10.1016/0022-2836(94)90007-8. [DOI] [PubMed] [Google Scholar]
  57. Wenzlau J. M., Saldanha R. J., Butow R. A., Perlman P. S. A latent intron-encoded maturase is also an endonuclease needed for intron mobility. Cell. 1989 Feb 10;56(3):421–430. doi: 10.1016/0092-8674(89)90245-6. [DOI] [PubMed] [Google Scholar]
  58. Winter A. J., van der Horst G., Tabak H. F. Characterization of products derived from self-splicing of intron aI5 alpha which is located in the mitochondrial COX I gene of Saccharomyces cerevisiae. Nucleic Acids Res. 1988 May 11;16(9):3845–3861. doi: 10.1093/nar/16.9.3845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Zaug A. J., Cech T. R. The intervening sequence excised from the ribosomal RNA precursor of Tetrahymena contains a 5-terminal guanosine residue not encoded by the DNA. Nucleic Acids Res. 1982 May 11;10(9):2823–2838. doi: 10.1093/nar/10.9.2823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Zhu H., Conrad-Webb H., Liao X. S., Perlman P. S., Butow R. A. Functional expression of a yeast mitochondrial intron-encoded protein requires RNA processing at a conserved dodecamer sequence at the 3' end of the gene. Mol Cell Biol. 1989 Apr;9(4):1507–1512. doi: 10.1128/mcb.9.4.1507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Zimmerly S., Guo H., Perlman P. S., Lambowitz A. M. Group II intron mobility occurs by target DNA-primed reverse transcription. Cell. 1995 Aug 25;82(4):545–554. doi: 10.1016/0092-8674(95)90027-6. [DOI] [PubMed] [Google Scholar]
  62. van der Horst G., Tabak H. F. Self-splicing of yeast mitochondrial ribosomal and messenger RNA precursors. Cell. 1985 Apr;40(4):759–766. doi: 10.1016/0092-8674(85)90335-6. [DOI] [PubMed] [Google Scholar]
  63. von Ahsen U., Davies J., Schroeder R. Antibiotic inhibition of group I ribozyme function. Nature. 1991 Sep 26;353(6342):368–370. doi: 10.1038/353368a0. [DOI] [PubMed] [Google Scholar]
  64. von Ahsen U., Davies J., Schroeder R. Non-competitive inhibition of group I intron RNA self-splicing by aminoglycoside antibiotics. J Mol Biol. 1992 Aug 20;226(4):935–941. doi: 10.1016/0022-2836(92)91043-o. [DOI] [PubMed] [Google Scholar]
  65. von Ahsen U., Schroeder R. Streptomycin inhibits splicing of group I introns by competition with the guanosine substrate. Nucleic Acids Res. 1991 May 11;19(9):2261–2265. doi: 10.1093/nar/19.9.2261. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from RNA are provided here courtesy of The RNA Society

RESOURCES