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Species relationships in the Hordeum murinum aggregate viewed from chloroplast DNA restriction fragment patterns

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Summary

Three annual widespread species of Hordeum were investigated by the fragment pattern method on their chloroplast (cp) DNA. The species were H. glaucum, H. leporinum and H. murinum; H. vulgare was surveyed for comparison. Twelve restriction enzymes were used, nine recognizing 6 bp, one 5 bp and two 4 bp, thus, randomly surveyed, a total of 2,113 bp or 1.6% of the cp genome. Differences in patterns were found in three enzymes, HindIII, CfoI and MspI. CfoI characterizes H. glaucum from the other two species. HindIII and MspI revealed polymorphisms within species. These results confirm previous numerical taxonomic relationships among these three closely related species. Furthermore, cpDNA polymorphism in Hordeum is discussed in view of earlier reports on cpDNA polymorphism in H. vulgare. The taxonomic implications of cpDNA polymorphism are discussed after reviewing several articles using the fragment pattern method on cpDNA. The importance of using material from several populations representative of a species is stressed.

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References

  • Baatout H, Marakchi M, Vedel F (1985) Variation of plastid and mitochondrial DNAs in the genus Hedysarum. Theor Appl Genet 70:577–584

    Google Scholar 

  • Banks JA, Birky Jr CW (1985) Chloroplast DNA diversity is low in a wild plant, Lupinus texensis. Proc Natl Acad Sci USA 82:6950–6954

    Google Scholar 

  • Baum BR, Bailey LG (1984 a) Taxonomic studies in wall barley (Hordeum murinum) and sea barley (Hordeum marinum). 1. Character investigation: assessment of new and traditional characters. Can J Bot 62:753–762

    Google Scholar 

  • Baum BR, Bailey LG (1984 b) Taxonomic studies in wall barley (Hordeum murinum sensu lato) and sea barley (Hordeum marinum senu lato). 2. Multivariate morphometrics. Can J Bot 62:2754–2764

    Google Scholar 

  • Baum BR, Bothmer R von, Jacobsen N, Fedak G, Craig I, Bailey LG (1984) Barley gene pool; a collection maintained by Agriculture Canada and by the Danish and Swedish agricultural universities (Nordic Gene Bank); Canadian-Scandinavian Hordeum Collection (CHC). Publication 1761/B, Communications Branch, Agriculture Canada, Ottawa

    Google Scholar 

  • Berthou F, Mathieu C, Vedel F (1983) Chloroplast and mitochondrial DNA variation as indicator of phylogenetic relationships in the genus Coffea L. Theor Appl Genet 65:77–84

    Google Scholar 

  • Buckner B, Hyde BB (1985) Chloroplast DNA variation between the common cultivated potato (Solanum tuberosum ssp. tuberosum) and several South American relatives. Theor Appl Genet 71:527–531

    Google Scholar 

  • Clegg MT, Brown AHD, Whitfeld PR (1984 a) Chloroplast DNA diversity in wild and cultivated barley: implications for genetic conservation. Genet Res 43:339–343

    Google Scholar 

  • Clegg MT, Rawson JRY, Thomas K (1984 b) Chloroplast DNA variation in Pearl millet and related species. Genetics 106:449–461

    Google Scholar 

  • Coates D, Cullis CA (1987) Chloroplast DNA variability among Linum species. Am J Bot 74:260–268

    Google Scholar 

  • Cockerill PN (1988) Two methods that facilitate autoradiography of small 32P-labeled DNA fragments following electrophoresis in agarose gels. Anal Biochem 168:451–454

    Google Scholar 

  • Enomoto S-I, Ogihara Y, Tsunewaki K (1985) Studies on the origin of crop species by restriction endonuclease analysis of organellar DNA. I. Phylogenetic relationships among ten cereals revealed by the restriction fragment patterns of chloroplast DNA. Jpn J Genet 60:411–424

    Google Scholar 

  • Fitch WM (1984) Cladistic and other methods: problems, pitfalls, and potentials. In: Duncan T, Stuessy TF (eds) Claditics: perspectives on the reconstruction of evolutionary history. Columbia University Press, New York, pp 221–252

    Google Scholar 

  • Holwerda BC, Jana S, Crosby WL (1986) Chloroplast DNA and mitochondrial DNA variation in Hordeum vulgare and Hordeum spontaneum. Genetics 114:1271–1291

    Google Scholar 

  • Hosaka K (1986) Who is the mother of the potato? — Restriction endonuclease analysis of chloroplast DNA of cultivated potatoes. Theor Appl Genet 72:606–618

    Google Scholar 

  • Jansen RK, Palmer JD (1988) Phylogenetic implications of chloroplast DNA restriction site variation in the Mutisieae (Asteraceae). Am J Bot 75:753–766

    Google Scholar 

  • Kataoka J, Ogihara Y, Tsunewaki K (1987) Chloroplast DNA variation observed among Hordeum species. Barley Genet 5:515–524

    Google Scholar 

  • Kung SD, Zhu YS, Shen GF (1982) Nicotiana chloroplast genome. 3. Chloroplast DNA evolution. Theor Appl Genet 61:73–79

    Google Scholar 

  • Lehväslaiho H, Saura A, Lokki J (1987) Chloroplast DNA variation in the grass tribe Festuceae. Theor Appl Genet 74:298–302

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor/NY

    Google Scholar 

  • Milo J, Levy A, Ladizinsky G, Palevitch D (1988) Phylogenetic and genetic studies in Papaver section Oxytona: cytogenetics, isozyme analysis and chloroplast DNA variation. Theor Appl Genet 75:795–802

    Google Scholar 

  • Ogihara Y, Tsunewaki K (1982) Molecular basis of the genetic diversity of the cytoplasm in Triticum and Aegilops. I. Diversity of the chloroplast genome and its lineage revealed by the restriction patterns of ctDNAs. Jpn J Genet 57:371–396

    Google Scholar 

  • Palmer JD (1987) Chloroplast DNA evolution and biosystematic uses of chloroplast DNA variation. Am Nat 130:S6-S29

    Google Scholar 

  • Palmer JD, Zamir D (1982) Chloroplast DNA evolution and phylogenetic relationships in Lycopersicon. Proc Natl Acad Sci USA 79:5006–5010

    Google Scholar 

  • Palmer JD, Shields CR, Cohen DB, Orton TJ (1983) Chloroplast DNA evolution and the origin of amphidiploid Brassica species. Theor Appl Genet 65:181–189

    Google Scholar 

  • Poulsen C (1983) The barley chloroplast genome: pyhsical structure and transcriptional activity in vivo. Carlsberg Res Commun 48:57–80

    Google Scholar 

  • Rogers SO, Bendich AJ (1988) Extraction of DNA from plant tissues. In: Gelvin SB, Schilperoort RA (eds) Plant molecular biology manual. Kluwer, Dordrecht, pp A6:1–10

    Google Scholar 

  • Snow R (1963) Alcoholic hydrochloric acid carmine as a stain for chromosomes in squash preparations. Stain Technol 38:9–13

    Google Scholar 

  • Swofford DL, Berlocher SH (1987) Inferring evolutionary trees from gene frequency data under the principle of maximum parsimony. Syst Zool 36:293–325

    Google Scholar 

  • Sytsma KJ, Gottlieb LD (1986 a) Chloroplast DNA evidence for the origin of the genus Heterogaura from a species of Clarkia (Onagraceae). Proc Natl Acad Sci USA 83:5554–5557

    Google Scholar 

  • Sytsma KJ, Gottlieb LD (1986 b) Chloroplast DNA evolution and phylogenetic relationships in Clarkia Sect. Perpetasma (Onagraceae). Evolution 40:1248–1261

    Google Scholar 

  • Sytsma KJ, Schaal BA (1985) Phylogenetics of the Lisianthius skinneri (Gentianaceae) species complex in Panama utilizing DNA restriction fragment analysis. Evolution 39:594–608

    Google Scholar 

  • Timothy DH, Levings III CS, Pring DR, Conde MF, Kermicle JL (1979) Organelle DNA variation and systematic relationships in the genus Zea: Teosinte. Proc Natl Acad Sci USA 76:4220–4224

    Google Scholar 

  • Vedel F, Lebacq P (1980) Cytoplasmic DNA variation and relationships in cereal genomes. Theor Appl Genet 58:219–224

    Google Scholar 

  • Vedel F, Quetier F, Dosba F, Dousinnault G (1978) Study of wheat phylogeny by EcoRI analysis of chloroplast and mitochondrial DNAs. Plant Sci Lett 13:97–102

    Google Scholar 

  • Yanagino T, Takahata Y, Hinata K (1987) Chloroplast DNA variation among diploid species in Brassica and allied genera. Jpn J Genet 62:119–125

    Google Scholar 

  • Zurawski G, Clegg MT (1987) Evolution of higher-plant chloroplast DNA-encoded genes: implications for structure-function and phylogentic studies. Annu Rev Plant Physiol 38:391–418

    Google Scholar 

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Communicated by K. Tsunewaki

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Baum, B.R., Bailey, L.G. Species relationships in the Hordeum murinum aggregate viewed from chloroplast DNA restriction fragment patterns. Theoret. Appl. Genetics 78, 311–317 (1989). https://doi.org/10.1007/BF00265289

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  • DOI: https://doi.org/10.1007/BF00265289

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