Skip to main content
Log in

Cloning of mtDNA fragments homologous to mitochondrial S2 plasmid-like DNA in maize

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

Mitochondria from S-type cytoplasmic male-sterile maize contain two small DNA species, S1 and S2, which are absent from other fertile and male-sterile cytoplasms. These species have been cloned in plasmid pBR322 by the homopolymer extension method. Probes made with these recombinant plasmids have been used to establish the homology between high molecular weight mitochondrial DNAs of fertile and male-sterile cytoplasms, and small mitochondrial plasmid-like molecules. Hybridization and mapping data show that S2 DNA copies are homologuous with sequences of the normal mitochondrial genome. A comparison of physical maps of different isolated mtDNA fragments indicates a heterogeneous arrangement of S2 sequences in the mtDNA population of normal fertile maize cytoplasm. The origin of this heterogeneity is discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • An G, Friesen JD (1979) Plasmid vehicles for direct cloning of Escherichia coli promoters. J Bacteriol 140:400–407

    Google Scholar 

  • Beckett JB (1971) Classification of male-sterile cytoplasms in maize (Zea maize L.). Crop Sci 11:724–727

    Google Scholar 

  • Blin N, Gabain AV, Bujard H (1975) Isolation of large molecular weight DNA from agarose gels for further digestion by restriction enzymes. FEBS Lett 53:84–86

    Google Scholar 

  • Borst P, Grivell LA (1978) The mitochondrial genome of yeast. Cell 15:705–723

    Google Scholar 

  • Chand ACY, Numberg LH, Kaufman RJ, Erlich HA, Schimke RT, Cohen S (1978) Phenotypic expression in E. coli of a DNA sequence coding for mouse dihydrofolate reductase. Nature 275:617–621

    Google Scholar 

  • Chang LMS, Bollum FJ (1971) Deoxynucleotide polymerizing enzyme of calf thymus gland V. Homogenous terminal deoxynucleotidyl transferase. J Biol Chem 246:909–916

    Google Scholar 

  • Clewell DBM, Helinski Dr (1969) Supercoiled circular DNA-protein complex in Escherichia coli: Purification and induced conversion to an open circular DNA form. Proc Natl Acad Sci USA 62:1159–1166

    Google Scholar 

  • Denhardt DT (1966) A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun 23:641–646

    Google Scholar 

  • Dujardin G, Pajot P, Groudinsky O, Slolimski PP (1980) Long range control circuits within mitochondria and between nucleus and mitochondria I Methodology and phenomenology of supressors. Mol Gen Genet 179:469–482

    Google Scholar 

  • Duvick DN (1965) Cytoplasmic pollen sterility in corn. Adv Genet 13:1–56

    Google Scholar 

  • Grunstein M, Hogness D (1975) Colony hybridization: A method for the isolation of cloned DNAs that contain a specific gene. Proc Natl Acad Sci USA 72:3961–3965

    Google Scholar 

  • Helling RB, Goodman HM, Boyer HW (1974) Analysis of endonuclease R.EcoRI fragments of DNA from lambdoid bacteriophages and other viruses by agarose-gel electrophoresis. J Virol 14:1235–1244

    Google Scholar 

  • Jovin TH, Englund PT, Bertsch LL (1969) Enzymatic synthesis of deoxyribonucleic acid XXVI Physical and chemical studies of a homogenous deoxyribonucleic acid polymerase. J Biol Chem 244:2996–3008

    Google Scholar 

  • Kemble RJ, Bedbrook JR (1980) Low molecular weight circular and linear DNA in mitochondria from normal and male-sterile Zea mays cytoplasm. Nature 284:565–566

    Google Scholar 

  • Kolodner R, Tewari KK (1972) Physicochemical characterization of mitochondrial DNA from pea leaves. Proc Natl Acad Sci USA 69:1830–1834

    Google Scholar 

  • Koncz Cs, Sain B (1980) Homology between rRNA of Escherichia coli and mitochondrial DNA of maize. FEBS Lett 109:141–144

    Google Scholar 

  • Koncz Cs, Sümegi J, Sain B, Kalman L, Dudits D (1980) Mitochondrial DNA of maize In: Zadrazil S, Sponar J (eds) DNA-recombination, interactions and repair, Pergamon Press Oxford and New York p 85

    Google Scholar 

  • Kushner SR (1979) An improved method for transformation of Escherichia coli with ColEl derived plasmids In: Boyer H, Nicosia S (eds) Genetic engineering. Elsevier North Holland Biomedical Press. Amsterdam-New York-Oxford p 17

    Google Scholar 

  • Laughnan JR, Gabay SJ (1973) Mutations leading to nuclear restoration of fertility in S male-sterile cytoplasm in maize. Theor Appl Genet 43:109–116

    Google Scholar 

  • Laughnan JR, Gabay SJ (1975) An episomal basis for instability of S male-sterility in maize and some implication for plant breeding In: Birky CW, Perlman JrPS, Byers TJ (eds). Genetics and the biogenesis of cell organelles, Ohio State Univ. Press, Columbus p 300

    Google Scholar 

  • Laughnan JR, Gabay SJ (1978) Nuclear and cytoplasmic mutations to fertility in S male-sterile maize In: Walden DB (ed) Maize breeding and genetics. John Wiley & Sons, New York-Chichester-Brisbane-Toronto p 427

    Google Scholar 

  • Lederberg EM, Cohen SN (1974) Transformation of Salmonella typhimurium by plasmid deoxyribonucleic acid. J Bacteriol 119:1072–1074

    Google Scholar 

  • Levings CSIII, Pring DR (1977) Diversity of mitochondrial genomes among normal cytoplasms of maize. J Hered 68:350–354

    Google Scholar 

  • Levings CSIII, Pring DR (1979) Mitochondrial DNA of higher plants and genetic engineering In: Setlow JK, Hollaender A (eds) Genetic engineering, vol 1. Plenum Press, New York p 205

    Google Scholar 

  • Levings CSIII, Hu WWL, Timothy DH, Pring DR (1979a) Terminal inverted repeats in the unique DNAs associated with the S cytoplasm. Maize News Lett 52:96–98

    Google Scholar 

  • Levings CSIII, Shah DM, Hu WWL, Pring DR, Timothy DH (1979b) Molecular heterogeneity among mitochondrial DNAs from different maize cytoplasms. In: Extrachromosomal DNA. Academic Press, New York (in press)

    Google Scholar 

  • Levings CSIII, Kim BD, Pring DR, Conde MF, Mans RJ, Laughnan JR, Gabay-Laughnan SJ (1980) Cytoplasmic reversion of cmsS in maize: Association with a transpositional event. Science 209:1021–1023

    Google Scholar 

  • Lewin AS, Morimoto R, Rabinowitz M (1979) Stable heterogenity of mitochondrial DNA in grande and petite strains of S. cerevisiae. Plasmid 2:474–484

    Google Scholar 

  • Murray NE, Bruce SA, Murray K (1979) Molecular cloning of the DNA ligase gene from bacteriophage T4 II. Amplification and preparation of the gene product. J Mol Biol 132:493–505

    Google Scholar 

  • Ojala D, Attardi G (1977) A detailed physical map of HeLa cell mitochondrial DNA and its alignment with the position of known genetic markers. Plasmid 1:78–105

    Google Scholar 

  • Pring DR, Levings CSIII, Hu WWL, Timothy DH (1977) Unique DNA associated with mitochondria in the “S”-type cytoplasm of male-sterile maize. Proc Natl Acad Sci USA 74:2904–2908

    Google Scholar 

  • Pring DR, Levings CSIII (1978) Heterogenity of maize cytoplasmic genomes among male-sterile cytoplasms. Genetics 89:121–136

    Google Scholar 

  • Pring DR, Levings CSIII, Conde MF (1980) The organelle genomes of cytoplasmic male-sterile maize and sorghum In: Davies DR, Hopwood DA (eds) The plant gehome. John Innes Charity, Norwich p 111

    Google Scholar 

  • Pring DR, Conde MF, Levings CSIII (1980) DNA heterogenity within the C group of maize male-sterile cytoplasms. Crop Sci 20:159–162

    Google Scholar 

  • Quetier F, Vedel F (1977) Heterogeneous population of mitochondrial DNA molecules in higher plants. Nature 268:365–368

    Google Scholar 

  • Reeve AE, Huang RCC (1979) A method for the enzymatic synthesis and purification of [α-32P] nucleoside triphosphates. Nucl Acids Res 6:81–90

    Google Scholar 

  • Rigby PWJ, Dieckmann M, Rhodes C, Berg P (1977) Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol 113:237–251

    Google Scholar 

  • Roberts RJ (1980) Restriction and modification enzymes and their recognition sequences. Nucl Acid Res 8:r63-r80

    Google Scholar 

  • Roychoudhury R, Jay E, Wu R (1976) Terminal labeling and addition of homopolymer tracts to duplex DNA fragments by terminal deoxynucleotidyl transferase. Nucl Acids Res 3:101–116

    Google Scholar 

  • Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–518

    Google Scholar 

  • Studier FW (1973) Analysis of bacteriophage T7 early RNAs and proteins on slab gels. J Mol Biol 79:237–248

    Google Scholar 

  • Tabak HF, Falvell RA (1978) A method for the recovery of DNA from agarose gels. Nucl Acids Res 5:2321–2332

    Google Scholar 

  • Thompson RD, Kemble RJ, Flavell R (1980) Variations in mitochondrial DNA organisation between normal and male-sterile cytoplasms of maize. Nucl Acids Res 8:1999–2008

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by J. Schell

Rights and permissions

Reprints and permissions

About this article

Cite this article

Koncz, C., Sümegi, J., Udvardy, A. et al. Cloning of mtDNA fragments homologous to mitochondrial S2 plasmid-like DNA in maize. Molec. Gen. Genet. 183, 449–458 (1981). https://doi.org/10.1007/BF00268764

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00268764

Keywords

Navigation