Skip to main content

Molecular Phylogenetic and Evolutionary Studies of Parasitic Plants

  • Chapter
Molecular Systematics of Plants II

Abstract

The parasitic nutritional mode is a frequently evolved adaptation in animals (Price, 1980), as well as in flowering plants (Kuijt, 1969). Heterotrophic angiosperms can be classified as either mycotrophs or as haustorial parasites. The former derive nutrients via a symbiotic relationship with mycorrhizal fungi. Haustorial parasites, in contrast, directly penetrate host tissues via a modified root called a haustorium and thereby obtain water and nutrients. Although such categories are often a matter of semantics, we use the term parasite in a strict sense to refer to haustorial parasites. Angiosperm parasites are restricted to the dicot subclasses Magnoliidae, Rosidae, and Asteridae; have evolved approximately 11 times; and represent approximately 22 families, 265 genera, and 4,000 species, that is, about 1% of all angiosperms (Fig. 8.1). Owing to their unique adaptations, parasitic plants have long been the focus of anatomical, morphological, biochemical, systematic, and ecological research (Kuijt, 1969; Press and Graves, 1995). For the vast majority of parasitic plants, negative effects upon the host are difficult to detect, yet others (e.g., Striga, Orobanche) are serious weeds of economically important crops (Kuijt, 1969; Musselman, 1980; Eplee, 1981; Stewart and Press, 1990; Press and Graves, 1995).

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 229.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 299.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 299.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature Cited

  • Adam, Z. 1995. A mutation in the small subunit of ribulose 1,5-biphosphate carboxylase/oxygenase that reduces the rate of its incorporation into holoenzyme. Photosynthesis Research 43:143–147.

    Article  CAS  Google Scholar 

  • An-Ming, L. 1990. A preliminary cladistic study of the families of the superorder Lamiiflorae. Botanical Journal of the Linnean Society 103:39–57.

    Article  Google Scholar 

  • Arts, G. J., and R. Benne. 1996. Mechanism and evolution of RNA editing in kinetoplastida. Biochimica Biophysica Acta 1307:39–54.

    Article  Google Scholar 

  • Barlow, B. A. 1964. Classification of the Loranthaceae and Viscaceae. Proceedings of the Linnaean Society of New South Wales 89:268–272.

    Google Scholar 

  • Barlow, B. A. 1983. Biogeography of Loranthaceae and Viscaceae. In The Biology of Mistletoes, eds. M. Calder and P. Bernhardt, pp. 19–45. Academic Press, New York.

    Google Scholar 

  • Barlow, B. A., and D. Wiens. 1971. The cytogeography of the loranthaceous mistletoes. Taxon 20:291–312.

    Article  Google Scholar 

  • Bhandari, N. N., and S. C. A. Vohra. 1983. Embryology and affinities of Viscaceae. In The Biology of Mistletoes, eds., M. Calder and P. Bernhardt, pp. 69–86. Academic Press, New York.

    Google Scholar 

  • Boeshore, I. 1920. The morphological continuity of Scrophulariaceae and Orobanchaceae. Contributions of the Botanical Laboratory of the Morris Arboretum 5:139–177.

    Google Scholar 

  • Bömmer, D., G. Haberhausen, and K. Zetsche. 1993. A large deletion in the plastid DNA of the holoparasitic flowering plant Cuscuta reflexa concerning two ribosomal proteins (rpl2, rpl23), one transfer RNA (trnl) and an ORF 2280 homologue. Current Genetics 24:171–176.

    Article  PubMed  Google Scholar 

  • Bousquet, J., S. H. Strauss, A. H. Doerksen, and R. A. Price. 1992. Extensive variation in evolutionary rate of rbcL gene sequences among seed plants. Proceedings of the National Academy of Sciences U.S.A. 89:7844–7848.

    Article  CAS  Google Scholar 

  • Bowe, L. M., and C. W. dePamphilis. 1996. Effects of RNA editing and gene processing on phylogenetic reconstruction. Molecular Biology and Evolution 13:1159–1166.

    Article  PubMed  CAS  Google Scholar 

  • Bricaud, C. H., P. Thalouarn, and S. Renaudin. 1986. Ribulose 1,5-bisphosphate carboxylase activity in the holoparasite Lathraea clandestina L. Journal of Plant Physiology 125:367–370.

    Article  CAS  Google Scholar 

  • Burtt, B. L. 1965. The transfer of Cyrtandromoea from Gesneriaceae to Scrophulariaceae, with notes on the classification of that family. Bulletin of the Botanical Survey 7:73–88.

    Google Scholar 

  • Chase, M. W., D. E. Soltis, R. G. Olmstead, D. Morgan, D. H. Les, B. D. Mishler, M. R. Duvall, R. A. Price, H. G. Hills, Y.-L. Qiu, K. A. Kron, J. H. Rettig, E. Conti, J. D. Palmer, J. R. Manhart, K. J. Sytsma, H. J. Michaels, W. J. Kress, K. G. Karol, W. D. Clark, M. Hedrén, B. S. Gaut, R. K. Jansen, K.-J. Kim, C. F. Wimpee, J. F. Smith, G. R. Furnier, S. H. Strauss, Q.-Y. Xiang, G. M. Plunkett, P. S. Soltis, S. M. Swensen, S. E. Williams, P. A. Gadek, C. J. Quinn, L. E. Eguiarte, E. Golenberg, G. H. Learn, Jr., S. W. Graham, S. C. H. Barrett, S. Dayanandan, and V. A. Albert. 1993. Phylogenetics of seed plants: an analysis of nucleotide sequences from the plastid gene rbcL. Annals of the Missouri Botanical Garden 80:528–580.

    Article  Google Scholar 

  • Cocucci, A. E. 1983. New evidence from embryology in angiosperm classification. Nordic Journal of Botany 3:67–73.

    Article  Google Scholar 

  • Colwell, A. E. 1994. Genome evolution in a non-photosynthetic plant, Conopholis Americana. Ph.D. dissertation, Washington University, St. Louis, Missouri.

    Google Scholar 

  • Cronquist, A. 1981. An Integrated System of Classification of Flowering Plants. Columbia University Press, New York.

    Google Scholar 

  • Cronquist, A. 1988. The Evolution and Classification of Flowering Plants. New York Botanical Garden, New York.

    Google Scholar 

  • Dayhoff, M. O., R. M. Schwartz, and B. C. Orcutt. 1978. A model of evolutionary change in proteins. In Atlas of Protein Sequence and Structure, ed. M. O. Dayhoff, pp. 345–352. National Biomedical Research Foundation, Silver Springs, Maryland.

    Google Scholar 

  • Delavault, P., V. Sakanyan, and P. Thalouarn. 1995. Divergent evolution of two plastid genes, rbcL and atpB, in a non-photosynthetic parasitic plant. Plant Molecular Biology 29:1071–1079.

    Article  PubMed  CAS  Google Scholar 

  • Delavault, P. ML, N. M. Russo, N. A. Lusson, and P. A. Thalouarn. 1996. Organization of the reduced plastid genome of Lathraea clandestina, an achlorophyllous parasitic plant. Physiologia Plantarum 96:674–682.

    Article  CAS  Google Scholar 

  • de Pamphilis, C. W. 1995. Genes and genomes. In Parasitic Plants, eds. M. C. Press and J. D. Graves, pp. 176–205. Chapman & Hall, London.

    Google Scholar 

  • de Pamphilis, C. W., and J. D. Palmer. 1989. Evolution and function of plastid DNA: a review with special reference to nonphotosynthetic plants. In Physiology, Biochemistry, and Genetics of Nongreen Plastids, eds. C. D. Boyer, J. C. Shannon, and R. C. Hardison, pp. 182–202. American Society of Plant Physiologists, Rockville, Maryland.

    Google Scholar 

  • de Pamphilis, C. W., and J. D. Palmer. 1990. Loss of photosynthetic and chlororespiratory genes from the plastid genome of a parasitic flowering plant. Nature (London) 348:337–339.

    Article  Google Scholar 

  • de Pamphilis, C. W., N. D. Young, and A. D. Wolfe. 1997. Evolution of plastid gene rps2 in a lineage of hemiparasitic and holoparasitic plants: many losses of photosynthesis and complex patterns of rate variation. Proceedings of the National Academy of Sciences U.S.A. 94:7367–7372.

    Article  Google Scholar 

  • Dodge, J. D. and G. B. Lawes. 1974. Plastid ultrastructure in some parasitic and semi-parasitic plants. Cytobiology 9:1–9.

    Google Scholar 

  • Donoghue, M. J., and J. A. Doyle, 1989. Phylogenetic analysis of angiosperms and the relationships of Hamamelidae. In Evolution, Systematics, and Fossil History of the Hamamelidae, eds. P. R. Crane and S. Blackmore, pp. 17–45. Clarendon Press, Oxford.

    Google Scholar 

  • Downie, S. R., and J. D. Palmer. 1992. Use of chloroplast DNA rearrangements in reconstructing plant phylogeny. In Molecular Plant Systematics, eds. P. S. Soltis, D. E. Soltis, and J. J. Doyle, pp. 14–35. Chapman & Hall, New York.

    Chapter  Google Scholar 

  • Duff, R. J., and D. L. Nickrent. 1997. Characterization of mitochondrial small-subunit ribosomal RNAs from holoparasitic plants. Journal of Molecular Evolution 45:631–639.

    Article  PubMed  CAS  Google Scholar 

  • Ems, S. C., C. W. Morden, C. K. Dixon, K. H. Wolfe, C. W. dePamphilis, and J. D. Palmer. 1995. Transcription, splicing and editing of plastid RNAs in the nonphotosynthetic plant Epifagus virginiana. Plant Molecular Biology 29:721–733.

    Article  PubMed  CAS  Google Scholar 

  • Eplee, R. E. 1981. Striga’s status as a plant parasite in the United States. Plant Disease 56:951–954.

    Article  Google Scholar 

  • Escalante, A. A., and F. J. Ayala. 1995. Evolutionary origin of Plasmodium and other Apicomplexa based on rRNA genes. Proceedings of the National Academy of Sciences U.S.A. 92:5793–5797.

    Article  CAS  Google Scholar 

  • Fagerlind, F. 1948. Beitrage zür Kenntnis der Gynaceummorphologie und Phylogenie der Santalales-Familien. Svensk Botanisk Tidskrift 42:195–229.

    Google Scholar 

  • Felsenstein, J. 1978. Cases in which parsimony or compatibility will be positively misleading. Systematic Zoology 27:401–410.

    Article  Google Scholar 

  • Freyer, R., K. Neckermann, R. M. Maier, and H. Kössel. 1995. Structural and functional analysis of plastid genomes from parasitic plants: loss of an intron within the genus Cuscuta. Current Genetics 27:580–586.

    Article  PubMed  CAS  Google Scholar 

  • Gaut, B., S. Muse, W. Clark, and M. Clegg. 1992. Relative rates of nucleotide substitution at the rbcL locus of monocotyledonous plants. Journal of Molecular Evolution 35:292–303.

    Article  PubMed  CAS  Google Scholar 

  • Gaut, B. S., B. R. Morton, B. C. McCaig, and M. T. Clegg. 1996. Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL. Proceedings of the National Academy of Sciences U.S.A. 93:10274–10279.

    Article  CAS  Google Scholar 

  • Gockel, G., W. Hachtel, S. Baier, C. Fliss, and M. Henke. 1994. Genes for components of the chloroplast translational apparatus are conserved in the reduced 73-kb plastid DNA of the nonphotosynthetic euglenoid flagellate Astasia longa. Current Genetics 26:256–262.

    Article  PubMed  CAS  Google Scholar 

  • Gutell, R. R. 1993. Collection of small subunit (16S and 16S-like) ribosomal RNA structures. Nucleic Acids Research 21:3051–3054.

    Article  PubMed  CAS  Google Scholar 

  • Haberhausen, G., and K. Zetsche. 1992. Nucleotide sequences of the rbcL gene and the intergenic promoter region between the divergently transcribed rbcL and atpB genes in Ipomoea purpurea (L.). Plant Molecular Biology 18:823–825.

    Article  PubMed  CAS  Google Scholar 

  • Haberhausen, G., and K. Zetsche. 1994. Functional loss of all ndh genes in an otherwise relatively unaltered plastid genome of the holoparasitic flowering plant Cuscuta reflexa. Plant Molecular Biology 24:217–222.

    Article  PubMed  CAS  Google Scholar 

  • Haberhausen, G. K., Valentin, and K. Zetsche. 1992. Organization and sequence of photosynthetic genes from the plastid genome of the holoparasitic flowering plant Cuscuta reflexa. Molecular and General Genetics 232:154–161.

    Article  PubMed  CAS  Google Scholar 

  • Harms, H. 1935. Hydnoraceae. In Die Natürlichen Pflanzenfamilien, eds. A. Engler and H. Harms, pp. 282–295. W. Engelmann, Leipzig.

    Google Scholar 

  • Hong, D.-Y. 1984. Taxonomy and evolution of the Veroniceae (Scrophulariaceae) with special reference to palynology. Opera Botanica 75:1–60.

    Google Scholar 

  • Hull, R. J., and O. A. Leonard. 1964. Physiological aspects of parasitism in mistletoes (Arceuthobium and Phoradendrori). 2. The photosynthetic capacity of mistletoes. Plant Physiology 39:1008–1017.

    Article  PubMed  CAS  Google Scholar 

  • Kellogg, E. A., and N. D. Juliano. 1997. The structure and function of RuBisCo and their implications for systematic studies. American Journal of Botany 84:413–428.

    Article  PubMed  CAS  Google Scholar 

  • Kuijt, J. 1968. Mutual affinities of Santalalean families. Brittonia 20:136–147.

    Article  Google Scholar 

  • Kuijt, J. 1969. The Biology of Parasitic Flowering Plants. University of California Press, Berkeley.

    Google Scholar 

  • Kumar, S., K. Tamura, and M. Nei. 1993. MEGA: Molecular Evolutionary Genetics Analysis, version 1.01. The Pennsylvania State University, University Park.

    Google Scholar 

  • Li, W.-H. 1983. Evolution of duplicate genes and pseudogenes. In Evolution of Genes and Proteins, eds. M. Nei and R. K. Koehn, pp. 14–37. Sinauer Associates, Sunderland, Massachusetts.

    Google Scholar 

  • Machado, M. A., and K. Zetsche. 1990. A structural, functional and molecular analysis of plastids of the holoparasites Cuscuta reflexa and Cuscuta europaea. Planta 181:91–96.

    Article  CAS  Google Scholar 

  • Maddison, W. P. 1989. Reconstructing character evolution on polytomous cladograms. Cladistics 5:365–377.

    Article  Google Scholar 

  • Maddison, W. P., and D. R. Maddison. 1992. MacClade, Analysis of Phylogeny and Character Evolution, version 3.01. Sinauer Associates, Sunderland, Massachusetts.

    Google Scholar 

  • Mayfield, S. P., C. B. Yohn, A. Cohen, and A. Danon. 1995. Regulation of chloroplast gene expression. Annual Review of Plant Physiology and Plant Molecular Biology 46:147–166.

    Article  CAS  Google Scholar 

  • Minkin, J. P., and W. H. Eshbaugh. 1989. Pollen morphology of the Orobanchaceae and rhinanthoid Scrophulariaceae. Grana 28:1–18.

    Article  Google Scholar 

  • Morden, C. W., K. H. Wolfe, C. W. de Pamphilis, and J. D. Palmer. 1991. Plastid translation and transcription genes in a nonphotosynthetic plant: intact, missing and pseudo genes. European Molecular Biology Organization Journal 10:3281–3288.

    CAS  Google Scholar 

  • Muller, J. 1981. Fossil pollen records of extant angiosperms. Botanical Review 47:1–142.

    Article  Google Scholar 

  • Musselman, L. J. 1980. The biology of Striga, Orobanche, and other root-parasitic weeds. Annual Review of Phytopathology 18:463–489.

    Article  Google Scholar 

  • Nelissen, B., Y. Van de Peer, A. Wilmotte, and R. De Wachter. 1995. An early origin of plastids within the cyanobacterial divergence is suggested by evolutionary trees based on complete 16S rRNA sequences. Molecular Biology and Evolution 12:1166–1173.

    PubMed  CAS  Google Scholar 

  • Nickrent, D. L., and R. J. Duff. 1996. Molecular studies of parasitic plants using ribosomal RNA. In Advances in Parasitic Plant Research, eds. M. T. Moreno, J. I. Cubero, D. Berner, D. Joel, L. J. Musselman, and C. Parker, pp. 28–52. Junta de Andalucia, Direction General de Investigation Agraria, Cordoba, Spain.

    Google Scholar 

  • Nickrent, D. L., and C. R. Franchina. 1990. Phylogenetic relationships of the Santalales and relatives. Journal of Molecular Evolution 31:294–301.

    Article  PubMed  CAS  Google Scholar 

  • Nickrent, D. L., and D. E. Soltis. 1995. A comparison of angiosperm phylogenies based upon complete 18S rDNA and rbcL sequences. Annals of the Missouri Botanical Garden 82:208–234.

    Article  Google Scholar 

  • Nickrent, D. L., and E. M. Starr. 1994. High rates of nucleotide substitution in nuclear small-subunit (18S) rDNA from holoparasitic flowering plants. Journal of Molecular Evolution 39:62–70.

    Article  PubMed  CAS  Google Scholar 

  • Nickrent, D. L., Y. Ouyang, and C. W. dePamphilis. 1995. Presence of plastid genes in representatives of the holoparasitic families Balanophoraceae, Hydnoraceae, and Rafflesiaceae. American Journal of Botany (suppl.) 82:75.

    Google Scholar 

  • Nickrent, D. L., R. J. Duff, and D. A. M. Konings. 1997a. Structural analyses of plastid-encoded 16S rRNAs in holoparasitic angiosperms. Plant Molecular Biology 74:731–743.

    Article  Google Scholar 

  • Nickrent, D. L., Y. Ouyang, R. J. Duff, and C. W. dePamphilis. 1997b. Do nonasterid holoparasitic flowering plants have plastid genomes? Plant Molecular Biology 34:717–729.

    Article  PubMed  CAS  Google Scholar 

  • Olmstead, R. G., and P. A. Reeves. 1995. Evidence for the polyphyly of the Scrophulariaceae based on chloroplast rbcL and ndhF sequences. Annals of the Missouri Botanical Garden 82:176–193.

    Article  Google Scholar 

  • Olsen, G. J. 1987. Earliest phylogenetic branchings: comparing rRNA-based evolutionary trees inferred with various techniques. Cold Spring Harbor Symposium on Quantitative Biology 52:825–837.

    Article  CAS  Google Scholar 

  • Palmer, J. D. 1990. Contrasting modes and tempos of genome evolution in land plant organelles. Trends in Genetics 6:115–120.

    Article  PubMed  CAS  Google Scholar 

  • Palmer, J. D. 1992. Mitochondrial DNA in plant systematics: applications and limitations. In Molecular Plant Systematics, eds. P. S. Soltis, D. E. Soltis, and J. J. Doyle, pp. 36–49. Chapman & Hall, New York.

    Chapter  Google Scholar 

  • Pazy, B., U. Plitmann, and O. Cohen. 1996. Bimodal karyotype in Cynomorium coccineum L. and its systematic implications. Journal of the Linnaean Society, London 120:279–281.

    Google Scholar 

  • Pennell, F. W. 1935. The Scrophulariaceae of Eastern Temperate North America. Academy of Natural Sciences, Philadelphia.

    Google Scholar 

  • Press, M. C., and J. D. Graves. 1995. Parasitic Plants. Chapman & Hall, London.

    Google Scholar 

  • Press, M. C., N. Shah, and G. R. Stewart. 1986. The parasitic habit: trends in metabolic reductionism. In Biology and Control of Orobanche, ed. S. J. ter Borg, pp. 96–106. LH/VPO, Wageningen, Netherlands.

    Google Scholar 

  • Press, M. C., S. Smith, and G. R. Stewart. 1991. Carbon acquisition and assimilation in parasitic plants. Functional Ecology 5:278–283.

    Article  Google Scholar 

  • Price, P. 1980. Evolutionary Biology of Parasites. Monographs in Population Biology No. 15. Princeton University Press, Princeton, New Jersey.

    Google Scholar 

  • Reed, C. F. 1955. The comparative morphology of the Olacaceae, Opiliaceae, and Octoknemaceae. Memorias da Sociedade Broteriana 10:29–79.

    Google Scholar 

  • Roy, H., and S. A. Nierzwicki-Bauer. 1991. RuBisCO: genes, structure, assembly, and evolution. In The Photosynthetic Apparatus: Molecular Biology and Operation, eds. L. Bogorad and I. K. Vasil, pp. 347–364. Academic Press, San Diego.

    Chapter  Google Scholar 

  • Schreuder, H. A., S. Knight, P. M. G. Curmi, I. Andersson, D. Cascio, C.-I. Brändén, and D. Eisenberg. 1993. Formation of the active site of ribulose-l,5-bisphosphate carboxylase/oxygenase by a disorder-order transition from the unactivated to the activated form. Proceedings of the National Academy of Sciences U.S.A. 90:9968–9972.

    Article  CAS  Google Scholar 

  • Schuster, W., R. Ternes, V. Knoop, R. Hiesel, B. Wissinger, and A. Brennicke. 1991. Distribution of RNA editing sites in Oenothera mitochondrial mRNAs and rRNAs. Current Genetics 20:397–404.

    Article  PubMed  CAS  Google Scholar 

  • Shimada, H., and M. Sugiura. 1991. Fine structural features of the chloroplast genome: comparison of the sequenced chloroplast genomes. Nucleic Acids Research 19:983–995.

    Article  PubMed  CAS  Google Scholar 

  • Sleumer, H. O. 1984. Flora Neotropica. Olacaceae Monograph No 38. New York Botanical Garden, New York.

    Google Scholar 

  • Solms-Laubach, H. 1894. Hydnoraceae. In Die Natürlichen Planzenfamilien, Part III, eds. A. Engler and K. Prantl, pp. 282–285. W. Engelmann, Leipzig.

    Google Scholar 

  • Soltis, D. E., P. S. Soltis, D. L. Nickrent, L. A. Johnson, W. J. Hahn, S. B. Hoot, J. A. Sweere, R. K. Kuzoff, K. A. Kron, M. W. Chase, S. M. Swensen, E. A. Zimmer, S.M. Chaw, L. J. Gillespie, W. J. Kress, and K. J. Sytsma. 1997. Angiosperm phylogeny inferred from 18S ribosomal DNA sequences. Annals of the Missouri Botanical Garden 84:1–49.

    Article  Google Scholar 

  • Sper-Whitis, G. L., J. L. Moody, and J. C. Vaughn. 1996. Universality of mitochondrial RNA editing in cytochrome-c oxidase subunit I (coxl) among the land plants. Biochimica Biophysica Acta 1307:301–308.

    Article  Google Scholar 

  • Stewart, G. R., and M. C. Press. 1990. The physiology and biochemistry of parasitic angiosperms. Annual Review of Plant Physiology and Plant Molecular Biology 41:127–151.

    Article  CAS  Google Scholar 

  • Susek, R. E., and J. Chory. 1992. A tale of two genomes: role of a chloroplast signal in coordinating nuclear and plastid genome expression. Australian Journal of Plant Physiology 19:387–399.

    Article  CAS  Google Scholar 

  • Takhtajan, A. L. 1987. Sistema magnoliofltov [in Russian]. Nauka, Leningrad.

    Google Scholar 

  • Takhtajan, A. L., N. R. Meyer, and V. N. Kosenko. 1985. Morfologiya pyl’tsy i klassifikatsiya semeystva Rafflesiaceae s. 1. Botanicheskii Zhurnal 70:153–162.

    Google Scholar 

  • Taylor, G. W., K. H. Wolfe, C. W. Morden, C. W dePamphilis, and J. D. Palmer. 1991. Lack of a functional plastid tRNAcys gene is associated with loss of photosynthesis in a lineage of parasitic plants. Current Genetics 20:515–518.

    Article  PubMed  CAS  Google Scholar 

  • Thalouarn, P., M.-C. Arnaud, and S. Renaudin. 1989. Evidence of ribulose-bisphosphate carboxylase in the Scrophulariaceae holoparasite Lathraea clandestina L. Comptes Rendu Academy of Science Paris 309:275–280.

    CAS  Google Scholar 

  • Thalouarn, P., C. Theodet, and S. Renaudin. 1991. Evidence of plastid and nuclear genes for the large and small subunits of Rubisco in the Scrophulariaceae holoparasite Lathraea clandesiina L. Comparison with the autotroph Digitalis purpurea L. and hemiparasite Melampyrum pratense L. Comptes Rendu Academy of Science Paris 312:1–6.

    CAS  Google Scholar 

  • Thalouarn, P., C. Theodet, N. Russo, and P. Delavault. 1994. The reduced plastid genome of a nonphotosynthetic angiosperm Orobanche hederae has retained the rbcL gene. Plant Physiology and Biochemistry 32:233–242.

    CAS  Google Scholar 

  • Thieret, J. W. 1967. Supraspecific classification in the Scrophulariceae: a review. Sida 387-106.

    Google Scholar 

  • Thorne, R. F. 1992. An updated phylogenetic classification of the flowering plants. Aliso 13:365–389.

    Google Scholar 

  • Tocher, R. D., S. W. Gustafson, and D. M. Knutson. 1984. Water metabolism and seedling photosynthesis in dwarf mistletoes. In Biology of Dwarf Mistletoes: Proceedings of the Symposium, eds. F. G. Hawksworth and R. F. Scharpf, pp. 62–69. USDA, Rocky Mt. Forest & Range Experimental Station, Ft. Collins, Colorado.

    Google Scholar 

  • van der Vies, S. M., P. V. Viitanen, A. A. Gatenby, G. H. Lorimer, and R. Jaenicke. 1992. Conformational states of ribulosebisphosphate carboxylase and their interaction with chaperonin 60. Biochemistry 31:3635–3644.

    Article  PubMed  Google Scholar 

  • Walsh, M. A., E. A. Rechel and T. M. Popovich. 1980. Observations of plastid fine structure in the holoparasitic angiosperm Epifagus virginiana. American Journal of Botany 67:833–837.

    Article  Google Scholar 

  • Weber, H. C. 1980. Evolution of parasitism in Scrophulariceae and Orobanchaceae. Plant Systematics and Evolution 136:217–232.

    Article  Google Scholar 

  • Wettstein, R. 1897. Scrophulariceae. In Die Natürlichen Pflanzenfamilien Nachtrage I-IV, eds. A. Engler and K. Prantl, pp. 293–299. W Engelmann, Leipzig.

    Google Scholar 

  • Wiens, D., and B. A. Barlow. 1971. The cytogeography and relationships of the viscaceous and eremolepidaceous mistletoes. Taxon 20:313–332.

    Article  Google Scholar 

  • Wilson, R. J. M., P. W. Denny, P. R. Preiser, K. Rangachari, K. Roberts, A. Roy, A. Whyte, M. Strath, D. J. Moore, P. W. Moore, and D. H. Williamson. 1996. Complete gene map of the plastid-like DNA of the malaria parasite Plasmodium falciparum. Journal of Molecular Biology 261:155–172.

    Article  PubMed  CAS  Google Scholar 

  • Wimpee, C. F., R. L. Wrobel, and D. K. Garvin. 1991. A divergent plastid genome in Conopholis americana, an achlorophyllous parasitic plant. Plant Molecular Biology 17:161–166.

    Article  PubMed  CAS  Google Scholar 

  • Wimpee, C. F., R. Morgan, and R. L. Wrobel. 1992a. An aberrant plastid ribosomal RNA gene cluster in the root parasite Conopholis Americana. Plant Molecular Biology 18:275–285.

    Article  PubMed  CAS  Google Scholar 

  • Wimpee, C. F, R. Morgan, and R. L. Wronel. 1992b. Loss of transfer RNA genes from the plastid 16S-23S ribosomal RNA gene spacer in a parasitic plant. Current Genetics 21:417–422.

    Article  PubMed  CAS  Google Scholar 

  • Wolfe, A. D., and C. W. dePamphilis. 1995. Systematic implications of relaxed functional constraints on the RUBISCO large subunit in parasitic plants of the Scrophulariaceae and Orobanchaceae. American Journal of Botany (suppl.) 82:6.

    Google Scholar 

  • Wolfe, A. D., and C. W. dePamphilis. 1997. Alternate paths of evolution for the photosynthetic gene rbcL in four nonphotosynthetic species of Orobanche. Plant Molecular Biology 33:965–977.

    Article  PubMed  CAS  Google Scholar 

  • Wolfe, K. H., D. S. Katz-Downie, C. W. Morden, and J. D. Palmer. 1992a. Evolution of the plastid ribosomal RNA operon in a nongreen parasitic plant: accelerated sequence evolution, altered promoter structure, and tRNA pseudogenes. Plant Molecular Biology 18:1037–1048.

    Article  PubMed  CAS  Google Scholar 

  • Wolfe, K. H., C. W. Morden, S. C. Ems, and J. D. Palmer. 1992b. Rapid evolution of the plastid translational apparatus in a nonphotosynthetic plant: loss or accelerated sequence evolution of tRNA and ribosomal protein genes. Journal of Molecular Evolution 35:304–317.

    Article  PubMed  CAS  Google Scholar 

  • Wolfe, K. H., C. W. Morden, and J. D. Palmer. 1992c. Function and evolution of a minimal plastid genome from a nonphotosynthetic parasitic plant. Proceedings of the National Academy of Sciences U.S.A. 89:10648–10652.

    Article  CAS  Google Scholar 

  • Wu, C.-L, and W.-H. Li. 1985. Evidence for higher rates of nucleotide substitution in rodents than in man. Proceedings of the National Academy of Sciences U.S.A. 82:1741–1745.

    Article  CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1998 Springer Science+Business Media New York

About this chapter

Cite this chapter

Nickrent, D.L. et al. (1998). Molecular Phylogenetic and Evolutionary Studies of Parasitic Plants. In: Soltis, D.E., Soltis, P.S., Doyle, J.J. (eds) Molecular Systematics of Plants II. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5419-6_8

Download citation

  • DOI: https://doi.org/10.1007/978-1-4615-5419-6_8

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-412-11131-0

  • Online ISBN: 978-1-4615-5419-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics